Novel Therapies for Unmet Clinical Needs in Myelodysplastic Syndromes

被引:9
作者
Cassanello, Giulio [1 ,2 ]
Pasquale, Raffaella [2 ]
Barcellini, Wilma [2 ]
Fattizzo, Bruno [1 ,2 ]
机构
[1] Univ Milan, Dept Oncol & Oncohematol, I-20122 Milan, Italy
[2] Fdn IRCCS Ca Granda Osped Maggiore Policlin, Hematol Unit, I-20122 Milan, Italy
关键词
myelodysplastic syndromes; unmet needs; target therapy; somatic mutations; immunotherapy; HEALTH-ORGANIZATION CLASSIFICATION; ACUTE MYELOID-LEUKEMIA; RANDOMIZED PHASE-III; LOW-DOSE DECITABINE; CELL TRANSPLANTATION; SUPPORTIVE CARE; SCORING SYSTEM; RISK; MDS; AZACITIDINE;
D O I
10.3390/cancers14194941
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Several novel therapies are being developed to improve the management of patients with myelodysplastic syndromes. They include drugs aimed at improving hematopoiesis and differentiation of myeloid precursors, hypomethylating agents, several compounds that target intracellular molecular pathways, and immunotherapies. In this review article, we discuss how the novel drugs may address the several unmet needs of lower- and higher-risk patients. Myelodysplastic syndromes (MDS) are a very heterogeneous disease, with extremely variable clinical features and outcomes. Current management relies on risk stratification based on IPSS and IPSS-R, which categorizes patients into low (LR-) and high-risk (HR-) MDS. Therapeutic strategies in LR-MDS patients mainly consist of erythropoiesis stimulating agents (ESAs), transfusion support, and luspatercept or lenalidomide for selected patients. Current unmet needs include the limited options available after treatment failure, and the consequent transfusion burden with several hospital admissions and poor quality of life. Therapeutic approaches in HR-MDS patients are aimed at changing the natural course of the disease and hypometylating agents (HMA) are the first choice. The only potentially curative treatment is allogeneic stem cell transplant (allo-HCT), restricted to a minority of young and fit candidates. Patients unfit for or those that relapse after the abovementioned options harbor an adverse prognosis, with limited overall survival and frequent leukemic evolution. Recent advances in genetic mutations and intracellular pathways that are relevant for MDS pathogenesis are improving disease risk stratification and highlighting therapeutic targets addressed by novel agents. Several drugs are under evaluation for LR and HR patients, which differ by their mechanism of action, reported efficacy, and phase of development. This review analyzes the current unmet clinical needs for MDS patients and provides a critical overview of the novel agents under development in this setting.
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页数:17
相关论文
共 93 条
[1]   Pevonedistat plus azacitidine vs azacitidine alone in higher-risk MDS/chronic myelomonocytic leukemia or low-blast-percentage AML [J].
Ades, Lionel ;
Girshova, Larisa ;
Doronin, Vadim A. ;
Diez-Campelo, Maria ;
Valcarcel, David ;
Kambhampati, Suman ;
Viniou, Nora-Athina ;
Woszczyk, Dariusz ;
De Paz Arias, Raquel ;
Symeonidis, Argiris ;
Anagnostopoulos, Achilles ;
Ciliao Munhoz, Eduardo ;
Platzbecker, Uwe ;
Santini, Valeria ;
Fram, Robert J. ;
Yuan, Ying ;
Friedlander, Sharon ;
Faller, Douglas, V ;
Sekeres, Mikkael A. .
BLOOD ADVANCES, 2022, 6 (17) :5132-5145
[2]   Myelodysplastic syndromes [J].
Ades, Lionel ;
Itzykson, Raphael ;
Fenaux, Pierre .
LANCET, 2014, 383 (9936) :2239-2252
[3]   Interim Results from the Phase I Deplethink Trial Evaluating the Infusion of a NKG2D CAR T-Cell Therapy Post a Non-Myeloablative Conditioning in Relapse or Refractory Acute Myeloid Leukemia and Myelodysplastic Syndrome Patients [J].
Al-Homsi, A. Samer ;
Purev, Enkhtsetseg ;
Lewalle, Philippe ;
Abdul-Hay, Maher ;
Pollyea, Daniel A. ;
Salaroli, Adriano ;
Lequertier, Thomas ;
Alcantar-Orozco, Erik ;
Borghese, Fabian ;
Lonez, Caroline ;
Braun, Nathalie ;
Renard, Florence ;
Flament, Anne ;
Moors, Ine ;
Kerre, Tessa .
BLOOD, 2019, 134
[4]   Efficacy of the combination of venetoclax and hypomethylating agents in relapsed/refractory acute myeloid leukemia [J].
Aldoss, Ibrahim ;
Yang, Dongyun ;
Aribi, Ahmed ;
Ali, Haris ;
Sandhu, Karamjeet ;
Al Malki, Monzr M. ;
Mei, Matthew ;
Salhotra, Amandeep ;
Khaled, Samer ;
Nakamura, Ryotaro ;
Snyder, David ;
O'Donnell, Margaret ;
Stein, Anthony S. ;
Forman, Stephen J. ;
Marcucci, Guido ;
Pullarkat, Vinod .
HAEMATOLOGICA, 2018, 103 (09) :E404-E407
[5]   Iron Chelation in Transfusion-Dependent Patients With Low- to Intermediate-1-Risk Myelodysplastic Syndromes A Randomized Trial [J].
Angelucci, Emanuele ;
Li, Junmin ;
Greenberg, Peter ;
Wu, Depei ;
Hou, Ming ;
Montano Figueroa, Efreen Horacio ;
Guadalupe Rodriguez, Maria ;
Dong, Xunwei ;
Ghosh, Jagannath ;
Izquierdo, Miguel ;
Garcia-Manero, Guillermo .
ANNALS OF INTERNAL MEDICINE, 2020, 172 (08) :513-+
[6]   Evidence for Selective Benefit of Sequential Treatment With Hypomethylating Agents in Patients With Myelodysplastic Syndrome [J].
Apuri, Susmitha ;
Al Ali, Najla ;
Padron, Eric ;
Lancet, Jeffrey E. ;
List, Alan F. ;
Komrokji, Rami S. .
CLINICAL LYMPHOMA MYELOMA & LEUKEMIA, 2017, 17 (04) :211-214
[7]   The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia [J].
Arber, Daniel A. ;
Orazi, Attilio ;
Hasserjian, Robert ;
Thiele, Jurgen ;
Borowitz, Michael J. ;
Le Beau, Michelle M. ;
Bloomfield, Clara D. ;
Cazzola, Mario ;
Vardiman, James W. .
BLOOD, 2016, 127 (20) :2391-2405
[8]   Azacitidine plus venetoclax in patients with high-risk myelodysplastic syndromes or chronic myelomonocytic leukaemia: phase 1 results of a single-centre, dose- escalation, dose-expansion, phase 1-2 study [J].
Bazinet, Alexandre ;
Darbaniyan, Faezeh ;
Jabbour, Elias ;
Montalban-Bravo, Guillermo ;
Ohanian, Maro ;
Chien, Kelly ;
Kadia, Tapan ;
Takahashi, Koichi ;
Masarova, Lucia ;
Short, Nicholas ;
Alvarado, Yesid ;
Yilmaz, Musa ;
Ravandi, Farhad ;
Andreeff, Michael ;
Kanagal-Shamanna, Rashmi ;
Ganan-Gomez, Irene ;
Colla, Simona ;
Qiao, Wei ;
Huang, Xuelin ;
McCue, Deborah ;
Mirabella, Bailey ;
Kantarjian, Hagop ;
Garcia-Manero, Guillermo .
LANCET HAEMATOLOGY, 2022, 9 (10) :E756-E765
[9]   Clinical Effect of Point Mutations in Myelodysplastic Syndromes [J].
Bejar, Rafael ;
Stevenson, Kristen ;
Abdel-Wahab, Omar ;
Galili, Naomi ;
Nilsson, Bjoern ;
Garcia-Manero, Guillermo ;
Kantarjian, Hagop ;
Raza, Azra ;
Levine, Ross L. ;
Neuberg, Donna ;
Ebert, Benjamin L. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 364 (26) :2496-2506
[10]  
Bernard Elsa, 2022, NEJM Evid, V1, pEVIDoa2200008, DOI 10.1056/EVIDoa2200008