First-Line Pembrolizumab + Chemotherapy Versus Placebo + Chemotherapy for Persistent, Recurrent, or Metastatic Cervical Cancer: Final Overall Survival Results of KEYNOTE-826

dc.contributor.authorMonk, Bradley J.
dc.contributor.authorColombo, Nicoletta
dc.contributor.authorTewari, Krishnansu S.
dc.contributor.authorDubot, Coraline
dc.contributor.authorCaceres, M. Valeria
dc.contributor.authorHasegawa, Kosei
dc.contributor.authorShapira-Frommer, Ronnie
dc.date.accessioned2025-05-10T15:24:14Z
dc.date.issued2023
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractClinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in JCO or elsewhere, for which the primary end point has already been reported.The phase III, double-blind KEYNOTE-826 trial of pembrolizumab 200 mg or placebo once every 3 weeks for up to 35 cycles plus platinum-based chemotherapy, with or without bevacizumab, showed statistically significant survival benefits with the addition of pembrolizumab for patients with persistent, recurrent, or metastatic cervical cancer (primary data cutoff: May 3, 2021). This article reports the protocol-specified final overall survival (OS) results tested in the PD-L1 combined positive score (CPS) ?1, all-comer, and CPS ?10 populations. At the final data cutoff (October 3, 2022), the median study follow-up duration was 39.1 months (range, 32.1-46.5 months). In the PD-L1 CPS ?1 (N = 548), all-comer (N = 617), and CPS ?10 (N = 317) populations, median OS with pembrolizumab-chemotherapy versus placebo-chemotherapy was 28.6 months versus 16.5 months (hazard ratio [HR] for death, 0.60 [95% CI, 0.49 to 0.74]), 26.4 months versus 16.8 months (HR, 0.63 [95% CI, 0.52 to 0.77]), and 29.6 months versus 17.4 months (HR, 0.58 [95% CI, 0.44 to 0.78]), respectively. The incidence of grade ?3 adverse events was 82.4% with pembrolizumab-chemotherapy and 75.4% with placebo-chemotherapy. These results show that pembrolizumab plus chemotherapy, with or without bevacizumab, continued to provide clinically meaningful improvements in OS for patients with persistent, recurrent, or metastatic cervical cancer. © American Society of Clinical Oncology.
dc.identifier.doi10.1200/JCO.23.00914
dc.identifier.endpage5511
dc.identifier.issn0732-183X
dc.identifier.issue36
dc.identifier.pmid37910822
dc.identifier.scopus2-s2.0-85178116765
dc.identifier.scopusqualityQ1
dc.identifier.startpage5505
dc.identifier.urihttps://doi.org/10.1200/JCO.23.00914
dc.identifier.urihttps://hdl.handle.net/20.500.14730/6644
dc.identifier.volume41
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherLippincott Williams and Wilkins
dc.relation.ispartofJournal of Clinical Oncology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_Scopus_20250302
dc.subjectAntineoplastic Combined Chemotherapy Protocols; B7-H1 Antigen; Bevacizumab; Carcinoma, Non-Small-Cell Lung; Female; Humans; Lung Neoplasms; Uterine Cervical Neoplasms; antineoplastic metal complex; bevacizumab; carboplatin; cisplatin; paclitaxel; pembrolizumab; placebo; antineoplastic agent; bevacizumab; pembrolizumab; programmed death 1 ligand 1; adenosquamous carcinoma; adult; aged; alopecia; anemia; Article; autoimmune encephalitis; autoimmune pancreatitis; cancer combination chemotherapy; cancer immunotherapy; cancer recurrence; cancer surgery; cancer survival; cervical metastasis; cervical squamous cell carcinoma; chemoradiotherapy; chronic disease; controlled study; disease duration; double blind procedure; drug efficacy; drug fatality; drug safety; ECOG Performance Status; female; first-line treatment; follow up; human; hypertension; immune mediated injury; major clinical study; monoclonal antibody therapy; multiple cycle treatment; nausea; overall survival; phase 3 clinical trial; progression free survival; randomized controlled trial; response evaluation criteria in solid tumors; treatment response time; uterine cervix adenocarcinoma; uterine cervix cancer; lung tumor; non small cell lung cancer; uterine cervix tumor
dc.titleFirst-Line Pembrolizumab + Chemotherapy Versus Placebo + Chemotherapy for Persistent, Recurrent, or Metastatic Cervical Cancer: Final Overall Survival Results of KEYNOTE-826
dc.typeArticle

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