No clinical evidence on the efficacy and safety of eribulin monotherapy has been obtained by a prospective clinical study in patients with metastatic breast cancer (MBC) who had well-defined taxane resistance. The present Phase II, multicenter, single-arm, open-label study aimed to obtain the evidence. Japanese female patients, aged 33–74 years who had the metastasis of taxane-resistant and histopathologically confirmed breast cancer, received eribulin mesylate 1.4 mg/m2 (equivalent to eribulin 1.23 mg/m2 [expressed as free base]) as a 2- to 5-min intravenous infusion on days 1 and 8 of each 21-day cycle. The primary endpoint was the clinical benefit rate (CBR) [complete response (CR), partial response (PR), and long-term stable disease (LSD) ≥24 weeks]. A total of 51 patients underwent chemotherapy cycles (median 4; range 1–42 cycles). The CBR was 39.2 % (CR 2.0 %; PR 23.5 %; and LSD 13.7 %), and the rate of progressive disease was 49.0 %. The median progression-free survival and the median overall survival were 3.6 months [95 % confidence interval (CI) 2.6–4.6 months] and 11.7 months (95 % CI 9.2–14.2 months), respectively. Grade 3 or greater adverse events were leukopenia (23.5 %), neutropenia (35.3 %), anemia (5.9 %), and febrile neutropenia (7.8 %). The incidences of grade 3 and 4 peripheral sensory neuropathy were 2.0 and 0 %, respectively. Eribulin showed a clinically manageable tolerability profile by dose adjustments or symptomatic treatment. Eribulin was effective and well tolerated in heavily pretreated patients with MBC who had well-defined taxane resistance, thus providing a potential therapeutic option in the clinical settings.
Introduction
Breast cancer is the most common cancer in American women, with estimated new cases and deaths of 231,840 (28.6 % of all new cancers in women) and 40,290 (14.5 % of all cancer deaths in women), respectively, for year 2015 [1]. Approximately 5–10 % of patients with breast cancer present metastasis at diagnosis, and up to 30 and 70 % of node-negative and -positive breast cancers will relapse, respectively [2]. In Japanese women, on the other hand, the estimated number of new cases and deaths were 86,700 (22.8 % of all new cases in women) and 13,400 (9.0 % of all cancer deaths in women), respectively, for year 2014. Breast cancer is the fifth most common malignancy causing cancer deaths, preceded by colon, lung, stomach, and pancreatic cancers in 2013 [3].
Chemotherapy constitutes a beneficial therapeutic armamentarium for patients with metastatic breast cancer (MBC) although the complete cure of the disease is difficult to attain, and anthracyclines and taxanes—two most active classes of cytotoxic agents that are commonly used for the treatment of breast cancer—are preferred as single agents for recurrent or metastatic breast cancer [4]. However, lifetime exposure to the former is restricted due to their cardiotoxicity, myelosuppression, and alopecia. On the other hand, the latter provokes alopecia, peripheral neuropathy, and other serious adverse events. Furthermore, the emergence of resistance to anthracyclines and taxanes has become a major clinical obstacle [5].
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Eribulin, which is a non-taxane microtubule dynamics inhibitor belonging to the halichondrin class of antineoplastic agents [6], has a unique end-poisoning mechanism that results predominantly in the inhibition of microtubule growth with no or little effect on shortening [7, 8]. Consequently, eribulin exerts its cytotoxicity by suppressing microtubule growth and sequestering tubulins, eventually causing G2-M cell cycle arrest and apoptosis [9‐11]. Eribulin has shown antitumor activity for a number of human cancer cell lines and xenografts with a variety of therapeutic indexes [12]. In addition to its pharmacological potency superior to other agents (e.g., paclitaxel and vinblastine), eribulin has potent activity against paclitaxel-resistant human cancer cell lines in vitro [13]. Apart from its cytotoxicity, eribulin induces the remodeling of tumor vasculature through a novel antivascular activity and a reversing effect on the epithelial–mesenchymal transition of cancer cells—a key process for metastatic promotion in cancer, thus inhibiting metastasis [14‐19]. This may also contribute to the extension of survival of patients with MBC.
In prior Phase II and III clinical studies of eribulin monotherapy, the drug has shown antitumor activity and a survival benefit for patients with MBC who had previously undergone anthracycline- or taxane-based chemotherapy regimens [20‐26]. Especially in a Phase III open-label randomized clinical study of eribulin (EMBRACE) [25], furthermore, eribulin monotherapy showed a significant and clinically meaningful improvement in the overall survival (OS) of patients with MBC compared to treatment of physician’s choice (TPC) in heavily pretreated patients with MBC. In 2010, consequently, the Food and Drug Administration approved eribulin mesylate as third-line treatment for MBC refractory to anthracyclines and taxanes [27]. By contrast, eribulin is approved as first or subsequent line therapy for the treatment of patients with MBC in Japan. As described above, prior clinical studies have examined the efficacy and safety of eribulin in patients with MBC who were previously treated with taxanes. However, no clinical evidence about these features of eribulin has been obtained in MBC patients who had well-defined taxane resistance. Therefore, we conducted the present study to obtain the evidence.
Methods
Study design
A Phase II, multicenter, single-arm, open-label clinical study (University Hospital Medical Information Network identifier: 000006965) was conducted at eight medical institutions in Japan and enrolled Japanese female patients with MBC who were found to have well-defined taxane resistance. The administration of colony-stimulating factors (G-CSFs) was allowed according to the Japanese Society of Clinical Oncology guidelines.
Patients
Female patients were considered eligible when meeting all of the following criteria: women aged 20–74 years with histopathologically confirmed breast cancer; prior chemotherapy regimens with taxanes and/or anthracyclines; Eastern Cooperative Oncology Group (ECOG) performance status: 0–2; lesions measurable by computed tomography or magnetic resonance imaging at least in one dimension; conserved functions of principle organs (bone marrow, liver, kidney, and lung)—neutrophil count: ≥1500/μL; platelet count: ≥100,000/μL; hemoglobin concentration: ≥8.0 g/dL; aspartate aminotransferase (AST) and alanine aminotransferase (ALT): ≤2.5-fold the upper limit of normal (ULN) or ≤5.0-fold the ULN in patients with hepatic metastasis; total bilirubin: ≤1.5-fold the ULN; and serum creatinine concentration: ≤1.5-fold the ULN; and written informed consent. A woman with MBC, who was already under chemotherapy, was considered to present well-defined taxane resistance when falling under either of the following cases: (1) breast cancer recurred during taxane treatment or within 1 year after the last administration when undergoing neo- or adjuvant chemotherapy with taxanes and 2) the tumor progressed (from CR/PR/SD to PD or PD) during taxane treatment.
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Women were excluded when falling under any of the following criteria: systemic infection involving fever (≥38 °C); a large volume of pleural fluid, ascites, or pericardial fluid requiring drainage; brain metastasis with clinical symptoms; serious complications including heart disease (e.g., poorly controlled ischemic disease and arrhythmias excluding left ventricular hypertrophy associated with hypertension, mild left ventricular load, and mild right bundle branch block), myocardial infarction within previous 6 months, hepatic cirrhosis, interstitial pneumonia, pulmonary fibrosis, and bleeding tendency; active double cancer; overexpression of the human epidermal growth factor receptor type 2 (HER2) at the primary or metastatic lesion as either (3+) by immunohistochemistry or (+) by fluorescence in situ hybridization (FISH); pregnancy, breast-feeding, or women with childbearing potential; and ineligibility for the study.
Patients underwent study treatment until disease progression, unacceptable toxicity, consent withdrawal, or investigator’s discretion to discontinue the treatment. All patients provided written informed consent before enrollment. The study was conducted in accordance with the Declaration of Helsinki, Good Clinical Practice, and local ethical and legal requirements. The study protocol was approved by the Institutional or Central Ethics Committee.
Treatment
Eribulin mesylate 1.4 mg/m2 (equivalent to eribulin 1.23 mg/m2 [expressed as free base]) was administered as a 2- to 5-min intravenous infusion on days 1 and 8 of each 21-day cycle. Successive dose reductions to 1.1 and 0.7 mg/m2 were permitted at the investigator’s discretion or to manage the following events: grade 3 or greater febrile neutropenia; grade 3 or greater neutropenia (<1000/μL) requiring antibiotic treatment; grade 4 thrombocytopenia (<25,000/μL); grade 3 or greater nonhematologic toxicities excluding nausea, vomiting, anorexia, and laboratory abnormalities without clinical symptoms; and administration on day 8 of the cycle was omitted because grade 3 or greater neutropenia (<1000/μL) or thrombocytopenia (<50,000/μL) occurred. The second or subsequent cycle was postponed for a maximum of 2 weeks (day 36 of the previous cycle) in the event that at least one of the following criteria for next cycle initiation was unmet: neutrophil count: ≥1000/μL; platelet count: ≥75,000/μL; AST or ALT: ≤2.5 fold the ULN; total bilirubin: ≤1.5-fold the ULN; serum creatinine: ≤1.5-fold the ULN; and nonhematologic toxicities: grade 2 or lower (excluding those caused by the disease and laboratory abnormalities without clinical symptoms). The dose delay or interruption was resumed after confirming that the criteria were met. Grade 3 or 4 adverse events (AEs) were managed by dose modifications (interruptions, delays, or reductions).
In principle, concomitant treatment for concurrent underlying disease was not restricted. However, the following concurrent or adjunctive therapy was not permitted: other anticancer treatments (e.g., immunotherapy, chemotherapy, and surgery); prophylactic administration of G-CSF; and other investigational drugs. Symptomatic treatment with G-CSFs was permitted for grade 4 neutropenia and grade 3 febrile neutropenia.
Assessments
Efficacy
Tumor lesions and markers were monitored at screening or day 1 and every 8 weeks thereafter. Subsequent monitoring could be rescheduled when a change in disease status was suspected. Tumor response was assessed according to Response Evaluation Criteria in Solid Tumors [28] at screening, week 8 (+2 weeks) after the day of first administration, and every 8 weeks (±2 weeks) after the day of previous observation of the tumor lesion. Tumor responses were categorized as follows: complete response (CR); partial response (PR); progressive disease (PD); stable disease (SD); and not evaluable (NE). CR and PR required two or more successive confirmations at 4-week or more intervals. The clinical benefit rate [CBR: CR + PR + long-term SD (LSD: SD ≥24 weeks)], the overall response rate (ORR: CR + PR), and the disease control rate (DCR: CR + PR + SD) were calculated. Progression-free survival (PFS) was defined as the span from enrollment to the earliest date of disease progression, death, or censoring. Overall survival (OS) was defined as the span from enrollment to death or to the date of censoring. The efficacy and safety evaluation panel reviewed the efficacy and safety data on the investigator-assessed patients.
Study endpoints
The primary endpoint was the CBR, and the secondary endpoints were PFS, OS, and safety.
Safety
AEs were recorded and graded according to the Common Terminology Criteria for Adverse Events Japanese version 4.0, and coded according to the Medical Dictionary for Regulatory Activities, Japanese version (MedDRA/J).
Vital signs and ECOG performance status were assessed; laboratory tests (hematology and blood biochemistry) and 12-lead electrocardiography at rest were conducted before recruitment and at the time of each visit, discontinuation, and completion.
Statistical analyses
PFS and the ORR (median with 95 % confidence interval [CI]) were calculated using Kaplan–Meier estimates. Safety data were evaluated using descriptive statistics. Sample size was estimated to be 52 based on previous clinical studies: in a Phase II study [21], the independently reviewed CBR was 17.1 % (95 % CI 12.8–22.1 %) and the investigator-reviewed CBR was 19.7 % (95 % CI 15.1–25.0 %); in a Phase III study [25], these CBRs were 23.0 % (95 % CI 18.9–26.7 %) and 28.0 % (95 % CI 23.8–32.1 %), respectively. We assumed that third-line therapy would produce antitumor activity comparable to that described in these previous studies and established an expected CBR of 23 % and a threshold CBR of 10 %, with 80 % power at a type I error of 5 % (two-sided alpha). These assumptions produced 52 samples for the detection of tumor response. SPSS version 19 (IBM, Armonk, NY) was used to make all statistical analyses.
Results
Patients
A total of 53 patients were recruited at eight institutions in Japan between February 2012 and November 2014, two of whom were subsequently excluded from the study because of not meeting the key inclusion criteria; consequently, 51 were enrolled. The baseline demographic and clinical characteristics of the patients are shown in Table 1. The median age was 55.0 years (range 33.9–74.4 years), 25 (49.0 %) had an ECOG performance status of 0, 31 (60.8 %) had estrogen receptor (ER)-positive breast cancer, 19 (37.3 %) had triple-negative breast cancer, 46 (90.2 %) had undergone chemotherapy after recurrence with a median of 2 regimens (range 0–7), 25 (49.0 %) had four or more metastases—predominantly in the bone, lung, and liver, and 37 (72.5 %) had grade 1 or greater peripheral sensory neuropathy.
Table 1
Baseline demographic and clinical characteristics of patients
Characteristics
N = 51
n (percentage)
Age, years
Median
55.0
Range
33.9–74.4
ECOG performance status
0
25 (49.0 %)
1
22 (43.1 %)
2
4 (7.8 %)
Hormone receptor status
ER-positive
31 (60.8 %)
Triple-negative (ER, PgR, HER2)
19 (37.3 %)
Unknown
1 (2.0 %)
Prior treatments
Neoadjuvant chemotherapy
20 (39.2 %)
Adjuvant chemotherapy
20 (39.2 %)
Chemotherapy after recurrence
46 (90.2 %)
Number of prior chemotherapy regimens after recurrence
0
5 (9.8 %)
1
8 (15.7 %)
2
15 (29.4 %)
3
10 (19.6 %)
4
4 (7.8 %)
≥5
9 (17.6 %)
Median
2
Range
0–7
Prior chemotherapy agent
Anthracycline
29 (56.9 %)
Paclitaxel
42 (82.4 %)
Docetaxel
8 (15.7 %)
Paclitaxel and docetaxel
1 (2.0 %)
Capecitabine/TS1
37 (72.5 %)
Vinorelbine
5 (9.8 %)
Gemcitabine
8 (15.7 %)
Site of metastasis
Bone
28 (54.9 %)
Lung
24 (47.1 %)
Liver
25 (49.0 %)
Distal/regional lymph node
20/18 (39.2/35.3 %)
Local lesion
15 (29.4 %)
Pleura
10 (19.6 %)
Skin
8 (15.7 %)
Brain
3 (5.8 %)
Number of metastases
1
5 (9.8 %)
2
7 (13.7 %)
3
14 (27.5 %)
≥4
25 (49.0 %)
ECOG Eastern Cooperative Oncology Group, ER estrogen receptor, PgR progesterone receptor, HER2 human epidermal growth factor receptor 2
Study drug exposure
The median of cycles delivered was 4 (range 1–42 cycles). Among 51 patients treated, 13 (25.5 %), 18 (35.3 %), and 11 (21.6 %) experienced dose interruptions, delays, and reductions during cycle 1, respectively, primarily as a result of neutropenia. One (2.0 %) of the patients discontinued eribulin administration who had a cerebrovascular accident. The median of relative dose intensity (RDI) was 85.6 % (range 31.0–101.3 %). Four patients (7.8 %) received G-CSFs for the treatment of grade 3 febrile neutropenia.
Efficacy
The following variables for efficacy were obtained (Table 2): the CBR was 39.2 % (95 % CI 25.8–53.9 %), and the median ORR was 25.5 % (95 % CI 14.3–39.6 %). However, six of enrolled patients were found to have not received an anthracycline: two patients each in those who presented PR, LSD, and PD. After excluding these six patients from the assessment of efficacy, the following variables for efficacy were obtained: the CBR was 35.6 % (95 % CI 21.9–51.2 %), and the median ORR was 24.4 % (95 % CI 12.9–39.5 %). The Kaplan–Meier curves for PFS and OS are shown in Fig. 1. The median PFS was 3.6 months (95 % CI 2.6–4.6 months) and the median OS was 11.7 months (95 % CI 9.2–14.2 months). Percent changes in metastatic tumor size (total sum of the longest single dimension for measurable target lesions) from baseline to the maximal tumor shrinkage regarding best overall responses in the overall, liver, and lung are shown in Fig. 2; eribulin caused tumor shrinkage in the target organs that were examined (e.g., the liver and lung).
Table 2
Best overall responses
n
%
CR
1
2.0
PR
12
23.5
SD
5
9.8
LSD
7
13.7
PD
25
49.0
NE
1
2.0
CBR (CR + PR + LSD)
20
39.2
95 % CI
25.8–53.9
ORR (CR + PR)
13
25.5
95 % CI
14.3–39.6
DCR (CR + PR + SD)
25
49.0
95 % CI
34.8–63.4
CR complete response, PR partial response, SD stable disease, LSD long-term stable disease ≥24 weeks, PD progressive disease, NE not evaluable, CI confidence interval
Fig. 1
Kaplan–Meier curves for progression-free survival (a) and overall survival (b)
Fig. 2
Waterfall plots of percent changes in metastatic tumor size (total sum of the longest single dimension for measurable target lesions) from baseline to the maximal tumor shrinkage regarding best overall responses: a overall, b liver, and c lung. CR complete response, PR partial response, SD stable disease, PD progressive disease, LSD long-term stable disease
×
×
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The CBRs were comparable between ER-positive and triple-negative patients (Table 3). Eribulin showed efficacy (CBR: ≥40 %) in the major organs of metastasis, e.g., lung and liver (Table 4). The rate of best overall response in patients who had undergone paclitaxel treatment was as high as 35.7 % in the CBR (Table 5). Among the patients examined, the CBR was highest in patients whose best overall response was qualified from SD to PD (Table 6).
†Defined as “tumor metastasis during taxane treatment or within 1 year after the last administration of a taxane” or “tumor progress (from CR/PR/SD to PD) during taxane treatment.”
No patient with CR in our study
Safety
All patients experienced treatment-related adverse events (TRAEs), but eribulin showed a clinically manageable tolerability profile by dose modifications or symptomatic treatment. One patient suffered from a cerebrovascular accident about whom causality with eribulin could not be ruled out, which led to the discontinuation of eribulin administration. However, no death occurred during the study period.
The most common TRAEs were neutropenia (35.3 %), leukopenia (33.3 %), and anemia (29.4 %) among hematologic AEs and were oral mucositis, alopecia, AST increased, fatigue, constipation, anorexia, and peripheral motor neuropathy (13.7 % each) among nonhematologic AEs (Table 7). The grade 3 TRAEs were leukopenia (19.6 %), neutropenia (17.6 %), febrile neutropenia (7.8 %), and anemia (5.9 %). Neutropenia was managed by dose interruptions/delays or dose reductions, or with G-CSFs, administered to 4 patients (7.8 %). Dose interruptions were caused most frequently by neutropenia, peripheral neuropathy, ALT increased, and pulmonary fibrosis (10, 1, 1, and 1 patients, respectively). On the other hand, dose reductions were required most frequently by neutropenia, peripheral neuropathy, and ALT increased (9, 1, and 1 patients, respectively). Furthermore, dose delays were necessitated most frequently by neutropenia, peripheral neuropathy, and others (10, 4, and 4, respectively). The incidence of grade 3 peripheral sensory neuropathy was 2.0 % (1/51), and neither grade 3 motor neuropathy nor grade 4 peripheral sensory/motor neuropathy was observed.
Table 7
Most common adverse events with an incidence of ≥10 % for all grades by CTCAE grade in the safety population (n = 51)
Adverse event
Severity
All grades
Grade 1
Grade 2
Grade 3
Grade 4
Hematologic
Neutropenia
29 (56.9 %)
1 (2.0 %)
10 (19.6 %)
9 (17.6 %)
9 (17.6 %)
Leukopenia
30 (58,8 %)
5 (9.8 %)
13 (25.5 %)
10 (19.6 %)
2 (3.9 %)
Anemia
15 (29.4 %)
10 (19.6 %)
2 (3.9 %)
3 (5.9 %)
Febrile neutropenia
4 (7.8 %)
4 (7.8 %)
Thrombocytopenia
2 (3.9 %)
1 (2.0 %)
1 (2.0 %)
Nonhematologic
Oral mucositis
7 (13.7 %)
7 (13.7 %)
Alopecia
7 (13.7 %)
6 (11.8 %)
1 (2.0 %)
AST increased
7 (13.7 %)
6 (11.8 %)
1 (2.0 %)
Fatigue
7 (13.7 %)
4 (7.8 %)
2 (3.9 %)
1 (2.0 %)
Constipation
7 (13.7 %)
4 (7.8 %)
3 (5.9 %)
Anorexia
7 (13.7 %)
5 (9.8 %)
2 (3.9 %)
Peripheral motor neuropathy
7 (13.7 %)
7 (13.7 %)
Nausea
6 (11.8 %)
5 (9.8 %)
1 (2.0 %)
Peripheral sensory neuropathy
6 (11.8 %)
2 (3.9 %)
3 (5.9 %)
1 (2.0 %)
ALT increased
5 (9.8 %)
3 (5.9 %)
2 (3.9 %)
Diarrhea
4 (7.8 %)
2 (3.9 %)
2 (3.9 %)
CTCAE common terminology criteria for adverse events, ALT alanine aminotransferase, AST aspartate aminotransferase
Discussion
In EMBRACE Study [25] that examined patients who had undergone anthracycline- and taxane-based treatment for locally recurrent breast cancer or MBC, the median OS was 13.1 months for eribulin monotherapy and 10.6 months for TPC; eribulin thus indicated a 2.5-month extension of the median OS in patients who were taxane refractory because of having shown disease progression within 6 months of latest chemotherapy. In view of the outcomes from the EMBRACE Study, we intended to examine the efficacy and safety of eribulin monotherapy in Japanese female patients with MBC who had stricter taxane resistance (tumor progression within 1 year after treatment with taxanes) than the study.
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Our study population consisted of heavily pretreated patients, the majority of whom (76.5 %) already had three or more sites of metastasis at baseline. Despite these facts, a certain level of anticancer activity was observed in our patients who had stricter taxane resistance than that in the study conducted by Aogi et al. [24]. After excluding six patients who had not received anthracyclines, the activity was demonstrated with a CBR of 35.6 % (vs. 27.5 %), a median ORR of 24.4 % (vs. 21.3 %), a median PFS of 3.5 months (vs. 3.7 months), and a median OS of 11.7 months (vs. 11.1 months). Compared with their study, namely, the efficacy profile of eribulin was better and equivalent with respect to variables for efficacy including the CBR.
Furthermore, the CBR in the present study was equivalent to the CBRs (17.1–32.9 %) described in other prior Phase II and III clinical studies of eribulin monotherapy in non-Japanese patients [20, 21, 25, 26]; however, the CBR in our study was much lower than 51.8 and 62.9 % in Phase II clinical studies of eribulin as first-line therapy conducted by McIntyre et al. [22] and Takashima et al. [23]—a sufficiently comprehensible fact when considering differences between the first- and late-line therapies. The median ORR in the present study was equivalent to 21.3 % [24] in Japanese patients and was higher than 9.3–16.1 % in non-Japanese patients [20‐22, 25, 26]. In addition, the median PFS and the median OS in this study were comparable to 2.6–4.1 months and 9.2–15.9 months in non-Japanese patients, respectively [20‐22, 25, 26].
The subgroup analyses of best overall responses revealed several novel insights into the efficacy profile of eribulin. The CBRs were comparable between the “ER-positive” and “triple-negative” categories in receptor status (Table 3); this might indicate that eribulin suppresses disease progression regardless of receptor status. The top three CBRs by organ in decreasing order were found for the regional lymph node (44.4 %), as well as for vital organs—lung (41.7 %) and liver (40.0 %) (Table 4) (Fig. 2). Namely, eribulin showed efficacy in nonvisceral and visceral organs as with the study conducted by Aogi et al. The waterfall plot analysis of maximal changes in metastatic tumor size by organ (Fig. 2, overall) revealed a markedly reduced proportion of patients who presented SD and LSD (23.5 %) as compared with 37.5 % in the study conducted by Aogi et al. Namely, our study suggested cross resistance in a proportion of the enrolled patients. On the other hand, eribulin also showed the ORR comparable to that in the study conducted by Aogi et al. in Japanese patients with MBC, thus possibly reflecting the preclinical evidence that eribulin has antitumor activity against taxane-resistant tumor cell lines [13]. Eribulin showed efficacy regardless of a difference in taxanes—paclitaxel and docetaxel (Table 5). In addition, the subgroup analysis of best overall responses by well-defined taxane resistance pattern in our patients revealed the following findings of interest (Table 6): (1) the predominant (about 80 %) pathogenesis of taxane resistance was tumor progression; (2) all subgroups of tumor progression patterns showed the CBRs of ≥20 %, i.e., eribulin provided a given level of tumor response regardless of taxane resistance pattern; and (3) the CBR was higher in patients whose tumor progression shifted from “SD” to “PD” than in those from “PR” to “SD” or whose tumor exhibited “PD.” Nevertheless, further study will be required to specify the factors involved in these findings through the acquisition of information on exposure to taxanes in prior chemotherapy regimens and others.
The safety profile of eribulin in the present study is in line with what has been described in the previous Phase II and III clinical trials of eribulin monotherapy [20‐26]. Concretely, leukopenia (58.8 %), neutropenia (56.9 %), and anemia (29.4 %) constituted major hematologic AEs as with the clinical trials conducted by Aogi et al., Cortes et al., and Kahfman et al. AEs requiring dose modifications were grade 3 febrile neutropenia and grade 4 neutropenia, the incidences of which in the present study were comparable to or lower than those described in the abovementioned studies which ranged between 25.0 and 95.1 % and between 21.0 and 24.6 %, respectively. Importantly, eribulin indicated an incidence of grade 3 febrile neutropenia (7.8 %), which was much lower than 13.6 % in Japanese patients [24] and was comparable to 2.0–5.5 % in non-Japanese patients [20‐22, 25, 26]. Both grade 3 febrile neutropenia and grade 4 neutropenia were successfully managed by dose modifications or with G-CSFs. Of note were the following facts: (1) the incidences of grade 1 peripheral neuropathy and grade 3 peripheral sensory neuropathy were as low as 13.7 and 2.0 %, respectively; and (2) grade 4 peripheral motor/sensory neuropathy did not develop as with the studies conducted by Vahdat et al., Cortes et al., and McIntyre et al. [20‐22].
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Apart from the clinical benefits of eribulin monotherapy described above, eribulin also offers therapeutic advantages because of necessitating an intravenous infusion time that is as short as 2–5 min, requiring no premedication to prevent hypersensitivity, and causing little infusion-related reactions during repeated administration.
Study limitations
The present study had several limitations. First, sample size is relatively small. However, our study provided the efficacy and safety profiles of eribulin monotherapy that were in accord with those described in a previous clinical study in Japanese patients with heavily pretreated MBC. Second, our study is not a randomized clinical study, thus affording practical insights of lower evidence level but reflecting the real-world clinical settings. Third, we could not obtain detailed information on the factors of prior chemotherapy regimens that might influence disease progression after the onset of eribulin monotherapy. The acquisition of the relevant information and the accumulation of new patients will help specify MBC patients presenting well-defined taxane resistance to whom eribulin is expected to be most effective.
Conclusions
Eribulin was effective for heavily pretreated patients with MBC who were found to have well-defined taxane resistance. Furthermore, eribulin exhibited the clinically manageable safety profile in the study population including patients with MBC who developed peripheral neuropathy. Together, eribulin is a potential therapeutic option in the clinical settings.
Acknowledgments
The authors thank Satoshi Sakima, MD, for his gracious review of the manuscript and Ms. Masako Nakamura for her technical assistance. The present study was supported by the National Cancer Center Research and Development Fund (23-A-16, 23-A-17, 26-A-4) and Health and Labour Sciences Research Expenses for Commission, Applied Research for Innovative Treatment of Cancer from the Ministry of Health, Labour and Welfare (H26-applied-general-043,046). Furthermore, this research was supported by the Practical Research for Innovative Cancer Control (15ck0106046h0002, 15ck0106049h0002) from Japan Agency for Medical Research and Development, AMED and by Saitama Breast Cancer Clinical Study Group (24). Medical writing was funded by Eisai Co., Ltd.
Author Contributions
KI conceived the study, participated in the design, and drafted the manuscript. KI, KK, and HY conducted the data analysis. KI, TS, KO, KK, HY, TS, KI, and SH played a significant role in the acquisition and interpretation of data and in the critical revision of the manuscript for important intellectual content. All authors read and approved the final manuscript.
Compliance with ethical standards
Conflict of interest
KI received lecture free from Eisai Co., Ltd. Other authors declare that they have no conflict of interest.
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