Combination therapy involving azacitidine for acute myeloid leukemia patients ineligible for intensive chemotherapy

被引:1
作者
Li, Juan [1 ,2 ]
Fu, Shuying [1 ,2 ]
Ye, Chunmei [1 ,2 ]
Li, Jun [1 ,2 ]
机构
[1] Yangzhou Univ, Dept Hematol, Taixing Peoples Hosp, Changzheng Rd, Taixing 225400, Peoples R China
[2] Yangzhou Univ, Inst Hematol, Affiliated Hosp, Taixing, Peoples R China
关键词
Acute myeloid leukemia; Azacitidine; Unfit; Combination therapy; RISK MYELODYSPLASTIC SYNDROMES; HYPOMETHYLATING AGENTS; OLDER PATIENTS; DOUBLE-BLIND; PHASE-II; LENALIDOMIDE; CYTOGENETICS; MULTICENTER; VORINOSTAT; IVOSIDENIB;
D O I
10.1016/j.leukres.2024.107638
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Acute myeloid leukemia (AML) is a complex hematological malignancy predominantly affecting the elderly, with a median diagnosis age of 68 years. Despite advances in treatment, elderly AML patients face suboptimal survival outcomes, with an estimated 5-year survival rate below 20 %. Epigenetic dysregulation, notably DNA methylation, is a key factor in the progression of myelodysplastic syndromes (MDS) to AML. This review examines various combination regimens involving azacitidine (AZA), including those with lenalidomide, histone deacetylase inhibitors (HDACi), kinase inhibitors, metabolic enzyme inhibitors, monoclonal antibodies, immune checkpoint inhibitors, and anti-apoptotic protein inhibitors. Notable among these are the combinations with venetoclax, which has demonstrated remarkable efficacy in phase III trials, and the emerging IDH inhibitors ivosidenib and enasidenib, which have shown significant clinical benefits in patients with IDH mutations. While combination therapies with AZA hold great promise, challenges persist, including translating in vitro synergies to in vivo efficacy and identifying optimal regimens for specific patient populations. Cumulative toxicities may also offset clinical benefits, necessitating rigorous clinical trial design. Future research must focus on refining combination strategies, optimizing dosages and sequences, and thoroughly evaluating therapeutic efficacy and safety to advance the treatment of AML and improve patient outcomes.
引用
收藏
页数:8
相关论文
共 91 条
[1]   Ivosidenib in IDH1-mutant, chemotherapy-refractory Croatia& cholangiocarcinoma (ClarlDHy): a multicentre, randomised, double-blind, placebo-controlled, phase 3 study [J].
Abou-Alfa, Ghassan K. ;
Macarulla, Teresa ;
Javle, Milind M. ;
Kelley, Robin K. ;
Lubner, Sam J. ;
Adeva, Jorge ;
Cleary, James M. ;
Catenacci, Daniel V. ;
Borad, Mitesh J. ;
Bridgewater, John ;
Harris, William P. ;
Murphy, Adrian G. ;
Oh, Do-Youn ;
Whisenant, Jonathan ;
Lowery, Maeve A. ;
Goyal, Lipika ;
Shroff, Rachna T. ;
El-Khoueiry, Anthony B. ;
Fan, Bin ;
Wu, Bin ;
Chamberlain, Christina X. ;
Jiang, Liewen ;
Gliser, Camelia ;
Pandya, Shuchi S. ;
Valle, Juan W. ;
Zhu, Andrew X. .
LANCET ONCOLOGY, 2020, 21 (06) :796-807
[2]   A retrospective study evaluating treatment patterns and survival outcomes in elderly patients with acute myeloid leukemia treated in the United States with either 7+3 or a hypomethylating agent [J].
Bell, Jill A. ;
Galaznik, Aaron ;
Farrelly, Eileen ;
Blazer, Marlo ;
Murty, Sharanya ;
Ogbonnaya, Augustina ;
Eaddy, Michael ;
Fram, Robert J. ;
Faller, Douglas V. ;
Kota, Vamsi K. .
LEUKEMIA RESEARCH, 2019, 78 :45-51
[3]   Clinical Practice Guidelines in Oncology [J].
Benson, Al B., III ;
Arnoletti, J. Pablo ;
Bekaii-Saab, Tanios ;
Chan, Emily ;
Chen, Yi-Jen ;
Choti, Michael A. ;
Cooper, Harry S. ;
Dilawari, Raza A. ;
Engstrom, Paul F. ;
Enzinger, Peter C. ;
Fleshman, James W., Jr. ;
Fuchs, Charles S. ;
Grem, Jean L. ;
Knol, James A. ;
Leong, Lucille A. ;
Lin, Edward ;
May, Kilian Salerno ;
Mulcahy, Mary F. ;
Murphy, Kate ;
Rohren, Eric ;
Ryan, David P. ;
Saltz, Leonard ;
Sharma, Sunil ;
Shibata, David ;
Skibber, John M. ;
Small, William, Jr. ;
Sofocleous, Constantinos T. ;
Venook, Alan P. ;
Willett, Christopher .
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK, 2011, 9 (11) :1238-1290
[4]   Bruton Tyrosine Kinase (BTK) and Its Role in B-cell Malignancy [J].
Buggy, Joseph J. ;
Elias, Laurence .
INTERNATIONAL REVIEWS OF IMMUNOLOGY, 2012, 31 (02) :119-132
[5]   Restoration of the tumor suppressor function to mutant p53 by a low-molecular-weight compound [J].
Bykov, VJN ;
Issaeva, N ;
Shilov, A ;
Hultcrantz, M ;
Pugacheva, E ;
Chumakov, P ;
Bergman, J ;
Wiman, KG ;
Selivanova, G .
NATURE MEDICINE, 2002, 8 (03) :282-288
[6]   Targeting LAG-3, TIM-3, and TIGIT for cancer immunotherapy [J].
Cai, Letong ;
Li, Yuchen ;
Tan, Jiaxiong ;
Xu, Ling ;
Li, Yangqiu .
JOURNAL OF HEMATOLOGY & ONCOLOGY, 2023, 16 (01)
[7]   Mutant IDH1 promotes leukemogenesis in vivo and can be specifically targeted in human AML [J].
Chaturvedi, Anuhar ;
Cruz, Michelle Maria Araujo ;
Jyotsana, Nidhi ;
Sharma, Amit ;
Yun, Haiyang ;
Goerlich, Kerstin ;
Wichmann, Martin ;
Schwarzer, Adrian ;
Preller, Matthias ;
Thol, Felicitas ;
Meyer, Johann ;
Haemmerle, Reinhard ;
Struys, Eduard A. ;
Jansen, Erwin E. ;
Modlich, Ute ;
Li, Zhixiong ;
Sly, Laura M. ;
Geffers, Robert ;
Lindner, Robert ;
Manstein, Dietmar J. ;
Lehmann, Ulrich ;
Krauter, Juergen ;
Ganser, Arnold ;
Heuser, Michael .
BLOOD, 2013, 122 (16) :2877-2887
[8]   Updates on DNA methylation modifiers in acute myeloid leukemia [J].
Contieri, Bruna ;
Duarte, Bruno Kosa Lino ;
Lazarini, Mariana .
ANNALS OF HEMATOLOGY, 2020, 99 (04) :693-701
[9]   Clinical Experience With Ibrutinib Alone or in Combination With Either Cytarabine or Azacitidine in Patients With Acute Myeloid Leukemia [J].
Cortes, Jorge E. ;
Jonas, Brian A. ;
Graef, Thorsten ;
Luan, Ying ;
Stein, Anthony S. .
CLINICAL LYMPHOMA MYELOMA & LEUKEMIA, 2019, 19 (08) :509-+
[10]   Outcome of Azacitidine Therapy in Acute Myeloid Leukemia Is not Improved by Concurrent Vorinostat Therapy but Is Predicted by a Diagnostic Molecular Signature [J].
Craddock, Charles F. ;
Houlton, Aimee E. ;
Quek, Lynn Swun ;
Ferguson, Paul ;
Gbandi, Emma ;
Roberts, Corran ;
Metzner, Marlen ;
Garcia-Martin, Natalia ;
Kennedy, Alison ;
Hamblin, Angela ;
Raghavan, Manoj ;
Nagra, Sandeep ;
Dudley, Louise ;
Wheatley, Keith ;
McMullin, Mary Frances ;
Pillai, Srinivas P. ;
Kelly, Richard J. ;
Siddique, Shamyla ;
Dennis, Michael ;
Cavenagh, Jamie D. ;
Vyas, Paresh .
CLINICAL CANCER RESEARCH, 2017, 23 (21) :6430-6440