KLENER, Pavel, Eva FRONKOVA, David BELADA, Kristina FORSTEROVA, Robert PYTLIK, Marketa KALINOVA, Martin SIMKOVIC, David ŠÁLEK, Heidi MOCIKOVA, Vít PROCHAZKA, Petra BLAHOVCOVA, Andrea JANÍKOVÁ, Jana MARKOVA, Ales OBR, Adela BERKOVA, Jozef KUBINYI, Martina VASKOVA, Ester MEJSTRIKOVA, Vít CAMPR, Radek JAKSA, Roman KODET, Kyra MICHALOVA, Jan TRKA and Marek TRNENY. Alternating R-CHOP and R-cytarabine is a safe and effective regimen for transplant-ineligible patients with a newly diagnosed mantle cell lymphoma. Hematological Oncology. MALDEN, USA: WILEY-BLACKWELL, 2018, vol. 36, No 1, p. 110-115. ISSN 0278-0232. Available from: https://dx.doi.org/10.1002/hon.2483.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name Alternating R-CHOP and R-cytarabine is a safe and effective regimen for transplant-ineligible patients with a newly diagnosed mantle cell lymphoma
Authors KLENER, Pavel (203 Czech Republic, guarantor), Eva FRONKOVA (203 Czech Republic), David BELADA (203 Czech Republic), Kristina FORSTEROVA (203 Czech Republic), Robert PYTLIK (203 Czech Republic), Marketa KALINOVA (203 Czech Republic), Martin SIMKOVIC (203 Czech Republic), David ŠÁLEK (203 Czech Republic, belonging to the institution), Heidi MOCIKOVA (203 Czech Republic), Vít PROCHAZKA (203 Czech Republic), Petra BLAHOVCOVA, Andrea JANÍKOVÁ (203 Czech Republic, belonging to the institution), Jana MARKOVA (203 Czech Republic), Ales OBR (203 Czech Republic), Adela BERKOVA (203 Czech Republic), Jozef KUBINYI (203 Czech Republic), Martina VASKOVA (203 Czech Republic), Ester MEJSTRIKOVA (203 Czech Republic), Vít CAMPR (203 Czech Republic), Radek JAKSA (203 Czech Republic), Roman KODET (203 Czech Republic), Kyra MICHALOVA (203 Czech Republic), Jan TRKA (203 Czech Republic) and Marek TRNENY (203 Czech Republic).
Edition Hematological Oncology, MALDEN, USA, WILEY-BLACKWELL, 2018, 0278-0232.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30204 Oncology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 3.439
RIV identification code RIV/00216224:14110/18:00104075
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1002/hon.2483
UT WoS 000425633300016
Keywords in English elderly patients; high-dose cytarabine; mantle cell lymphoma; PET-CT; rituximab maintenance
Tags 14110212, rivok
Tags International impact, Reviewed
Changed by Changed by: Soňa Böhmová, učo 232884. Changed: 9/2/2019 20:18.
Abstract
Implementation of cytarabine into induction therapy became standard of care for younger patients with mantle cell lymphoma (MCL). On the basis of its beneficial impact, many centers incorporated cytarabine at lower doses also into first-line treatments of elderly patients. We conducted a multicenter observational study that prospectively analyzed safety and efficacy of alternating 3+3cycles of R-CHOP and R-cytarabine for newly diagnosed transplant-ineligible MCL patients. A total of 73 patients were enrolled with median age 70years. Most patients had intermediate (39.7%) and high-risk (50.7%) disease according to MCL international prognostic index. Rituximab maintenance was initiated in 58 patients. Overall response rate reached 89% by positron emission tomography-computed tomography, including 75.3% complete remissions. Two patients (2.7%) did not complete the induction therapy because of toxicity. Three patients (4.1%) were considered nonresponders, which led to therapy change before completion of induction. Estimated progression-free survival and overall survival were 51.3% and 68.6% at 4years, respectively. Mantle cell lymphoma international prognostic index, bulky disease ( 5cm), and achievement of positron emission tomography-negativity independently correlated with progression-free survival. Grade 3 to 4 hematologic and nonhematologic toxicity was documented in 48% and 20.5% patients, respectively. Alternation of R-CHOP and R-cytarabine represents feasible and very effective regimen for elderly/comorbid MCL patients. This study was registered at GovTrial () NCT03054883.
PrintDisplayed: 29/6/2024 04:19