Future Directions in Chronic Phase CML Treatment

被引:11
作者
Javidi-Sharifi, Nathalie [1 ]
Hobbs, Gabriela [2 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, 450 Brookline Ave, Boston, MA 02215 USA
[2] Massachusetts Gen Hosp, Leukemia Ctr, 55 Fruit St, Boston, MA 02114 USA
关键词
Chronic myeloid leukemia; Tyrosine kinase inhibitor; Treatment-free remission; Leukemia stem cell; Interferon; BH3; mimetics; Immune checkpoint inhibitor; PPAR ligand; CHRONIC MYELOID-LEUKEMIA; IMATINIB; INHIBITOR; RUXOLITINIB; COMBINATION; NILOTINIB; DEATH; TRIAL;
D O I
10.1007/s11899-021-00658-w
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of Review This review will focus on recent and emerging treatment paradigms in chronic phase CML. The discussion of each novel treatment or drug combination will include a brief overview of scientific rational and pre-clinical data, followed by recently published or ongoing clinical trial efforts. The review will be divided into three focus areas in CML treatment: new frontline approaches and approaches to deepen remission, second treatment-free remission studies, and the treatment of refractory disease. Recent Findings The section on new frontline approaches will highlight several strategies of combination therapy. These can be grouped into immunomodulatory approaches with interferons and immune checkpoint inhibitors, targeting of leukemia stem cells with compounds such as venetoclax and pioglitazone, and BCR-ABL1-intrinsic combination therapy with asciminib. The chance at a second treatment-free remission is an important emerging clinical trial concept, and again combination approaches are under investigation. Lastly, in advanced disease, the development of novel tyrosine kinase inhibitors remains a major focus. This review will provide an overview and perspective of treatment strategies on the horizon for chronic phase CML. Despite the already excellent clinical outcomes for most patients, challenges remain with regard to deepening initial responses, prolonging treatment-free remission, and providing efficacious and tolerable options for patients with refractory disease and resistance mutations.
引用
收藏
页码:500 / 508
页数:9
相关论文
共 34 条
[1]   BCR-ABL1 tyrosine kinase inhibitor K0706 exhibits preclinical activity in Philadelphia chromosome-positive leukemia [J].
Antelope, Orlando ;
Vellore, Nadeem A. ;
Pomicter, Anthony D. ;
Patel, Ami B. ;
Van Scoyk, Alexandria ;
Clair, Phillip M. ;
Deininger, Michael W. ;
O'Hare, Thomas .
EXPERIMENTAL HEMATOLOGY, 2019, 77 :36-40
[2]   Imatinib and pegylated human recombinant interferon-α2b in early chronic-phase chronic myeloid leukemia [J].
Baccarani, M ;
Martinelli, G ;
Rosti, G ;
Trabacchi, E ;
Testoni, N ;
Bassi, S ;
Amabile, M ;
Soverini, S ;
Castagnetti, F ;
Cilloni, D ;
Izzo, B ;
de Vivo, A ;
Messa, E ;
Bonifazi, F ;
Poerio, A ;
Luatti, S ;
Giugliano, E ;
Alberti, D ;
Fincato, G ;
Russo, D ;
Pane, F ;
Saglio, G .
BLOOD, 2004, 104 (13) :4245-4251
[3]   Stat3 contributes to resistance toward BCR-ABL inhibitors in a bone marrow microenvironment model of drug resistance [J].
Bewry, Nadine N. ;
Nair, Rajesh R. ;
Emmons, Michael F. ;
Boulware, David ;
Pinilla-Ibarz, Javier ;
Hazlehurst, Lori A. .
MOLECULAR CANCER THERAPEUTICS, 2008, 7 (10) :3169-3175
[4]   Combined targeting of BCL-2 and BCR-ABL tyrosine kinase eradicates chronic myeloid leukemia stem cells [J].
Carter, Bing Z. ;
Mak, Po Yee ;
Mu, Hong ;
Zhou, Hongsheng ;
Mak, Duncan H. ;
Schober, Wendy ;
Leverson, Joel D. ;
Zhang, Bin ;
Bhatia, Ravi ;
Huang, Xuelin ;
Cortes, Jorge ;
Kantarjian, Hagop ;
Konopleva, Marina ;
Andreeff, Michael .
SCIENCE TRANSLATIONAL MEDICINE, 2016, 8 (355)
[5]   Discontinuation of Tyrosine Kinase Inhibitors in Chronic Myeloid Leukemia With Losing Major Molecular Response as a Definition for Molecular Relapse: A Systematic Review and Meta-Analysis [J].
Chen, Kang-kang ;
Du, Tai-feng ;
Xiong, Pei-sheng ;
Fan, Guan-hua ;
Yang, Wei .
FRONTIERS IN ONCOLOGY, 2019, 9
[6]   Increased Level of Myeloid-Derived Suppressor Cells, Programmed Death Receptor Ligand 1/Programmed Death Receptor 1, and Soluble CD25 in Sokal High Risk Chronic Myeloid Leukemia [J].
Christiansson, Lisa ;
Soderlund, Stina ;
Svensson, Emma ;
Mustjoki, Satu ;
Bengtsson, Mats ;
Simonsson, Bengt ;
Olsson-Stromberg, Ulla ;
Loskog, Angelica S. I. .
PLOS ONE, 2013, 8 (01)
[7]   Ponatinib efficacy and safety in Philadelphia chromosome-positive leukemia: final 5-year results of the phase 2 PACE trial [J].
Cortes, Jorge E. ;
Kim, Dong-Wook ;
Pinilla-Ibarz, Javier ;
le Coutre, Philipp D. ;
Paquette, Ronald ;
Chuah, Charles ;
Nicolini, Franck E. ;
Apperley, Jane F. ;
Khoury, H. Jean ;
Talpaz, Moshe ;
DeAngelo, Daniel J. ;
Abruzzese, Elisabetta ;
Rea, Delphine ;
Baccarani, Michele ;
Mueller, Martin C. ;
Gambacorti-Passerini, Carlo ;
Lustgarten, Stephanie ;
Rivera, Victor M. ;
Haluska, Frank G. ;
Guilhot, Francois ;
Deininger, Michael W. ;
Hochhaus, Andreas ;
Hughes, Timothy P. ;
Shah, Neil P. ;
Kantarjian, Hagop M. .
BLOOD, 2018, 132 (04) :393-404
[8]   Long-term data from a phase 3 study of radotinib versus imatinib in patients with newly diagnosed, chronic myeloid leukaemia in the chronic phase (RERISE) [J].
Do, Young Rok ;
Kwak, Jae-Yong ;
Kim, Jeong A. ;
Kim, Hyeoung Joon ;
Chung, Joo Seop ;
Shin, Ho-Jin ;
Kim, Sung-Hyun ;
Bunworasate, Udomsak ;
Choi, Chul Won ;
Zang, Dae Young ;
Oh, Suk Joong ;
Jootar, Saengsuree ;
Reksodiputro, Ary Harryanto ;
Lee, Won Sik ;
Mun, Yeung-Chul ;
Kong, Jee Hyun ;
Caguioa, Priscilla B. ;
Kim, Hawk ;
Park, Jinny ;
Kim, Dong-Wook .
BRITISH JOURNAL OF HAEMATOLOGY, 2020, 189 (02) :303-312
[9]   Ropeginterferon alfa-2b versus standard therapy for polycythaemia vera (PROUD-PV and CONTINUATION-PV): a randomised, non-inferiority, phase 3 trial and its extension study [J].
Gisslinger, Heinz ;
Klade, Christoph ;
Georgiev, Pencho ;
Krochmalczyk, Dorota ;
Gercheva-Kyuchukova, Liana ;
Egyed, Miklos ;
Rossiev, Viktor ;
Dulicek, Petr ;
Illes, Arpad ;
Pylypenko, Halyna ;
Sivcheva, Lylia ;
Mayer, Jiri ;
Yablokova, Vera ;
Krejcy, Kurt ;
Grohmann-Izay, Barbara ;
Hasselbalch, Hans C. ;
Kralovics, Robert ;
Kiladjian, Jean-Jacques .
LANCET HAEMATOLOGY, 2020, 7 (03) :E196-E208
[10]   PPARγ ligands increase antileukemic activity of second- and third-generation tyrosine kinase inhibitors in chronic myeloid leukemia cells [J].
Glodkowska-Mrowka, E. ;
Manda-Handzlik, A. ;
Stelmaszczyk-Emmel, A. ;
Seferynska, I. ;
Stoklosa, T. ;
Przybylski, J. ;
Mrowka, P. .
BLOOD CANCER JOURNAL, 2016, 6 :e377-e377