Safety and efficacy of venetoclax for acute myeloid leukaemia in real-world clinical practice

被引:2
作者
Fukumoto, Ami [1 ,2 ]
Narita, Kentaro [1 ]
Ikeda, Daisuke [1 ]
Uesugi, Yuka [1 ]
Tabata, Rikako [1 ]
Miura, Daisuke [1 ]
Takeuchi, Masami [1 ]
Matsue, Kosei [1 ]
机构
[1] Kameda Med Ctr, Dept Internal Med, Div Hematol Oncol, Chiba, Japan
[2] Kameda Med Ctr, Dept Internal Med, Div Hematol Oncol, 929 Higashi Chou, Kamogawa, Chiba 2968602, Japan
关键词
acute myeloid leukaemia; venetoclax; chemotherapy; AZACITIDINE; RECOMMENDATIONS; DIAGNOSIS;
D O I
10.1093/jjco/hyad075
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Venetoclax combined with low-intensity chemotherapy has led to longer survival and higher remission rates in patients with untreated acute myeloid leukaemia who are ineligible for intensive chemotherapy. We reviewed 41 newly diagnosed and relapse/refractory acute myeloid leukaemia patients who received venetoclax at our institute. Complete remission or complete remission with incomplete recovery was achieved in 73.1% of patients. A total of 95.1% of patients discontinued venetoclax, mainly because of severe cytopenia, disease progression and haematopoietic stem cell transplantation. The median number of courses of venetoclax was 2. In all, 92.6% of the patients experienced grade & GE; 3 neutropenia. The median overall survival was 287 days. Venetoclax dose reduction resulted in better continuity of treatment with fewer complications. In conclusion, venetoclax and low-intensity chemotherapy led to high remission rates, but survival was restrained because of the large number of venetoclax discontinuations. Dose reduction of venetoclax may mitigate cytopenia while maintaining efficacy. Venetoclax combined with low-intensity chemotherapy achieved high remission rates in acute myeloid leukaemia patients of real-world settings, but discontinuations of venetoclax limited survival. Reduced venetoclax improved treatment continuity and mitigated complications.
引用
收藏
页码:991 / 995
页数:5
相关论文
共 18 条
[1]   Venetoclax combinations induce high response rates in newly diagnosed acute myeloid leukemia patients ineligible for intensive chemotherapy in routine practice [J].
Apel, Arie ;
Moshe, Yakir ;
Ofran, Yishai ;
Gural, Alexander ;
Wolach, Ofir ;
Ganzel, Chezi ;
Canaani, Jonathan ;
Zektser, Miri ;
Duek, Adrian ;
Stemer, Galia ;
Hellman, Ilana ;
Basood, May ;
Frisch, Avraham ;
Leibovitch, Chiya ;
Koren-Michowitz, Maya .
AMERICAN JOURNAL OF HEMATOLOGY, 2021, 96 (07) :790-795
[2]   Revised recommendations of the international working group for diagnosis, standardization of response criteria, treatment outcomes, and reporting standards for therapeutic trials in acute myeloid leukemia [J].
Cheson, BD ;
Bennett, JM ;
Kopecky, KJ ;
Büchner, T ;
Willman, CL ;
Estey, EH ;
Schiffer, CA ;
Döhner, H ;
Tallman, MS ;
Lister, TA ;
LoCocco, F ;
Willemze, R ;
Biondi, A ;
Hiddemann, W ;
Larson, RA ;
Löwenberg, B ;
Sanz, MA ;
Head, DR ;
Ohno, R ;
Bloomfield, CD .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (24) :4642-4649
[3]   Azacitidine and Venetoclax in Previously Untreated Acute Myeloid Leukemia [J].
DiNardo, C. D. ;
Jonas, B. A. ;
Pullarkat, V. ;
Thirman, M. J. ;
Garcia, J. S. ;
Wei, A. H. ;
Konopleva, M. ;
Doehner, H. ;
Letai, A. ;
Fenaux, P. ;
Koller, E. ;
Havelange, V. ;
Leber, B. ;
Esteve, J. ;
Wang, J. ;
Pejsa, V. ;
Hajek, R. ;
Porkka, K. ;
Illes, A. ;
Lavie, D. ;
Lemoli, R. M. ;
Yamamoto, K. ;
Yoon, S. -S. ;
Jang, J. -H. ;
Yeh, S. -P. ;
Turgut, M. ;
Hong, W. -J. ;
Zhou, Y. ;
Potluri, J. ;
Pratz, K. W. .
NEW ENGLAND JOURNAL OF MEDICINE, 2020, 383 (07) :617-629
[4]   How I treat acute myeloid leukemia in the era of new drugs [J].
DiNardo, Courtney D. ;
Wei, Andrew H. .
BLOOD, 2020, 135 (02) :85-96
[5]   Diagnosis and management of acute myeloid leukemia in adults: recommendations from an international expert panel, on behalf of the European LeukemiaNet [J].
Doehner, Hartmut ;
Estey, Elihu H. ;
Amadori, Sergio ;
Appelbaum, Frederick R. ;
Buechner, Thomas ;
Burnett, Alan K. ;
Dombret, Herve ;
Fenaux, Pierre ;
Grimwade, David ;
Larson, Richard A. ;
Lo-Coco, Francesco ;
Naoe, Tomoki ;
Niederwieser, Dietger ;
Ossenkoppele, Gert J. ;
Sanz, Miguel A. ;
Sierra, Jorge ;
Tallman, Martin S. ;
Loewenberg, Bob ;
Bloomfield, Clara D. .
BLOOD, 2010, 115 (03) :453-474
[6]   Real-world treatment patterns of venetoclax and azacytidine therapy in Japanese patients with acute myeloid leukemia [J].
Gando, Yoshito ;
Yasu, Takeo .
ANNALS OF HEMATOLOGY, 2023, 102 (05) :1283-1285
[7]   How we use venetoclax with hypomethylating agents for the treatment of newly diagnosed patients with acute myeloid leukemia [J].
Jonas, Brian A. ;
Pollyea, Daniel A. .
LEUKEMIA, 2019, 33 (12) :2795-2804
[8]   Intensive chemotherapy does not benefit most older patients (age 70 years or older) with acute myeloid leukemia [J].
Kantarjian, Hagop ;
Ravandi, Farhad ;
O'Brien, Susan ;
Cortes, Jorge ;
Faderl, Stefan ;
Garcia-Manero, Guillermo ;
Jabbour, Elias ;
Wierda, William ;
Kadia, Tapan ;
Pierce, Sherry ;
Shan, Jianqin ;
Keating, Michael ;
Freireich, Emil J. .
BLOOD, 2010, 116 (22) :4422-4429
[9]   Utility of therapeutic drug monitoring of venetoclax in acute myeloid leukemia [J].
Kobayashi, Masayuki ;
Yasu, Takeo ;
Suzaki, Ken ;
Kosugi, Nobuharu .
MEDICAL ONCOLOGY, 2022, 39 (12)
[10]   Real-world effectiveness of CPX-351 vs venetoclax and azacitidine in acute myeloid leukemia [J].
Matthews, Andrew H. ;
Perl, Alexander E. ;
Luger, Selina M. ;
Loren, Alison W. ;
Gill, Saar I. ;
Porter, David L. ;
Babushok, Daria V. ;
Maillard, Ivan P. ;
Carroll, Martin P. ;
Frey, Noelle V. ;
Hexner, Elizabeth O. ;
Martin, Mary Ellen ;
McCurdy, Shannon R. ;
Stadtmauer, Edward A. ;
Paralkar, Vikram R. ;
Bruno, Ximena Jordan ;
Hwang, Wei -Ting ;
Margolis, David ;
Pratz, Keith W. .
BLOOD ADVANCES, 2022, 6 (13) :3997-4005