Azacitidine in the Front-line Treatment of Therapy-related Myeloid Neoplasms: A Multicenter Case Series

被引:1
作者
Minoia, Carla [1 ]
Sgherza, Nicola [1 ]
Loseto, Giacomo [1 ]
Greco, Giuseppina [2 ]
Buquicchio, Caterina [3 ]
Merchionne, Francesca [4 ]
Toldo, Chandrakala [5 ]
Galise, Ida [6 ]
Melpignano, Angela [4 ]
Tarantini, Giuseppe [3 ]
Pavone, Vincenzo [2 ]
Guarini, Attilio [1 ]
机构
[1] IRCCS Natl Canc Res Ctr Giovanni Paolo II, Haematol Unit, I-70124 Bari, Italy
[2] G Panico Hosp, Haematol Unit, Lecce, Italy
[3] Dimiccoli Hosp, Haematol Unit, Barletta, Italy
[4] Antonio Perrino Hosp, Haematol Unit, Brindisi, Italy
[5] S Chiara di Trento Hosp, Dept Hematol, Internal Med Unit, Trento, Italy
[6] IRCCS Natl Canc Res Ctr Giovanni Paolo II, Registro Tumori Puglia, I-70124 Bari, Italy
关键词
Therapy-related myeloid neosplasm; azacitidine; outcome; safety; MYELODYSPLASTIC SYNDROMES; LEUKEMIA; RISK; EFFICACY; AML;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: A continued increase in the incidence of therapy-related myeloid neoplasnis (t-MN) is expected due to the improvement of chemotherapeutic treatments for solid and haematological malignancies. The use of 5-azacytidine (AZA) is emerging in these patients. We, therefore, analyzed the outcome of patients with t-MN ineligible for intensive chemotherapy treated in the front-line with AZA. Patients and Methods: We retrospectively collected clinical data from consecutive patients with t-MN treated in the front-line with AZA at five Haematology Centers. Response to therapy, overall survival (OS) and safety were considered. Results: The overall response rate was of 35.7% with a median OS of 9.6 months. Patients who were heavily pre-treated for their primary malignancy (more than 3 lines of chemotherapy) presented a significant inferior OS (4.9 months). The principal reported toxicity was haematological with severe infections occurring in a minority of patients. Fatigue was the most common extra-haematological toxicity. Conclusion: New aspects emerged on the management of t-MN. AZA may represent a reasonable choice for patients ineligible for intensive treatment, with the exception of heavily pre-treated patients who presented -anyway- a worse outcome.
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收藏
页码:461 / 466
页数:6
相关论文
共 26 条
[1]   Azacitidine in the treatment of therapy related myelodysplastic syndrome and acute myeloid leukemia (tMDS/AML): A report on 54 patients by the Groupe Francophone Des Myelodysplasies (GFM) [J].
Bally, Cecile ;
Thepot, Sylvain ;
Quesnel, Bruno ;
Vey, Norbert ;
Dreyfus, Francois ;
Fadlallah, Jehane ;
Turlure, Pascal ;
de Botton, Stephane ;
Dartigeas, Caroline ;
de Renzis, Benoit ;
Itzykson, Raphael ;
Fenaux, Pierre ;
Ades, Lionel .
LEUKEMIA RESEARCH, 2013, 37 (06) :637-640
[2]   Treatment-related myelodysplastic syndrome: molecular characteristics and therapy [J].
Bhatia, Ravi ;
Deeg, H. Joachim .
CURRENT OPINION IN HEMATOLOGY, 2011, 18 (02) :77-82
[3]   Therapy-Related Myelodysplasia and Acute Myeloid Leukemia [J].
Bhatia, Smita .
SEMINARS IN ONCOLOGY, 2013, 40 (06) :666-675
[4]   11q23 balanced chromosome aberrations in treatment- related myelodysplastic syndromes and acute leukemia:: Report from an international workshop [J].
Bloomfield, CD ;
Archer, KJ ;
Mrózek, K ;
Lillington, DM ;
Kaneko, Y ;
Head, DR ;
Dal Cin, P ;
Raimondi, SC .
GENES CHROMOSOMES & CANCER, 2002, 33 (04) :362-378
[5]   NMR-Based Metabolomic Analysis of the Molecular Pathogenesis of Therapy-Related Myelodysplasia/Acute Myeloid Leukemia [J].
Cano, Kristin E. ;
Li, Liang ;
Bhatia, Smita ;
Bhatia, Ravi ;
Forman, Stephen J. ;
Chen, Yuan .
JOURNAL OF PROTEOME RESEARCH, 2011, 10 (06) :2873-2881
[6]   Accelerated Telomere Shortening Precedes Development of Therapy-Related Myelodysplasia or Acute Myelogenous Leukemia After Autologous Transplantation for Lymphoma [J].
Chakraborty, Sujata ;
Sun, Can-Lan ;
Francisco, Liton ;
Sabado, Melanie ;
Li, Liang ;
Chang, Karen L. ;
Forman, Stephen ;
Bhatia, Smita ;
Bhatia, Ravi .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (05) :791-798
[7]   Clinical application and proposal for modification of the International Working Group (IWG) response criteria in myelodysplasia [J].
Cheson, Bruce D. ;
Greenberg, Peter L. ;
Bennett, John M. ;
Lowenberg, Bob ;
Wijermans, Pierre W. ;
Nimer, Stephen D. ;
Pinto, Antonio ;
Beran, Miloslav ;
de Witte, Theo M. ;
Stone, Richard M. ;
Mittelman, Moshe ;
Sanz, Guillermo F. ;
Gore, Steven D. ;
Schiffer, Charles A. ;
Kantarjian, Hagop .
BLOOD, 2006, 108 (02) :419-425
[8]   The evolving challenge of therapy-related myeloid neoplasms [J].
Churpek, Jane E. ;
Larson, Richard A. .
BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY, 2013, 26 (04) :309-317
[9]   Identification of methylguanine methyltransferase polymorphisms as genetic markers of individual susceptibility to therapy-related myeloid neoplasms [J].
Dubois, Julie ;
Etienne, Gabriel ;
Laroche-Clary, Audrey ;
Lascaux, Axelle ;
Bidet, Audrey ;
Lippert, Eric ;
Ait-ouferoukh, Sofiane ;
Saada, Veronique ;
Micol, Jean-Baptiste ;
Bouabdallah, Krimo ;
Robert, Jacques .
EUROPEAN JOURNAL OF CANCER, 2014, 50 (02) :418-424
[10]   Outcome of azacitidine treatment in patients with therapy-related myeloid neoplasms with assessment of prognostic risk stratification models [J].
Duong, Vu H. ;
Lancet, Jeffrey E. ;
Alrawi, Ezzideen ;
Al-Ali, Najla H. ;
Perkins, Janelle ;
Field, Teresa ;
Epling-Burnette, Pearlie K. ;
Zhang, Ling ;
List, Alan F. ;
Komrokji, Rami S. .
LEUKEMIA RESEARCH, 2013, 37 (05) :510-515