Academic Journal

Outcomes and toxicity of allogeneic hematopoietic cell transplantation in chronic myeloid leukemia patients previously treated with second-generation tyrosine kinase inhibitors: a prospective non-interventional study from the Chronic Malignancy Working Party of the EBMT

التفاصيل البيبلوغرافية
العنوان: Outcomes and toxicity of allogeneic hematopoietic cell transplantation in chronic myeloid leukemia patients previously treated with second-generation tyrosine kinase inhibitors: a prospective non-interventional study from the Chronic Malignancy Working Party of the EBMT
المؤلفون: Masouridi-Levrat, Stavroula, Olavarria, Eduardo, Iacobelli, Simona, Aljurf, Mahmoud, Morozova, Elena, Niittyvuopio, Riitta, Sengeloev, Henrik, Reményi, Peter, Helbig, Grzegorz, Browne, Paul, Ganser, Arnold, Nagler, Arnon, Snowden, John A., Robin, Marie, Passweg, Jakob, Van Gorkom, Gwendolyn, Wallet, Hélène Labussière, Hoek, Jennifer, Blok, Henric-Jan, De Witte, Theo, Kroeger, Nicolaus, Hayden, Patrick, Chalandon, Yves, Yakoub-Agha, Ibrahim
المساهمون: Université de Lille, Inserm, CHU Lille, Hopital Saint-Louis AP-HP AP-HP, Hospices Civils de Lyon HCL, Institut de Recherche Translationnelle sur l'Inflammation (INFINITE) - U1286
سنة النشر: 2024
المجموعة: LillOA (Lille Open Archive - Université de Lille)
الوصف: Allogeneic hematopoietic cell transplantation (allo-HCT) remains a treatment option for patients with chronic myeloid leukemia (CML) who fail to respond to tyrosine kinase inhibitors (TKIs). While imatinib seems to have no adverse impact on outcomes after transplant, little is known on the effects of prior use of second-generation TKI (2GTKI). We present the results of a prospective non-interventional study performed by the EBMT on 383 consecutive CML patients previously treated with dasatinib or nilotinib undergoing allo-HCT from 2009 to 2013. The median age was 45 years (18–68). Disease status at transplant was CP1 in 139 patients (38%), AP or >CP1 in 163 (45%), and BC in 59 (16%). The choice of 2GTKI was: 40% dasatinib, 17% nilotinib, and 43% a sequential treatment of dasatinib and nilotinib with or without bosutinib/ponatinib. With a median follow-up of 37 months (1–77), 8% of patients developed either primary or secondary graft failure, 34% acute and 60% chronic GvHD. There were no differences in post-transplant complications between the three different 2GTKI subgroups. Non-relapse mortality was 18% and 24% at 12 months and at 5 years, respectively. Relapse incidence was 36%, overall survival 56% and relapse-free survival 40% at 5 years. No differences in post-transplant outcomes were found between the three different 2GTKI subgroups. This prospective study demonstrates the feasibility of allo-HCT in patients previously treated with 2GTKI with a post-transplant complications rate comparable to that of TKI-naive or imatinib-treated patients. ; 57
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/octet-stream; application/rdf+xml; charset=utf-8; application/pdf
اللغة: English
Relation: Bone Marrow Transplantation; Bone Marrow Transplant.; http://hdl.handle.net/20.500.12210/114126
الاتاحة: https://hdl.handle.net/20.500.12210/114126
Rights: Attribution 3.0 United States ; info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.CCC13900
قاعدة البيانات: BASE