Phase II study of multidisciplinary therapy combined with pembrolizumab for patients with synchronous oligometastatic non-small cell lung cancer: TRAP-OLIGO study (WJOG11118L).

H Hideyuki Harada (Division of Radiation and Proton Therapy Center, Shizuoka Cancer Center, Nagaizumi, Japan) T Taichi Miyawaki (Department of Respiratory Medicine, Juntendo University Hospital, Tokyo, Japan) Y Yasuhisa Ohde Y Yasutaka Chiba (Clinical Research Center, Kindai University Hospital, Osaka, Japan) H Hidetoshi Hayashi Y Yasuhiro Tsutani (Kindai University, Osaka, Japan) K Kentaro Tanaka K Keiji Matsumoto M Masaki Oshima (Department of Radiation Oncology, Juntendo University, Graduate School of Medicine, Tokyo, Japan) S Satoru Miura T Tadashi Aoki (Department of Chest Surgery, Niigata Cancer Center Hospital, Niigata, Japan) Y Yuki Sato T Tomoiki Aiba (Department of Pulmonary Medicine, Sendai Kousei Hospital, Sendai, Japan) K Koichi Azuma M Masafumi Yamaguchi (Department of Thoracic Oncology, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan) N Nobuyuki Yamamoto (Department of Chemistry) H Hirotsugu Kenmotsu

Abstract

8571 Background: Several clinical trials have demonstrated that local ablative therapy (LAT) to all lesions, including primary site, may provide a survival benefit for patients with oligometastatic non-small cell lung cancer (NSCLC). However, few studies have evaluated the efficacy of integrating immune checkpoint inhibitors with chemotherapy and LAT. This study aimed to evaluate the efficacy of multimodal therapy combining platinum-doublet chemotherapy plus pembrolizumab followed by LAT to all sites of disease in patients with synchronous oligometastatic NSCLC. Methods: This multicenter, single-arm, phase II trial enrolled treatment-naive patients with stage IV NSCLC and three or fewer metastatic lesions. Patients received 4 cycles of induction therapy consisting of pembrolizumab plus platinum-doublet chemotherapy. Patients then received LAT to all residual lesions, followed by maintenance therapy with pembrolizumab. The primary endpoint was the 24-month progression-free survival (PFS) rate from the initiation of LAT. Secondary endpoints included safety, response to induction therapy, PFS, overall survival (OS), and the proportion of patients who underwent LAT. The threshold and expected 24-month PFS rates were set at 25% and 60%, respectively, with a one-sided alpha of 0.025 and 80% power. Results: Between October 30, 2020, and August 12, 2022, 30 patients were enrolled. At enrollment, seven patients had one metastasis (23.3%), 14 had two (46.7%), and 9 had three (30%). Twenty-three patients (76.7%) received LAT to all residual disease sites. The 24-month PFS rate from the initiation of LAT was 56.5% (95% CI, 34.3–79.8%). The median PFS from the initiation of LAT was 25.8 months (95% CI, 11.7–not reached). The OS rates at 24 and 36 months from the initiation of LAT were 78.0% (95% CI, 55.0–90.2%) and 61.6% (95% CI, 37.2–78.9%), respectively. During the LAT phase, grade 3/4 adverse events occurred in 3 patients (13.0%). No treatment-related deaths were observed. Conclusions: The TRAP-OLIGO study met its primary endpoint with the lower limit of the 95% CI exceeding the threshold, demonstrating that multimodal therapy combining platinum-based chemotherapy plus pembrolizumab and LAT provides favorable efficacy for patients with synchronous oligometastatic NSCLC. These findings suggest that this integrated approach is a promising treatment strategy for this population. Trial registration: Japan Registry of Clinical Trials, jRCTs041200046. Clinical trial information: jRCTs041200046 .

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
Pages 8571-8571
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (17)

H

Hideyuki Harada

Division of Radiation and Proton Therapy Center, Shizuoka Cancer Center, Nagaizumi, Japan

T

Taichi Miyawaki

Department of Respiratory Medicine, Juntendo University Hospital, Tokyo, Japan

Y

Yasuhisa Ohde

Y

Yasutaka Chiba

Clinical Research Center, Kindai University Hospital, Osaka, Japan

H

Hidetoshi Hayashi

Y

Yasuhiro Tsutani

Kindai University, Osaka, Japan

K

Kentaro Tanaka

K

Keiji Matsumoto

M

Masaki Oshima

Department of Radiation Oncology, Juntendo University, Graduate School of Medicine, Tokyo, Japan

S

Satoru Miura

T

Tadashi Aoki

Department of Chest Surgery, Niigata Cancer Center Hospital, Niigata, Japan

Y

Yuki Sato

T

Tomoiki Aiba

Department of Pulmonary Medicine, Sendai Kousei Hospital, Sendai, Japan

K

Koichi Azuma

M

Masafumi Yamaguchi

Department of Thoracic Oncology, National Hospital Organization Kyushu Cancer Center, Fukuoka, Japan

N

Nobuyuki Yamamoto

Department of Chemistry

H

Hirotsugu Kenmotsu