TY - JOUR
T1 - First-line management of metastatic castrate-resistant prostate cancer patients
T2 - Audit of real-life practices
AU - Turpin, Anthony
AU - Pasquier, David
AU - Massard, Christophe
AU - Berdah, Jean François
AU - Culine, Stéphane
AU - Penel, Nicolas
N1 - Publisher Copyright:
© 2017 Société Française du Cancer
PY - 2017/6/1
Y1 - 2017/6/1
N2 - Background No reliable guidelines are available for choosing the best option between docetaxel and new hormonal therapies (NHTs) (i.e., abiraterone and enzalutamide) in first-line therapy for metastatic castration-resistant prostate cancer (mCRPC) patients. We performed an audit of real-life practices. Methods We built an online questionnaire and distributed it with the help of French oncology networks. This questionnaire was sent to 481 physicians who treat patients with mCRPC. All of the answers were declarative, individual, and anonymized. A descriptive analysis was done. A univariate logistic regression analysis was performed for the criteria of choice between docetaxel and NHTs. Results From March to July 2015, 109/481 physicians (22.6%) completed the questionnaire. The selection criteria for initially choosing docetaxel were as follows: presence of visceral metastases (79.8%), heavy tumor burden (68.8%), aggressive tumor disease (66.1%), and short-term efficacy of castration (66.1%). The selection criteria for initially choosing NHTs were as follows: long-term efficacy of castration (66.1%), higher age (67.9%), low tumor grade (56.9%), and absence of symptoms (54.1%). With docetaxel, the first tumor assessment was typically performed after three (1–6) cycles, including prostate-specific antigen (PSA) testing (96.3%), a thoraco-abdominopelvic CT scan (68.8%), and bone scintigraphy (59.6%). With NHTs, tumor assessment was mainly performed after 3 months of treatment (1–6) and included PSA testing, a thoraco-abdominopelvic CT, and bone scintigraphy in 90.8%, 61.5%, and 63.3% of cases, respectively. Conclusions This is the first study assessing real-life practices among physicians who treat patients with mCRPC. These practices were found to be homogeneous.
AB - Background No reliable guidelines are available for choosing the best option between docetaxel and new hormonal therapies (NHTs) (i.e., abiraterone and enzalutamide) in first-line therapy for metastatic castration-resistant prostate cancer (mCRPC) patients. We performed an audit of real-life practices. Methods We built an online questionnaire and distributed it with the help of French oncology networks. This questionnaire was sent to 481 physicians who treat patients with mCRPC. All of the answers were declarative, individual, and anonymized. A descriptive analysis was done. A univariate logistic regression analysis was performed for the criteria of choice between docetaxel and NHTs. Results From March to July 2015, 109/481 physicians (22.6%) completed the questionnaire. The selection criteria for initially choosing docetaxel were as follows: presence of visceral metastases (79.8%), heavy tumor burden (68.8%), aggressive tumor disease (66.1%), and short-term efficacy of castration (66.1%). The selection criteria for initially choosing NHTs were as follows: long-term efficacy of castration (66.1%), higher age (67.9%), low tumor grade (56.9%), and absence of symptoms (54.1%). With docetaxel, the first tumor assessment was typically performed after three (1–6) cycles, including prostate-specific antigen (PSA) testing (96.3%), a thoraco-abdominopelvic CT scan (68.8%), and bone scintigraphy (59.6%). With NHTs, tumor assessment was mainly performed after 3 months of treatment (1–6) and included PSA testing, a thoraco-abdominopelvic CT, and bone scintigraphy in 90.8%, 61.5%, and 63.3% of cases, respectively. Conclusions This is the first study assessing real-life practices among physicians who treat patients with mCRPC. These practices were found to be homogeneous.
KW - Abiraterone
KW - Castrate-resistant prostate cancer
KW - Docetaxel
KW - Enzalutamide
KW - First-line therapy
UR - http://www.scopus.com/inward/record.url?scp=85017158073&partnerID=8YFLogxK
U2 - 10.1016/j.bulcan.2017.02.002
DO - 10.1016/j.bulcan.2017.02.002
M3 - Article
C2 - 28390646
AN - SCOPUS:85017158073
SN - 0007-4551
VL - 104
SP - 552
EP - 558
JO - Bulletin du Cancer
JF - Bulletin du Cancer
IS - 6
ER -