Impact of Sequential Ramucirumab Plus Docetaxel After <scp>PD</scp> ‐1 Inhibitors on Anti‐ <scp>PD</scp> ‐1 Antibody‐Bound T‐Cell Dynamics and Clinical Outcomes
Ramucirumab plus docetaxel (RAM+DOC) demonstrates clinical activity after programmed cell death-1 (PD-1) inhibitors in advanced non-small cell lung cancer (NSCLC); however, the underlying mechanisms remain unclear. We aimed to evaluate clinical efficacy and explore immunologic dynamics and benefit-associated biomarkers. Patients treated with RAM+DOC after PD-1 inhibitors were enrolled in a multicenter prospective cohort. Anti-PD-1 antibody bound (IgG4<sup>+</sup>) T-cell subsets were measured at baseline (T0) and after 2-3 cycles (T1), reflecting residual anti-PD-1 antibody binding on circulating T cells. T1/T0 ratios of immune subsets were calculated to assess dynamics. Landmark analyses at T1 evaluated associations with progression-free survival (PFS) and overall survival (OS). Prognostic biomarkers were assessed at baseline. Among 27 evaluable patients, the objective response rate was 37.0%, median PFS 5.1 months, and OS 10.4 months. RAM + DOC responders had higher IgG4<sup>+</sup>CD8<sup>+</sup> T-cell and lower IgG4<sup>+</sup> Treg T1/T0 ratios (both p < 0.001). Higher IgG4<sup>+</sup>CD8<sup>+</sup> ratios were associated with longer landmark PFS (p = 0.002) and OS (p = 0.016) and were inversely correlated with IgG4<sup>+</sup> Treg ratios (p = 0.008). Among the baseline factors, high IgG4<sup>+</sup>CD8<sup>+</sup> Temra conferred survival benefits (OS, not reached vs. 8.2 months; p = 0.006), and low vascular endothelial growth factor (VEGF)-C levels were associated with longer OS (not reached vs. 8.5 months, p = 0.044). Both variables remained independent prognostic factors of PFS and OS in multivariable analysis. Our findings suggest that sequential strategy administering RAM+DOC during persistent binding of anti-PD-1 antibody to T cells may be beneficial. IgG4<sup>+</sup>CD8<sup>+</sup> Temra and VEGF-C levels at RAM+DOC initiation may serve as biomarkers of survival benefit. Trial Registration: UMIN-Clinical Trials Registry (UMIN000050478).
Authors
- A. Tamiya
- Yujiro Naito
- N. Takakura
- Toshie Niki
- Yuhei Kinehara
- K. Matsumoto
- Shingo Satoh
- Masahide Mori (ORCID: https://orcid.org/0009-0007-9223-3854)
- K. Okishio
- Yoshito Takeda
- Tomoki Kuge
- Akio Osa
- Hidekazu Suzuki
- Atsushi Kumanogoh
- Motohiro Tamiya
- Yasuhiko Suga
- Shohei Koyama
- Toshiyuki Minami
- Satoshi Tetsumoto
- Kazumi Nishino
- Takayuki Shiroyama
Institutions
- Japan Agency for Medical Research and Development (JP)
- Osaka Prefectural Medical Center (JP)
- Osaka City University (JP)
- Nishinomiya Municipal Central Hospital (JP)
- Osaka International Cancer Institute (JP)
- Toneyama National Hospital (JP)
- Chiba Cancer Center (JP)
- Suita Municipal Hospital (JP)
- Osaka Hospital (JP)
- Kinki Central Hospital (JP)
- Osaka International Cancer Institute (JP)
- Nippon Medical School Hospital (JP)
- NHO Kinki Chuo Chest Medical Center (JP)
- Osaka International University (JP)
- National Cancer Research Institute (GB)
- Hyogo University (JP)
- The University of Osaka (JP)
Publication Details
- Journal
- Cancer Science
- Published
- 2026-01-30
- DOI
- https://doi.org/10.1111/cas.70336
- Primary Topic
- Cancer Immunotherapy and Biomarkers
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Eli Lilly and Company
- Japan Agency for Medical Research and Development
- Ministry of Education, Culture, Sports, Science and Technology
- Eli Lilly Japan
- Japan Society for the Promotion of Science
- Japan Science and Technology Agency