Ibrutinib and Venetoclax for First-Line Treatment of CLL

被引:428
作者
Jain, Nitin [1 ]
Keating, Michael [1 ]
Thompson, Philip [1 ]
Ferrajoli, Alessandra [1 ]
Burger, Jan [1 ]
Borthakur, Gautam [1 ]
Takahashi, Koichi [1 ]
Estrov, Zeev [1 ]
Fowler, Nathan [2 ]
Kadia, Tapan [1 ]
Konopleva, Marina [1 ]
Alvarado, Yesid [1 ]
Yilmaz, Musa [1 ]
DiNardo, Courtney [1 ]
Bose, Prithviraj [1 ]
Ohanian, Maro [1 ]
Pemmaraju, Naveen [1 ]
Jabbour, Elias [1 ]
Sasaki, Koji [1 ]
Kanagal-Shamanna, Rashmi [3 ]
Patel, Keyur [3 ]
Jorgensen, Jeffrey [3 ]
Garg, Naveen [4 ]
Wang, Xuemei [5 ]
Sondermann, Katrina [1 ]
Cruz, Nichole [1 ]
Wei, Chongjuan [1 ]
Ayala, Ana [1 ]
Plunkett, William [6 ]
Kantarjian, Hagop [1 ]
Gandhi, Varsha [6 ]
Wierda, William [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Lymphoma & Myeloma, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Hematopathol, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Diagnost Radiol, Houston, TX 77030 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Houston, TX 77030 USA
关键词
CHRONIC LYMPHOCYTIC-LEUKEMIA; PROGRESSION-FREE; INITIAL THERAPY; RITUXIMAB; CHEMOIMMUNOTHERAPY; CYCLOPHOSPHAMIDE; FLUDARABINE; SURVIVAL;
D O I
10.1056/NEJMoa1900574
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Ibrutinib, an inhibitor of Bruton's tyrosine kinase, and venetoclax, an inhibitor of B-cell lymphoma 2 protein, have been approved for patients with chronic lymphocytic leukemia (CLL). Preclinical investigations have indicated potential synergistic interaction of their combination. Methods We conducted an investigator-initiated phase 2 study of combined ibrutinib and venetoclax involving previously untreated high-risk and older patients with CLL. All patients had at least one of the following features: chromosome 17p deletion, mutated TP53, chromosome 11q deletion, unmutated IGHV, or an age of 65 years or older. Patients received ibrutinib monotherapy (420 mg once daily) for 3 cycles, followed by the addition of venetoclax (weekly dose escalation to 400 mg once daily). Combined therapy was administered for 24 cycles. Response assessments were performed according to International Workshop on Chronic Lymphocytic Leukemia 2008 criteria. Minimal residual disease was assessed by means of multicolor flow cytometry in bone marrow (sensitivity, 10(-4)). Results A total of 80 patients were treated. The median age was 65 years (range, 26 to 83). A total of 30% of the patients were 70 years of age or older. Overall, 92% of the patients had unmutated IGHV, TP53 aberration, or chromosome 11q deletion. With combined treatment, the proportions of patients who had complete remission (with or without normal blood count recovery) and remission with undetectable minimal residual disease increased over time. After 12 cycles of combined treatment, 88% of the patients had complete remission or complete remission with incomplete count recovery, and 61% had remission with undetectable minimal residual disease. Responses were noted in older adults and across all high-risk subgroups. Three patients had laboratory evidence of tumor lysis syndrome. The adverse-event profile was similar to what has been reported with ibrutinib and venetoclax. Conclusions In this study, combined venetoclax and ibrutinib was an effective oral regimen for high-risk and older patients with CLL.
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收藏
页码:2095 / 2103
页数:9
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