PANOVSKÁ, Anna, Lucie BEZDĚKOVÁ, Lucie NEKVINDOVÁ, Martin SPACEK, Martin SIMKOVIC, Tomas PAPAJIK, Martin BREJCHA, Daniel LYSAK, Jana ZUCHNICKA, Jan NOVAK, David STAROSTKA, Hynek POUL, Filip VRBACKY, Pavel VODAREK, Renata URBANOVA, Karla PLEVOVÁ, Šárka POSPÍŠILOVÁ, Stanislava MASLEJOVA, Yvona BRYCHTOVÁ, Eva KORIŤÁKOVÁ, Lukas SMOLEJ and Michael DOUBEK. Real-world data on efficacy and safety of obinutuzumab plus chlorambucil, rituximab plus chlorambucil, and rituximab plus bendamustine in the frontline treatment of chronic lymphocytic leukemia: TheGO-CLLEARStudy by the CzechCLLStudy Group. Hematological Oncology. MALDEN, USA: WILEY-BLACKWELL, 2020, vol. 38, No 4, p. 509-516. ISSN 0278-0232. Available from: https://dx.doi.org/10.1002/hon.2744.
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Basic information
Original name Real-world data on efficacy and safety of obinutuzumab plus chlorambucil, rituximab plus chlorambucil, and rituximab plus bendamustine in the frontline treatment of chronic lymphocytic leukemia: TheGO-CLLEARStudy by the CzechCLLStudy Group
Authors PANOVSKÁ, Anna (203 Czech Republic, belonging to the institution), Lucie BEZDĚKOVÁ (203 Czech Republic, belonging to the institution), Lucie NEKVINDOVÁ (203 Czech Republic), Martin SPACEK (203 Czech Republic), Martin SIMKOVIC (203 Czech Republic), Tomas PAPAJIK (203 Czech Republic), Martin BREJCHA (203 Czech Republic), Daniel LYSAK (203 Czech Republic), Jana ZUCHNICKA (203 Czech Republic), Jan NOVAK (203 Czech Republic), David STAROSTKA (203 Czech Republic), Hynek POUL (203 Czech Republic), Filip VRBACKY (203 Czech Republic), Pavel VODAREK (203 Czech Republic), Renata URBANOVA (203 Czech Republic), Karla PLEVOVÁ (203 Czech Republic, belonging to the institution), Šárka POSPÍŠILOVÁ (203 Czech Republic, belonging to the institution), Stanislava MASLEJOVA (203 Czech Republic), Yvona BRYCHTOVÁ (203 Czech Republic, belonging to the institution), Eva KORIŤÁKOVÁ (203 Czech Republic), Lukas SMOLEJ (203 Czech Republic) and Michael DOUBEK (203 Czech Republic, guarantor, belonging to the institution).
Edition Hematological Oncology, MALDEN, USA, WILEY-BLACKWELL, 2020, 0278-0232.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30205 Hematology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 5.271
RIV identification code RIV/00216224:14740/20:00116170
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1002/hon.2744
UT WoS 000539416600001
Keywords in English CIRS; CLL; frontline treatment; obinutuzumab-chlorambucil; rituximab-bendamustine; rituximab-chlorambucil
Tags 14110212, podil, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 9/11/2020 10:38.
Abstract
Until recently, a combination of anti-CD20 antibody plus less intensive chemotherapy was a standard of care in elderly population with previously untreated chronic lymphocytic leukemia (CLL). The aim of this observational study was to retrospectively assess efficacy and safety of obinutuzumab + chlorambucil (G-Clb), rituximab + chlorambucil (R-Clb), and bendamustine + rituximab (BR) given as the frontline therapy within routine practice. The final analyzed dataset included 398 consecutive CLL patients from 10 hematology centers cooperating within the Czech CLL Study Group: 63 treated with G-Clb, 78 with R-Clb, and 257 with BR. There were no significant differences in prognostic and predictive markers among the groups. On the contrary, median age at the start of therapy and cumulative illness rating scale (CIRS) score was significantly higher in R-Clb group. Obinutuzumab plus chlorambucil regimen was preferably offered to elderly patients (compared to BR) with less severe comorbidities and lower CIRS score (compared to R-Clb). A time period when a treatment was indicated had also a strong impact on the choice of the regimen. The overall response rate reached 76% (30% complete remissions, CRs) in G-Clb, 75% (22% CRs) in R-Clb, and 85% (47% CRs) in BR group. Median event-free survival was 49.0 months for G-Clb, 20.3 months for R-Clb, and 37.0 months for BR group. Neutropenia grade >= 3 developed in 43% of G-Clb, 31% of R-Clb and in 49% of BR patients, grade >= 3 infections were recorded in 17% of G-Clb, 6.4% of R-Clb, and 17% of BR patients. In conclusion, real-world therapeutic activity of G-Clb appears to be at least comparable to prospective clinical trial data. R-Clb yields relatively good results in very old and severely comorbid patients.
Links
LQ1601, research and development projectName: CEITEC 2020 (Acronym: CEITEC2020)
Investor: Ministry of Education, Youth and Sports of the CR
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