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Dostarlimab or pembrolizumab plus chemotherapy in previously untreated metastatic non-squamous non-small cell lung cancer: the randomized PERLA phase II trial
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lim, Sun Min | - |
| dc.contributor.author | Peters, Solange | - |
| dc.contributor.author | Granados, Ana Laura Ortega | - |
| dc.contributor.author | Pinto, Gustavo dix Junqueira | - |
| dc.contributor.author | Fuentes, Christian Sebastian | - |
| dc.contributor.author | Lo Russo, Giuseppe | - |
| dc.contributor.author | Schenker, Michael | - |
| dc.contributor.author | Ahn, Jin Seok | - |
| dc.contributor.author | Reck, Martin | - |
| dc.contributor.author | Szijgyarto, Zsolt | - |
| dc.contributor.author | Huseinovic, Neda | - |
| dc.contributor.author | Zografos, Eleftherios | - |
| dc.contributor.author | Buss, Elena | - |
| dc.contributor.author | Stjepanovic, Neda | - |
| dc.contributor.author | ODonnell, Sean | - |
| dc.contributor.author | de Marinis, Filippo | - |
| dc.date.accessioned | 2024-02-15T06:45:45Z | - |
| dc.date.available | 2024-02-15T06:45:45Z | - |
| dc.date.created | 2024-02-22 | - |
| dc.date.issued | 2023-11 | - |
| dc.identifier.issn | 2041-1723 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/198024 | - |
| dc.description.abstract | PERLA is a global, double-blind, parallel phase II trial (NCT04581824) comparing efficacy and safety of anti-PD-1 antibodies dostarlimab and pembrolizumab, plus chemotherapy (DCT and PCT, respectively) as first-line treatment in patients with metastatic non-squamous NSCLC without known targetable genomic aberrations. Patients stratified by PD-L1 tumor proportion score and smoking status were randomized 1:1, receiving <= 35 cycles 500 mg dostarlimab or 200 mg pembrolizumab, <= 35 cycles 500 mg/m2 pemetrexed and <= 4 cycles cisplatin (75 mg/m2) or carboplatin (AUC 5 mg/ml/min) Q3W. Primary endpoint was overall response rate (ORR) (blinded independent central review). Secondary endpoints include progression-free survival (PFS) based on investigator assessment, overall survival (OS) and safety. Exploratory endpoints include ORR by PD-L1 subgroup and duration of response. PERLA met its pre-specified endpoint. ORR (n/N; 95% CI) is 45% (55/121; 36.4-54.8) for DCT and 39% (48/122; 30.6-48.6) for PCT (data cut-off: 07 July 23), numerically favoring dostarlimab in PD-L1-positive subgroups. Median PFS (months [95% CI]) is 8.8 (6.7-10.4) for DCT and 6.7 (4.9-7.1) for PCT (HR 0.70 [95% CI: 0.50-0.98]; data cut-off: 04 August 22). Median OS (months [95% CI]) is 19.4 (14.5-NR) for DCT and 15.9 (11.6-19.3) for PCT (HR 0.75 [95% CI: 0.53-1.05]) (data cut-off: 07 July 23). Safety profiles are similar between groups. In this study, DCT shows similar efficacy to PCT and demonstrates clinical efficacy as first-line treatment for patients with metastatic non-squamous NSCLC. Several PD-(L)1 inhibitors have been approved or are in development for the treatment of NSCLC, showing promising efficacy and tolerable safety profiles. Here, the authors present a randomized phase II clinical trial comparing two different anti-PD-1 antibodies, dostarlimab and pembrolizumab, both combined with chemotherapy as first-line treatment in patients with metastatic NSCLC. | - |
| dc.description.statementOfResponsibility | open | - |
| dc.language | English | - |
| dc.publisher | Nature Pub. Group | - |
| dc.relation.isPartOf | NATURE COMMUNICATIONS | - |
| dc.relation.isPartOf | NATURE COMMUNICATIONS | - |
| dc.rights | CC BY-NC-ND 2.0 KR | - |
| dc.title | Dostarlimab or pembrolizumab plus chemotherapy in previously untreated metastatic non-squamous non-small cell lung cancer: the randomized PERLA phase II trial | - |
| dc.type | Article | - |
| dc.contributor.college | College of Medicine (의과대학) | - |
| dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
| dc.contributor.googleauthor | Lim, Sun Min | - |
| dc.contributor.googleauthor | Peters, Solange | - |
| dc.contributor.googleauthor | Granados, Ana Laura Ortega | - |
| dc.contributor.googleauthor | Pinto, Gustavo dix Junqueira | - |
| dc.contributor.googleauthor | Fuentes, Christian Sebastian | - |
| dc.contributor.googleauthor | Lo Russo, Giuseppe | - |
| dc.contributor.googleauthor | Schenker, Michael | - |
| dc.contributor.googleauthor | Ahn, Jin Seok | - |
| dc.contributor.googleauthor | Reck, Martin | - |
| dc.contributor.googleauthor | Szijgyarto, Zsolt | - |
| dc.contributor.googleauthor | Huseinovic, Neda | - |
| dc.contributor.googleauthor | Zografos, Eleftherios | - |
| dc.contributor.googleauthor | Buss, Elena | - |
| dc.contributor.googleauthor | Stjepanovic, Neda | - |
| dc.contributor.googleauthor | ODonnell, Sean | - |
| dc.contributor.googleauthor | de Marinis, Filippo | - |
| dc.identifier.doi | 10.1038/s41467-023-42900-4 | - |
| dc.relation.journalcode | J02293 | - |
| dc.identifier.eissn | 2041-1723 | - |
| dc.identifier.pmid | 37951954 | - |
| dc.contributor.alternativeName | Lim, Sun Min | - |
| dc.contributor.affiliatedAuthor | Lim, Sun Min | - |
| dc.identifier.scopusid | 2-s2.0-85176577090 | - |
| dc.identifier.wosid | 001103534100004 | - |
| dc.citation.volume | 14 | - |
| dc.citation.number | 1 | - |
| dc.identifier.bibliographicCitation | NATURE COMMUNICATIONS, Vol.14(1), 2023-11 | - |
| dc.identifier.rimsid | 82268 | - |
| dc.type.rims | ART | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalWebOfScienceCategory | Multidisciplinary Sciences | - |
| dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
| dc.identifier.articleno | 7301 | - |
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