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- Publisher Website: 10.1016/S0140-6736(18)31257-1
- Scopus: eid_2-s2.0-85048592368
- PMID: 29880231
- WOS: WOS:000438501300027
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Article: Pembrolizumab versus paclitaxel for previously treated, advanced gastric or gastro-oesophageal junction cancer (KEYNOTE-061): a randomised, open-label, controlled, phase 3 trial
Title | Pembrolizumab versus paclitaxel for previously treated, advanced gastric or gastro-oesophageal junction cancer (KEYNOTE-061): a randomised, open-label, controlled, phase 3 trial |
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Authors | |
Issue Date | 2018 |
Publisher | The Lancet Publishing Group. The Journal's web site is located at http://www.elsevier.com/locate/lancet |
Citation | The Lancet, 2018, v. 392 n. 10142, p. 123-133 How to Cite? |
Abstract | Background:
Patients with advanced gastric or gastro-oesophageal junction cancer that progresses on chemotherapy have poor outcomes. We compared pembrolizumab with paclitaxel in patients with advanced gastric or gastro-oesophageal junction cancer that progressed on first-line chemotherapy with a platinum and fluoropyrimidine.
Methods:
This randomised, open-label, phase 3 study was done at 148 medical centres in 30 countries. Eligible patients were randomised (1:1) in blocks of four per stratum with an interactive voice-response and integrated web-response system to receive either pembrolizumab 200 mg every 3 weeks for up to 2 years or standard-dose paclitaxel. Primary endpoints were overall survival and progression-free survival in patients with a programmed cell death ligand 1 (PD-L1) combined positive score (CPS) of 1 or higher. Safety was assessed in all patients, irrespective of CPS. The significance threshold for overall survival was p=0·0135 (one-sided). This trial is registered at ClinicalTrials.gov, number NCT02370498.
Findings:
Between June 4, 2015, and July 26, 2016, 592 patients were enrolled. Of the 395 patients who had a PD-L1 CPS of 1 or higher, 196 patients were assigned to receive pembrolizumab and 199 patients were assigned to receive paclitaxel. As of Oct 26, 2017, 326 patients in the population with CPS of 1 or higher had died (151 [77%] of 196 patients in the pembrolizumab group and 175 [88%] of 199 patients in the paclitaxel group). Median overall survival was 9·1 months (95% CI 6·2–10·7) with pembrolizumab and 8·3 months (7·6–9·0) with paclitaxel (hazard ratio [HR] 0·82, 95% CI 0·66–1·03; one-sided p=0·0421). Median progression-free survival was 1·5 months (95% CI 1·4–2·0) with pembrolizumab and 4·1 months (3·1–4·2) with paclitaxel (HR 1·27, 95% CI 1·03–1·57). In the total population, grade 3–5 treatment-related adverse events occurred in 42 (14%) of the 294 patients treated with pembrolizumab and 96 (35%) of the 276 patients treated with paclitaxel.
Interpretation:
Pembrolizumab did not significantly improve overall survival compared with paclitaxel as second-line therapy for advanced gastric or gastro-oesophageal junction cancer with PD-L1 CPS of 1 or higher. Pembrolizumab had a better safety profile than paclitaxel. Additional trials of pembrolizumab in gastric and gastro-oesophageal cancer are ongoing.
Funding:
Merck Sharp & Dohme, a subsidiary of Merck & Co. |
Persistent Identifier | http://hdl.handle.net/10722/281023 |
ISSN | 2023 Impact Factor: 98.4 2023 SCImago Journal Rankings: 12.113 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Shitara, K | - |
dc.contributor.author | Ozguroglu, M | - |
dc.contributor.author | Bang, Y-J | - |
dc.contributor.author | Bartolmeo, MD | - |
dc.contributor.author | Mandala, M | - |
dc.contributor.author | Ryu, M-H | - |
dc.contributor.author | Fornaro, L | - |
dc.contributor.author | Olesinski, T | - |
dc.contributor.author | Caglevic, C | - |
dc.contributor.author | Chung, HC | - |
dc.contributor.author | Muro, K | - |
dc.contributor.author | Goekkurt, E | - |
dc.contributor.author | Mansoor, W | - |
dc.contributor.author | McDermott, RS | - |
dc.contributor.author | Shacham-Shumueli, E | - |
dc.contributor.author | Chen, X | - |
dc.contributor.author | Mayo, C | - |
dc.contributor.author | Kang, SP | - |
dc.contributor.author | Ohtsu, A | - |
dc.contributor.author | Fuchs, CS | - |
dc.contributor.author | KEYNOTE-061 investigators | - |
dc.contributor.author | Lam, KO | - |
dc.date.accessioned | 2020-02-28T01:22:31Z | - |
dc.date.available | 2020-02-28T01:22:31Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | The Lancet, 2018, v. 392 n. 10142, p. 123-133 | - |
dc.identifier.issn | 0140-6736 | - |
dc.identifier.uri | http://hdl.handle.net/10722/281023 | - |
dc.description.abstract | Background: Patients with advanced gastric or gastro-oesophageal junction cancer that progresses on chemotherapy have poor outcomes. We compared pembrolizumab with paclitaxel in patients with advanced gastric or gastro-oesophageal junction cancer that progressed on first-line chemotherapy with a platinum and fluoropyrimidine. Methods: This randomised, open-label, phase 3 study was done at 148 medical centres in 30 countries. Eligible patients were randomised (1:1) in blocks of four per stratum with an interactive voice-response and integrated web-response system to receive either pembrolizumab 200 mg every 3 weeks for up to 2 years or standard-dose paclitaxel. Primary endpoints were overall survival and progression-free survival in patients with a programmed cell death ligand 1 (PD-L1) combined positive score (CPS) of 1 or higher. Safety was assessed in all patients, irrespective of CPS. The significance threshold for overall survival was p=0·0135 (one-sided). This trial is registered at ClinicalTrials.gov, number NCT02370498. Findings: Between June 4, 2015, and July 26, 2016, 592 patients were enrolled. Of the 395 patients who had a PD-L1 CPS of 1 or higher, 196 patients were assigned to receive pembrolizumab and 199 patients were assigned to receive paclitaxel. As of Oct 26, 2017, 326 patients in the population with CPS of 1 or higher had died (151 [77%] of 196 patients in the pembrolizumab group and 175 [88%] of 199 patients in the paclitaxel group). Median overall survival was 9·1 months (95% CI 6·2–10·7) with pembrolizumab and 8·3 months (7·6–9·0) with paclitaxel (hazard ratio [HR] 0·82, 95% CI 0·66–1·03; one-sided p=0·0421). Median progression-free survival was 1·5 months (95% CI 1·4–2·0) with pembrolizumab and 4·1 months (3·1–4·2) with paclitaxel (HR 1·27, 95% CI 1·03–1·57). In the total population, grade 3–5 treatment-related adverse events occurred in 42 (14%) of the 294 patients treated with pembrolizumab and 96 (35%) of the 276 patients treated with paclitaxel. Interpretation: Pembrolizumab did not significantly improve overall survival compared with paclitaxel as second-line therapy for advanced gastric or gastro-oesophageal junction cancer with PD-L1 CPS of 1 or higher. Pembrolizumab had a better safety profile than paclitaxel. Additional trials of pembrolizumab in gastric and gastro-oesophageal cancer are ongoing. Funding: Merck Sharp & Dohme, a subsidiary of Merck & Co. | - |
dc.language | eng | - |
dc.publisher | The Lancet Publishing Group. The Journal's web site is located at http://www.elsevier.com/locate/lancet | - |
dc.relation.ispartof | The Lancet | - |
dc.title | Pembrolizumab versus paclitaxel for previously treated, advanced gastric or gastro-oesophageal junction cancer (KEYNOTE-061): a randomised, open-label, controlled, phase 3 trial | - |
dc.type | Article | - |
dc.identifier.email | Lam, KO: lamkaon@hku.hk | - |
dc.identifier.authority | Lam, KO=rp01501 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/S0140-6736(18)31257-1 | - |
dc.identifier.pmid | 29880231 | - |
dc.identifier.scopus | eid_2-s2.0-85048592368 | - |
dc.identifier.hkuros | 303031 | - |
dc.identifier.volume | 392 | - |
dc.identifier.issue | 10142 | - |
dc.identifier.spage | 123 | - |
dc.identifier.epage | 133 | - |
dc.identifier.isi | WOS:000438501300027 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 0140-6736 | - |