Detailed Information on Publication Record
2022
Polatuzumab vedotin plus bendamustine and rituximab in patients with relapsed/refractory diffuse large B-cell lymphoma in the real world
VODICKA, Prokop, Katerina BENESOVA, Andrea JANÍKOVÁ, Vit PROCHAZKA, David BELADA et. al.Basic information
Original name
Polatuzumab vedotin plus bendamustine and rituximab in patients with relapsed/refractory diffuse large B-cell lymphoma in the real world
Authors
VODICKA, Prokop (203 Czech Republic), Katerina BENESOVA (203 Czech Republic), Andrea JANÍKOVÁ (203 Czech Republic, belonging to the institution), Vit PROCHAZKA (203 Czech Republic), David BELADA (203 Czech Republic), Heidi MOCIKOVA (203 Czech Republic), Katerina STEINEROVA (203 Czech Republic), Juraj DURAS (203 Czech Republic), Josef KARBAN (203 Czech Republic), Veronika HANACKOVA (203 Czech Republic), Alice SYKOROVA (203 Czech Republic), Ales OBR (203 Czech Republic) and Marek TRNENY (203 Czech Republic, guarantor)
Edition
European Journal of Haematology, Hoboken, Wiley-Blackwell, 2022, 0902-4441
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30205 Hematology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 3.100
RIV identification code
RIV/00216224:14110/22:00128259
Organization unit
Faculty of Medicine
UT WoS
000793085400001
Keywords in English
DLBCL; polatuzumab vedotin; real world
Tags
International impact, Reviewed
Změněno: 25/1/2023 09:54, Mgr. Tereza Miškechová
Abstract
V originále
Objectives Polatuzumab vedotin with bendamustine and rituximab (Pola-BR) was approved for treatment of transplant-ineligible patients with relapsed/refractory DLBCL (R/R DLBCL). However, the number of patients treated in the GO29365 trial including the extension cohort was limited, and more data evaluating the efficacy of this treatment regimen is needed. Methods We analyzed 21 patients with R/R DLBCL to determine real-life efficacy and safety of Pola-BR regimen. Data of all patients entered the database of the NiHiL project (NCT03199066). Results Median overall survival was 8.7 months, and progression-free survival 3.8 months. The overall response rate was 33%. Grade 3-4 neutropenia was detected in 29%, thrombocytopenia in 38%, anemia in 19%, infections in 24% cases, and peripheral neuropathy in 5%. Discontinuation of treatment was caused by progression in 50%, adverse events in 31%, and intended bridging to CAR-T therapy in 19%. Conclusion Although the outcome of patients is worse than in GO29365 trial, the use of Pola-BR regimen in the real world demonstrates tolerable toxicity profile and efficacy in transplant-ineligible patients with R/R DLBCL. Moreover, this regimen might represent a perspective option as a bridge to CAR-T therapy.