TY - JOUR
T1 - Efficacy and safety of pemetrexed maintenance therapy versus best supportive care in patients from East Asia with advanced, nonsquamous non-small cell lung cancer
T2 - An exploratory subgroup analysis of a global, randomized, phase 3 clinical trial
AU - Belani, Chandra Prakash
AU - Wu, Yi Long
AU - Chen, Yuh Min
AU - Kim, Joo Hang
AU - Yang, Sung Hyun
AU - Zhang, Li
AU - Peterson, Patrick
AU - Orlando, Mauro
N1 - Funding Information:
The authors acknowledge the independent medical writing assistance provided by Serina Stretton, PhD, and Janelle Keys, PhD, of ProScribe Medical Communications, funded from an unrestricted financial grant from Eli Lilly. ProScribe's services complied with international guidelines for Good Publication Practice (GPP2). The authors also gratefully acknowledge the contribution of the patients, investigators, and investigative site assistants who participated in the trial. The authors also thank Susanna Holt (Eli Lilly) for her editorial and administrative assistance and Yashan Zhou (Eli Lilly) for his assistance with the statistical analysis.
PY - 2012/3
Y1 - 2012/3
N2 - In a recent global phase 3 trial, patients with advanced non-small cell lung cancer (NSCLC), who had not progressed after four cycles of platinum-based induction chemotherapy, were randomized to maintenance therapy with pemetrexed or placebo. The objective of this retrospective, exploratory, post hoc subgroup analysis was to compare outcomes of East Asian patients with non-East Asian patients treated with pemetrexed or placebo. Methods: Only patients with nonsquamous histology were analyzed. Patients were grouped by enrollment location (East Asian = China, Korea, or Taiwan; non-East Asian = all other countries). The Kaplan-Meier method was used to calculate median progression-free survival (PFS) and overall survival (OS) times. Hazard ratios (HRs) were calculated using unadjusted Cox proportional hazard models. Results: Of the 663 patients enrolled in the study, 481 patients had nonsquamous NSCLC: East Asian = 27% and non-East Asian = 73%. In the East Asian subgroup, there were more women, never smokers, and patients with adenocarcinoma. PFS was similar between the subgroups and significantly prolonged in patients treated with pemetrexed than placebo (median PFS: East Asian, 4.4 versus 1.6 months, HR = 0.42, p < 0.001; non-East Asian, 4.5 versus 2.8 months, HR = 0.45, p < 0.001). OS was numerically prolonged in East Asians (median OS: pemetrexed, 19.7 months; placebo, 16.4 months) compared with non-East Asians (pemetrexed, 13.2 months; placebo, 8.5 months). Pemetrexed was reasonably well tolerated with few severe adverse events reported. Conclusion: The results of this subgroup analysis support pemetrexed as maintenance therapy for East Asian patients with advanced, nonsquamous NSCLC.
AB - In a recent global phase 3 trial, patients with advanced non-small cell lung cancer (NSCLC), who had not progressed after four cycles of platinum-based induction chemotherapy, were randomized to maintenance therapy with pemetrexed or placebo. The objective of this retrospective, exploratory, post hoc subgroup analysis was to compare outcomes of East Asian patients with non-East Asian patients treated with pemetrexed or placebo. Methods: Only patients with nonsquamous histology were analyzed. Patients were grouped by enrollment location (East Asian = China, Korea, or Taiwan; non-East Asian = all other countries). The Kaplan-Meier method was used to calculate median progression-free survival (PFS) and overall survival (OS) times. Hazard ratios (HRs) were calculated using unadjusted Cox proportional hazard models. Results: Of the 663 patients enrolled in the study, 481 patients had nonsquamous NSCLC: East Asian = 27% and non-East Asian = 73%. In the East Asian subgroup, there were more women, never smokers, and patients with adenocarcinoma. PFS was similar between the subgroups and significantly prolonged in patients treated with pemetrexed than placebo (median PFS: East Asian, 4.4 versus 1.6 months, HR = 0.42, p < 0.001; non-East Asian, 4.5 versus 2.8 months, HR = 0.45, p < 0.001). OS was numerically prolonged in East Asians (median OS: pemetrexed, 19.7 months; placebo, 16.4 months) compared with non-East Asians (pemetrexed, 13.2 months; placebo, 8.5 months). Pemetrexed was reasonably well tolerated with few severe adverse events reported. Conclusion: The results of this subgroup analysis support pemetrexed as maintenance therapy for East Asian patients with advanced, nonsquamous NSCLC.
UR - http://www.scopus.com/inward/record.url?scp=84857910629&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84857910629&partnerID=8YFLogxK
U2 - 10.1097/JTO.0b013e31823d4f9d
DO - 10.1097/JTO.0b013e31823d4f9d
M3 - Article
C2 - 22157370
AN - SCOPUS:84857910629
SN - 1556-0864
VL - 7
SP - 567
EP - 573
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
IS - 3
ER -