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Phase 2 study of first‐line pembrolizumab monotherapy in elderly patients with non‐small‐cell lung cancer expressing high PD‐L1
BACKGROUND: Pembrolizumab is the recommended first‐line therapy for patients with advanced non‐small‐cell lung cancer (NSCLC) and a programmed death ligand‐1 (PD‐L1) tumor proportion score (TPS) of ≥50% without driver mutations. However, its efficacy and safety for patients ≥75 years have not been p...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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John Wiley & Sons Australia, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161325/ https://www.ncbi.nlm.nih.gov/pubmed/35488720 http://dx.doi.org/10.1111/1759-7714.14428 |
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author | Masuda, Takeshi Fujitaka, Kazunori Suzuki, Tomoko Hamai, Kosuke Matsumoto, Naoko Matsumura, Mirai Isoyama, Shoko Ueno, Sayaka Mito, Mineyo Yamaguchi, Kakuhiro Sakamoto, Shinjiro Kawano, Reo Masuda, Ken Nishino, Ryohei Ishikawa, Nobuhisa Yamasaki, Masahiro Hattori, Noboru |
author_facet | Masuda, Takeshi Fujitaka, Kazunori Suzuki, Tomoko Hamai, Kosuke Matsumoto, Naoko Matsumura, Mirai Isoyama, Shoko Ueno, Sayaka Mito, Mineyo Yamaguchi, Kakuhiro Sakamoto, Shinjiro Kawano, Reo Masuda, Ken Nishino, Ryohei Ishikawa, Nobuhisa Yamasaki, Masahiro Hattori, Noboru |
author_sort | Masuda, Takeshi |
collection | PubMed |
description | BACKGROUND: Pembrolizumab is the recommended first‐line therapy for patients with advanced non‐small‐cell lung cancer (NSCLC) and a programmed death ligand‐1 (PD‐L1) tumor proportion score (TPS) of ≥50% without driver mutations. However, its efficacy and safety for patients ≥75 years have not been prospectively investigated; this was the aim of this study. METHODS: This multicenter and open‐label single‐arm phase II study was conducted at 12 institutions. Chemotherapy‐naïve patients with advanced NSCLC and a PD‐L1 TPS of ≥50% without EGFR mutations or translocation of the ALK received pembrolizumab every 3 weeks. The primary endpoint was progression‐free survival (PFS) with a threshold of 4.3 months. The secondary endpoints were overall survival (OS), objective response rate (ORR), disease control rate (DCR), safety, and quality of life. RESULTS: Twenty‐six patients were enrolled between October 2017 and March 2020. The median PFS was 9.6 (95% confidence interval [CI] 2.1–20.6) months. The lower limit of the 95% CI did not exceed the target. The median OS was 21.6 months. The ORR and DCR were 41.7% and 70.8%, respectively. The proportion of patients with grade ≥3 treatment‐related adverse events was 15.4%. The quality of life score did not change significantly during treatment. CONCLUSION: While this study showed that pembrolizumab was a tolerable treatment for elderly patients, the safety requires further confirmation in a larger study. Although the primary endpoint, the median PFS (9.6 months), was slightly shorter than that (10.3 months) of the previous phase III study (KEYNOTE‐024 study), the median PFS did not achieve the expected value. |
format | Online Article Text |
id | pubmed-9161325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-91613252022-06-04 Phase 2 study of first‐line pembrolizumab monotherapy in elderly patients with non‐small‐cell lung cancer expressing high PD‐L1 Masuda, Takeshi Fujitaka, Kazunori Suzuki, Tomoko Hamai, Kosuke Matsumoto, Naoko Matsumura, Mirai Isoyama, Shoko Ueno, Sayaka Mito, Mineyo Yamaguchi, Kakuhiro Sakamoto, Shinjiro Kawano, Reo Masuda, Ken Nishino, Ryohei Ishikawa, Nobuhisa Yamasaki, Masahiro Hattori, Noboru Thorac Cancer Original Articles BACKGROUND: Pembrolizumab is the recommended first‐line therapy for patients with advanced non‐small‐cell lung cancer (NSCLC) and a programmed death ligand‐1 (PD‐L1) tumor proportion score (TPS) of ≥50% without driver mutations. However, its efficacy and safety for patients ≥75 years have not been prospectively investigated; this was the aim of this study. METHODS: This multicenter and open‐label single‐arm phase II study was conducted at 12 institutions. Chemotherapy‐naïve patients with advanced NSCLC and a PD‐L1 TPS of ≥50% without EGFR mutations or translocation of the ALK received pembrolizumab every 3 weeks. The primary endpoint was progression‐free survival (PFS) with a threshold of 4.3 months. The secondary endpoints were overall survival (OS), objective response rate (ORR), disease control rate (DCR), safety, and quality of life. RESULTS: Twenty‐six patients were enrolled between October 2017 and March 2020. The median PFS was 9.6 (95% confidence interval [CI] 2.1–20.6) months. The lower limit of the 95% CI did not exceed the target. The median OS was 21.6 months. The ORR and DCR were 41.7% and 70.8%, respectively. The proportion of patients with grade ≥3 treatment‐related adverse events was 15.4%. The quality of life score did not change significantly during treatment. CONCLUSION: While this study showed that pembrolizumab was a tolerable treatment for elderly patients, the safety requires further confirmation in a larger study. Although the primary endpoint, the median PFS (9.6 months), was slightly shorter than that (10.3 months) of the previous phase III study (KEYNOTE‐024 study), the median PFS did not achieve the expected value. John Wiley & Sons Australia, Ltd 2022-04-30 2022-06 /pmc/articles/PMC9161325/ /pubmed/35488720 http://dx.doi.org/10.1111/1759-7714.14428 Text en © 2022 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Masuda, Takeshi Fujitaka, Kazunori Suzuki, Tomoko Hamai, Kosuke Matsumoto, Naoko Matsumura, Mirai Isoyama, Shoko Ueno, Sayaka Mito, Mineyo Yamaguchi, Kakuhiro Sakamoto, Shinjiro Kawano, Reo Masuda, Ken Nishino, Ryohei Ishikawa, Nobuhisa Yamasaki, Masahiro Hattori, Noboru Phase 2 study of first‐line pembrolizumab monotherapy in elderly patients with non‐small‐cell lung cancer expressing high PD‐L1 |
title | Phase 2 study of first‐line pembrolizumab monotherapy in elderly patients with non‐small‐cell lung cancer expressing high PD‐L1
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title_full | Phase 2 study of first‐line pembrolizumab monotherapy in elderly patients with non‐small‐cell lung cancer expressing high PD‐L1
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title_fullStr | Phase 2 study of first‐line pembrolizumab monotherapy in elderly patients with non‐small‐cell lung cancer expressing high PD‐L1
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title_full_unstemmed | Phase 2 study of first‐line pembrolizumab monotherapy in elderly patients with non‐small‐cell lung cancer expressing high PD‐L1
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title_short | Phase 2 study of first‐line pembrolizumab monotherapy in elderly patients with non‐small‐cell lung cancer expressing high PD‐L1
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title_sort | phase 2 study of first‐line pembrolizumab monotherapy in elderly patients with non‐small‐cell lung cancer expressing high pd‐l1 |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161325/ https://www.ncbi.nlm.nih.gov/pubmed/35488720 http://dx.doi.org/10.1111/1759-7714.14428 |
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