Response to chemotherapy is predictive in relation to longer overall survival in an individual patient combined-analysis with pleural mesothelioma

被引:23
作者
Blayney, Jaine K. [2 ]
Ceresoli, Giovanni L. [3 ]
Castagneto, Bruno [4 ]
O'Brien, Mary E. R. [5 ,6 ]
Hasan, Baktiar
Sylvester, Richard
Rudd, Robin [7 ]
Steele, Jeremy [8 ]
Busacca, Sara [1 ]
Porta, Camillo [9 ]
Mutti, Luciano [10 ]
O'Byrne, Kenneth J. [11 ]
Scullin, Paula [12 ]
Gaafar, Rabab [6 ,13 ]
Baas, Paul [6 ,14 ]
Van Meerbeeck, Jan [6 ,15 ]
Fennell, Dean A. [1 ]
机构
[1] Univ Leicester, Leicester LE1 9HN, Leics, England
[2] Queens Univ Belfast, Ctr Canc Res & Cell Biol, Belfast BT7 1NN, Antrim, North Ireland
[3] Clin Humanitas Gavazzeni, Thorac & Genito Urinary Oncol Unit, Bergamo, Italy
[4] San Giacamo Hosp, Dept Oncol, Novi Ligure, Italy
[5] Royal Marsden Hosp, Sutton, Surrey, England
[6] European Org Res & Treatment Canc EORTC, Lung Canc Grp, Brussels, Belgium
[7] London Lung Canc Grp, London, England
[8] St Bartholomews Hosp, London, England
[9] San Matteo Univ Hosp Fdn, IRCCS, Dept Med Oncol, Pavia, Italy
[10] Vercelli Natl Hlth Trust, Lab Clin Oncol, Vercelli, Italy
[11] St James Hosp, Dublin, Ireland
[12] No Ireland Canc Ctr, Belfast, Antrim, North Ireland
[13] Cairo Univ, Natl Canc Inst, Cairo, Egypt
[14] Netherlands Canc Inst, Dept Thorac Oncol, Amsterdam, Netherlands
[15] Ghent Univ Hosp, Lung Oncol Network, Ghent, Belgium
关键词
Mesothelioma; Survival; Prognosis; Landmark analysis; CANCER COOPERATIVE GROUP; PEMETREXED PLUS CARBOPLATIN; PROGRESSION-FREE SURVIVAL; PHASE-II TRIALS; LUNG-CANCER; MALIGNANT MESOTHELIOMA; TUMOR RESPONSE; EORTC; VINORELBINE; CISPLATIN;
D O I
10.1016/j.ejca.2012.05.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background: There is currently no early predictive marker of survival for patients receiving chemotherapy for malignant pleural mesothelioma (MPM). Tumour response may be predictive for overall survival (OS), though this has not been explored. We have thus undertaken a combined-analysis of OS, from a 42 day landmark, of 526 patients receiving systemic therapy for MPM. We also validate published progression-free survival rates (PFSRs) and a progression-free survival (PFS) prognostic-index model. Methods: Analyses included nine MPM clinical trials incorporating six European Organisation for Research and Treatment of Cancer (EORTC) studies. Analysis of OS from landmark (from day 42 post-treatment) was considered regarding tumour response. PFSR analysis data included six non-EORTC MPM clinical trials. Prognostic index validation was performed on one non-EORTC data-set, with available survival data. Results: Median OS, from landmark, of patients with partial response (PR) was 12.8 months, stable disease (SD), 9.4 months and progressive disease (PD), 3.4 months. Both PR and SD were associated with longer OS from landmark compared with disease progression (both p < 0.0001). PFSRs for platinum-based combination therapies were consistent with published significant clinical activity ranges. Effective separation between PFS and OS curves provided a validation of the EORTC prognostic model, based on histology, stage and performance status. Conclusion: Response to chemotherapy is associated with significantly longer OS from landmark in patients with MPM. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2983 / 2992
页数:10
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