Detailed Information on Publication Record
2020
Allogeneic hematopoietic cell transplantation improves outcome of adults with t(6;9) acute myeloid leukemia: results from an international collaborative study
KAYSER, Sabine, Robert K. HILLS, Marlise R. LUSKIN, Andrew M. BRUNNER, Christine TERRE et. al.Basic information
Original name
Allogeneic hematopoietic cell transplantation improves outcome of adults with t(6;9) acute myeloid leukemia: results from an international collaborative study
Authors
KAYSER, Sabine (276 Germany, guarantor), Robert K. HILLS (826 United Kingdom of Great Britain and Northern Ireland), Marlise R. LUSKIN (840 United States of America), Andrew M. BRUNNER (840 United States of America), Christine TERRE (250 France), Jorg WESTERMANN (276 Germany), Kamal MENGHRAJANI (840 United States of America), Carole SHAW (840 United States of America), Maria R. BAER (840 United States of America), Michelle A. ELLIOTT (840 United States of America), Alexander E. PERL (840 United States of America), Zdeněk RÁČIL (203 Czech Republic, belonging to the institution), Jiří MAYER (203 Czech Republic, belonging to the institution), Pavel ZAK (203 Czech Republic), Tomas SZOTKOWSKI (203 Czech Republic), Stephane DE BOTTON (250 France), David GRIMWADE (826 United Kingdom of Great Britain and Northern Ireland), Karin MAYER (276 Germany), Roland B. WALTER (840 United States of America), Alwin KRAMER (276 Germany), Alan K. BURNETT (826 United Kingdom of Great Britain and Northern Ireland), Anthony D. HO (276 Germany), Uwe PLATZBECKER (276 Germany), Christian THIEDE (276 Germany), Gerhard EHNINGER (276 Germany), Richard M. STONE (840 United States of America), Christoph ROLLIG (276 Germany), Martin S. TALLMAN (840 United States of America), Elihu H. ESTEY (840 United States of America), Carsten MULLER-TIDOW (276 Germany), Nigel H. RUSSELL (826 United Kingdom of Great Britain and Northern Ireland), Richard F. SCHLENK (276 Germany) and Mark J. LEVIS (840 United States of America)
Edition
Haematologica, PAVIA, FERRATA STORTI FOUNDATION, 2020, 0390-6078
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30205 Hematology
Country of publisher
Italy
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 9.941
RIV identification code
RIV/00216224:14110/20:00118595
Organization unit
Faculty of Medicine
UT WoS
000505041200031
Keywords in English
HIGH-DOSE CYTARABINE; ACUTE MYELOGENOUS LEUKEMIA; FLT3 GENE; AML; T(6/9)(P23_Q34); INDUCTION; CONSOLIDATION; CHEMOTHERAPY; PROGNOSIS; SURVIVAL
Tags
International impact, Reviewed
Změněno: 17/2/2020 15:35, Mgr. Tereza Miškechová
Abstract
V originále
A cute myeloid leukemia (AML) with t(6;9)(p22;q34) is a distinct entity accounting for 1-2% of AML cases. A substantial proportion of these patients have a concomitant FLT3-ITD. While outcomes are dismal intensive chemotherapy, limited evidence suggests allogeneic hematopoietic cell transplantation (allo-HCT) may improve survival if performed early during first complete remission. We report on a cohort of 178 patients with t(6;9)(p22;q34) within an international, multicenter collaboration. Median age was 46 years (range: 16-76), AML was de novo in 88%, FLT3-ITD was present in 62%, and additional cytogenetic abnormalities in 21%. Complete remission was achieved in 81% (n=144), including 14 patients who received high-dose cytarabine after initial induction failure. With a median follow up of 5.43 years, estimated overall survival at five years was 38% (95%CI: 31-47%). Allo-HCT was performed in 117 (66%) patients, including 89 in first complete remission. Allo-HCT in first complete remission was associated with higher 5-year relapse-free and overall survival as compared to consolidation chemotherapy: 45% (95%CI: 35-59%) and 53% (95%CI: 42-66%) versus 7% (95%CI: 3-19%) and 23% (95%CI: 13-38%), respectively. For patients undergoing allo-HCT, there was no difference in overall survival rates at five years according to whether it was performed in first [53% (95%CI: 42-66%)], or second [58% (95%CI: 31-100%); n=10] complete remission or with active disease/relapse [54% (95%CI: 34-84%); n=18] (P=0.67). Neither FLT3-ITD nor additional chromosomal abnormalities impacted survival. In conclusion, outcomes of t(6;9)(p22;q34) AML are poor with chemotherapy, and can be substantially improved with allo-HCT.
Links
NV15-25809A, research and development project |
|