کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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5882744 | 1149597 | 2013 | 5 صفحه PDF | دانلود رایگان |
IntroductionThe standard of care for locoregionally advanced non-small-cell lung cancer is concurrent platinum-based chemoradiation. Many patients relapse, and subsequent systemic treatment may involve platinum-doublet chemotherapy. It is not known if prior platinum-based chemoradiation influences the response to platinum-based chemotherapy given subsequently for relapse. Therefore, we compared outcomes in these patients with those in patients without prior treatment.MethodsA retrospective study of patients who had been treated with carboplatin and gemcitabine chemotherapy for de novo metastatic disease or recurrent non-small-cell lung cancer after receiving platinum-based chemoradiation. The primary outcome was progression-free survival (PFS).ResultsA total of 104 patients were analyzed. The median age was 63 years (range, 35-81 years), with 63 (61%) patients with newly diagnosed disease and with 41 (39%) who were previously treated. The response rate was significantly lower for those previously exposed to chemoradiation (10% vs. 29%: PÂ = .001), as was the median PFS (3.6 months vs. 5.7 months; PÂ = .002), and median overall survival (OS) (8.6 months vs. 12.1 months; PÂ = .007). Only the treatment group was a significant predictor (PÂ = .032) of PFS by univariate analysis. In univariate analysis; sex (men; PÂ = .04), histology (squamous cell; PÂ = .04), Eastern Cooperative Oncology Group Performance Status Scale (PÂ = .002), and treatment group (PÂ = .023) predicted significantly inferior OS. Multivariate analysis showed that performance status was the only significant predictor of inferior OS.ConclusionOutcomes were inferior in patients previously exposed to platinum-based chemoradiation. An approach of stratifying such patients in future trials of chemotherapy should be adopted. Alternative options such as non-platinum-based agents or targeted therapies should be considered in this group.
Journal: Clinical Lung Cancer - Volume 14, Issue 5, September 2013, Pages 508-512