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Erschienen in: BMC Cancer 1/2014

Open Access 01.12.2014 | Research article

Adherence to hormone therapy among women with breast cancer

verfasst von: Claudia Brito, Margareth Crisóstomo Portela, Mauricio Teixeira Leite de Vasconcellos

Erschienen in: BMC Cancer | Ausgabe 1/2014

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Abstract

Background

Despite the excellent results obtained with hormone therapy, the long treatment period and the side effects associated with its use make patient adherence difficult. Moreover, certain aspects of health care can mitigate or exacerbate non-adherence. This study aimed to identify the factors associated with adherence to hormone therapy for breast cancer, with the goal of contributing to the reformulation of the care process and to improvements in outcomes.

Method

This was a retrospective longitudinal study based on secondary data. The study integrated and analyzed data from a cohort of 5,861 women with breast cancer who were identified in the databases of the Brazilian National Cancer Institute [Instituto Nacional de Câncer - INCA] and the Unified Health System [Sistema Único de Saúde - SUS]. All of the patients were treated at INCA, which dispenses free medication, and the follow-up period lasted from 01/01/2004 to 10/29/2010. The outcome of interest was hormone treatment adherence, which was defined as the possession of medication, and a logistic regression model was employed to identify the socio-demographic, behavioral, clinical, and health care variables that were independently associated with the variations in this outcome.

Results

The proportion of women who adhered to hormone therapy was 76.3%. The likelihood of adherence to hormone therapy increased with each additional year of age, as well as among women with a secondary or higher level education, those with a partner, those who underwent surgery, those who had more consultations with a breast specialist and clinical oncologist, and those who underwent psychotherapy; the effect for the latter increased with each additional consultation. Conversely, the likelihood of adherence was lower among patients at a non-curable stage, those who were alcohol drinkers, those who received chemotherapy, those who had undergone more tests and had more hospitalizations, and those who used tamoxifen and combined aromatase inhibitors.

Conclusion

This study shows that approximately a quarter of the women with breast cancer did not adhere to hormone treatment, thus risking clinical responses below the expected standards. It also identifies the most vulnerable subgroups in the treatment process and the aspects of care that provide better results.
Hinweise

Electronic supplementary material

The online version of this article (doi:10.​1186/​1471-2407-14-397) contains supplementary material, which is available to authorized users.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

All authors participated in study design, dataset preparation by combining the databases, statistical analysis, and drafting and/or reviewing the manuscript. All authors read and approved the final manuscript.
Abkürzungen
AIS
Aromatase inhibitors
CT
Chemotherapy
DTS
Diagnostic and therapeutic services
HT
Hormone therapy
INCA
National cancer institute
MPR
Medication possession ratio
MTS
Multi-professional therapeutic support
OR
Odds ratio
RHC
Hospital-based cancer registry
RT
Radiotherapy
SHI
Integrated hospital system
SUS
Unified health system
TMX
Tamoxifen.

Background

Studies of endocrine therapy for breast cancer treatment have been increasingly performed throughout the world [1] due to the large patient volume [2], the long treatment duration [3], the optimal obtained results [4, 5], and the adverse drug effects [6, 7].
Adjuvant endocrine therapy or hormone therapy for breast cancer involves the use of hormone suppressants or similar substances to inhibit tumor growth [7]. This type of therapy is associated with lower rates of disease recurrence and metastasis and, thus, improves mortality rates and disease-free survival [4, 8]. Consequently, its use and related expenses have increased significantly in recent decades [2].
The duration of hormone treatment is relatively long, and patients are required to use the medication daily for 5 years [3] to obtain the maximum benefits [9]. The increase in oral medication use has highlighted a potential problem in the adherence to cancer treatment in both health and economic terms. If patients do not take their medications, they will not benefit from them, thus resulting in increased mortality and morbidity as well as increased costs and consumption of care resources. Moreover, if the doctor is unaware of the patient’s non-adherence to oral therapy, he/she might attribute the disease progression to the ineffectiveness of the drug and change the regimen unnecessarily [10] or prescribe a second- or third-line medicine with greater side effects or costs. In Brazil, breast cancer is the leading cause of cancer deaths among women (12,852 deaths in 2010), and it is estimated that in 2013, 52,680 women will be diagnosed with this type of tumor [11].
Despite the excellent results obtained with hormone therapy, the long treatment period and the side effects associated with its use make patient adherence difficult, which can lead to adverse clinical outcomes [12, 13]. Moreover, certain aspects of health care (e.g., the doctor-patient relationship and the management of side effects) can mitigate or exacerbate non-adherence [1, 8], even for patients with a good prognosis [14, 15].
This study aimed to identify the factors associated with adherence to hormone therapy for breast cancer, with the goal of contributing to the reformulation of the care process and to improved outcomes.

Methods

A hospital-based population retrospective longitudinal study was conducted with secondary data from women with breast cancer who received hormone therapy prescriptions from the National Cancer Institute (Instituto Nacional de Câncer; INCA) of Brazil.
INCA is the Ministry of Health reference center for cancer policies and care [16] and as such, INCA integrates the public health system and provides all inpatient and outpatient oncological treatment modalities free of charge. It is also the largest breast cancer care provider in the state of Rio de Janeiro, which has the highest incidence of this disease in Brazil [11].
The study included all women with breast cancer who appeared in the hospital-based cancer registry (hospital-based cancer registry; RHC) between 2002 and 2008 who started hormone treatment with tamoxifen (TMX) and/or the aromatase inhibitors (AIS) letrozole or anastrozole on or after 01/01/2004, and who received dispensed medication more than once before 10/29/2010, according to the INCA pharmacy (the only medicine dispensary for those women).
An integration and analysis of the information found in the following databases was performed as follows:
a.
The dispensing database from the INCA pharmacy aggregated data about medicine dispensation, including the date, type (TMX, letrozole and anastrozole) and quantity. It permitted the acquisition and delivery control of medicine with satisfactory accuracy. Only patients who started hormone therapy after 01/01/2004 were considered because this database was established in October 2003 and thus included patients who required continuous treatment. The last included dispensing date was 10/29/2010.
 
b.
The RHC database was implemented at INCA according to the recommendations of the International Agency for Research on Cancer (IARC) and was employed in the study to obtain sociodemographic and clinical variables.
The study inclusion criteria for women with breast cancer tumors who were enrolled between 2002 and 2008 relied on data availability at the time of the study. The RHC was organized by tumor, which meant that a single patient with more than 1 primary malignant tumor (excluding recurrence or metastasis) could be registered more than once. For patients with multiple recorded tumors, we used the more complete observation, the observation with the highest stage if the diagnosis dates were the same or the earliest observation if the diagnosis dates were different.
 
c.
The Integrated Hospital System (Sistema Hospitalar Integrado; SHI) and the INCA Absolute System databases were used to record the procedures provided to women with breast cancer. The SHI was established in 1998 and was used at INCA until 2004, at which time it was replaced by the Absolute system. We evaluated data from 01/01/2002 to 10/29/2010. The Absolute system had more data categories than the SHI and thus required data cleaning to make the records compatible. The option for the use of both SHI and Absolute as sources of health care variables relied on their comprehensiveness; this was in contrast to RHC, which only included data concerning chemotherapy, radiotherapy, and oncological surgery.
 
After combining the databases, the differences in dates between the beginning of hormone treatment and the diagnosis of breast cancer were calculated. There were 198 cases with negative values; these were most likely due to typographical errors, and the data were subsequently corrected according to the following procedures. (1) If the initial hormone treatment date was ≤ 3 months earlier than the date of diagnosis, the diagnosis and the initiation of hormone treatment were assumed to coincide (i.e., the difference was equal to 0). (2) If the negative difference between the start of hormone therapy and the diagnosis was > 3 months, and if the second medication dispensing date was consistent with the diagnosis date, the first dispensing date was ignored and replaced with the second date, and the amount dispensed on the discarded date was deducted from the total. With these procedures, it was possible to retain 185 cases in the analysis; however, 13 women were eliminated due to a complete lack of consistency in the data.
Thus, data for 5,861 women were retained for analysis in the integrated database. There was no systematic association between the excluded cases and the variables of interest; thus, there is a low probability that data exclusion due to operational issues might have introduced bias into the study.
Adherence is defined as the extent to which a patient acts in accordance with the prescribed interval and dose of a dosing regimen, and is operationalized, in a retrospective assessment, as the number of doses dispensed in relation to the dispensing period, often called the “medication possession ratio (MPR)” [12, 1719].
It was calculated, for each woman, by summing up all quantities dispensed, and dividing the sum by her time in the cohort, that, in turn, was given by the difference between the last and the first dispensing date summed to the last dispensed quantity, for those that did not die, and between the death and the first dispensing date, for those that died [12, 1719]. We considered the recommendation of a daily hormone therapy (HT) pill for five years. The drugs that INCA dispensed free of charge were TMX and AIS.
Patients with an MPR ≥ 80% were considered adherent, which is a criterion widely applied [2022].
The independent variables of interest included socio-demographic variables (RHC) such as the age at diagnosis, education, and marital status; clinical variables (RHC) such as the histological tumor type, stage, laterality, family history of cancer, smoking, and alcohol consumption; and treatment and health care variables (SHI/Absolute). The latter included the type of hormone therapy (e.g., TMX only, AIS only, letrozole or anastrozole, or both TMX and AIS, which indicated a switch from one form of therapy to the other), surgery, chemotherapy (CT), radiation therapy (RT), hospitalizations, clinical consultations with mastologists, clinical oncologists and other doctors, psychotherapy, multi-professional therapeutic support (MTS) (including nursing ambulatory care, nutrition services, physical therapy, speech therapy and psychology), services from a social worker, dentist or pharmacist, diagnostic and therapeutic services (DTS), and the time between the diagnosis and the initiation of hormone treatment.
Bivariate analyses of adherence were conducted with the chi-squared (χ2) test for categorical independent variables and Student’s t-test for continuous variables. Multivariate logistic regression was also used, while excluding variables without independent effects (p ≥ 0.15) for parsimoniousness. The analyses were performed with the SAS® statistical software package, version 9.1 (SAS Institute Inc., 2003; Cary, NC, USA).
The study was approved by the Research Ethics Committee of INCA under number 84/2010.

Results

The patient age at diagnosis ranged from 21 to 103 years, with a mean of 57.5 (SD = 13.6) years and a median of 56.6 years. Approximately 50% of the women were between 40 and 59 years old, and only a minority was younger than 40 years. Half of the women in the cohort had a low level of education (e.g., they were illiterate or had an incomplete elementary education), and 10% had completed a higher education level.
The adherence rate was compiled from the information for each time frame as follows:
The mean and median follow-up periods were 1225 (SD = 631) and 1209 days, respectively. The cohort showed a mean and median adherence of 86.3% and 94.3%, respectively. If the patients with at least 80% adherence to treatment were assumed to be adherent, the proportion of adherent patients was 76.3%.
The group of adherent women was slightly older than the group of non-adherent women, with mean ages of 58.0 and 56.0 years, respectively (student’s t-test, p < 0.0001). Based on the chi-square test, we found associations of adherence with all categorical variables except the histological primary tumor type (p = 0.6049) and laterality (p = 0.2690; Tables 1, 2 and 3).
Table 1
Distribution of socio-demographic characteristics according to adherence to hormone treatment (N = 5,861)
Variable
Adherent
Non-adherent
χ2(p)
N
%
N
%
Age (years)
    
<0.0001
< 40
342
65.9
177
34.1
 
40 - 49
1,052
74.4
362
25.6
 
50 - 59
1,165
77.7
334
22.3
 
60 - 69
950
79.0
253
21.0
 
> 70
961
78.4
265
21.6
 
Education
    
0.0530
Illiterate + incomplete 1st grade
2,219
75.4
724
24.6
 
Complete 1st grade
772
74.8
260
25.2
 
2nd grade + higher education
1,444
78.5
395
21.5
 
No information
35
74.5
12
25.5
 
Relationship status at start of treatment
   
0.0022
With a partner
2,135
78.3
590
21.6
 
Without a partner
2,307
74.5
791
25.5
 
No information
28
73.7
10
26.3
 
Table 2
Distribution of clinical characteristics according to adherence to hormone treatment (N = 5,861)
Variable
Adherent
Non-adherent
χ2(p)
N
%
N
%
Family history of cancer
    
0.0454
Yes
2,519
77.5
732
22.5
 
No
1,816
74.9
610
25.1
 
No information
135
73.4
49
26.6
 
Alcohol consumption
    
0.0082
Yes
1,181
73.6
424
26.4
 
No
3,164
77.4
924
22.6
 
No information
125
74.4
43
25.4
 
Smoker
    
0.0014
Yes
1,503
73.9
530
26.1
 
No
2,902
77.7
832
22.3
 
No information
65
69.1
29
30.8
 
Histological type of primary tumor
    
0.6049
Invasive ductal carcinoma (IDC)
3,561
76.1
1117
23.9
 
Other tumors
909
76.8
274
23.2
 
Laterality
    
0.2690
Unilateral
4,293
76.4
1325
23.6
 
Bilateral
173
73.3
63
26.7
 
No information
4
57.1
3
42.8
 
Stage
    
< 0.0001
Curable
2,742
83.4
544
16.6
 
Non-curable
1,549
65.3
822
34.7
 
No information
179
87.7
25
12.2
 
Table 3
Distribution of breast cancer treatment procedures according to adherence to hormone treatment (N = 5,861)
Variable
Adherent
Non-adherent
χ2(p)
N
%
N
%
Type of hormone therapy
    
<0.0001
TMX only
3,014
79.8
762
20.2
 
AIS only
256
75.5
83
24.5
 
Both (TMX + AIS)
1,200
68.7
546
31.3
 
Surgery
    
0.0007
Yes
2,720
77.8
775
22.2
 
No
1,750
74.0
616
26.0
 
Chemotherapy
    
< 0.0001
Yes
2,553
72.3
978
27.7
 
No
1,917
82.3
413
17.7
 
Radiotherapy
    
< 0.0001
Yes
2,036
73.4
736
26.5
 
No
2,434
78.8
655
21.2
 
Therapeutic combination
    
< 0.0001
HT only
447
80.9
105
19.0
 
HT and surgery
762
84.8
137
15.2
 
HT and CT
395
68.2
184
31.8
 
HT and RT
405
80.5
98
19.5
 
HT, CT and surgery
830
78.4
229
21.6
 
HT, RT and surgery
303
80.6
73
19.4
 
HT, CT and RT
503
68.7
229
31.3
 
HT, CT, RT and surgery
825
71.1
336
28.9
 
CT frequency
   
< 0.0001
No procedure
1,917
82.3
413
17.7
 
1 to 3 procedures
560
81.2
130
18.8
 
4 to 6 procedures
1,463
82.3
314
17.7
 
≥ 7procedures
530
49.8
534
50.2
 
Frequency of hospitalization
    
< 0.0001
None
752
78.2
209
21.7
 
One
2,250
80.5
544
19.5
 
Two
909
76.9
273
23.1
 
≥ 3
559
60.5
365
39.5
 
Mastologist consultations
    
< 0.0001
None
343
55.6
274
44.4
 
1 to 4 consultations
693
69.2
308
30.8
 
5 to 13 consultations
2,473
83.2
498
16.8
 
≥14 consultations
961
75.5
311
24.5
 
Clinical oncologist consultations
   
< 0.0001
None
1,006
80.3
251
20.0
 
1 to 4 consultations
1,325
79.1
349
20.8
 
5 to 12 consultations
1,126
74.6
384
25.4
 
≥13 consultations
1,013
71.3
407
28.7
 
Other physician consultations
   
< 0.0001
≤ 9 consultations
410
67.9
194
32.1
 
10 to 22 consultations
1,683
78.0
475
22.0
 
23 to 34 consultations
1,316
80.5
319
19.5
 
≥35 consultations
1,061
72.5
403
27.5
 
Psychotherapy consultations
    
< 0.0001
None
2,422
72.7
909
27.3
 
1 to 3 consultations
1,577
80.0
394
20.0
 
≥4 consultations
471
84.3
88
15.7
 
Therapeutic support consultations
   
< 0.0001
None
994
70.8
410
29.2
 
1 to 3 consultations
1,553
77.3
457
22.7
 
4 to 7 consultations
872
77.2
258
22.8
 
≥8 consultations
1,051
79.8
266
20.2
 
DATS (tests)
    
< 0.0001
None
870
78.2
242
21.8
 
1 test
1,587
79.1
420
20.9
 
2 to 3 tests
1,377
75.8
439
24.2
 
≥4 tests
636
68.7
290
31.3
 
Table 1 presents the results according to sociodemographic variables and shows the lower likelihood of adherence among younger women (<40 years). Table 1 also shows the higher likelihood of adherence among women who had completed second grade or higher and among those with a partner; these factors were found to have borderline associations.
In relation to the clinical variables (Table 2), the results show a higher likelihood of adherence among women with a family history of cancer and a lower likelihood of adherence among women who were alcohol drinkers or smokers. The likelihood of adherence was especially low among those who were diagnosed with cancer at a non-curable stage (III and IV).
With regard to the variables related to patient care (Table 3), there was a higher likelihood of adherence in women who were treated with TMX alone, as well as those who underwent surgery. In contrast, women who were treated with both types of hormone therapy (switching from 1 form of therapy to the other), who underwent radiotherapy, who had more consultations with clinical oncologists, or who underwent seven or more chemotherapy procedures, hospitalizations, and tests all had a lower likelihood of adherence. The results also revealed a lower frequency of adherence among women who had not consulted with a mastologist and among those who had not received professional therapeutic support or psychotherapy.
Table 4 shows the multiple logistic regression model that identified the effects of the explanatory variables on adherence to hormone therapy.
Table 4
Multiple logistic regression model for adherence to hormone treatment (N = 5,861)
Variable
Coefficient
Standard error
Pr > χ2
Odds ratio
95% CI
Intercept
−0.3642
0.2591
0.1598
  
Age* (years)
0.0117
0.0029
<0.0001
1.012
1.006 – 1.018
Education
     
  High school diploma
0.2216
0.0858
0.0098
1.248
1.055 – 1.477
  Bachelor’s degree
0.3087
0.1197
0.0099
1.362
1.077 - 1.722
Conjugal status - with a partner
0.2341
0.0681
0.0006
1.264
1.106 – 1.444
Disease stage - non-curable
−0.7329
0.0711
<0.0001
0.481
0.418 – 0.552
Alcohol consumption (yes)
−0.2266
0.0735
0.0020
0.797
0.690 – 0.921
Breast cancer surgery (yes)
0.2478
0.0686
0.0003
1.281
1.120 – 1.466
Chemotherapy (yes)
−0.2686
0.0816
0.0010
0.764
0.651 – 0.897
Hospitalizations (≥3)
−0.5322
0.0842
<0.0001
0.587
0.498 – 0.693
Mastologist visits
     
  1-4
0.4215
0.1135
0.0002
1.524
1.220 – 1.904
  ≥ 5
1.2805
0.1081
<0.0001
3.598
2.911 – 4.447
Oncologist visits
     
  1-4
0.2446
0.0989
0.0134
1.277
1.052 – 1.550
  ≥ 5
0.3203
0.0958
0.0008
1.378
1.142 – 1.662
Diagnostic and therapeutic services
     
  ≤1 exam
0.2557
0.0788
0.0012
1.291
1.107 – 1.507
  ≥ 4 exams
−0.3284
0.0968
0.0007
0.720
0.596 – 0.871
Psychotherapy* (consultations)
0.0534
0.0147
0.0003
1.055
1.025 – 1.086
Type of hormone therapy - both (TMX + AIS)
−0.3148
0.0751
<0.0001
0.730
0.630 – 0.846
CI = Confidence interval. *Continuous variables. References for categorical variables: education – incomplete high school or lower, no information; conjugal status at start of treatment – without a partner, no information; disease stage – curable, no information; alcohol consumption – no, no information; breast cancer surgery – no; chemotherapy – no; hospitalization – <3; mastologist consultations – none; clinical oncologist consultations – none; DTS – 2–3 exams; type of hormone therapy - TMX only, AIS only.
The likelihood of adherence increased with increasing age (OR = 1.012, 95% CI = 1.006-1.018) and with the number of psychotherapy consultations (OR = 1.055, 95% CI = 1.025-1.086). It was greater among women with a mid-level education (OR = 1.248, 95% CI = 1.055-1.477) or higher education (OR = 1.362, 95% CI = 1.07-1.722), as well as among those with a partner (OR = 1.264, 95% CI = 1.106-1.444), those who underwent breast cancer surgery (OR = 1.281, 95% CI = 1.120-1.466), those who consulted with a mastologist (1–4 visits, OR = 1.524, 95% CI = 1.220-1.904; ≥5 visits, OR = 3.598, 95% CI = 2.911- 4.447) or an oncologist (1–4 visits, OR = 1.277, 95% CI = 1.052-1.550; ≥ 5 visits, OR = 1.378; 95% CI = 1.142-1.662), and those who underwent one or no exams (OR = 1.291, 95% CI = 1.107-1.507). On the other hand, the likelihood of adherence was lower among patients diagnosed at a non-curable stage (OR = 0.481, 95% CI = 0.418-0.552), those who were alcohol drinkers (OR = 0.797, 95% CI = 0.690-0.921), those who received chemotherapy (OR = 0.764; 95% CI = 0.651-0.897), those who had three or more hospitalizations (OR = 0.587, 95% CI = 0.498-0.693) or at least four exams (OR = 0.720, 95% CI = 0.596-0.871), and those who were treated with both TMX and AIS (OR = 0.730, 95% CI = 0.630-0.846).

Discussion

The observed level of adherence to hormone therapy (76.3%) in this study was consistent with those found in other published studies, that indicated, considering the same criteria to define adherence, proportions of 75% [20] and 72% [22], or a mean adherence of 93% [12]. However, we underline the difficulties of correlating some available previous studies due to differences in adherence definitions, eligibility criteria (e.g., patients with early tumors or only either young or elderly women), analysis methods, and the types of drugs used (only TMX, only IAS, or both).
The method employed in this study, as in others, accounts for medication delivery as a proxy for medication use, what may result in an overestimation of adherence rates. It is a limitation, but it is believed that the bias can be attenuated when estimations are made on the basis of secondary data from large populations [23].
Another limit of this study was the absence of individual information regarding treatment side effects, which could certainly affect hormone therapy adherence [24].
The truncation of adherence in cases where it reached levels above 100% is justified by the awareness of situations such as the occurrence of deaths, change of medication, and anticipated drug deliveries to meet patient needs.
Only women who received drugs at least twice were included in the study, once the MPR formula requires two dispensing dates. This procedure could have contributed to over or underestimations of the adherence rates, since who received the medication only one time could have been adherent or not to treatment in another place.
Moreover, we underline the difference between the concepts of treatment adherence and persistence, indicating that adherent patients may be non-persistent if they interrupt the treatment before the recommended period of five years.
This study was based on data from a single hospital, and we acknowledge that this might be a limitation. Nevertheless, it is important to emphasize that the hospital allows universal access, restricting entrance only to patients who was treated previously in other locations.
The observed association between adherence and age in this study agrees with some studies [12, 19, 21, 25] yet contradicting others [26]. It can be speculated that the observed lower adherence rate among younger patients is related to the adverse effects of hormone therapy on the women’s sexuality, which include fertility issues and menopausal symptoms [13]. Moreover, the association of greater treatment compliance with having a partner, also found in other studies [22, 26], might be linked to support reception. This result is consistent with the idea that social support is highly predictive of adherence [1].
In this cohort, there was greater adherence among women with higher education levels, contrasting to findings of Wigertz et al.[26], who did not identify a statistically significant association between adherence and education. Anyway, it must be noted that it is very difficult to ensure that education in the Brazilian context is comparable to that of developed countries, and there are few other national studies on the subject. It is plausible the observation of greater adherence among patients with higher education while considering, among other things, that socioeconomic status has also been identified as predictive of adherence [21].
With regard to the disease stage, the observation of lower compliance among patients at non-curable stages (III and IV) contradicts Wigertz et al. [26], who found greater adherence among women with larger tumors. Kimmick et al. [20] found no association between these variables. Importantly, however, the majority of studies on this topic were based only on cohorts of women with early stage disease, which reflects the reality in developed countries, wherein 60% of tumors are diagnosed at a localized stage and thus women who are fighting the disease are at a great advantage.
In Brazil, despite the efforts of the Ministry of Health to implement national policies for earlier breast cancer detection, the proportion of advanced-stage diagnoses is very high, compared to that in developed countries [27]. The lower adherence rates among women with a non-curable stage at diagnosis emphasize the importance of investments in early diagnosis since it has a direct effect on patient survival [4, 8] and also an indirect effect by facilitating treatment compliance.
Bivariate analyses conducted in this study identified the association between both smoking and alcohol consumption and lower treatment adherence [21], while the multivariate analysis ratified only the effect of alcohol consumption on the dependent variable.
This study reinforces the importance of surgery in breast cancer treatment. Previously, surgery had been associated with longer survival [27, 28], and herein, it was associated with greater patient adherence to hormone therapy. The current study also revealed that patient monitoring by mastologists and oncologists had a positive association effect on hormone therapy adherence [19]. However, a more intensive use of health care resources such as chemotherapy, exams and hospitalizations appeared to associate with lower adherence. This result was not directly observed in other studies but may be indirectly related to the association between lower adherence and comorbidities, observed in other studies [15, 20]. Additionally, it should be emphasized that the independent effects of these clinical variables, even after controlling for the disease stage at diagnosis, might reflect the different levels of tumor aggressiveness, different levels of treatment responses, and the presence of comorbidities.
Another notable finding in this study was the independent positive effect of psychotherapy consultations on the likelihood of treatment adherence. This result might be related to those of studies that related psychological problems, particularly depression, to lower treatment adherence [1].
For Kim & Toge [29], a multidisciplinary approach to breast cancer treatment broke down barriers to access, facilitated cooperation between doctors to produce better treatment proposals, and improved the quality of care and patient satisfaction. Although the multidisciplinary team approach to oncology is required by the Brazilian Ministry of Health [16] and is a necessary condition to hospital certification for the provision of oncological care in the Unified Health System (Sistema Único de Saúde; SUS), the present study indicates that between 24.0% and 57.0% of women who were treated at INCA had no records of multidisciplinary therapeutic support consultations or psychotherapy, respectively. Thus, more consultations with nurses, psychologists, social workers and physiotherapists should be encouraged in the clinical monitoring phase. Steps that facilitate the patient’s understanding of the need for treatment and that promote and monitor adherence should be valued. Multidisciplinary therapeutic support consultations were associated with greater adherence to hormone therapy in the bivariate analysis, but were not significant in the multivariate model when psychotherapy consultations were considered separately. The role of such consultations should be further explored in other studies, which may provide more information about their effects and indicate potential changes in their objectives and uses.
With regard to the type of hormone therapy, the poor adherence among patients who used both TMX and AIS has been corroborated in others studies [19, 26]. This finding might be due to the frequent musculoskeletal toxicity associated with AIS [30]. Other studies have found no statistically significant differences between the different types of hormone therapy and adherence [31, 32], although a lower adherence rate has been noted for anastrozole than for TMX [32]. It is noteworthy that in the current study cohort, the majority (64.4%) of the women were treated with TMX alone, while 29.8% received a combination of TMX and AIS and a few women (5.8%) were treated only with AIS. The indication of each drug according to the patient’s morbidity profile was not analyzed.

Conclusion

In this cohort, approximately 25% of the breast cancer patients were considered to be non-adherent to hormone treatment, thus risking a clinical response below the expected standards. Moreover, this study identified the patient characteristics that are associated with greater vulnerability while receiving hormone therapy for breast cancer and reveals the health care practices that facilitate adherence to treatment. Interventions based on these results may help improve patient adherence, quality of care and outcomes.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

All authors participated in study design, dataset preparation by combining the databases, statistical analysis, and drafting and/or reviewing the manuscript. All authors read and approved the final manuscript.
Anhänge

Authors’ original submitted files for images

Literatur
1.
Zurück zum Zitat Ruddy K, Mayer E, Partridge A: Patient adherence and persistence with oral anticancer treatment. CA Cancer J Clin. 2009, 59: 56-66. 10.3322/caac.20004.CrossRefPubMed Ruddy K, Mayer E, Partridge A: Patient adherence and persistence with oral anticancer treatment. CA Cancer J Clin. 2009, 59: 56-66. 10.3322/caac.20004.CrossRefPubMed
2.
Zurück zum Zitat Vervoort MM, Draisma G, Fracheboud J, Van de Poll-Franse LV, Koning HJ: Trends in the usage of adjuvant systemic therapy for breast cancer in the Netherlands and its effect on mortality. Br J Cancer. 2004, 91: 242-247.PubMedPubMedCentral Vervoort MM, Draisma G, Fracheboud J, Van de Poll-Franse LV, Koning HJ: Trends in the usage of adjuvant systemic therapy for breast cancer in the Netherlands and its effect on mortality. Br J Cancer. 2004, 91: 242-247.PubMedPubMedCentral
3.
Zurück zum Zitat Early Breast Cancer Trialists’ Collaborative Group (EBCTCG): Tamoxifen for early breast cancer: an over- view of the randomized trials. Lancet. 1998, 351: 1451-1467.CrossRef Early Breast Cancer Trialists’ Collaborative Group (EBCTCG): Tamoxifen for early breast cancer: an over- view of the randomized trials. Lancet. 1998, 351: 1451-1467.CrossRef
4.
Zurück zum Zitat Early Breast Cancer Trialists’ Collaborative Group (EBCTCG): Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: an overview of the randomised trials. Lancet. 2005, 365: 1687-1717.CrossRef Early Breast Cancer Trialists’ Collaborative Group (EBCTCG): Effects of chemotherapy and hormonal therapy for early breast cancer on recurrence and 15-year survival: an overview of the randomised trials. Lancet. 2005, 365: 1687-1717.CrossRef
5.
Zurück zum Zitat Forbes JF, Cuzick J, Buzdar A, Howell A, Tobias JS, Baum M, Arimidex, Tamoxifen, Alone or in Combination (ATAC) Trialists’ Group: Effect of anastrozole and tamoxifen as adjuvant treatment for early stage breast cancer: 100-month analysis of the ATAC trial. Lancet Oncol. 2008, 9: 45-53.CrossRefPubMed Forbes JF, Cuzick J, Buzdar A, Howell A, Tobias JS, Baum M, Arimidex, Tamoxifen, Alone or in Combination (ATAC) Trialists’ Group: Effect of anastrozole and tamoxifen as adjuvant treatment for early stage breast cancer: 100-month analysis of the ATAC trial. Lancet Oncol. 2008, 9: 45-53.CrossRefPubMed
6.
Zurück zum Zitat Thürlimann B, Keshaviah A, Coates AS, Mouridsen H, Mauriac L, Forbes JF, Paridaens R, Castiglione-Gertsch M, Gelber RD, Rabaglio M, Smith I, Wardley A, Price KN, Goldhirsch A, Breast International Group (BIG) 1–98 Collaborative Group: A comparison of letrozole and tamoxifen in postmenopausal women with early breast cancer. N Engl J Med. 2005, 353: 2747-2757.CrossRefPubMed Thürlimann B, Keshaviah A, Coates AS, Mouridsen H, Mauriac L, Forbes JF, Paridaens R, Castiglione-Gertsch M, Gelber RD, Rabaglio M, Smith I, Wardley A, Price KN, Goldhirsch A, Breast International Group (BIG) 1–98 Collaborative Group: A comparison of letrozole and tamoxifen in postmenopausal women with early breast cancer. N Engl J Med. 2005, 353: 2747-2757.CrossRefPubMed
8.
Zurück zum Zitat WHO (World Health Organization): National Cancer Control Programmes: Policies and Managerial Guidelines. 2002, Geneva: WHO, 2 WHO (World Health Organization): National Cancer Control Programmes: Policies and Managerial Guidelines. 2002, Geneva: WHO, 2
9.
Zurück zum Zitat Burstein HJ, Winer EP: Primary care for survivors of breast cancer. N Engl J Med. 2000, 343: 1086-1094. 10.1056/NEJM200010123431506.CrossRefPubMed Burstein HJ, Winer EP: Primary care for survivors of breast cancer. N Engl J Med. 2000, 343: 1086-1094. 10.1056/NEJM200010123431506.CrossRefPubMed
10.
Zurück zum Zitat Avorn J, Monette J, Lacour A, Bohn RL, Monane M, Mogun H, LeLorier J: Persistence of use of lipid-lowering medications: a cross-national study. JAMA. 1998, 279: 1458-1462. 10.1001/jama.279.18.1458.CrossRefPubMed Avorn J, Monette J, Lacour A, Bohn RL, Monane M, Mogun H, LeLorier J: Persistence of use of lipid-lowering medications: a cross-national study. JAMA. 1998, 279: 1458-1462. 10.1001/jama.279.18.1458.CrossRefPubMed
11.
Zurück zum Zitat Ministério da Saúde (MS)/ Instituto Nacional de Câncer: Estimativa 2012: Incidência de Câncer no Brasil. 2011, Rio de Janeiro: INCA/MS, 2011- Ministério da Saúde (MS)/ Instituto Nacional de Câncer: Estimativa 2012: Incidência de Câncer no Brasil. 2011, Rio de Janeiro: INCA/MS, 2011-
12.
Zurück zum Zitat McCowan C, Shearer J, Donnan PT, Dewar JA, Crilly M, Thompson AM, Fahey TP: Cohort study examining tamoxifen adherence and its relationship to mortality in women with breast cancer. Br J Cancer. 2008, 99: 1763-1768. 10.1038/sj.bjc.6604758.CrossRefPubMedPubMedCentral McCowan C, Shearer J, Donnan PT, Dewar JA, Crilly M, Thompson AM, Fahey TP: Cohort study examining tamoxifen adherence and its relationship to mortality in women with breast cancer. Br J Cancer. 2008, 99: 1763-1768. 10.1038/sj.bjc.6604758.CrossRefPubMedPubMedCentral
13.
Zurück zum Zitat Pellegrini I, Sarradon-Eck A, Soussan PB, Lacour AC, Largillier R, Tallet A, Tarpin C, Julian-Reynier C: Women’s perceptions and experience of adjuvant tamoxifen therapy account for their adherence: breast cancer patients’ point of view. Psychooncology. 2009, 19: 472-479.CrossRef Pellegrini I, Sarradon-Eck A, Soussan PB, Lacour AC, Largillier R, Tallet A, Tarpin C, Julian-Reynier C: Women’s perceptions and experience of adjuvant tamoxifen therapy account for their adherence: breast cancer patients’ point of view. Psychooncology. 2009, 19: 472-479.CrossRef
14.
Zurück zum Zitat Partridge AH, LaFountain A, Mayer E, Taylor BS, Winer E, Asnis-Alibozek A: Adherence to initial adjuvant anastrozole therapy among women with early-stage breast cancer. JCO. 2008, 26 (4): 556-562. 10.1200/JCO.2007.11.5451.CrossRef Partridge AH, LaFountain A, Mayer E, Taylor BS, Winer E, Asnis-Alibozek A: Adherence to initial adjuvant anastrozole therapy among women with early-stage breast cancer. JCO. 2008, 26 (4): 556-562. 10.1200/JCO.2007.11.5451.CrossRef
15.
Zurück zum Zitat Hershman DL, Kushi LH, Shao T, Buono D, Kershenbaum A, Tsai WY, Fehrenbacher L, Gomez SL, Miles S, Neugut AI: Early Discontinuation and Nonadherence to Adjuvant Hormonal Therapy in a Cohort of 8.769 Early-Stage Breast Cancer Patients. JCO. 2010, 28 (27): 4120-4128. 10.1200/JCO.2009.25.9655.CrossRef Hershman DL, Kushi LH, Shao T, Buono D, Kershenbaum A, Tsai WY, Fehrenbacher L, Gomez SL, Miles S, Neugut AI: Early Discontinuation and Nonadherence to Adjuvant Hormonal Therapy in a Cohort of 8.769 Early-Stage Breast Cancer Patients. JCO. 2010, 28 (27): 4120-4128. 10.1200/JCO.2009.25.9655.CrossRef
16.
Zurück zum Zitat Ministério da Saúde (MS): Portaria nº 741, de 19 de dezembro de 2005. Definir as unidades de assistência de alta complexidade em oncologia, os centros de assistência de alta complexidade em oncologia (CACON) e os centros de referência de alta complexidade em oncologia e suas aptidões e qualidades. Diário Oficial União. 2005, 246 (1): 113-124. Ministério da Saúde (MS): Portaria nº 741, de 19 de dezembro de 2005. Definir as unidades de assistência de alta complexidade em oncologia, os centros de assistência de alta complexidade em oncologia (CACON) e os centros de referência de alta complexidade em oncologia e suas aptidões e qualidades. Diário Oficial União. 2005, 246 (1): 113-124.
17.
Zurück zum Zitat Cramer JA, Roy A, Burrell A, Fairchild CJ, Fuldeore MJ, Ollendorf DA, Wong PK: Medication compliance and persistence: terminology and definitions. Value Health. 2008, 11: 44-47. 10.1111/j.1524-4733.2007.00213.x.CrossRefPubMed Cramer JA, Roy A, Burrell A, Fairchild CJ, Fuldeore MJ, Ollendorf DA, Wong PK: Medication compliance and persistence: terminology and definitions. Value Health. 2008, 11: 44-47. 10.1111/j.1524-4733.2007.00213.x.CrossRefPubMed
18.
Zurück zum Zitat Peterson AM, Nau DP, Cramer JA, Benner J, Gwadry-Sridhar F, Nichol M, International Society for Pharmacoeconomics and Outcomes Research (ISPOR): A checklist for medication compliance and persistence studies using retrospective databases. Value Health. 2007, 10 (1): 3-12. 10.1111/j.1524-4733.2006.00139.x.CrossRefPubMed Peterson AM, Nau DP, Cramer JA, Benner J, Gwadry-Sridhar F, Nichol M, International Society for Pharmacoeconomics and Outcomes Research (ISPOR): A checklist for medication compliance and persistence studies using retrospective databases. Value Health. 2007, 10 (1): 3-12. 10.1111/j.1524-4733.2006.00139.x.CrossRefPubMed
19.
Zurück zum Zitat Murphy CC, Bartholomew LK, Carpentier MY, Bluethmann SM, Vernon SW: Adherence to adjuvant hormonal therapy among breast cancer survivors in clinical practice: a systematic review. Breast Cancer Res Treat. 2012, 134: 459-478. 10.1007/s10549-012-2114-5.CrossRefPubMedPubMedCentral Murphy CC, Bartholomew LK, Carpentier MY, Bluethmann SM, Vernon SW: Adherence to adjuvant hormonal therapy among breast cancer survivors in clinical practice: a systematic review. Breast Cancer Res Treat. 2012, 134: 459-478. 10.1007/s10549-012-2114-5.CrossRefPubMedPubMedCentral
20.
Zurück zum Zitat Kimmick G, Anderson R, Camacho F, Bhosle M, Hwang W, Balkrishnan R: Adjuvant Hormonal Therapy Use Among Insured, Low-Income Women With Breast Cancer. J Clin Oncol. 2009, 27: 3445-3451. 10.1200/JCO.2008.19.2419.CrossRefPubMedPubMedCentral Kimmick G, Anderson R, Camacho F, Bhosle M, Hwang W, Balkrishnan R: Adjuvant Hormonal Therapy Use Among Insured, Low-Income Women With Breast Cancer. J Clin Oncol. 2009, 27: 3445-3451. 10.1200/JCO.2008.19.2419.CrossRefPubMedPubMedCentral
21.
Zurück zum Zitat Lin JH, Zhang SM, Manson JE: Predicting adherence to tamoxifen for breast cancer adjuvant therapy and prevention. Cancer Prev Res (Phila). 2011, 4: 1360-1365. 10.1158/1940-6207.CAPR-11-0380.CrossRef Lin JH, Zhang SM, Manson JE: Predicting adherence to tamoxifen for breast cancer adjuvant therapy and prevention. Cancer Prev Res (Phila). 2011, 4: 1360-1365. 10.1158/1940-6207.CAPR-11-0380.CrossRef
22.
Zurück zum Zitat Hershman DL, Shao T, Kushi LH, Buono D, Tsai WY, Fehrenbacher L, Kwan M, Gomez SL, Neugut AI: Early discontinuation and non-adherence to adjuvant hormonal therapy are associated with increased mortality in women with breast cancer. Breast Cancer Res Treat. 2011, 126 (2): 529-537. 10.1007/s10549-010-1132-4.CrossRefPubMed Hershman DL, Shao T, Kushi LH, Buono D, Tsai WY, Fehrenbacher L, Kwan M, Gomez SL, Neugut AI: Early discontinuation and non-adherence to adjuvant hormonal therapy are associated with increased mortality in women with breast cancer. Breast Cancer Res Treat. 2011, 126 (2): 529-537. 10.1007/s10549-010-1132-4.CrossRefPubMed
24.
Zurück zum Zitat Guth U, Myrick ME, Schotzau A, Kilic N, Schmid SM: Drug switch because of treatment-related adverse side effects in endocrine adjuvant breast cancer therapy: how often and how often does it work?. Breast Cancer Res Treat. 2011, 129: 799-807. 10.1007/s10549-011-1668-y.CrossRefPubMed Guth U, Myrick ME, Schotzau A, Kilic N, Schmid SM: Drug switch because of treatment-related adverse side effects in endocrine adjuvant breast cancer therapy: how often and how often does it work?. Breast Cancer Res Treat. 2011, 129: 799-807. 10.1007/s10549-011-1668-y.CrossRefPubMed
25.
Zurück zum Zitat Güth U, Myrick ME, Kilic N, Eppenberger-Castori S, Schmid SM: Compliance and persistence of endocrine adjuvant breast cancer therapy. Breast Cancer Res Treat. 2012, 131: 491-499. 10.1007/s10549-011-1801-y.CrossRefPubMed Güth U, Myrick ME, Kilic N, Eppenberger-Castori S, Schmid SM: Compliance and persistence of endocrine adjuvant breast cancer therapy. Breast Cancer Res Treat. 2012, 131: 491-499. 10.1007/s10549-011-1801-y.CrossRefPubMed
26.
Zurück zum Zitat Wigertz A, Ahlgren J, Holmqvist M, Fornander T, Adolfsson J, Lindman H, Bergkvist L, Lambe M: Adherence and discontinuation of adjuvant hormonal therapy in breast cancer patients: a population-based study. Breast Cancer Res Treat. 2012, 133: 367-373. 10.1007/s10549-012-1961-4.CrossRefPubMed Wigertz A, Ahlgren J, Holmqvist M, Fornander T, Adolfsson J, Lindman H, Bergkvist L, Lambe M: Adherence and discontinuation of adjuvant hormonal therapy in breast cancer patients: a population-based study. Breast Cancer Res Treat. 2012, 133: 367-373. 10.1007/s10549-012-1961-4.CrossRefPubMed
27.
Zurück zum Zitat Brito C, Portela MC, Vasconcellos MTL: Sobrevida de mulheres tratadas por câncer de mama no estado do Rio de Janeiro. Rev Saude Publica. 2009, 43: 481-489. 10.1590/S0034-89102009000300012.CrossRefPubMed Brito C, Portela MC, Vasconcellos MTL: Sobrevida de mulheres tratadas por câncer de mama no estado do Rio de Janeiro. Rev Saude Publica. 2009, 43: 481-489. 10.1590/S0034-89102009000300012.CrossRefPubMed
28.
Zurück zum Zitat Rao VS, Jameel JK, Mahapatra TK, McManus PL, Fox JN, Drew PJ: Surgery is associated with lower morbidity and longer survival in elderly breast cancer patients over 80. Breast J. 2007, 13: 368-373. 10.1111/j.1524-4741.2007.00444.x.CrossRefPubMed Rao VS, Jameel JK, Mahapatra TK, McManus PL, Fox JN, Drew PJ: Surgery is associated with lower morbidity and longer survival in elderly breast cancer patients over 80. Breast J. 2007, 13: 368-373. 10.1111/j.1524-4741.2007.00444.x.CrossRefPubMed
29.
Zurück zum Zitat Kim R, Toge T: Multidisciplinary approach to cancer treatment: a model for breast cancer treatment at the M. D. Anderson Cancer Center. Int J Clin Oncol. 2004, 9: 356-363. 10.1007/s10147-004-0411-7.CrossRefPubMed Kim R, Toge T: Multidisciplinary approach to cancer treatment: a model for breast cancer treatment at the M. D. Anderson Cancer Center. Int J Clin Oncol. 2004, 9: 356-363. 10.1007/s10147-004-0411-7.CrossRefPubMed
30.
Zurück zum Zitat Henry NL, Azzouz F, Desta Z, Li L, Nguyen AT, Lemler S, Hayden J, Tarpinian K, Yakim E, Flockhart DA, Stearns V, Hayes DF, Storniolo AM: Predictors of aromatase inhibitor discontinuation as a result of treatment-emergent symptoms in early-stage breast cancer. J Clin Oncol. 2012, 30: 936-942. 10.1200/JCO.2011.38.0261.CrossRefPubMedPubMedCentral Henry NL, Azzouz F, Desta Z, Li L, Nguyen AT, Lemler S, Hayden J, Tarpinian K, Yakim E, Flockhart DA, Stearns V, Hayes DF, Storniolo AM: Predictors of aromatase inhibitor discontinuation as a result of treatment-emergent symptoms in early-stage breast cancer. J Clin Oncol. 2012, 30: 936-942. 10.1200/JCO.2011.38.0261.CrossRefPubMedPubMedCentral
31.
Zurück zum Zitat Chlebowski RT, Geller ML: Adherence to Endocrine Therapy for Breast Cancer. Oncology. 2006, 71: 1-9.PubMed Chlebowski RT, Geller ML: Adherence to Endocrine Therapy for Breast Cancer. Oncology. 2006, 71: 1-9.PubMed
32.
Zurück zum Zitat Ziller V, Kalder M, Albert US, Holzhauer W, Ziller M, Wagner U, Hadji P: Adherence to adjuvant endocrine therapy in postmenopausal women with breast cancer. Ann Oncol. 2009, 20: 431-436.CrossRefPubMed Ziller V, Kalder M, Albert US, Holzhauer W, Ziller M, Wagner U, Hadji P: Adherence to adjuvant endocrine therapy in postmenopausal women with breast cancer. Ann Oncol. 2009, 20: 431-436.CrossRefPubMed
Metadaten
Titel
Adherence to hormone therapy among women with breast cancer
verfasst von
Claudia Brito
Margareth Crisóstomo Portela
Mauricio Teixeira Leite de Vasconcellos
Publikationsdatum
01.12.2014
Verlag
BioMed Central
Erschienen in
BMC Cancer / Ausgabe 1/2014
Elektronische ISSN: 1471-2407
DOI
https://doi.org/10.1186/1471-2407-14-397

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