Cited 1 times in
Adjuvant Pembrolizumab in Patients with Stage IIIA/N2 Non-Small Cell Lung Cancer Completely Resected after Neoadjuvant Concurrent Chemoradiation: A Prospective, Open-Label, Single-Arm, Phase 2 Trial
DC Field | Value | Language |
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dc.contributor.author | 김경환 | - |
dc.date.accessioned | 2025-02-03T09:13:58Z | - |
dc.date.available | 2025-02-03T09:13:58Z | - |
dc.date.issued | 2024-10 | - |
dc.identifier.issn | 1598-2998 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/202309 | - |
dc.description.abstract | Purpose: Optimal treatment for stage IIIA/N2 non-small cell lung cancer (NSCLC) is controversial. We aimed to assess the efficacy and safety of adjuvant pembrolizumab for stage IIIA/N2 NSCLC completely resected after neoadjuvant concurrent chemoradiation therapy (CCRT). Materials and methods: In this open-label, single-center, single-arm phase 2 trial, patients with stage IIIA/N2 NSCLC received adjuvant pembrolizumab for up to 2 years after complete resection following neoadjuvant CCRT. The primary endpoint was disease-free survival (DFS). Secondary endpoints included overall survival (OS) and safety. As an exploratory biomarker analysis, we evaluated the proliferative response of blood CD39+PD-1+CD8+ T cells using fold changes in the percentage of proliferating Ki-67+ cells from days 1 to 7 of cycle 1 (Ki-67D7/D1). Results: Between October 2017 and October 2018, 37 patients were enrolled. Twelve (32%) and three (8%) patients harbored EGFR and ALK alterations, respectively. Of 34 patients with programmed cell death ligand 1 assessment, 21 (62%), nine (26%), and four (12%) had a tumor proportion score of < 1%, 1%-50%, and ≥ 50%, respectively. The median follow-up was 71 months. The median DFS was 22.4 months in the overall population, with a 5-year DFS rate of 29%. The OS rate was 86% at 2 years and 76% at 5 years. Patients with tumor recurrence within 6 months had a significantly lower Ki-67D7/D1 among CD39+PD-1+CD8+ T cells than those without (p=0.036). No new safety signals were identified. Conclusion: Adjuvant pembrolizumab may offer durable disease control in a subset of stage IIIA/N2 NSCLC patients after neoadjuvant CCRT and surgery. | - |
dc.description.statementOfResponsibility | open | - |
dc.language | English, Korean | - |
dc.publisher | Official journal of Korean Cancer Association | - |
dc.relation.isPartOf | CANCER RESEARCH AND TREATMENT | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Antibodies, Monoclonal, Humanized* / administration & dosage | - |
dc.subject.MESH | Antibodies, Monoclonal, Humanized* / therapeutic use | - |
dc.subject.MESH | Antineoplastic Agents, Immunological / pharmacology | - |
dc.subject.MESH | Antineoplastic Agents, Immunological / therapeutic use | - |
dc.subject.MESH | Carcinoma, Non-Small-Cell Lung* / mortality | - |
dc.subject.MESH | Carcinoma, Non-Small-Cell Lung* / pathology | - |
dc.subject.MESH | Carcinoma, Non-Small-Cell Lung* / therapy | - |
dc.subject.MESH | Chemoradiotherapy* / methods | - |
dc.subject.MESH | Chemotherapy, Adjuvant / methods | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Lung Neoplasms* / mortality | - |
dc.subject.MESH | Lung Neoplasms* / pathology | - |
dc.subject.MESH | Lung Neoplasms* / therapy | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Neoadjuvant Therapy* / methods | - |
dc.subject.MESH | Neoplasm Staging* | - |
dc.subject.MESH | Prospective Studies | - |
dc.title | Adjuvant Pembrolizumab in Patients with Stage IIIA/N2 Non-Small Cell Lung Cancer Completely Resected after Neoadjuvant Concurrent Chemoradiation: A Prospective, Open-Label, Single-Arm, Phase 2 Trial | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Radiation Oncology (방사선종양학교실) | - |
dc.contributor.googleauthor | Junghoon Shin | - |
dc.contributor.googleauthor | Sehhoon Park | - |
dc.contributor.googleauthor | Kyung Hwan Kim | - |
dc.contributor.googleauthor | Eui-Cheol Shin | - |
dc.contributor.googleauthor | Hyun Ae Jung | - |
dc.contributor.googleauthor | Jong Ho Cho | - |
dc.contributor.googleauthor | Jong-Mu Sun | - |
dc.contributor.googleauthor | Se-Hoon Lee | - |
dc.contributor.googleauthor | Yong Soo Choi | - |
dc.contributor.googleauthor | Jin Seok Ahn | - |
dc.contributor.googleauthor | Jhingook Kim | - |
dc.contributor.googleauthor | Keunchil Park | - |
dc.contributor.googleauthor | Young Mog Shim | - |
dc.contributor.googleauthor | Hong Kwan Kim | - |
dc.contributor.googleauthor | Jae Myoung Noh | - |
dc.contributor.googleauthor | Yong Chan Ahn | - |
dc.contributor.googleauthor | Hongryull Pyo | - |
dc.contributor.googleauthor | Myung-Ju Ahn | - |
dc.identifier.doi | 10.4143/crt.2024.084 | - |
dc.contributor.localId | A05226 | - |
dc.relation.journalcode | J00453 | - |
dc.identifier.eissn | 2005-9256 | - |
dc.identifier.pmid | 38697848 | - |
dc.subject.keyword | Adjuvant chemotherapy | - |
dc.subject.keyword | Chemoradiotherapy | - |
dc.subject.keyword | Non-small-cell lung carcinoma | - |
dc.subject.keyword | Pembrolizumab | - |
dc.contributor.alternativeName | Kim, Kyung Hwan | - |
dc.contributor.affiliatedAuthor | 김경환 | - |
dc.citation.volume | 56 | - |
dc.citation.number | 4 | - |
dc.citation.startPage | 1084 | - |
dc.citation.endPage | 1095 | - |
dc.identifier.bibliographicCitation | CANCER RESEARCH AND TREATMENT, Vol.56(4) : 1084-1095, 2024-10 | - |
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