Sequencing strategies with ramucirumab and docetaxel following prior treatments for advanced non-small cell lung cancer: a multicenter retrospective cohort study

Author:

Tanizaki Satoshi1,Matsumoto Kinnosuke2,Tamiya Akihiro2,Taniguchi Yoshihiko2,Matsuda Yoshinobu2,Uchida Junji1,Ueno Kiyonobu1,Kawachi Hayato3,Tamiya Motohiro3,Yanase Takafumi4,Suzuki Hidekazu4,Okishio Kyoichi2

Affiliation:

1. Osaka General Medical Center

2. National Hospital Organization Kinki-Chuo Chest Medical Center

3. Osaka International Cancer Institute

4. Osaka Prefectural Medical Center for Respiratory and Allergic Disease

Abstract

Abstract Objectives Ramucirumab (RAM) and docetaxel (DOC) are commonly used after first-line therapy for advanced non-small-cell lung cancer (NSCLC). Therefore, we aimed to elucidate sequencing strategies of RAM and DOC following prior treatments, including immune checkpoint inhibitor (ICI), cytotoxic agent (CTx) alone, bevacizumab (BEV), and tyrosine kinase inhibitor (TKI). Methods We recruited patients with NSCLC who received RAM and DOC and compared the groups with and without prior ICI, CTx alone, BEV, and TKI, respectively. By tumor response to such treatments, the patients were further classified into “complete response (CR) + partial response (PR),” “stable disease,” and “progressive disease” groups, respectively. We compared RAM and DOC efficacy among these groups. Results In total, 237 patients were registered. In the group with prior ICI, the objective response rate and disease control rate were significantly higher than those without prior ICI (p = 0.012 and 0.028, respectively), and the median progression-free survival (PFS) was also significantly longer (p = 0.027). There were no significant differences in PFS between the groups with and without CTx alone, BEV, and TKI. Multivariate analysis revealed that prior ICI was an independent factor associated with better PFS. Furthermore, the prior ICI group with CR + PR significantly prolonged PFS compared to the group without prior ICI (p = 0.013). Conclusion RAM and DOC may be preferably administered after ICI, rather than after CTx alone, BEV, or TKI, and furthermore, enhanced if the prior ICI has a favorable tumor response.

Publisher

Research Square Platform LLC

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