Detailed Information on Publication Record
2019
Prospective observational study in comorbid patients with chronic lymphocytic leukemia receiving first-line bendamustine with rituximab
ŠPAČEK, Martin, Petra OBRTLÍKOVÁ, Stanislava HROBKOVÁ, Eduard CMUNT, Josef KARBAN et. al.Basic information
Original name
Prospective observational study in comorbid patients with chronic lymphocytic leukemia receiving first-line bendamustine with rituximab
Authors
ŠPAČEK, Martin (203 Czech Republic, guarantor), Petra OBRTLÍKOVÁ (203 Czech Republic), Stanislava HROBKOVÁ (703 Slovakia, belonging to the institution), Eduard CMUNT (203 Czech Republic), Josef KARBAN (203 Czech Republic), Jan MOLINSKÝ (203 Czech Republic), Martin ŠIMKOVIČ (203 Czech Republic), Heidi MOCIKOVÁ (203 Czech Republic), Lekaa MOHAMMADOVÁ (203 Czech Republic), Anna PANOVSKÁ (203 Czech Republic, belonging to the institution), Jan NOVÁK (203 Czech Republic), Marek TRNĚNÝ (203 Czech Republic), Lukáš SMOLEJ (203 Czech Republic) and Michael DOUBEK (203 Czech Republic, belonging to the institution)
Edition
Leukemia Research, OXFORD, PERGAMON-ELSEVIER SCIENCE LTD, 2019, 0145-2126
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30205 Hematology
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 2.214
RIV identification code
RIV/00216224:14110/19:00108491
Organization unit
Faculty of Medicine
UT WoS
000460898400004
Keywords in English
CLL; Bendamustine; Rituximab; Comorbid patients; CIRS; First-line treatment
Tags
International impact, Reviewed
Změněno: 31/3/2020 22:16, Mgr. Pavla Foltynová, Ph.D.
Abstract
V originále
Chemoimmunotherapy with bendamustine and rituximab is an alternative treatment for elderly patients with CLL. The aim of this observational multicenter study was to prospectively assess efficacy and safety of bendamustine and rituximab in front-line therapy in patients with CLL and significant comorbidities in real hematological practice. Eighty-three consecutive patients with cumulative illness rating scale (CIRS) > 6 who received at least one cycle of BR as first-line treatment were included in the study. The median age was 71 years (range, 53-83), the median CIRS was 8 (range, 7-17), and 60.2% of patients had a creatinine clearance <= 70 mL/min. FISH analysis, available for 78 cases, showed a del(17p) in 11.5% and del(11q) in 20.5% of patients. Overall response rate was 88.0% with a complete response rate of 20.5%. With median follow-up time of 22 months, the estimated median progression free survival was 35.9 months. Progression free survival and overall survival rates at 2 years were 69.9% and 96.2%, respectively. Grade 3 or 4 neutropenia, thrombocytopenia, and anemia were documented in 40 (48.2%), 14 (16.9%), and 8 (9.6%) patients, respectively. Grade 3 or 4 infections occurred in 14.5% of patients. Chemoimmunotherapy with BR is an effective therapeutic option with manageable toxicity for the initial treatment of CLL patients with significant comorbidities. ClinicalTrials.gov Identifier: NCT02381899.
Links
NV15-30015A, research and development project |
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