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- Publisher Website: 10.1200/JCO.21.01308
- Scopus: eid_2-s2.0-85125441729
- PMID: 35108059
- WOS: WOS:000799692000006
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Article: Five-Year Survival Outcomes From the PACIFIC Trial: Durvalumab After Chemoradiotherapy in Stage III Non-Small-Cell Lung Cancer
Title | Five-Year Survival Outcomes From the PACIFIC Trial: Durvalumab After Chemoradiotherapy in Stage III Non-Small-Cell Lung Cancer |
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Authors | Spigel, David R.Faivre-Finn, CorinneGray, Jhanelle E.Vicente, DavidPlanchard, DavidPaz-Ares, LuisVansteenkiste, Johan F.Garassino, Marina C.Hui, RinaQuantin, XavierRimner, AndreasWu, Yi LongÖzgüroǧlu, MustafaLee, Ki H.Kato, TerufumiDe Wit, MaikeKurata, TakayasuReck, MartinCho, Byoung C.Senan, SureshNaidoo, JarushkaMann, HelenNewton, MichaelThiyagarajah, PirunthaAntonia, Scott J. |
Issue Date | 2022 |
Citation | Journal of Clinical Oncology, 2022, v. 40, n. 12, p. 1301-1311 How to Cite? |
Abstract | PURPOSEThe phase III PACIFIC trial compared durvalumab with placebo in patients with unresectable, stage III non-small-cell lung cancer and no disease progression after concurrent chemoradiotherapy. Consolidation durvalumab was associated with significant improvements in the primary end points of overall survival (OS; stratified hazard ratio [HR], 0.68; 95% CI, 0.53 to 0.87; P =.00251) and progression-free survival (PFS [blinded independent central review; RECIST v1.1]; stratified HR, 0.52; 95% CI, 0.42 to 0.65; P <.0001), with manageable safety. We report updated, exploratory analyses of survival, approximately 5 years after the last patient was randomly assigned.METHODSPatients with WHO performance status 0 or 1 (any tumor programmed cell death-ligand 1 status) were randomly assigned (2:1) to durvalumab (10 mg/kg intravenously; administered once every 2 weeks for 12 months) or placebo, stratified by age, sex, and smoking history. Time-to-event end point analyses were performed using stratified log-rank tests. Medians and landmark survival rates were estimated using the Kaplan-Meier method.RESULTSSeven hundred and nine of 713 randomly assigned patients received durvalumab (473 of 476) or placebo (236 of 237). As of January 11, 2021 (median follow-up, 34.2 months [all patients]; 61.6 months [censored patients]), updated OS (stratified HR, 0.72; 95% CI, 0.59 to 0.89; median, 47.5 v 29.1 months) and PFS (stratified HR, 0.55; 95% CI, 0.45 to 0.68; median, 16.9 v 5.6 months) remained consistent with the primary analyses. Estimated 5-year rates (95% CI) for durvalumab and placebo were 42.9% (38.2 to 47.4) versus 33.4% (27.3 to 39.6) for OS and 33.1% (28.0 to 38.2) versus 19.0% (13.6 to 25.2) for PFS.CONCLUSIONThese updated analyses demonstrate robust and sustained OS and durable PFS benefit with durvalumab after chemoradiotherapy. An estimated 42.9% of patients randomly assigned to durvalumab remain alive at 5 years and 33.1% of patients randomly assigned to durvalumab remain alive and free of disease progression, establishing a new benchmark for standard of care in this setting. |
Persistent Identifier | http://hdl.handle.net/10722/326433 |
ISSN | 2023 Impact Factor: 42.1 2023 SCImago Journal Rankings: 10.639 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Spigel, David R. | - |
dc.contributor.author | Faivre-Finn, Corinne | - |
dc.contributor.author | Gray, Jhanelle E. | - |
dc.contributor.author | Vicente, David | - |
dc.contributor.author | Planchard, David | - |
dc.contributor.author | Paz-Ares, Luis | - |
dc.contributor.author | Vansteenkiste, Johan F. | - |
dc.contributor.author | Garassino, Marina C. | - |
dc.contributor.author | Hui, Rina | - |
dc.contributor.author | Quantin, Xavier | - |
dc.contributor.author | Rimner, Andreas | - |
dc.contributor.author | Wu, Yi Long | - |
dc.contributor.author | Özgüroǧlu, Mustafa | - |
dc.contributor.author | Lee, Ki H. | - |
dc.contributor.author | Kato, Terufumi | - |
dc.contributor.author | De Wit, Maike | - |
dc.contributor.author | Kurata, Takayasu | - |
dc.contributor.author | Reck, Martin | - |
dc.contributor.author | Cho, Byoung C. | - |
dc.contributor.author | Senan, Suresh | - |
dc.contributor.author | Naidoo, Jarushka | - |
dc.contributor.author | Mann, Helen | - |
dc.contributor.author | Newton, Michael | - |
dc.contributor.author | Thiyagarajah, Piruntha | - |
dc.contributor.author | Antonia, Scott J. | - |
dc.date.accessioned | 2023-03-10T02:19:15Z | - |
dc.date.available | 2023-03-10T02:19:15Z | - |
dc.date.issued | 2022 | - |
dc.identifier.citation | Journal of Clinical Oncology, 2022, v. 40, n. 12, p. 1301-1311 | - |
dc.identifier.issn | 0732-183X | - |
dc.identifier.uri | http://hdl.handle.net/10722/326433 | - |
dc.description.abstract | PURPOSEThe phase III PACIFIC trial compared durvalumab with placebo in patients with unresectable, stage III non-small-cell lung cancer and no disease progression after concurrent chemoradiotherapy. Consolidation durvalumab was associated with significant improvements in the primary end points of overall survival (OS; stratified hazard ratio [HR], 0.68; 95% CI, 0.53 to 0.87; P =.00251) and progression-free survival (PFS [blinded independent central review; RECIST v1.1]; stratified HR, 0.52; 95% CI, 0.42 to 0.65; P <.0001), with manageable safety. We report updated, exploratory analyses of survival, approximately 5 years after the last patient was randomly assigned.METHODSPatients with WHO performance status 0 or 1 (any tumor programmed cell death-ligand 1 status) were randomly assigned (2:1) to durvalumab (10 mg/kg intravenously; administered once every 2 weeks for 12 months) or placebo, stratified by age, sex, and smoking history. Time-to-event end point analyses were performed using stratified log-rank tests. Medians and landmark survival rates were estimated using the Kaplan-Meier method.RESULTSSeven hundred and nine of 713 randomly assigned patients received durvalumab (473 of 476) or placebo (236 of 237). As of January 11, 2021 (median follow-up, 34.2 months [all patients]; 61.6 months [censored patients]), updated OS (stratified HR, 0.72; 95% CI, 0.59 to 0.89; median, 47.5 v 29.1 months) and PFS (stratified HR, 0.55; 95% CI, 0.45 to 0.68; median, 16.9 v 5.6 months) remained consistent with the primary analyses. Estimated 5-year rates (95% CI) for durvalumab and placebo were 42.9% (38.2 to 47.4) versus 33.4% (27.3 to 39.6) for OS and 33.1% (28.0 to 38.2) versus 19.0% (13.6 to 25.2) for PFS.CONCLUSIONThese updated analyses demonstrate robust and sustained OS and durable PFS benefit with durvalumab after chemoradiotherapy. An estimated 42.9% of patients randomly assigned to durvalumab remain alive at 5 years and 33.1% of patients randomly assigned to durvalumab remain alive and free of disease progression, establishing a new benchmark for standard of care in this setting. | - |
dc.language | eng | - |
dc.relation.ispartof | Journal of Clinical Oncology | - |
dc.title | Five-Year Survival Outcomes From the PACIFIC Trial: Durvalumab After Chemoradiotherapy in Stage III Non-Small-Cell Lung Cancer | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1200/JCO.21.01308 | - |
dc.identifier.pmid | 35108059 | - |
dc.identifier.scopus | eid_2-s2.0-85125441729 | - |
dc.identifier.volume | 40 | - |
dc.identifier.issue | 12 | - |
dc.identifier.spage | 1301 | - |
dc.identifier.epage | 1311 | - |
dc.identifier.eissn | 1527-7755 | - |
dc.identifier.isi | WOS:000799692000006 | - |