Skip to main content
Erschienen in: BMC Cancer 1/2018

Open Access 01.12.2018 | Research article

Prognostic value of an automated bone scan index for men with metastatic castration-resistant prostate cancer treated with cabazitaxel

verfasst von: Koichi Uemura, Yasuhide Miyoshi, Takashi Kawahara, Jikuya Ryosuke, Daisuke Yamashita, Shuko Yoneyama, Yumiko Yokomizo, Kazuki Kobayashi, Takeshi Kishida, Masahiro Yao, Hiroji Uemura

Erschienen in: BMC Cancer | Ausgabe 1/2018

Abstract

Background

A computer-assisted diagnostic system for analyzing bone scans (BONENAVI) calculates the automated bone scan index (aBSI). Here we evaluated the aBSI as a prognostic imaging biomarker for men with metastatic castration-resistant prostate cancer (mCRPC) treated with cabazitaxel.

Methods

We retrospectively analyzed 48 patients who received cabazitaxel for mCRPC and evaluated the ability of the aBSI to predict overall survival (OS). The Cox proportional hazards model was used to investigate the associations between baseline aBSI at cabazitaxel treatment and OS with the clinical variables as follows: age, number of cycles of docetaxel, serum prostate-specific antigen, hemoglobin (Hb), lactate dehydrogenase (LDH), and alkaline phosphatase. We determined the C-index to evaluate the discriminatory ability of our models when we included or excluded the aBSI from the analyses.

Results

The median OS after cabazitaxel treatment was 10.0 months, and patients with aBSI ≤1% achieved significantly longer OS compared with patients with aBSI ≥1%. Multivariate analysis showed that age, Hb, LDH, and aBSI were independent prognostic factors of OS. Adding aBSI to the base model increased the C-index from 0.78 to 0.80.

Conclusions

The aBSI may serve as a useful imaging biomarker for predicting OS among men with mCRPC treated with cabazitaxel. Prospective studies are required to establish the value of aBSI as prognostic imaging biomarker.
Abkürzungen
aBSI
Automated bone scan index
ALP
Alkaline phosphatase
CI
Confidence interval
EOD
Extent of disease
Hb
Hemoglobin
HR
Hazard ratio
LDH
Lactate dehydrogenase
mCRPC
Metastatic castration-resistant prostate cancer
OS
Overall survival
PSA
Prostate-specific antigen

Background

Although 80%–90% of prostate cancers with metastasis respond to initial hormone therapy, most patients finally develop to metastatic castration-resistant prostate cancer (mCRPC) [1, 2]. Sipuleucel-T, abiraterone acetate, enzalutamide, docetaxel, cabazitaxel, and radium-223 have all improved survival among men with mCRPC and have been approved in western countries [3, 4].
Cabazitaxel is the first chemotherapeutic agent to prolong overall survival (OS) of patients with mCRPC who are administered docetaxel. A phase III randomized controlled clinical trial (TROPIC) found that cabazitaxel prolongs OS compared with mitoxantrone and reduces the relative risk of death by 30% [5]. Accordingly, cabazitaxel is widely used for patients with mCRPC. However, no clinical biomarkers are available for predicting survival.
A computer-assisted diagnostic system for analyzing bone scans (BONENAVI; Fujifilm RI Pharma Co. Ltd., Tokyo, Japan) calculates the automated bone scan index (aBSI) that provides an objective and quantitative evaluation of the burden imposed by bone metastasis [6]. The prognostic value of aBSI as a biomarker was evaluated for predicting the survival of men treated with life-prolonging agents such as enzalutamide [7], abiraterone [7, 8], docetaxel [911], and radium-223 [12]. Here we conducted a retrospective analysis of the relationship between OS and baseline aBSI of patients with mCRPC treated with cabazitaxel.

Methods

Study design, patients, and treatment

We retrospectively analyzed 48 patients who were treated with cabazitaxel for bone-metastatic mCRPC between 2014 and 2016 at Yokohama City University Medical Center, Yokohama City University Hospital, and their associated hospitals. All patients had histologically confirmed prostate adenocarcinoma. The 2009 TNM clinical staging system and the 2005 International Society of Urologic Pathology Gleason grading system were used [13]. The clinical stages of all patients were evaluated using chest and body computed tomography as well as bone scans upon initiation of cabazitaxel treatment.
All patients were initially treated with androgen deprivation therapy (medical or surgical castration with an antiandrogen). After failure to CRPC, all patients were administered enzalutamide, abiraterone, or both, followed by docetaxel with dexamethasone, before cabazitaxel was administered. All patients received continuous androgen ablation therapy (an LH-RH analog) and oral dexamethasone (0.5–1.0 mg). Cabazitaxel treatment was continued until disease progression or unacceptable adverse events occurred.
Some patients received bisphosphonate or denosumab after the development of mCRPC. Patients were not administered sipuleucel-T and radium-223. For terminally ill patients, palliative therapy and pain control using morphine and palliative external beam radiotherapy were used as appropriate. Serum prostate-specific antigen (PSA) levels were measured using the Elecsys Total PSA Assay (Roche Diagnostics Corp., Basle, Switzerland).

Bone scan index

Bone scan images were obtained within 1 month before or after initiating cabazitaxel treatment and analyzed using BONENAVI version 2 [14]. The automated method for analysis of anterior and posterior whole-body bone scan images was previously described [15]. The aBSI was calculated as the percentage of the sum of all hot-spots classified as bone metastases using the artificial neural network (ANN) values [14].

Statistical analysis

The Cox proportional hazards model with stepwise regression analysis was used to investigate the association between aBSI, OS, and clinical variables of patients treated with cabazitaxel as follows: age, number of cycles of docetaxel, serum PSA, hemoglobin (Hb), lactate dehydrogenase (LDH), and alkaline phosphatase (ALP). The cut-off values for age, number of cycles of docetaxel, serum PSA, Hb, LDH, and ALP were determined according to the median value of each variable. The cut-off value of aBSI was defined as 1.0% according to published studies [10, 15]. The relative risks and 95% confidence intervals (CIs) were calculated, and the C-index was used to assess the discriminatory ability of our models.
The Kaplan–Meier product-limit was used to estimate the survival distribution. The log-rank test was used for the analysis of survival differences. All statistical tests were two-sided, and the significance level was defined as alpha = 0.05. All analyses were conducted using IBM SPSS Statistics software for Windows, version 24 (IBM Corp., Armonk, NY, USA) and the R package (R Foundation for Statistical Computing, Vienna, Austria).
The experimental procedures were conducted in accordance with the ethical standards of the Helsinki Declaration.

Results

Patients’ characteristics are shown in Table 1. Among the 48 patients, the sites of metastasis were as follows: 13, only bone; 12, lymph node + bone; 3, visceral + bone; and 20, visceral + lymph node + bone. The median baseline PSA value was 152.1 ng/ml, and the median aBSI was 3.5% (range, 0.0%–12.9%). Twenty-five (56.2%) patients died, and all deaths were caused by prostate cancer. The median OS after cabazitaxel treatment was initiated was 10.0 months (95%CI, 7.8–12.2) (Fig. 1). A Kaplan–Meier curve of OS after cabazitaxel treatment as a function of aBSI is shown in Fig. 2. The median OS of patients with aBSI < 1% (n = 17) and aBSI ≥1% (n = 31) was not reached and 7.8 months (95%CI: 4.6–10.9), respectively. Patients with aBSI < 1% had a significantly longer OS compared with patients with aBSI ≥1% (p = 0.027).
Table 1
Patients’ characteristics
Variables
 
Median age, years (range)
71.2 (52.5–82.9)
Cycles of docetaxel, cycles (range)
9 (1–55)
Use of enzalutamide, n (%)
35 (72.9)
Use of abiraterone acetate, n (%)
26 (54.1)
Median aBSI, %, (range)
3.5 (0.0–12.9)
Median baseline PSA, ng/mL (range)
152.1 (1.6–3564.0)
Median baseline Hb, g/dL (range)
11.0 (8.1–14.2)
Median baseline LDH, IU/L (range)
262 (124–3509)
Median baseline ALP, IU/L (range)
414 (111–3653)
Lymph node metastasis, n (%)
32 (66.6)
Visceral metastasis, n (%)
23 (47.9)
Cycles of cabazitaxel, cycles (range)
4 (1–15)
Median observation period, months (range)
7.2 (0.6–25.0)
Cancer death, n (%)
25 (56.2)
aBSI automated bone scan index, ALP alkaline phosphatase, Hb hemoglobin, LDH lactate dehydrogenase, PSA prostate-specific antigen
Univariate analysis revealed that age (hazard ratio [HR], 2.6; 95%CI, 1.1–6.0; p = 0.023), Hb (HR, 3.6; 95%CI, 1.6–8.1; p = 0.002), LDH (HR, 3.0; 95%CI 1.3–6.5; p = 0.008), and aBSI (HR, 3.1; 95%CI, 1.1–9.2; p = 0.036) were prognostic factors for OS (Table 2). Multivariate analysis demonstrated that age (HR, 3.4; 95%CI, 1.3–9.1; p = 0.013), Hb (HR, 2.6; 95%CI, 1.1–6.2; p = 0.034), LDH (HR, 3.3; 95%CI, 1.3–8.6; p = 0.014), and aBSI (HR, 5.8; 95%CI, 1.1–30.3; p = 0.031) were independent prognostic factors of OS (Table 3).
Table 2
Univariate analysis of predictions of overall survival of men with metastatic castration-resistant prostate cancer treated with cabazitaxel
 
HR
95% CI
P value
Lower
Upper
Age (≥71.2 years vs < 71.2)
2.6
1.1
6.0
0.023
Number of cycles of docetaxel (≥10 cycles vs ≤9)
0.8
0.4
1.7
0.533
Baseline aBSI (≥1.0% vs < 1.0)
3.1
1.1
9.2
0.036
Baseline PSA (≥152.1 ng/mL vs < 152.1)
1.7
0.7
3.7
0.218
Baseline Hb (<  11.0 g/dL vs ≥11.0)
3.6
1.6
8.1
0.002
Baseline LDH (≥262 IU/L vs < 262)
3.0
1.3
6.5
0.008
Baseline ALP (≥414 IU/L vs < 414)
2.0
0.9
4.5
0.100
aBSI automated bone scan index, ALP alkaline phosphatase, Hb hemoglobin, LDH lactate dehydrogenase, PSA prostate-specific antigen
Table 3
Multivariate analysis of predictions of overall survival of men with metastatic castration-resistant prostate cancer treated with cabazitaxel
 
HR
95% CI
P value
Lower
Upper
Age (≥71.2 years vs < 71.2)
3.4
1.3
9.1
0.013
Number of cycles of docetaxel (≥10 cycles vs ≤9)
0.8
0.3
2.8
0.781
Baseline aBSI (≥1.0% vs < 1.0)
5.8
1.1
30.3
0.031
Baseline PSA (≥152.1 ng/mL vs < 152.1)
0.8
0.2
2.9
0.769
Baseline Hb (<  11.0 g/dL vs ≥11.0)
2.6
1.1
6.2
0.034
Baseline LDH (≥262 IU/L vs < 262)
3.3
1.3
8.6
0.014
Baseline ALP (≥414 IU/L vs < 414)
0.5
0.2
1.6
0.255
aBSI automated bone scan index, ALP alkaline phosphatase, Hb hemoglobin, LDH lactate dehydrogenase, PSA prostate-specific antigen
We evaluated the discriminatory ability of our models by determining the C-index. The C-index in our model when aBSI was included was 0.80 for predicting OS after cabazitaxel treatment was initiated. When we analyzed the discriminatory ability of the model after excluding aBSI, we found that the C-index was 0.78 for predicting OS.
Finally, we stratified the patients into cohorts at low risk (0–2 risk factor, n = 26) or high risk (3–4 risk factors, n = 22) (Table 4). There was a statistically significant difference in OS between these groups (p < 0.001) (Fig. 3).
Table 4
Distributions of the risk factors in the low and high risk groups
 
Age ≥ 71.2 years
Hb < 11.0 g/dL
LDH ≥ 262 IU/L
aBSI≥1.0%
Low risk (n = 26), n (%)
8 (30.8)
5 (19.2)
6 (23.1)
13 (50.0)
High risk (n = 22), n (%)
16(72.7)
18 (81.8)
18 (81.8)
18 (81.8)
aBSI automated bone scan index, Hb hemoglobin, LDH lactate dehydrogenase

Discussion

The aBSI is useful imaging biomarker for predicting the survival of men with prostate cancer, including those with hormone-naïve prostate cancer or mCRPC [6, 9, 11, 1620]. For example, the survival of patients with mCRPC with aBSI ≥3% is shorter compared with men with aBSI < 3% who are treated with taxane-based chemotherapy [9]. Further, men with mCRPC with aBSI > 1% survive for shorter times compared with those with aBSI ≤1% who are treated with docetaxel [10]. Moreover, the aBSI is superior compared with the EOD score as a prognostic imaging biomarker [10].
Recent study demonstrated that not only baseline aBSI before treatment, but also aBSI change after treatment could be useful for prognostic imaging biomarker. Miyoshi et al. reported that decreased aBSI after abirateone acetate or enzalutamide was an independent predictor for longer OS among men with mCRPC [7]. Reza et al. also reported that aBSI change after abirateone acetate was related to survival time in mCRPC patients [8]. On the other hand, Fosbol et al. reported that aBSI was a prognostic biomarker for mCRPC patients received with Ra-223, although there was no significant association between aBSI change during Ra-223 therapy and OS [12].
Here we analyzed the association between OS, aBSI, and clinical variables of patients with mCRPC who were treated with cabazitaxel. We identified age, Hb, LDH, and aBSI as independent prognostic factors of OS. Including the aBSI in the base model improved the C-index from 0.78 to 0.80. Therefore, the aBSI may serve as a promising imaging biomarker for predicting OS among men with mCRPC who are treated with cabazitaxel. Further, the aBSI may provide useful information about such patients.
Although we show here that the aBSI played an important role in evaluating bone metastases, our study has several limitations. For example, our study was retrospective, the number of subjects was small, and the observation periods were relatively short. Prospective evaluation of larger patient populations and longer observations are warranted to establish the usefulness of the aBSI as a prognostic imaging biomarker.

Conclusion

Our analyses strongly indicate that the aBSI may serve as a useful tool for risk stratification of patients with mCRPC undergoing treatment with cabazitaxel.

Availability of data and materials

All data used for this study are available from the corresponding author upon reasonable request.
The Institutional Review Board of Yokohama City University Medical Center approved this study. Informed consent to participate in the study was obtained from the subjects.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
Literatur
1.
Zurück zum Zitat Small EJ, Vogelzang NJ. Second-line hormonal therapy for advanced prostate cancer: a shifting paradigm. J Clin Oncol. 1997;15(1):382–8.CrossRefPubMed Small EJ, Vogelzang NJ. Second-line hormonal therapy for advanced prostate cancer: a shifting paradigm. J Clin Oncol. 1997;15(1):382–8.CrossRefPubMed
2.
Zurück zum Zitat Oh WK, Kantoff PW. Management of hormone refractory prostate cancer: current standards and future prospects. J Urol. 1998;160(4):1220–9.CrossRefPubMed Oh WK, Kantoff PW. Management of hormone refractory prostate cancer: current standards and future prospects. J Urol. 1998;160(4):1220–9.CrossRefPubMed
3.
Zurück zum Zitat Agarwal N, Di Lorenzo G, Sonpavde G, Bellmunt J. New agents for prostate cancer. Ann Oncol. 2014;25(9):1700–9.CrossRefPubMed Agarwal N, Di Lorenzo G, Sonpavde G, Bellmunt J. New agents for prostate cancer. Ann Oncol. 2014;25(9):1700–9.CrossRefPubMed
4.
5.
Zurück zum Zitat de Bono JS, Oudard S, Ozguroglu M, Hansen S, Machiels JP, Kocak I, Gravis G, Bodrogi I, Mackenzie MJ, Shen L, et al. Prednisone plus cabazitaxel or mitoxantrone for metastatic castration-resistant prostate cancer progressing after docetaxel treatment: a randomised open-label trial. Lancet (London, England). 2010;376(9747):1147–54.CrossRef de Bono JS, Oudard S, Ozguroglu M, Hansen S, Machiels JP, Kocak I, Gravis G, Bodrogi I, Mackenzie MJ, Shen L, et al. Prednisone plus cabazitaxel or mitoxantrone for metastatic castration-resistant prostate cancer progressing after docetaxel treatment: a randomised open-label trial. Lancet (London, England). 2010;376(9747):1147–54.CrossRef
6.
Zurück zum Zitat Horikoshi H, Kikuchi A, Onoguchi M, Sjostrand K, Edenbrandt L. Computer-aided diagnosis system for bone scintigrams from Japanese patients: importance of training database. Ann Nucl Med. 2012;26(8):622–6.CrossRefPubMedPubMedCentral Horikoshi H, Kikuchi A, Onoguchi M, Sjostrand K, Edenbrandt L. Computer-aided diagnosis system for bone scintigrams from Japanese patients: importance of training database. Ann Nucl Med. 2012;26(8):622–6.CrossRefPubMedPubMedCentral
7.
Zurück zum Zitat Miyoshi Y, Uemura K, Kawahara T, Yoneyama S, Hattori Y, Teranishi JI, Ohta JI, Takebayashi S, Yokomizo Y, Hayashi N, et al. Prognostic value of automated bone scan index in men with metastatic castration-resistant prostate Cancer treated with Enzalutamide or Abiraterone acetate. Clin Genitourin Cancer. 2017;15(4):472–8.CrossRefPubMed Miyoshi Y, Uemura K, Kawahara T, Yoneyama S, Hattori Y, Teranishi JI, Ohta JI, Takebayashi S, Yokomizo Y, Hayashi N, et al. Prognostic value of automated bone scan index in men with metastatic castration-resistant prostate Cancer treated with Enzalutamide or Abiraterone acetate. Clin Genitourin Cancer. 2017;15(4):472–8.CrossRefPubMed
8.
Zurück zum Zitat Reza M, Ohlsson M, Kaboteh R, Anand A, Franck-Lissbrant I, Damber JE, Widmark A, Thellenberg-Karlsson C, Budaus L, Steuber T, et al. Bone scan index as an imaging biomarker in metastatic castration-resistant prostate Cancer: a multicentre study based on patients treated with Abiraterone acetate (Zytiga) in clinical practice. Eur Urol Focus. 2016;2(5):540–6.CrossRefPubMed Reza M, Ohlsson M, Kaboteh R, Anand A, Franck-Lissbrant I, Damber JE, Widmark A, Thellenberg-Karlsson C, Budaus L, Steuber T, et al. Bone scan index as an imaging biomarker in metastatic castration-resistant prostate Cancer: a multicentre study based on patients treated with Abiraterone acetate (Zytiga) in clinical practice. Eur Urol Focus. 2016;2(5):540–6.CrossRefPubMed
9.
Zurück zum Zitat Mitsui Y, Shiina H, Yamamoto Y, Haramoto M, Arichi N, Yasumoto H, Kitagaki H, Igawa M. Prediction of survival benefit using an automated bone scan index in patients with castration-resistant prostate cancer. BJU Int. 2012;110(11 Pt B):E628–34.CrossRefPubMed Mitsui Y, Shiina H, Yamamoto Y, Haramoto M, Arichi N, Yasumoto H, Kitagaki H, Igawa M. Prediction of survival benefit using an automated bone scan index in patients with castration-resistant prostate cancer. BJU Int. 2012;110(11 Pt B):E628–34.CrossRefPubMed
10.
Zurück zum Zitat Uemura K, Miyoshi Y, Kawahara T, Yoneyama S, Hattori Y, Teranishi J, Kondo K, Moriyama M, Takebayashi S, Yokomizo Y, et al. Prognostic value of a computer-aided diagnosis system involving bone scans among men treated with docetaxel for metastatic castration-resistant prostate cancer. BMC Cancer. 2016;16:109.CrossRefPubMedPubMedCentral Uemura K, Miyoshi Y, Kawahara T, Yoneyama S, Hattori Y, Teranishi J, Kondo K, Moriyama M, Takebayashi S, Yokomizo Y, et al. Prognostic value of a computer-aided diagnosis system involving bone scans among men treated with docetaxel for metastatic castration-resistant prostate cancer. BMC Cancer. 2016;16:109.CrossRefPubMedPubMedCentral
11.
Zurück zum Zitat Kaboteh R, Gjertsson P, Leek H, Lomsky M, Ohlsson M, Sjostrand K, Edenbrandt L. Progression of bone metastases in patients with prostate cancer - automated detection of new lesions and calculation of bone scan index. EJNMMI Res. 2013;3(1):64.CrossRefPubMedPubMedCentral Kaboteh R, Gjertsson P, Leek H, Lomsky M, Ohlsson M, Sjostrand K, Edenbrandt L. Progression of bone metastases in patients with prostate cancer - automated detection of new lesions and calculation of bone scan index. EJNMMI Res. 2013;3(1):64.CrossRefPubMedPubMedCentral
12.
Zurück zum Zitat Fosbol MO, Petersen PM, Daugaard G, Holm S, Kjaer A, Mortensen J. Impact of treatment delay in Radium-223 therapy of metastatic castration-resistant prostate cancer patients. Ann Nucl Med. 2018;32(1):16–21.CrossRefPubMed Fosbol MO, Petersen PM, Daugaard G, Holm S, Kjaer A, Mortensen J. Impact of treatment delay in Radium-223 therapy of metastatic castration-resistant prostate cancer patients. Ann Nucl Med. 2018;32(1):16–21.CrossRefPubMed
13.
Zurück zum Zitat Epstein JI, Allsbrook WC Jr, Amin MB, Egevad LL, Committee IG. The 2005 International Society of Urological Pathology (ISUP) consensus conference on Gleason grading of prostatic carcinoma. Am J Surg Pathol. 2005;29(9):1228–42.CrossRefPubMed Epstein JI, Allsbrook WC Jr, Amin MB, Egevad LL, Committee IG. The 2005 International Society of Urological Pathology (ISUP) consensus conference on Gleason grading of prostatic carcinoma. Am J Surg Pathol. 2005;29(9):1228–42.CrossRefPubMed
14.
Zurück zum Zitat Koizumi M, Wagatsuma K, Miyaji N, Murata T, Miwa K, Takiguchi T, Makino T, Koyama M. Evaluation of a computer-assisted diagnosis system, BONENAVI version 2, for bone scintigraphy in cancer patients in a routine clinical setting. Ann Nucl Med. 2015;29(2):138–48.CrossRefPubMed Koizumi M, Wagatsuma K, Miyaji N, Murata T, Miwa K, Takiguchi T, Makino T, Koyama M. Evaluation of a computer-assisted diagnosis system, BONENAVI version 2, for bone scintigraphy in cancer patients in a routine clinical setting. Ann Nucl Med. 2015;29(2):138–48.CrossRefPubMed
15.
Zurück zum Zitat Ulmert D, Kaboteh R, Fox JJ, Savage C, Evans MJ, Lilja H, Abrahamsson PA, Bjork T, Gerdtsson A, Bjartell A, et al. A novel automated platform for quantifying the extent of skeletal tumour involvement in prostate cancer patients using the bone scan index. Eur Urol. 2012;62(1):78–84.CrossRefPubMedPubMedCentral Ulmert D, Kaboteh R, Fox JJ, Savage C, Evans MJ, Lilja H, Abrahamsson PA, Bjork T, Gerdtsson A, Bjartell A, et al. A novel automated platform for quantifying the extent of skeletal tumour involvement in prostate cancer patients using the bone scan index. Eur Urol. 2012;62(1):78–84.CrossRefPubMedPubMedCentral
16.
Zurück zum Zitat Armstrong AJ, Kaboteh R, Carducci MA, Damber JE, Stadler WM, Hansen M, Edenbrandt L, Forsberg G, Nordle O, Pili R, et al. Assessment of the bone scan index in a randomized placebo-controlled trial of tasquinimod in men with metastatic castration-resistant prostate cancer (mCRPC). Urol Oncol. 2014;32(8):1308–16.CrossRefPubMed Armstrong AJ, Kaboteh R, Carducci MA, Damber JE, Stadler WM, Hansen M, Edenbrandt L, Forsberg G, Nordle O, Pili R, et al. Assessment of the bone scan index in a randomized placebo-controlled trial of tasquinimod in men with metastatic castration-resistant prostate cancer (mCRPC). Urol Oncol. 2014;32(8):1308–16.CrossRefPubMed
17.
Zurück zum Zitat Dennis ER, Jia X, Mezheritskiy IS, Stephenson RD, Schoder H, Fox JJ, Heller G, Scher HI, Larson SM, Morris MJ. Bone scan index: a quantitative treatment response biomarker for castration-resistant metastatic prostate cancer. J Clin Oncol. 2012;30(5):519–24.CrossRefPubMedPubMedCentral Dennis ER, Jia X, Mezheritskiy IS, Stephenson RD, Schoder H, Fox JJ, Heller G, Scher HI, Larson SM, Morris MJ. Bone scan index: a quantitative treatment response biomarker for castration-resistant metastatic prostate cancer. J Clin Oncol. 2012;30(5):519–24.CrossRefPubMedPubMedCentral
18.
Zurück zum Zitat Kaboteh R, Damber JE, Gjertsson P, Hoglund P, Lomsky M, Ohlsson M, Edenbrandt L. Bone scan index: a prognostic imaging biomarker for high-risk prostate cancer patients receiving primary hormonal therapy. EJNMMI Res. 2013;3(1):9.CrossRefPubMedPubMedCentral Kaboteh R, Damber JE, Gjertsson P, Hoglund P, Lomsky M, Ohlsson M, Edenbrandt L. Bone scan index: a prognostic imaging biomarker for high-risk prostate cancer patients receiving primary hormonal therapy. EJNMMI Res. 2013;3(1):9.CrossRefPubMedPubMedCentral
19.
Zurück zum Zitat Kalderstam J, Sadik M, Edenbrandt L, Ohlsson M. Analysis of regional bone scan index measurements for the survival of patients with prostate cancer. BMC Med Imaging. 2014;14:24.CrossRefPubMedPubMedCentral Kalderstam J, Sadik M, Edenbrandt L, Ohlsson M. Analysis of regional bone scan index measurements for the survival of patients with prostate cancer. BMC Med Imaging. 2014;14:24.CrossRefPubMedPubMedCentral
20.
Zurück zum Zitat Poulsen MH, Rasmussen J, Edenbrandt L, Hoilund-Carlsen PF, Gerke O, Johansen A, Lund L. Bone scan index predicts outcome in patients with metastatic hormone sensitive prostate cancer. BJU Int. 2015; Poulsen MH, Rasmussen J, Edenbrandt L, Hoilund-Carlsen PF, Gerke O, Johansen A, Lund L. Bone scan index predicts outcome in patients with metastatic hormone sensitive prostate cancer. BJU Int. 2015;
Metadaten
Titel
Prognostic value of an automated bone scan index for men with metastatic castration-resistant prostate cancer treated with cabazitaxel
verfasst von
Koichi Uemura
Yasuhide Miyoshi
Takashi Kawahara
Jikuya Ryosuke
Daisuke Yamashita
Shuko Yoneyama
Yumiko Yokomizo
Kazuki Kobayashi
Takeshi Kishida
Masahiro Yao
Hiroji Uemura
Publikationsdatum
01.12.2018
Verlag
BioMed Central
Erschienen in
BMC Cancer / Ausgabe 1/2018
Elektronische ISSN: 1471-2407
DOI
https://doi.org/10.1186/s12885-018-4401-y

Weitere Artikel der Ausgabe 1/2018

BMC Cancer 1/2018 Zur Ausgabe

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.