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Docetaxel, bevacizumab, and androgen deprivation therapy for biochemical disease recurrence after definitive local therapy for prostate cancer.
McKay, Rana R; Gray, Kathryn P; Hayes, Julia H; Bubley, Glenn J; Rosenberg, Jonathan E; Hussain, Arif; Kantoff, Philip W; Taplin, Mary-Ellen.
Affiliation
  • McKay RR; Lank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Gray KP; Lank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Hayes JH; Lank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Bubley GJ; Genitourinary Medical Oncology, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
  • Rosenberg JE; Genitourinary Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, New York.
  • Hussain A; Medical Oncology/Hematology Program, Greenebaum Cancer Center, Baltimore, Maryland.
  • Kantoff PW; Lank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Taplin ME; Lank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Cancer ; 121(15): 2603-11, 2015 Aug 01.
Article in En | MEDLINE | ID: mdl-25903013
ABSTRACT

BACKGROUND:

Patients with biochemical disease recurrence (BCR) after definitive treatment for prostate cancer comprise a heterogeneous population for whom standard therapy options are lacking. The purpose of the current trial was to evaluate the feasibility, toxicity, and efficacy of early multimodality systemic therapy in men with BCR.

METHODS:

Eligible patients had an increasing prostate-specific antigen (PSA) level, a PSA doubling time ≤10 months, and no evidence of metastases after radical prostatectomy (RP) and/or radiotherapy (RT) for localized disease. Treatment consisted of docetaxel at a dose of 75 mg/m(2) every 3 weeks for 4 cycles, bevacizumab at a dose of 15 mg/kg every 3 weeks for 8 cycles, and androgen deprivation therapy (ADT) for 18 months. The primary endpoint was the percentage of patients who were free from PSA progression 1 year after the completion of therapy.

RESULTS:

A total of 41 patients were included in the analysis. At 1 year after the completion of ADT, 45% of patients (13 of 29 patients) and 29% of patients (5 of 17 patients) with a testosterone level ≥100 ng/dL and ≥240 ng/dL, respectively, had a PSA <0.2 ng/mL. The median follow-up was 27.5 months (interquartile range, 21.8-38.1 months). Eight patients (20%) were free from PSA progression, 19 patients (46%) did not reinitiate ADT, and 34 patients (83%) were free from metastasis. Sixteen patients (39%) experienced grade 3 and 5 patients (12%) experienced grade 4 toxicities (toxicity was assessed using the National Cancer Institute Common Terminology Criteria for Adverse Events [version 3.0]).

CONCLUSIONS:

Multimodality systemic therapy with docetaxel, bevacizumab, and ADT is feasible and produces PSA responses in men with BCR. Long-term follow-up is needed to determine the percentage of patients with a durable PSA response who are able to avoid having to reinitiate prostate cancer therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Adenocarcinoma / Antineoplastic Combined Chemotherapy Protocols / Taxoids / Antibodies, Monoclonal, Humanized / Androgen Antagonists / Neoplasm Recurrence, Local Type of study: Clinical_trials Limits: Humans / Male / Middle aged Language: En Journal: Cancer Year: 2015 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Adenocarcinoma / Antineoplastic Combined Chemotherapy Protocols / Taxoids / Antibodies, Monoclonal, Humanized / Androgen Antagonists / Neoplasm Recurrence, Local Type of study: Clinical_trials Limits: Humans / Male / Middle aged Language: En Journal: Cancer Year: 2015 Type: Article