Original Articles
Treatment-by-Histology Interaction Analyses in Three Phase III Trials Show Superiority of Pemetrexed in Nonsquamous Non-small Cell Lung Cancer

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Introduction:

Recently, histology has emerged as a predictive factor for pemetrexed efficacy in non-small cell lung cancer (NSCLC). These analyses evaluate whether the differential efficacy of pemetrexed by NSCLC histology is reproducible and consistent across three registration studies of different lines of therapy (first-line/second-line and maintenance settings).

Methods:

The reported studies for patients with advanced NSCLC were pemetrexed versus docetaxel in previously treated patients (N = 571), cisplatin plus pemetrexed versus cisplatin plus gemcitabine in chemotherapy-naive patients (N = 1725), and maintenance pemetrexed plus best supportive care versus placebo plus best supportive care (N = 663). Cox models of overall survival (OS) and progression-free survival (PFS) were used to test for a significant treatment-by-histology interaction (THI). A significant THI indicates that the efficacy benefit for pemetrexed relative to the control arm is greater in patients with nonsquamous histology than in those with squamous histology. Subsequent Cox models were used to estimate hazard ratios for OS and PFS according to histology.

Results:

Histology was well balanced between treatment arms in each study. Across all three studies, no clinically relevant differences were observed for the safety profile of pemetrexed among histologic groups. THIs were statistically significant in all three studies for OS (p = 0.001, 0.002, and 0.033, respectively) and PFS (p = 0.004, 0.002, and 0.036, respectively).

Conclusions:

These analyses demonstrate a statistically significant interaction between treatment effect and NSCLC histology, indicating superior efficacy of pemetrexed in nonsquamous patients compared with other standard treatment options. Thus, histology is consistently predictive of the improved efficacy of pemetrexed in patients with nonsquamous NSCLC.

Key Words:

Non-small cell lung cancer
Pemetrexed
Histology
Adenocarcinoma
Squamous cell carcinoma
Large cell carcinoma
Nonsquamous
Thymidylate synthase

Cited by (0)

Disclosure: Giorgio Scagliotti, MD, Honoraria from AstraZeneca, Sanofi-Aventis, and Roche; Thomas Brodowicz, MD, Honoraria from Eli Lilly; Frances A. Shepherd, MD, Honoraria and stock ownership, Eli Lilly; Christoph Zielinski, MD, Honoraria: None during last 2 years; Johan Vansteenkiste, MD, Holder of the Eli-Lilly L. Hertel Chair at the Catholic University Leuven, Belgium (research funding); Christian Manegold, MD, Honorarium: Lilly, Roche, Merck-Darmstadt, Boehringer-Ingelheim, and AstraZeneca; Lorinda Simms, MSc, PStat, Employee of Eli Lilly and own Lilly stock; Frank Fossella, MD, None; Katherine Sugarman, MD, Employed by and holds stock in Eli Lilly and Company, the makers of pemetrexed; and Chandra P. Belani, MD, Consultant, Eli Lilly.