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Efficacy of metronomic oral cyclophosphamide with low dose dexamethasone and celecoxib in metastatic castration‐resistant prostate cancer
Author(s) -
Jeong Yumun,
Lee Jae Lyun
Publication year - 2017
Publication title -
asia‐pacific journal of clinical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.73
H-Index - 29
eISSN - 1743-7563
pISSN - 1743-7555
DOI - 10.1111/ajco.12583
Subject(s) - medicine , docetaxel , prostate cancer , cyclophosphamide , adverse effect , celecoxib , chemotherapy , urology , prostate specific antigen , oncology , dexamethasone , cancer
Aim This study aimed to assess the efficacy and safety of oral metronomic chemotherapy in patients with metastatic castration‐resistant prostate cancer (mCRPC). Methods From January 2011 to February 2013, 60 patients with mCRPC received daily metronomic oral cyclophosphamide (50 mg qd), dexamethasone (1 mg qd) and celecoxib (200 mg bid). Among them 49 patients who met the preset inclusion criteria were included in this retrospective study. Adverse events and activity for reducing serum prostate‐specific antigen (PSA) levels, Response Evaluation Criteria in Solid Tumor responses and symptomatic responses were reviewed. The primary endpoints were PSA response rate and time to PSA progression (TTPSA). Results Twenty‐two patients had previous exposure to docetaxel. The median age was 71 years (range, 49–88) with a median Eastern Cooperative Oncology Group performance of 1 (range, 0–2). The Gleason score was 8 or more in 41 patients (84%) with a median baseline serum PSA of 32.1 ng/mL (range, 1.2–743.0). The PSA response rate was 39%. With a median follow‐duration of 17.5 months, the median TTPSA was 5.2 months (95% CI: 3.1–7.4). The median time to composite progression was 3.9 months (95% CI: 2.2–5.6) and a median overall survival was 13.3 months (95% CI: 9.5–17.1 months). There were no significant differences in the TTPSA between the pre‐ and post‐docetaxel groups. Grade 3–4 AEs occurred only in six patients. Conclusion Metronomic oral cyclophosphamide chemotherapy is safe, well‐tolerated and shows promising activity against mCRPC.