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Pembrolizumab After Two or More Lines of Previous Therapy in Patients With Recurrent or Metastatic SCLC: Results From the KEYNOTE-028 and KEYNOTE-158 Studies
DC Field | Value | Language |
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dc.contributor.author | 정현철 | - |
dc.date.accessioned | 2020-06-17T00:32:29Z | - |
dc.date.available | 2020-06-17T00:32:29Z | - |
dc.date.issued | 2020-04 | - |
dc.identifier.issn | 1556-0864 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/176014 | - |
dc.description.abstract | Introduction: Pembrolizumab has shown clinical benefit in patients with previously treated recurrent or metastatic SCLC in the phase 1b multicohort study KEYNOTE-028 (NCT02054806) and the phase 2 multicohort study KEYNOTE-158 (NCT02628067). We present a pooled analysis of patients from KEYNOTE-028 and KEYNOTE-158 who had received two or more lines of previous therapy for SCLC. Methods: Eligible patients were aged 18 years and above, had histologically or cytologically confirmed incurable recurrent or metastatic SCLC, had an Eastern Cooperative Oncology Group performance status of 1 and below, and had received two or more lines of previous therapy. Patients in KEYNOTE-028 were required to have a programmed death ligand 1 (PD-L1)-positive tumor. Patients received pembrolizumab (10 mg/kg every 2 weeks in KEYNOTE-028 or 200 mg every 3 weeks in KEYNOTE-158) for up to 2 years. The primary end point was objective response rate per Response Evaluation Criteria in Solid Tumors version 1.1, which is presented here per independent review. Results: Eighty-three patients who had received two or more lines of previous therapy (KEYNOTE-028, n = 19; KEYNOTE-158, n = 64) were included. Median follow-up duration was 7.7 (range, 0.5-48.7) months. Objective response rate was 19.3% (95% confidence interval: 11.4-29.4); two patients had complete response (one with a PD-L1-positive tumor), and 14 patients had partial response (13 with PD-L1-positive tumors). The median duration of response was not reached (range, 4.1‒35.8+ mo; plus sign indicates ongoing response); 61% of responders had responses lasting 18 months or longer. Fifty-one patients (61.4%) experienced any-grade treatment-related adverse events; eight patients (9.6%) had grade 3 or higher events. Conclusions: Pembrolizumab exhibited durable antitumor activity in a subset of patients with recurrent or metastatic SCLC who had undergone two or more previous lines of therapy, regardless of PD-L1 expression. Pembrolizumab was well tolerated. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Elsevier | - |
dc.relation.isPartOf | JOURNAL OF THORACIC ONCOLOGY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.title | Pembrolizumab After Two or More Lines of Previous Therapy in Patients With Recurrent or Metastatic SCLC: Results From the KEYNOTE-028 and KEYNOTE-158 Studies | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
dc.contributor.googleauthor | Hyun Cheol Chung | - |
dc.contributor.googleauthor | Sarina A Piha-Paul | - |
dc.contributor.googleauthor | Jose Lopez-Martin | - |
dc.contributor.googleauthor | Jan H M Schellens | - |
dc.contributor.googleauthor | Steven Kao | - |
dc.contributor.googleauthor | Wilson H Miller Jr | - |
dc.contributor.googleauthor | Jean-Pierre Delord | - |
dc.contributor.googleauthor | Bo Gao | - |
dc.contributor.googleauthor | David Planchard | - |
dc.contributor.googleauthor | Maya Gottfried | - |
dc.contributor.googleauthor | Alona Zer | - |
dc.contributor.googleauthor | Shadia I Jalal | - |
dc.contributor.googleauthor | Nicolas Penel | - |
dc.contributor.googleauthor | Janice M Mehnert | - |
dc.contributor.googleauthor | Ignacio Matos | - |
dc.contributor.googleauthor | Jaafar Bennouna | - |
dc.contributor.googleauthor | Dong-Wan Kim | - |
dc.contributor.googleauthor | Lei Xu | - |
dc.contributor.googleauthor | Suba Krishnan | - |
dc.contributor.googleauthor | Kevin Norwood | - |
dc.contributor.googleauthor | Patrick A Ott | - |
dc.identifier.doi | 10.1016/j.jtho.2019.12.109 | - |
dc.contributor.localId | A03773 | - |
dc.relation.journalcode | J01909 | - |
dc.identifier.eissn | 1556-1380 | - |
dc.identifier.pmid | 31870883 | - |
dc.identifier.url | https://www.sciencedirect.com/science/article/pii/S155608641933850X | - |
dc.subject.keyword | Immunotherapy | - |
dc.subject.keyword | Pembrolizumab | - |
dc.subject.keyword | SCLC | - |
dc.subject.keyword | Third-line therapy | - |
dc.contributor.alternativeName | Chung, Hyun Cheol | - |
dc.contributor.affiliatedAuthor | 정현철 | - |
dc.citation.volume | 15 | - |
dc.citation.number | 4 | - |
dc.citation.startPage | 618 | - |
dc.citation.endPage | 627 | - |
dc.identifier.bibliographicCitation | JOURNAL OF THORACIC ONCOLOGY, Vol.15(4) : 618-627, 2020-04 | - |
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