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[Metronomic chemotherapy with oral cyclophosphamide : An individual option for the metastatic castration-resistant prostate cancer patient?] / Metronomische Chemotherapie mit oralem Cyclophosphamid : Eine individuelle Option für den metastasierten kastrationsresistenten Prostatakarzinompatienten?
Knipper, S; Mandel, P; V Amsberg, G; Strölin, P; Graefen, M; Steuber, T.
Affiliation
  • Knipper S; Martini-Klinik, UKE, Martinistraße 52, 20246, Hamburg, Deutschland. a.knipper@uke.de.
  • Mandel P; Klinik für Urologie, Universitätsklinikum Frankfurt, Frankfurt am Main, Deutschland.
  • V Amsberg G; Klinik und Poliklinik für Onkologie, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Deutschland.
  • Strölin P; Martini-Klinik, UKE, Martinistraße 52, 20246, Hamburg, Deutschland.
  • Graefen M; Martini-Klinik, UKE, Martinistraße 52, 20246, Hamburg, Deutschland.
  • Steuber T; Martini-Klinik, UKE, Martinistraße 52, 20246, Hamburg, Deutschland.
Urologe A ; 58(4): 410-417, 2019 Apr.
Article in De | MEDLINE | ID: mdl-29808369
ABSTRACT

BACKGROUND:

Multiple experimental approaches are meanwhile available for progressive metastatic castration resistant prostate cancer (mCRPC) patients after failure of guideline recommended therapy (i. e., chemotherapy and/or hormonal treatment). We evaluated the outcome of metronomic chemotherapy with cyclophosphamide (CY) in combination with low-dose prednisolone. MATERIALS AND

METHODS:

A total of 14 mCRPC-patients were treated with CY 50 mg/day (plus prednisolone 10 mg/day) between November 2012 and September 2017 after being resistant or unfit for chemotherapy and/or further hormonal treatment. Time to progression and overall survival (OS) were retrospectively determined by using Kaplan-Meier curves.

RESULTS:

Eight of 14 (57.1%) patients had undergone radical prostatectomy and 2 (14.3%) external beam radiation. All patients had at least three therapy lines and 50% had ≥5 mCRPC therapies. The median time from first diagnosis to mCRPC was 88 months; the median age was 78 years with a median baseline serum prostate-specific antigen (PSA) level of 341 ng/ml. With a median follow-up of 16.4 months, progression-free survival (PFS) was 71, 64, and 43% after 2, 4, and 6 months, respectively. Median OS was 8.1 months. No relevant adverse events occurred.

CONCLUSION:

Since CY is a well-tolerated medication with partially good clinical tumor control, it seems to be a convenient, individual treatment option in progressive mCRPC patients after failure of guideline recommended therapy.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antineoplastic Agents, Alkylating / Cyclophosphamide / Prostatic Neoplasms, Castration-Resistant Type of study: Guideline / Observational_studies / Risk_factors_studies Limits: Aged / Humans / Male Language: De Journal: Urologe A Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antineoplastic Agents, Alkylating / Cyclophosphamide / Prostatic Neoplasms, Castration-Resistant Type of study: Guideline / Observational_studies / Risk_factors_studies Limits: Aged / Humans / Male Language: De Journal: Urologe A Year: 2019 Document type: Article