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Polatuzumab vedotin in previously untreated diffuse large B-cell lymphoma
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.)
| cris.lastimport.wos | 2024-04-10T02:16:00Z | |
| dc.abstract.en | 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.) | pl |
| dc.cm.id | 106761 | |
| dc.cm.idOmega | UJCM7c368728f7a34c87988b485631454129 | pl |
| dc.contributor.author | Tilly, Herve | pl |
| dc.contributor.author | Morschhauser, Franck | pl |
| dc.contributor.author | Sehn, Laurie H. | pl |
| dc.contributor.author | Friedberg, Jonathan W. | pl |
| dc.contributor.author | Trneny, Marek | pl |
| dc.contributor.author | Sharman, Jeff P. | pl |
| dc.contributor.author | Herbaux, Charles | pl |
| dc.contributor.author | Burke, John M. | pl |
| dc.contributor.author | Matasar, Matthew | pl |
| dc.contributor.author | Rai, Shinya | pl |
| dc.contributor.author | Izutsu, Koji | pl |
| dc.contributor.author | Mehta-Shah, Neha | pl |
| dc.contributor.author | Oberic, Lucie | pl |
| dc.contributor.author | Chauchet, Adrien | pl |
| dc.contributor.author | Jurczak, Wojciech - 129923 | pl |
| dc.contributor.author | Song, Yuqin | pl |
| dc.contributor.author | Greil, Richard | pl |
| dc.contributor.author | Mykhalska, Larysa | pl |
| dc.contributor.author | Bergua-Burgues, Juan M. | pl |
| dc.contributor.author | Cheung, Matthew C. | pl |
| dc.contributor.author | Pinto, Antonio | pl |
| dc.contributor.author | Shin, Ho-Jin | pl |
| dc.contributor.author | Hapgood, Greg | pl |
| dc.contributor.author | Munhoz, Eduardo | pl |
| dc.contributor.author | Abrisqueta, Pau | pl |
| dc.contributor.author | Gau, Jyh-Pyng | pl |
| dc.contributor.author | Hirata, Jamie | pl |
| dc.contributor.author | Jiang, Yanwen | pl |
| dc.contributor.author | Yan, Mark | pl |
| dc.contributor.author | Lee, Calvin | pl |
| dc.contributor.author | Flowers, Christopher R. | pl |
| dc.contributor.author | Salles, Gilles | pl |
| dc.date.accession | 2022-02-10 | pl |
| dc.date.accessioned | 2022-02-10T11:38:44Z | |
| dc.date.available | 2022-02-10T11:38:44Z | |
| dc.date.issued | 2021 | pl |
| dc.description.number | 4 | pl |
| dc.description.physical | 351-363 | pl |
| dc.description.volume | 386 | pl |
| dc.identifier.doi | 10.1056/NEJMoa2115304 | pl |
| dc.identifier.eissn | 1533-4406 | pl |
| dc.identifier.issn | 0028-4793 | pl |
| dc.identifier.uri | https://ruj.uj.edu.pl/xmlui/handle/item/287990 | |
| dc.identifier.weblink | https://www.nejm.org/doi/10.1056/NEJMoa2115304 | pl |
| dc.language | eng | pl |
| dc.language.container | eng | pl |
| dc.rights | Dodaję tylko opis bibliograficzny | * |
| dc.rights.licence | Bez licencji otwartego dostępu | |
| dc.source.integrator | false | |
| dc.subtype | Article | pl |
| dc.title | Polatuzumab vedotin in previously untreated diffuse large B-cell lymphoma | pl |
| dc.title.journal | New England Journal of Medicine | pl |
| dc.type | JournalArticle | pl |
| dspace.entity.type | Publication |
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