TY - JOUR
T1 - Activity of cabazitaxel after docetaxel and abiraterone acetate therapy in patients with castration-resistant prostate cancer
AU - Sella, Avishay
AU - Sella, Tal
AU - Peer, Avivit
AU - Berger, Raanan
AU - Frank, Stephen Jay
AU - Gez, Eli
AU - Sharide, David
AU - Hayat, Henry
AU - Hanovich, Ekaterina
AU - Kovel, Svetlana
AU - Rosenbaum, Eli
AU - Neiman, Victoria
AU - Keizman, Daniel
N1 - Publisher Copyright:
© 2014 Elsevier Inc. All rights reserved.
PY - 2014
Y1 - 2014
N2 - The efficacy of cabazitaxel (CAB) after abiraterone acetate (AA) inmetastatic castration-resistant prostate cancer (mCRPC) is unknown. Because both affect the androgen receptor (AR) there is a concern about the activity of this sequence.We retrospectively demonstrated a prostate-specific antigen (PSA) response of 31.5%, partial response of 15.3%, and median survival of 8.2 months with CAB. CAB was active after AA and docetaxel in mCRPC. Patients and Methods: One hundred thirty mCRPC patients received AA after docetaxel treatment in compassionate programs. Of them, 24 (18.4%) subsequently received CAB. We retrospectively reviewed their data using conventional methods. Results: Twenty-four patients received a median of 4 (range, 1-13) CAB cycles. Nineteen (79.1%) of them received primary prophylaxis with growth factors. Median patient characteristics were: age 65 (range, 57-85) years; Gleason score: 8 (range, 6-10); and PSA: 128.1 (range, 0.01-1700) ng/mL. A PSA response (≥ 50% decrease from baseline) occurred in 6 (31.5%) of 19 evaluable patients (95% confidence interval [CI], 11.8-54.2%). CAB therapy obtained a partial response in 2 of the 13 (15.3%) evaluable patients (95% CI, 2.9-45.4%). Median survival from initiation of CAB was 8.2 (95% CI, 3.34-13.05) months, from AA 16.1 (95% CI, 11.56-20.64) and from docetaxel 32.0 (95% CI, 11.56-39.69). Conclusion: A limited number of patients with mCRPC received CAB after docetaxel and AA treatment. In this selected population, CAB was active.
AB - The efficacy of cabazitaxel (CAB) after abiraterone acetate (AA) inmetastatic castration-resistant prostate cancer (mCRPC) is unknown. Because both affect the androgen receptor (AR) there is a concern about the activity of this sequence.We retrospectively demonstrated a prostate-specific antigen (PSA) response of 31.5%, partial response of 15.3%, and median survival of 8.2 months with CAB. CAB was active after AA and docetaxel in mCRPC. Patients and Methods: One hundred thirty mCRPC patients received AA after docetaxel treatment in compassionate programs. Of them, 24 (18.4%) subsequently received CAB. We retrospectively reviewed their data using conventional methods. Results: Twenty-four patients received a median of 4 (range, 1-13) CAB cycles. Nineteen (79.1%) of them received primary prophylaxis with growth factors. Median patient characteristics were: age 65 (range, 57-85) years; Gleason score: 8 (range, 6-10); and PSA: 128.1 (range, 0.01-1700) ng/mL. A PSA response (≥ 50% decrease from baseline) occurred in 6 (31.5%) of 19 evaluable patients (95% confidence interval [CI], 11.8-54.2%). CAB therapy obtained a partial response in 2 of the 13 (15.3%) evaluable patients (95% CI, 2.9-45.4%). Median survival from initiation of CAB was 8.2 (95% CI, 3.34-13.05) months, from AA 16.1 (95% CI, 11.56-20.64) and from docetaxel 32.0 (95% CI, 11.56-39.69). Conclusion: A limited number of patients with mCRPC received CAB after docetaxel and AA treatment. In this selected population, CAB was active.
KW - Androgen receptor
KW - Chemotherapy
KW - Docetaxel and Abiraterone failure
KW - Metastatic castration-resistant prostate cancer
KW - Sequential therapy
UR - http://www.scopus.com/inward/record.url?scp=84922707661&partnerID=8YFLogxK
U2 - 10.1016/j.clgc.2014.06.007
DO - 10.1016/j.clgc.2014.06.007
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C2 - 25066221
AN - SCOPUS:84922707661
SN - 1558-7673
VL - 12
SP - 428
EP - 432
JO - Clinical Genitourinary Cancer
JF - Clinical Genitourinary Cancer
IS - 6
ER -