TY - JOUR
T1 - Response to chemotherapy is predictive in relation to longer overall survival in an individual patient combined-analysis with pleural mesothelioma
AU - Blayney, Jaine K.
AU - Ceresoli, Giovanni L.
AU - Castagneto, Bruno
AU - O'Brien, Mary E.R.
AU - Hasan, Baktiar
AU - Sylvester, Richard
AU - Rudd, Robin
AU - Steele, Jeremy
AU - Busacca, Sara
AU - Porta, Camillo
AU - Mutti, Luciano
AU - O'Byrne, Kenneth J.
AU - Scullin, Paula
AU - Gaafar, Rabab
AU - Baas, Paul
AU - Van Meerbeeck, Jan
AU - Fennell, Dean A.
PY - 2012/11/1
Y1 - 2012/11/1
N2 - 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.
AB - 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.
KW - Landmark analysis
KW - Mesothelioma
KW - Prognosis
KW - Survival
UR - http://www.scopus.com/inward/record.url?scp=84867575578&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2012.05.018
DO - 10.1016/j.ejca.2012.05.018
M3 - Article
C2 - 22704893
AN - SCOPUS:84867575578
VL - 48
SP - 2983
EP - 2992
JO - European Journal of Cancer
JF - European Journal of Cancer
SN - 0959-8049
IS - 16
ER -