Symptoms and patient-reported well-being : do they predict survival in malignant pleural mesothelioma? A prognostic factor analysis of EORTC-NCIC 08983 : randomized phase III study of cisplatin with or without raltitrexed in patients with malignant pleural mesothelioma
Faculty of Medicine and Health Sciences
Journal of clinical oncology. - New York
, p. 5770-5776
Purpose Malignant pleural mesothelioma (MPM) is a rare disease. Unlike other advanced cancer types, little is known about patient-reported symptoms or health-related quality of life (HRQOL) and their possible prognostic value. This study reports an evaluation of the prognostic value of these factors using data gathered from a recent randomized controlled trial. Patients and Methods Patients were entered onto this trial if they had a histologically proven unresectable MPM, not pretreated with chemotherapy, WHO performance status <= 2, and adequate hematologic, renal, and hepatic function. Patients were randomly assigned to receive cisplatin 80 mg/m(2) intravenously on day 1, without or with preceding infusion of raltitrexed 3 mg/m(2). HRQOL was assessed using the European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30/Lung Cancer 13 tool. The Cox proportional hazards regression model was used for the univariate and multivariate analyses of survival, along with a bootstrap validation technique. Included were the EORTC prognostic index (PI) composed of stage of disease, histology type, time since diagnosis, and WBC, and, in addition, 10 selected key symptoms and HRQOL scales. Results Two hundred fifty patients were randomly assigned (80% male; median age, 58 years; WHO performance status 0, 1, 2 in 25%, 62%, and 13% of cases, respectively). Two hundred twenty-nine patients (91.6%) had a valid HRQOL assessment. The final multivariate model retained the PI, pain (P = .0001), and appetite loss (P = .0100) as independent prognostic indicators of survival. Conclusion Results suggest that the PI, pain, and appetite loss may be independent prognostic factors in patients with advanced MPM.