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.Základní údaje
Originální název
Prospective observational study in comorbid patients with chronic lymphocytic leukemia receiving first-line bendamustine with rituximab
Autoři
ŠPAČEK, Martin (203 Česká republika, garant), Petra OBRTLÍKOVÁ (203 Česká republika), Stanislava HROBKOVÁ (703 Slovensko, domácí), Eduard CMUNT (203 Česká republika), Josef KARBAN (203 Česká republika), Jan MOLINSKÝ (203 Česká republika), Martin ŠIMKOVIČ (203 Česká republika), Heidi MOCIKOVÁ (203 Česká republika), Lekaa MOHAMMADOVÁ (203 Česká republika), Anna PANOVSKÁ (203 Česká republika, domácí), Jan NOVÁK (203 Česká republika), Marek TRNĚNÝ (203 Česká republika), Lukáš SMOLEJ (203 Česká republika) a Michael DOUBEK (203 Česká republika, domácí)
Vydání
Leukemia Research, OXFORD, PERGAMON-ELSEVIER SCIENCE LTD, 2019, 0145-2126
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30205 Hematology
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 2.214
Kód RIV
RIV/00216224:14110/19:00108491
Organizační jednotka
Lékařská fakulta
UT WoS
000460898400004
Klíčová slova anglicky
CLL; Bendamustine; Rituximab; Comorbid patients; CIRS; First-line treatment
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 31. 3. 2020 22:16, Mgr. Pavla Foltynová, Ph.D.
Anotace
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.
Návaznosti
NV15-30015A, projekt VaV |
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