BJU International 2014-12-01

Radiographic progression by Prostate Cancer Working Group (PCWG)-2 criteria as an intermediate endpoint for drug development in metastatic castration-resistant prostate cancer.

Guru Sonpavde, Gregory R Pond, Andrew J Armstrong, Matthew D Galsky, Lance Leopold, Brian A Wood, Shaw-Ling Wang, Jolanda Paolini, Isan Chen, Edna Chow-Maneval, David J Mooney, Mariajose Lechuga, Matthew R Smith, M Dror Michaelson

Index: BJU Int. 114(6b) , E25-31, (2014)

Full Text: HTML

Abstract

To investigate the association of radiographic progression defined by Prostate Cancer Working Group (PCWG)-2 guidelines and overall survival (OS) in men with metastatic castration-resistant prostate cancer (mCRPC).Two trials that used PCWG-2 guidelines to define progression were analysed: a randomized phase II trial (n = 221) comparing first-line docetaxel-prednisone plus AT-101 or placebo, and a phase III trial (n = 873) comparing prednisone plus sunitinib or placebo after docetaxel-based chemotherapy. Cox proportional hazards regression models were used to estimate the association of radiographic progression with OS. Landmark analyses compared progressing patients with those who had not progressed. Sub-analyses compared patients removed from trial for progression vs other reasons.An increased risk of death was seen for radiographic progression at landmark times from 6 to 12 months with docetaxel-based therapy (hazard ratio [HR] >1.7 at all time-points). An increased risk of death was also seen with post-docetaxel prednisone alone or with sunitinib for progression at landmark times from 2 to 8 months (HR >2.7 at all time-points). Kendall's τ was 0.50 (P < 0.001) in the setting of docetaxel-based therapy and 0.34 (P < 0.001) in the post-docetaxel setting for association between radiographic progression and death amongst patients with both events. Removal from study due to radiographic progression was associated with a significantly lower OS compared with removal for other reasons in both trials. Limitations of a retrospective analysis apply and there was no central radiology review.Radiographic progression by PCWG-2 criteria was significantly associated with OS in patients with mCRPC receiving first-line docetaxel-based chemotherapy or post-docetaxel therapy. With external validation as a surrogate endpoint in trials showing survival benefits, the use of radiographic progression-free survival may expedite drug development in mCRPC, which has been hampered by the lack of intermediate endpoints.© 2013 The Authors. BJU International © 2013 BJU International.


Related Compounds

  • Gossypol
  • AT-101
  • Docetaxel
  • Acetate gossypol

Related Articles:

Male contraception: history and development.

2014-02-01

[Urol. Clin. North Am. 41(1) , 145-61, (2014)]

The investigational agent MLN2238 induces apoptosis and is cytotoxic to CLL cells in vitro, as a single agent and in combination with other drugs.

2014-04-01

[Br. J. Haematol. 165(1) , 78-88, (2014)]

(-)-Gossypol-enriched cottonseed oil inhibits proliferation and adipogenesis of human breast pre-adipocytes.

2013-03-01

[Anticancer Res. 33(3) , 949-55, (2013)]

Di(phenylpropylamino)gossypol: a derivative of the dimeric natural product gossypol.

2013-04-01

[Acta Crystallogr. C 69(Pt 4) , 439-43, (2013)]

Gossypol overcomes stroma-mediated resistance to the BCL2 inhibitor ABT-737 in chronic lymphocytic leukemia cells ex vivo.

2013-11-01

[Leukemia 27(11) , 2262-4, (2013)]

More Articles...