Azacitidine front-line in 339 patients with myelodysplastic syndromes and acute myeloid leukaemia: comparison of French-American-British and World Health Organization classifications

Abstract Background The MDS-IWG and NCCN currently endorse both FAB and WHO classifications of MDS and AML, thus allowing patients with 20–30 % bone marrow blasts (AML20–30, formerly MDS-RAEB-t) to be categorised and treated as either MDS or AML. In addition, an artificial distinction between AML20–...

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Main Authors: Lisa Pleyer, Sonja Burgstaller, Reinhard Stauder, Michael Girschikofsky, Heinz Sill, Konstantin Schlick, Josef Thaler, Britta Halter, Sigrid Machherndl-Spandl, Armin Zebisch, Angelika Pichler, Michael Pfeilstöcker, Eva-Maria Autzinger, Alois Lang, Klaus Geissler, Daniela Voskova, Dietmar Geissler, Wolfgang R. Sperr, Sabine Hojas, Inga M. Rogulj, Johannes Andel, Richard Greil
Format: Article
Language:English
Published: BMC 2016-04-01
Series:Journal of Hematology & Oncology
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13045-016-0263-4
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author Lisa Pleyer
Sonja Burgstaller
Reinhard Stauder
Michael Girschikofsky
Heinz Sill
Konstantin Schlick
Josef Thaler
Britta Halter
Sigrid Machherndl-Spandl
Armin Zebisch
Angelika Pichler
Michael Pfeilstöcker
Eva-Maria Autzinger
Alois Lang
Klaus Geissler
Daniela Voskova
Dietmar Geissler
Wolfgang R. Sperr
Sabine Hojas
Inga M. Rogulj
Johannes Andel
Richard Greil
author_facet Lisa Pleyer
Sonja Burgstaller
Reinhard Stauder
Michael Girschikofsky
Heinz Sill
Konstantin Schlick
Josef Thaler
Britta Halter
Sigrid Machherndl-Spandl
Armin Zebisch
Angelika Pichler
Michael Pfeilstöcker
Eva-Maria Autzinger
Alois Lang
Klaus Geissler
Daniela Voskova
Dietmar Geissler
Wolfgang R. Sperr
Sabine Hojas
Inga M. Rogulj
Johannes Andel
Richard Greil
author_sort Lisa Pleyer
collection DOAJ
description Abstract Background The MDS-IWG and NCCN currently endorse both FAB and WHO classifications of MDS and AML, thus allowing patients with 20–30 % bone marrow blasts (AML20–30, formerly MDS-RAEB-t) to be categorised and treated as either MDS or AML. In addition, an artificial distinction between AML20–30 and AML30+ was made by regulatory agencies by initially restricting approval of azacitidine to AML20–30. Thus, uncertainty prevails regarding the diagnosis, prognosis and optimal treatment timing and strategy for patients with AML20–30. Here, we aim to provide clarification for patients treated with azacitidine front-line. Methods The Austrian Azacitidine Registry is a multicentre database (ClinicalTrials.gov: NCT01595295). For this analysis, we selected 339 patients treated with azacitidine front-line. According to the WHO classification 53, 96 and 190 patients had MDS-RAEB-I, MDS-RAEB-II and AML (AML20–30: n = 79; AML30+: n = 111), respectively. According to the FAB classification, 131, 101 and 111 patients had MDS-RAEB, MDS-RAEB-t and AML, respectively. Results The median ages of patients with MDS and AML were 72 (range 37–87) and 77 (range 23–93) years, respectively. Overall, 80 % of classifiable patients (≤30 % bone marrow blasts) had intermediate-2 or high-risk IPSS scores. Most other baseline, treatment and response characteristics were similar between patients diagnosed with MDS or AML. WHO-classified patients with AML20–30 had significantly worse OS than patients with MDS-RAEB-II (13.1 vs 18.9 months; p = 0.010), but similar OS to patients with AML30+ (10.9 vs 13.1 months; p = 0.238). AML patients that showed MDS-related features did not have worse outcomes compared with patients who did not (13.2 vs 8.9 months; p = 0.104). FAB-classified patients with MDS-RAEB-t had similar survival to patients with AML30+ (12.8 vs 10.9 months; p = 0.376), but significantly worse OS than patients with MDS-RAEB (10.9 vs 24.4 months; p < 0.001). Conclusions Our data demonstrate the validity of the WHO classification of MDS and AML, and its superiority over the former FAB classification, for patients treated with azacitidine front-line. Neither bone marrow blast count nor presence of MDS-related features had an adverse prognostic impact on survival. Patients with AML20–30 should therefore be regarded as having ‘true AML’ and in our opinion treatment should be initiated without delay.
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spelling doaj.art-b40b7ac28a984159b4bb8b27ecd446582022-12-22T01:10:43ZengBMCJournal of Hematology & Oncology1756-87222016-04-019111610.1186/s13045-016-0263-4Azacitidine front-line in 339 patients with myelodysplastic syndromes and acute myeloid leukaemia: comparison of French-American-British and World Health Organization classificationsLisa Pleyer0Sonja Burgstaller1Reinhard Stauder2Michael Girschikofsky3Heinz Sill4Konstantin Schlick5Josef Thaler6Britta Halter7Sigrid Machherndl-Spandl8Armin Zebisch9Angelika Pichler10Michael Pfeilstöcker11Eva-Maria Autzinger12Alois Lang13Klaus Geissler14Daniela Voskova15Dietmar Geissler16Wolfgang R. Sperr17Sabine Hojas18Inga M. Rogulj19Johannes Andel20Richard Greil213rd Medical Department with Hematology and Medical Oncology, Hemostaseology, Rheumatology and Infectious Diseases, Laboratory for Immunological and Molecular Cancer Research, Oncologic Center, Paracelsus Medical University SalzburgDepartment of Internal Medicine IV, Klinikum Wels-GrieskirchenDepartment of Internal Medicine V, Innsbruck Medical UniversityDepartment of Hematology and Oncology, Elisabethinen HospitalDepartment of Hematology, Medical University of Graz3rd Medical Department with Hematology and Medical Oncology, Hemostaseology, Rheumatology and Infectious Diseases, Laboratory for Immunological and Molecular Cancer Research, Oncologic Center, Paracelsus Medical University SalzburgDepartment of Internal Medicine IV, Klinikum Wels-GrieskirchenDepartment of Internal Medicine V, Innsbruck Medical UniversityDepartment of Hematology and Oncology, Elisabethinen HospitalDepartment of Hematology, Medical University of GrazDepartment for Hematology and Oncology, LKH Leoben3rd Medical Department for Hematology and Oncology, Hanusch HospitalFirst Medical Department, Center for Oncology, Hematology and Palliative Care, WilhelminenspitalDepartment of Internal Medicine, LKH Feldkirch5th Medical Department, Hospital HietzingDepartment of Internal Medicine III, General Hospital1st Medical department, Klinikum KlagenfurtDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of ViennaDepartment of Internal Medicine, LKH FürstenfeldDepartment of Hematology, Clinical Hospital MerkurDepartment of Internal Medicine II, LKH Steyr3rd Medical Department with Hematology and Medical Oncology, Hemostaseology, Rheumatology and Infectious Diseases, Laboratory for Immunological and Molecular Cancer Research, Oncologic Center, Paracelsus Medical University SalzburgAbstract Background The MDS-IWG and NCCN currently endorse both FAB and WHO classifications of MDS and AML, thus allowing patients with 20–30 % bone marrow blasts (AML20–30, formerly MDS-RAEB-t) to be categorised and treated as either MDS or AML. In addition, an artificial distinction between AML20–30 and AML30+ was made by regulatory agencies by initially restricting approval of azacitidine to AML20–30. Thus, uncertainty prevails regarding the diagnosis, prognosis and optimal treatment timing and strategy for patients with AML20–30. Here, we aim to provide clarification for patients treated with azacitidine front-line. Methods The Austrian Azacitidine Registry is a multicentre database (ClinicalTrials.gov: NCT01595295). For this analysis, we selected 339 patients treated with azacitidine front-line. According to the WHO classification 53, 96 and 190 patients had MDS-RAEB-I, MDS-RAEB-II and AML (AML20–30: n = 79; AML30+: n = 111), respectively. According to the FAB classification, 131, 101 and 111 patients had MDS-RAEB, MDS-RAEB-t and AML, respectively. Results The median ages of patients with MDS and AML were 72 (range 37–87) and 77 (range 23–93) years, respectively. Overall, 80 % of classifiable patients (≤30 % bone marrow blasts) had intermediate-2 or high-risk IPSS scores. Most other baseline, treatment and response characteristics were similar between patients diagnosed with MDS or AML. WHO-classified patients with AML20–30 had significantly worse OS than patients with MDS-RAEB-II (13.1 vs 18.9 months; p = 0.010), but similar OS to patients with AML30+ (10.9 vs 13.1 months; p = 0.238). AML patients that showed MDS-related features did not have worse outcomes compared with patients who did not (13.2 vs 8.9 months; p = 0.104). FAB-classified patients with MDS-RAEB-t had similar survival to patients with AML30+ (12.8 vs 10.9 months; p = 0.376), but significantly worse OS than patients with MDS-RAEB (10.9 vs 24.4 months; p < 0.001). Conclusions Our data demonstrate the validity of the WHO classification of MDS and AML, and its superiority over the former FAB classification, for patients treated with azacitidine front-line. Neither bone marrow blast count nor presence of MDS-related features had an adverse prognostic impact on survival. Patients with AML20–30 should therefore be regarded as having ‘true AML’ and in our opinion treatment should be initiated without delay.http://link.springer.com/article/10.1186/s13045-016-0263-4AMLMDSWHOFABClassificationRAEB-t
spellingShingle Lisa Pleyer
Sonja Burgstaller
Reinhard Stauder
Michael Girschikofsky
Heinz Sill
Konstantin Schlick
Josef Thaler
Britta Halter
Sigrid Machherndl-Spandl
Armin Zebisch
Angelika Pichler
Michael Pfeilstöcker
Eva-Maria Autzinger
Alois Lang
Klaus Geissler
Daniela Voskova
Dietmar Geissler
Wolfgang R. Sperr
Sabine Hojas
Inga M. Rogulj
Johannes Andel
Richard Greil
Azacitidine front-line in 339 patients with myelodysplastic syndromes and acute myeloid leukaemia: comparison of French-American-British and World Health Organization classifications
Journal of Hematology & Oncology
AML
MDS
WHO
FAB
Classification
RAEB-t
title Azacitidine front-line in 339 patients with myelodysplastic syndromes and acute myeloid leukaemia: comparison of French-American-British and World Health Organization classifications
title_full Azacitidine front-line in 339 patients with myelodysplastic syndromes and acute myeloid leukaemia: comparison of French-American-British and World Health Organization classifications
title_fullStr Azacitidine front-line in 339 patients with myelodysplastic syndromes and acute myeloid leukaemia: comparison of French-American-British and World Health Organization classifications
title_full_unstemmed Azacitidine front-line in 339 patients with myelodysplastic syndromes and acute myeloid leukaemia: comparison of French-American-British and World Health Organization classifications
title_short Azacitidine front-line in 339 patients with myelodysplastic syndromes and acute myeloid leukaemia: comparison of French-American-British and World Health Organization classifications
title_sort azacitidine front line in 339 patients with myelodysplastic syndromes and acute myeloid leukaemia comparison of french american british and world health organization classifications
topic AML
MDS
WHO
FAB
Classification
RAEB-t
url http://link.springer.com/article/10.1186/s13045-016-0263-4
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