Literature DB >> 29473209

Bendamustine-based conditioning prior to autologous stem cell transplantation (ASCT): Results of a French multicenter study of 474 patients from LYmphoma Study Association (LYSA) centers.

Sylvain P Chantepie1, Sylvain Garciaz2, Emmanuelle Tchernonog3, Frederic Peyrade4, Marie-Virginie Larcher5, Momar Diouf6, Luc-Mathieu Fornecker7, Roch Houot8, Thomas Gastinne9, Carole Soussain10, Sandra Malak10, Richard Lemal11, Caroline Delette12, Ahmad Ibrahim13, Anne-Claire Gac1, Emilie Reboursière1, Jean-Pierre Vilque14, Mohamed-Amine Bekadja15, Rene-Olivier Casasnovas16, Remy Gressin17, Stéphanie Guidez18, Diane Coso2, Charles Herbaux19, Ibrahim Yakoub-Agha19, Krimo Bouabdallah20, Eric Durot21, Gandhi Damaj1,22.   

Abstract

Carmustine shortage has led to an increase use of alternative conditioning regimens prior to autologous stem cell transplantation for the treatment of lymphoma, including Bendamustine-based (BeEAM). The aim of this study was to evaluate the safety of the BeEAM regimen in a large cohort of patients. A total of 474 patients with a median age of 56 years were analyzed. The majority of patients had diffuse large B-cell lymphoma (43.5%). Bendamustine was administered at a median dose of 197 mg/m2 /day (50-250) on days-7 and -6. The observed grade 1-4 toxicities included mucositis (83.5%), gastroenteritis (53%), skin toxicity (34%), colitis (29%), liver toxicity (19%), pneumonitis (5%), and cardiac rhythm disorders (4%). Nonrelapse mortality (NRM) was reported in 3.3% of patients. Acute renal failure (ARF) was reported in 132 cases (27.9%) (G ≥2; 12.3%). Organ toxicities and death were more frequent in patients with post conditioning renal failure. In a multivariate analysis, pretransplant chronic renal failure, bendamustine dose >160 mg/m2 and age were independent prognostic factors for ARF. Pretransplant chronic renal failure, hyperhydration volume, duration of hyperhydration, and etoposide dose were predictive factors of NRM. A simple, four-point scoring system can stratify patients by levels of risk for ARF and may allow for a reduction in the bendamustine dose to avoid toxicity. Drugs shortage may have dangerous consequences. Prospective, comparative studies are needed to confirm the toxicity/efficacy extents from this conditioning regimen compared to other types of high dose therapy.
© 2018 Wiley Periodicals, Inc.

Entities:  

Mesh:

Substances:

Year:  2018        PMID: 29473209     DOI: 10.1002/ajh.25077

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  5 in total

1.  BeEAM High-Dose Chemotherapy with Polatuzumab (Pola-BeEAM) before ASCT in Patients with DLBCL-A Pilot Study.

Authors:  Tanja Stoffel; Ulrike Bacher; Yara Banz; Michael Daskalakis; Urban Novak; Thomas Pabst
Journal:  J Clin Med       Date:  2022-06-28       Impact factor: 4.964

Review 2.  Strategies to improve outcomes of autologous hematopoietic cell transplant in lymphoma.

Authors:  Parastoo B Dahi; Hillard M Lazarus; Craig S Sauter; Sergio A Giralt
Journal:  Bone Marrow Transplant       Date:  2018-11-02       Impact factor: 5.174

3.  [Safety and the short-term efficacy of bendamustine in the conditioning regimen for autologous stem cell transplantation in patients with lymphoma].

Authors:  L C An; Y H Liu; J Y Wang; J J Ma; J Q Xu; K M Li; R X Wei; J R Sui; X Y Feng; X Q Liu; L M Chen; X X Chu
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2022-01-14

4.  Comparison of CEAC, BEAM and IEAC conditioning regimens followed by autologous stem cell transplantation in peripheral T-cell lymphoma patients.

Authors:  Yi-Ying Xiong; Jing Wang; Li Wang; Jian-Bin Chen; Lin Liu; Xiao-Qiong Tang; Xin Wang; Hong-Bin Zhang
Journal:  Sci Rep       Date:  2022-08-23       Impact factor: 4.996

5.  Bendamustine-induced nephrogenic diabetes insipidus - A case report.

Authors:  Audrey Desjardins; Viviane Le-Nguyen; Léa Turgeon-Mallette; Chloé Vo; Jean-Samuel Boudreault; Jean-Philippe Rioux; Xue Feng; Amélie Veilleux
Journal:  J Oncol Pharm Pract       Date:  2021-05-14       Impact factor: 1.809

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.