Polatuzumab vedotin in previously untreated diffuse large B-cell lymphoma

2021
journal article
article
705
cris.lastimport.wos2024-04-10T02:16:00Z
dc.abstract.enBackground: Diffuse large B-cell lymphoma (DLBCL) is typically treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP). However, only 60% of patients are cured with R-CHOP. Polatuzumab vedotin is an antibody–drug conjugate targeting CD79b, which is ubiquitously expressed on the surface of malignant B cells. Methods: We conducted a double-blind, placebo-controlled, international phase 3 trial to evaluate a modified regimen of R-CHOP (pola-R-CHP), in which vincristine was replaced with polatuzumab vedotin, as compared with standard R-CHOP, in patients with previously untreated intermediate-risk or high-risk DLBCL. Patients 18 to 80 years of age were randomly assigned in a 1:1 ratio to receive six cycles of either pola-R-CHP or R-CHOP, plus two cycles of rituximab alone. The primary end point was investigator-assessed progression-free survival. Secondary end points included overall survival and safety. Results: Overall, 879 patients underwent randomization: 440 were assigned to the pola-R-CHP group and 439 to the R-CHOP group. After a median follow-up of 28.2 months, the percentage of patients surviving without progression was significantly higher in the pola-R-CHP group than in the R-CHOP group (76.7% [95% confidence interval (CI), 72.7 to 80.8] vs. 70.2% [95% CI, 65.8 to 74.6] at 2 years; stratified hazard ratio for progression, relapse, or death, 0.73 by Cox regression; 95% CI, 0.57 to 0.95; P=0.02). Overall survival at 2 years did not differ significantly between the groups (88.7% [95% CI, 85.7 to 91.6] in the pola-R-CHP group and 88.6% [95% CI, 85.6 to 91.6] in the R-CHOP group; hazard ratio for death, 0.94; 95% CI, 0.65 to 1.37; P=0.75). The safety profile was similar in the two groups. Conclusions: Among patients with previously untreated intermediate-risk or high-risk DLBCL, the risk of disease progression, relapse, or death was lower among those who received pola-R-CHP than among those who received R-CHOP. (Funded by F. Hoffmann–La Roche/Genentech; POLARIX ClinicalTrials.gov number, NCT03274492. opens in new tab.)pl
dc.cm.id106761
dc.cm.idOmegaUJCM7c368728f7a34c87988b485631454129pl
dc.contributor.authorTilly, Hervepl
dc.contributor.authorMorschhauser, Franckpl
dc.contributor.authorSehn, Laurie H.pl
dc.contributor.authorFriedberg, Jonathan W.pl
dc.contributor.authorTrneny, Marekpl
dc.contributor.authorSharman, Jeff P.pl
dc.contributor.authorHerbaux, Charlespl
dc.contributor.authorBurke, John M.pl
dc.contributor.authorMatasar, Matthewpl
dc.contributor.authorRai, Shinyapl
dc.contributor.authorIzutsu, Kojipl
dc.contributor.authorMehta-Shah, Nehapl
dc.contributor.authorOberic, Luciepl
dc.contributor.authorChauchet, Adrienpl
dc.contributor.authorJurczak, Wojciech - 129923 pl
dc.contributor.authorSong, Yuqinpl
dc.contributor.authorGreil, Richardpl
dc.contributor.authorMykhalska, Larysapl
dc.contributor.authorBergua-Burgues, Juan M.pl
dc.contributor.authorCheung, Matthew C.pl
dc.contributor.authorPinto, Antoniopl
dc.contributor.authorShin, Ho-Jinpl
dc.contributor.authorHapgood, Gregpl
dc.contributor.authorMunhoz, Eduardopl
dc.contributor.authorAbrisqueta, Paupl
dc.contributor.authorGau, Jyh-Pyngpl
dc.contributor.authorHirata, Jamiepl
dc.contributor.authorJiang, Yanwenpl
dc.contributor.authorYan, Markpl
dc.contributor.authorLee, Calvinpl
dc.contributor.authorFlowers, Christopher R.pl
dc.contributor.authorSalles, Gillespl
dc.date.accession2022-02-10pl
dc.date.accessioned2022-02-10T11:38:44Z
dc.date.available2022-02-10T11:38:44Z
dc.date.issued2021pl
dc.description.number4pl
dc.description.physical351-363pl
dc.description.volume386pl
dc.identifier.doi10.1056/NEJMoa2115304pl
dc.identifier.eissn1533-4406pl
dc.identifier.issn0028-4793pl
dc.identifier.urihttps://ruj.uj.edu.pl/xmlui/handle/item/287990
dc.identifier.weblinkhttps://www.nejm.org/doi/10.1056/NEJMoa2115304pl
dc.languageengpl
dc.language.containerengpl
dc.rightsDodaję tylko opis bibliograficzny*
dc.rights.licenceBez licencji otwartego dostępu
dc.source.integratorfalse
dc.subtypeArticlepl
dc.titlePolatuzumab vedotin in previously untreated diffuse large B-cell lymphomapl
dc.title.journalNew England Journal of Medicinepl
dc.typeJournalArticlepl
dspace.entity.typePublication
cris.lastimport.wos
2024-04-10T02:16:00Z
dc.abstract.enpl
Background: Diffuse large B-cell lymphoma (DLBCL) is typically treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP). However, only 60% of patients are cured with R-CHOP. Polatuzumab vedotin is an antibody–drug conjugate targeting CD79b, which is ubiquitously expressed on the surface of malignant B cells. Methods: We conducted a double-blind, placebo-controlled, international phase 3 trial to evaluate a modified regimen of R-CHOP (pola-R-CHP), in which vincristine was replaced with polatuzumab vedotin, as compared with standard R-CHOP, in patients with previously untreated intermediate-risk or high-risk DLBCL. Patients 18 to 80 years of age were randomly assigned in a 1:1 ratio to receive six cycles of either pola-R-CHP or R-CHOP, plus two cycles of rituximab alone. The primary end point was investigator-assessed progression-free survival. Secondary end points included overall survival and safety. Results: Overall, 879 patients underwent randomization: 440 were assigned to the pola-R-CHP group and 439 to the R-CHOP group. After a median follow-up of 28.2 months, the percentage of patients surviving without progression was significantly higher in the pola-R-CHP group than in the R-CHOP group (76.7% [95% confidence interval (CI), 72.7 to 80.8] vs. 70.2% [95% CI, 65.8 to 74.6] at 2 years; stratified hazard ratio for progression, relapse, or death, 0.73 by Cox regression; 95% CI, 0.57 to 0.95; P=0.02). Overall survival at 2 years did not differ significantly between the groups (88.7% [95% CI, 85.7 to 91.6] in the pola-R-CHP group and 88.6% [95% CI, 85.6 to 91.6] in the R-CHOP group; hazard ratio for death, 0.94; 95% CI, 0.65 to 1.37; P=0.75). The safety profile was similar in the two groups. Conclusions: Among patients with previously untreated intermediate-risk or high-risk DLBCL, the risk of disease progression, relapse, or death was lower among those who received pola-R-CHP than among those who received R-CHOP. (Funded by F. Hoffmann–La Roche/Genentech; POLARIX ClinicalTrials.gov number, NCT03274492. opens in new tab.)
dc.cm.id
106761
dc.cm.idOmegapl
UJCM7c368728f7a34c87988b485631454129
dc.contributor.authorpl
Tilly, Herve
dc.contributor.authorpl
Morschhauser, Franck
dc.contributor.authorpl
Sehn, Laurie H.
dc.contributor.authorpl
Friedberg, Jonathan W.
dc.contributor.authorpl
Trneny, Marek
dc.contributor.authorpl
Sharman, Jeff P.
dc.contributor.authorpl
Herbaux, Charles
dc.contributor.authorpl
Burke, John M.
dc.contributor.authorpl
Matasar, Matthew
dc.contributor.authorpl
Rai, Shinya
dc.contributor.authorpl
Izutsu, Koji
dc.contributor.authorpl
Mehta-Shah, Neha
dc.contributor.authorpl
Oberic, Lucie
dc.contributor.authorpl
Chauchet, Adrien
dc.contributor.authorpl
Jurczak, Wojciech - 129923
dc.contributor.authorpl
Song, Yuqin
dc.contributor.authorpl
Greil, Richard
dc.contributor.authorpl
Mykhalska, Larysa
dc.contributor.authorpl
Bergua-Burgues, Juan M.
dc.contributor.authorpl
Cheung, Matthew C.
dc.contributor.authorpl
Pinto, Antonio
dc.contributor.authorpl
Shin, Ho-Jin
dc.contributor.authorpl
Hapgood, Greg
dc.contributor.authorpl
Munhoz, Eduardo
dc.contributor.authorpl
Abrisqueta, Pau
dc.contributor.authorpl
Gau, Jyh-Pyng
dc.contributor.authorpl
Hirata, Jamie
dc.contributor.authorpl
Jiang, Yanwen
dc.contributor.authorpl
Yan, Mark
dc.contributor.authorpl
Lee, Calvin
dc.contributor.authorpl
Flowers, Christopher R.
dc.contributor.authorpl
Salles, Gilles
dc.date.accessionpl
2022-02-10
dc.date.accessioned
2022-02-10T11:38:44Z
dc.date.available
2022-02-10T11:38:44Z
dc.date.issuedpl
2021
dc.description.numberpl
4
dc.description.physicalpl
351-363
dc.description.volumepl
386
dc.identifier.doipl
10.1056/NEJMoa2115304
dc.identifier.eissnpl
1533-4406
dc.identifier.issnpl
0028-4793
dc.identifier.uri
https://ruj.uj.edu.pl/xmlui/handle/item/287990
dc.identifier.weblinkpl
https://www.nejm.org/doi/10.1056/NEJMoa2115304
dc.languagepl
eng
dc.language.containerpl
eng
dc.rights*
Dodaję tylko opis bibliograficzny
dc.rights.licence
Bez licencji otwartego dostępu
dc.source.integrator
false
dc.subtypepl
Article
dc.titlepl
Polatuzumab vedotin in previously untreated diffuse large B-cell lymphoma
dc.title.journalpl
New England Journal of Medicine
dc.typepl
JournalArticle
dspace.entity.type
Publication
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