2015
DOI: 10.1200/jco.2015.33.15_suppl.5001
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Docetaxel and/or zoledronic acid for hormone-naïve prostate cancer: First overall survival results from STAMPEDE (NCT00268476).

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Cited by 105 publications
(82 citation statements)
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“…In contrast, adding zoledronic acid to standard therapy did not affect survival, and adding the combination of zoledronic acid and docetaxel was not more effective than adding just docetaxel. These findings were presented on 13 May at a presscast in advance of the ASCO 2015 [39]. These and other upcoming trials will begin to define the role of more effective systemic therapy in hormone-sensitive prostate cancer.…”
Section: Role Of Chemotherapy In Hormone-sensitive Diseasementioning
confidence: 80%
“…In contrast, adding zoledronic acid to standard therapy did not affect survival, and adding the combination of zoledronic acid and docetaxel was not more effective than adding just docetaxel. These findings were presented on 13 May at a presscast in advance of the ASCO 2015 [39]. These and other upcoming trials will begin to define the role of more effective systemic therapy in hormone-sensitive prostate cancer.…”
Section: Role Of Chemotherapy In Hormone-sensitive Diseasementioning
confidence: 80%
“…The STAMPEDE trial uses a novel, multi-arm, multi-stage design, enrolling men with locally advanced or metastatic prostate cancer being started on long-term ADT. The addition of docetaxel to long-term ADT in this heterogeneous cohort improved median survival by 10 months (77 vs. 67 months) and resulted in a statistically significant improvement in survival (hazard ratio 0.76 [95 % CI 0.63-0.91; p = 0.003]) [52]. Interestingly, a French multicenter trial also evaluating early docetaxel and ADT for hormone-naïve metastatic prostate cancer, GETUG-15, failed to demonstrate a survival advantage compared to ADT alone [53].…”
Section: Neoadjuvant Chemotherapy and Chemohormonal Therapymentioning
confidence: 91%
“…Preliminary data in the Systemic Therapy in Advancing or Metastatic Prostate cancer: Evaluation of Drug Efficacy (STAMPEDE) trial observed a median overall survival benefit of docetaxel 1 ADT of 10 months (HR, 0.76; 95% CI, 0.63-0.91; P 5 .003) versus standard of care. 80 Of note, the median age of patients in this study is 65 years, and among those randomized to the docetaxel 1 ADT arm, 50% experienced a grade 3 to 5 toxicity versus 31% patients receiving standard of care (no P value available). 80 Certainly, more work is needed in this area to clarify the benefit of adding docetaxel to ADT for high-risk locally advanced PCa and mCRPC.…”
Section: Chemotherapymentioning
confidence: 98%
“…80 Of note, the median age of patients in this study is 65 years, and among those randomized to the docetaxel 1 ADT arm, 50% experienced a grade 3 to 5 toxicity versus 31% patients receiving standard of care (no P value available). 80 Certainly, more work is needed in this area to clarify the benefit of adding docetaxel to ADT for high-risk locally advanced PCa and mCRPC. In addition, it is important to consider the generalizability of such results to older adults, especially considering the high incidence of grade 3 to 5 toxicity reported among a relatively younger, fitter study population.…”
Section: Chemotherapymentioning
confidence: 98%