<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Spicer JD</submitter><funding>Health Research Board</funding><funding>NCI NIH HHS</funding><pagination>1240-1252</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11512588</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>404(10459)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>At the first interim analysis of the KEYNOTE-671 trial, adding perioperative pembrolizumab to neoadjuvant chemotherapy significantly improved event-free survival in participants with early-stage non-small-cell lung cancer (NSCLC). We report overall survival and health-related quality of life outcomes from the second interim analysis.&lt;h4>Methods&lt;/h4>KEYNOTE-671 was a global phase 3 trial done at 189 medical centres. Eligible participants (aged ≥18 years) with resectable stage II, IIIA, or IIIB (N2) NSCLC were randomly assigned (1:1) to four cycles of neoadjuvant pembrolizumab (200 mg administered intravenously every 3 weeks) plus cisplatin-based chemotherapy followed by surgery and 13 cycles of adjuvant pembrolizumab (200 mg administered intravenously every 3 weeks) or to</pubmed_abstract><journal>Lancet (London, England)</journal><pubmed_title>Neoadjuvant pembrolizumab plus chemotherapy followed by adjuvant pembrolizumab compared with neoadjuvant chemotherapy alone in patients with early-stage non-small-cell lung cancer (KEYNOTE-671): a randomised, double-blind, placebo-controlled, phase 3 trial.</pubmed_title><pmcid>PMC11512588</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>CTIC-2021-002</funding_grant_id><pubmed_authors>Teixeira C</pubmed_authors><pubmed_authors>Wesseler C</pubmed_authors><pubmed_authors>Cicenas S</pubmed_authors><pubmed_authors>Grohe C</pubmed_authors><pubmed_authors>Rathnasabapathy C</pubmed_authors><pubmed_authors>Alves G</pubmed_authors><pubmed_authors>Alekshun T</pubmed_authors><pubmed_authors>Zurawski B</pubmed_authors><pubmed_authors>Siegel R</pubmed_authors><pubmed_authors>Pastor A</pubmed_authors><pubmed_authors>Sakao Y</pubmed_authors><pubmed_authors>Levenko O</pubmed_authors><pubmed_authors>Chaft JE</pubmed_authors><pubmed_authors>Vogel G</pubmed_authors><pubmed_authors>Deschepper K</pubmed_authors><pubmed_authors>Jain S</pubmed_authors><pubmed_authors>Hui R</pubmed_authors><pubmed_authors>Duchemann B</pubmed_authors><pubmed_authors>Delmonte A</pubmed_authors><pubmed_authors>Horio Y</pubmed_authors><pubmed_authors>Kuroda H</pubmed_authors><pubmed_authors>Rodriguez-Abreu D</pubmed_authors><pubmed_authors>Jain K</pubmed_authors><pubmed_authors>Serke M</pubmed_authors><pubmed_authors>Furqan M</pubmed_authors><pubmed_authors>Hu J</pubmed_authors><pubmed_authors>Bylicki O</pubmed_authors><pubmed_authors>Martinengo G</pubmed_authors><pubmed_authors>Gilli M</pubmed_authors><pubmed_authors>Huang HC</pubmed_authors><pubmed_authors>Saji H</pubmed_authors><pubmed_authors>Makles K</pubmed_authors><pubmed_authors>Martinez Marti A</pubmed_authors><pubmed_authors>Spicer JD</pubmed_authors><pubmed_authors>Gal C</pubmed_authors><pubmed_authors>Guisier F</pubmed_authors><pubmed_authors>Kaywin P</pubmed_authors><pubmed_authors>Zhu Y</pubmed_authors><pubmed_authors>Puig J</pubmed_authors><pubmed_authors>Faria L</pubmed_authors><pubmed_authors>Iordan I</pubmed_authors><pubmed_authors>Hegmane A</pubmed_authors><pubmed_authors>Berceanu-Ion R</pubmed_authors><pubmed_authors>Sibille A</pubmed_authors><pubmed_authors>Zhao Q</pubmed_authors><pubmed_authors>Zhao G</pubmed_authors><pubmed_authors>Shio Y</pubmed_authors><pubmed_authors>Bonnet R</pubmed_authors><pubmed_authors>Bai J</pubmed_authors><pubmed_authors>Berard H</pubmed_authors><pubmed_authors>Wong 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F</pubmed_authors><pubmed_authors>Srkalovic G</pubmed_authors><pubmed_authors>Yu KL</pubmed_authors><pubmed_authors>Costin D</pubmed_authors><pubmed_authors>Spicer J</pubmed_authors><pubmed_authors>Girard N</pubmed_authors><pubmed_authors>Okada M</pubmed_authors><pubmed_authors>Liberman M</pubmed_authors><pubmed_authors>Begin P</pubmed_authors><pubmed_authors>Ganea D</pubmed_authors><pubmed_authors>Nesterova A</pubmed_authors><pubmed_authors>Liu-Dumlao T</pubmed_authors><pubmed_authors>Kato T</pubmed_authors><pubmed_authors>De Marchi PRM</pubmed_authors><pubmed_authors>Yan X</pubmed_authors><pubmed_authors>Bryl M</pubmed_authors><pubmed_authors>KEYNOTE-671 Investigators</pubmed_authors><pubmed_authors>Mazilu L</pubmed_authors><pubmed_authors>Lo Russo G</pubmed_authors><pubmed_authors>Zasadny X</pubmed_authors><pubmed_authors>Lang S</pubmed_authors><pubmed_authors>Nadal Alforja E</pubmed_authors><pubmed_authors>Dias J</pubmed_authors><pubmed_authors>Gianni L</pubmed_authors><pubmed_authors>Khan S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Neoadjuvant pembrolizumab plus chemotherapy followed by adjuvant pembrolizumab compared with neoadjuvant chemotherapy alone in patients with early-stage non-small-cell lung cancer (KEYNOTE-671): a randomised, double-blind, placebo-controlled, phase 3 trial.</name><description>&lt;h4>Background&lt;/h4>At the first interim analysis of the KEYNOTE-671 trial, adding perioperative pembrolizumab to neoadjuvant chemotherapy significantly improved event-free survival in participants with early-stage non-small-cell lung cancer (NSCLC). We report overall survival and health-related quality of life outcomes from the second interim analysis.&lt;h4>Methods&lt;/h4>KEYNOTE-671 was a global phase 3 trial done at 189 medical centres. Eligible participants (aged ≥18 years) with resectable stage II, IIIA, or IIIB (N2) NSCLC were randomly assigned (1:1) to four cycles of neoadjuvant pembrolizumab (200 mg administered intravenously every 3 weeks) plus cisplatin-based chemotherapy followed by surgery and 13 cycles of adjuvant pembrolizumab (200 mg administered intravenously every 3 weeks) or to</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Sep</publication><modification>2026-06-03T23:24:00.785Z</modification><creation>2026-05-03T03:10:48.182Z</creation></dates><accession>S-EPMC11512588</accession><cross_references><pubmed>39288781</pubmed><doi>10.1016/s0140-6736(24)01756-2</doi><doi>10.1016/S0140-6736(24)01756-2</doi></cross_references></HashMap>