Cytoreductive radical prostatectomy in metastatic prostate cancer: Does it really make sense? Review uri icon

Overview

abstract

  • PURPOSE: Surgical removal of the primary tumor in metastatic prostate cancer (mPCa) is becoming a hotly debated issue. The purpose of this review was to summarize the current knowledge on cytoreductive radical prostatectomy (cRP) in this setting. MATERIALS AND METHODS: We performed a non-systematic Medline/PubMed literature search of articles published in the field between January 2000 and April 2015. RESULTS: Cytoreductive surgery has demonstrated its benefit in various malignancies with a solid biological rationale to justify its assessment in mPCa. cRP appears as a safe and feasible procedure in expert hands and well-selected patients. A growing body of evidence suggests a survival benefit for patients undergoing cRP as a part of a multimodal approach compared to those treated with systemic treatment alone. Nevertheless, little is known about the best clinical and tumor characteristics for the selection of patients most likely to benefit from cRP. The current literature is based on retrospective studies with small cohorts and limited follow-up or large uncontrolled population-based studies. CONCLUSIONS: Data from various other malignancies together with the biological rationale and preliminary results in PCa suggest that cytoreductive surgery may be an option in some mPCa patients. The lack of randomized controlled trials and the low level of evidence in the current literature preclude any firms conclusion on the benefit of cRP in mPCa. Ongoing phase II and future phase III studies are mandatory to define the exact role of cRP in mPCa and to identify the patients who are most likely to benefit from cRP.

publication date

  • August 8, 2016

Research

keywords

  • Bone Neoplasms
  • Carcinoma
  • Cytoreduction Surgical Procedures
  • Prostatectomy
  • Prostatic Neoplasms

Identity

Scopus Document Identifier

  • 84981161394

Digital Object Identifier (DOI)

  • 10.1007/s00345-016-1906-3

PubMed ID

  • 27502935

Additional Document Info

volume

  • 35

issue

  • 4