Literature DB >> 25301760

Survival with Newly Diagnosed Metastatic Prostate Cancer in the "Docetaxel Era": Data from 917 Patients in the Control Arm of the STAMPEDE Trial (MRC PR08, CRUK/06/019).

Nicholas David James1, Melissa R Spears2, Noel W Clarke3, David P Dearnaley4, Johann S De Bono4, Joanna Gale5, John Hetherington6, Peter J Hoskin7, Robert J Jones8, Robert Laing9, Jason F Lester10, Duncan McLaren11, Christopher C Parker4, Mahesh K B Parmar2, Alastair W S Ritchie2, J Martin Russell12, Räto T Strebel13, George N Thalmann14, Malcolm D Mason10, Matthew R Sydes2.   

Abstract

BACKGROUND: Prostate cancer (PCa) is the second most common disease among men worldwide. It is important to know survival outcomes and prognostic factors for this disease. Recruitment for the largest therapeutic randomised controlled trial in PCa--the Systemic Therapy in Advancing or Metastatic Prostate Cancer: Evaluation of Drug Efficacy: A Multi-Stage Multi-Arm Randomised Controlled Trial (STAMPEDE)--includes men with newly diagnosed metastatic PCa who are commencing long-term androgen deprivation therapy (ADT); the control arm provides valuable data for a prospective cohort.
OBJECTIVE: Describe survival outcomes, along with current treatment standards and factors associated with prognosis, to inform future trial design in this patient group. DESIGN, SETTING, AND PARTICIPANTS: STAMPEDE trial control arm comprising men newly diagnosed with M1 disease who were recruited between October 2005 and January 2014. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Overall survival (OS) and failure-free survival (FFS) were reported by primary disease characteristics using Kaplan-Meier methods. Hazard ratios and 95% confidence intervals (CIs) were derived from multivariate Cox models. RESULTS AND LIMITATIONS: A cohort of 917 men with newly diagnosed M1 disease was recruited to the control arm in the specified interval. Median follow-up was 20 mo. Median age at randomisation was 66 yr (interquartile range [IQR]: 61-71), and median prostate-specific antigen level was 112 ng/ml (IQR: 34-373). Most men (n=574; 62%) had bone-only metastases, whereas 237 (26%) had both bone and soft tissue metastases; soft tissue metastasis was found mainly in distant lymph nodes. There were 238 deaths, 202 (85%) from PCa. Median FFS was 11 mo; 2-yr FFS was 29% (95% CI, 25-33). Median OS was 42 mo; 2-yr OS was 72% (95% CI, 68-76). Survival time was influenced by performance status, age, Gleason score, and metastases distribution. Median survival after FFS event was 22 mo. Trial eligibility criteria meant men were younger and fitter than general PCa population.
CONCLUSIONS: Survival remains disappointing in men presenting with M1 disease who are started on only long-term ADT, despite active treatments being available at first failure of ADT. Importantly, men with M1 disease now spend the majority of their remaining life in a state of castration-resistant relapse. PATIENT
SUMMARY: Results from this control arm cohort found survival is relatively short and highly influenced by patient age, fitness, and where prostate cancer has spread in the body.
Copyright © 2014 The Authors. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Control arm cohort; Hormone-naïve; Metastatic; Natural history; Prognostic factors; Prospective data; Prostate cancer; Survival; Time to progression

Mesh:

Substances:

Year:  2014        PMID: 25301760     DOI: 10.1016/j.eururo.2014.09.032

Source DB:  PubMed          Journal:  Eur Urol        ISSN: 0302-2838            Impact factor:   20.096


  123 in total

Review 1.  Multidisciplinary intervention of early, lethal metastatic prostate cancer: Report from the 2015 Coffey-Holden Prostate Cancer Academy Meeting.

Authors:  Andrea K Miyahira; Joshua M Lang; Robert B Den; Isla P Garraway; Tamara L Lotan; Ashley E Ross; Tanya Stoyanova; Steve Y Cho; Jonathan W Simons; Kenneth J Pienta; Howard R Soule
Journal:  Prostate       Date:  2015-10-19       Impact factor: 4.104

2.  Prostate Cancer Screening and Management in Solid Organ Transplant Candidates and Recipients.

Authors:  Ezequiel Becher; Alex Wang; Herbert Lepor
Journal:  Rev Urol       Date:  2019

3.  Loss of KMT2D induces prostate cancer ROS-mediated DNA damage by suppressing the enhancer activity and DNA binding of antioxidant transcription factor FOXO3.

Authors:  Shidong Lv; Haoran Wen; Xiongwei Shan; Jianhua Li; Yaobin Wu; Xinpei Yu; Wenhua Huang; Qiang Wei
Journal:  Epigenetics       Date:  2019-06-28       Impact factor: 4.528

Review 4.  The roles of microRNAs in the progression of castration-resistant prostate cancer.

Authors:  Satoko Kojima; Yusuke Goto; Yukio Naya
Journal:  J Hum Genet       Date:  2016-06-09       Impact factor: 3.172

Review 5.  Should docetaxel be standard of care for patients with metastatic hormone-sensitive prostate cancer? Pro and contra.

Authors:  K Fizazi; C Jenkins; I F Tannock
Journal:  Ann Oncol       Date:  2015-05-22       Impact factor: 32.976

6.  Androgen receptor splice variant V7 (AR-V7) in circulating tumor cells: a coming of age for AR splice variants?

Authors:  C Sprenger; T Uo; S Plymate
Journal:  Ann Oncol       Date:  2015-07-21       Impact factor: 32.976

Review 7.  [Chemohormonal therapy for metastatic prostate cancer : Taxane-based approaches].

Authors:  Annabel Spek
Journal:  Urologe A       Date:  2019-04       Impact factor: 0.639

8.  V-ATPase Inhibition Decreases Mutant Androgen Receptor Activity in Castrate-resistant Prostate Cancer.

Authors:  Bradleigh Whitton; Haruko Okamoto; Matthew Rose-Zerilli; Graham Packham; Simon J Crabb
Journal:  Mol Cancer Ther       Date:  2021-02-09       Impact factor: 6.261

Review 9.  Treatment of the primary tumor in metastatic prostate cancer.

Authors:  Ye Yuan; Amar U Kishan; Nicholas G Nickols
Journal:  World J Urol       Date:  2018-11-19       Impact factor: 4.226

Review 10.  The role of surgery in high risk and advanced prostate cancer: A narrative review.

Authors:  Chloe Sheila Dayan Roy; Ashwin Sachdeva; Gokul Vignesh Kandaswamy; Bhavan Prasad Rai
Journal:  Turk J Urol       Date:  2020-10-30
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.