Cited 0 time in
A Phase II Study of Durvalumab, Doxorubicin, and Ifosfamide in Recurrent and/or Metastatic Pulmonary Sarcomatoid Carcinoma (KCSG LU-19-24)
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Miso | - |
| dc.contributor.author | Youk, Jeonghwan | - |
| dc.contributor.author | Kim, Tae Min | - |
| dc.contributor.author | Lee, Gyeong-Won | - |
| dc.contributor.author | Kim, Dong-Wan | - |
| dc.contributor.author | Keam, Bhumsuk | - |
| dc.date.accessioned | 2026-01-28T01:30:15Z | - |
| dc.date.available | 2026-01-28T01:30:15Z | - |
| dc.date.issued | 2025-10 | - |
| dc.identifier.issn | 1525-7304 | - |
| dc.identifier.issn | 1938-0690 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/82156 | - |
| dc.description.abstract | Background Pulmonary sarcomatoid carcinomas (PSCs) are rare, aggressive tumors with a poor prognosis. Conventional chemotherapy shows limited efficacy, whereas immune checkpoint inhibitors and doxorubicin have shown potential. This study evaluated the efficacy and safety of durvalumab, doxorubicin, and ifosfamide in recurrent and/or metastatic PSC. Patients and Methods Patients with recurrent or metastatic PSC received durvalumab (1500 mg, day 1), doxorubicin (20 mg/m² intravenously, days 1-3), and ifosfamide (1.5 g/m² intravenously with mesna, days 2-4) every 3 weeks for up to four cycles, followed by durvalumab monotherapy until disease progression or unacceptable toxicity, for up to 12 months. The primary endpoint was objective response rate (ORR). Secondary endpoints included progression-free survival (PFS), overall survival (OS), duration of response (DOR), and toxicity. Results The study was prematurely terminated due to low recruitment rates, with 20 patients enrolled (15 male, 5 female; median age: 63.5 years). Among 18 evaluable cases, 16 (88.9%) were programmed death-ligand 1 positive. Six patients (30.0%) had prior palliative chemotherapy. ORR was 35.0% (95% CI, 17.7%-55.8%). The median DOR was 5.3 months (95% CI, 1.7-not estimated). After a median follow-up of 7.0 months (1.2-37.6), the median PFS and OS were 4.8 months (95% CI, 2.0-6.5) and 9.4 months (95% CI, 5.5-26.8), respectively. Adverse events (AEs) occurred in 19 patients, with serious AEs in 10 patients. Conclusion Durvalumab combined with doxorubicin and ifosfamide suggested clinical activity in recurrent and/or metastatic PSC. Larger studies are warranted to confirm benefits and refine treatment strategies. © 2025 The Authors. | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Elsevier Inc. | - |
| dc.title | A Phase II Study of Durvalumab, Doxorubicin, and Ifosfamide in Recurrent and/or Metastatic Pulmonary Sarcomatoid Carcinoma (KCSG LU-19-24) | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1016/j.cllc.2025.10.003 | - |
| dc.identifier.scopusid | 2-s2.0-105024994842 | - |
| dc.identifier.bibliographicCitation | Clinical Lung Cancer | - |
| dc.citation.title | Clinical Lung Cancer | - |
| dc.type.docType | Article in press | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.subject.keywordAuthor | Clinical trial | - |
| dc.subject.keywordAuthor | Combination therapy | - |
| dc.subject.keywordAuthor | Cytotoxic chemotherapy | - |
| dc.subject.keywordAuthor | Immune checkpoint inhibitor | - |
| dc.subject.keywordAuthor | Rare lung cancer | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
Gyeongsang National University Central Library, 501, Jinju-daero, Jinju-si, Gyeongsangnam-do, 52828, Republic of Korea+82-55-772-0534
COPYRIGHT 2022 GYEONGSANG NATIONAL UNIVERSITY LIBRARY. ALL RIGHTS RESERVED.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.
