Literature DB >> 33593877

Venetoclax and Navitoclax in Combination with Chemotherapy in Patients with Relapsed or Refractory Acute Lymphoblastic Leukemia and Lymphoblastic Lymphoma.

Vinod A Pullarkat1, Norman J Lacayo2, Elias Jabbour3, Jeffrey E Rubnitz4,5, Ashish Bajel6, Theodore W Laetsch7,8, Jessica Leonard9, Susan I Colace10, Seong Lin Khaw11, Shaun A Fleming12, Ryan J Mattison13, Robin Norris14, Joseph T Opferman15, Kathryn G Roberts16, Yaqi Zhao16, Chunxu Qu16, Mohamed Badawi17, Michelle Schmidt17, Bo Tong17, John C Pesko17, Yan Sun17, Jeremy A Ross17, Deeksha Vishwamitra17, Lindsey Rosenwinkel17, Su Young Kim17, Amanda Jacobson17, Charles G Mullighan16, Thomas B Alexander18, Wendy Stock19.   

Abstract

Combining venetoclax, a selective BCL2 inhibitor, with low-dose navitoclax, a BCL-XL/BCL2 inhibitor, may allow targeting of both BCL2 and BCL-XL without dose-limiting thrombocytopenia associated with navitoclax monotherapy. The safety and preliminary efficacy of venetoclax with low-dose navitoclax and chemotherapy was assessed in this phase I dose-escalation study (NCT03181126) in pediatric and adult patients with relapsed/refractory (R/R) acute lymphoblastic leukemia or lymphoblastic lymphoma. Forty-seven patients received treatment. A recommended phase II dose of 50 mg navitoclax for adults and 25 mg for patients <45 kg with 400 mg adult-equivalent venetoclax was identified. Delayed hematopoietic recovery was the primary safety finding. The complete remission rate was 60%, including responses in patients who had previously received hematopoietic cell transplantation or immunotherapy. Thirteen patients (28%) proceeded to transplantation or CAR T-cell therapy on study. Venetoclax with navitoclax and chemotherapy was well tolerated and had promising efficacy in this heavily pretreated patient population. SIGNIFICANCE: In this phase I study, venetoclax with low-dose navitoclax and chemotherapy was well tolerated and had promising efficacy in patients with relapsed/refractory acute lymphoblastic leukemia or lymphoblastic lymphoma. Responses were observed in patients across histologic and genomic subtypes and in those who failed available therapies including stem cell transplant.See related commentary by Larkin and Byrd, p. 1324.This article is highlighted in the In This Issue feature, p. 1307. ©2021 American Association for Cancer Research.

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Year:  2021        PMID: 33593877      PMCID: PMC9533326          DOI: 10.1158/2159-8290.CD-20-1465

Source DB:  PubMed          Journal:  Cancer Discov        ISSN: 2159-8274            Impact factor:   38.272


  49 in total

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Journal:  Nat Med       Date:  2013-01-06       Impact factor: 53.440

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Review 5.  Virus-Mediated Inhibition of Apoptosis in the Context of EBV-Associated Diseases: Molecular Mechanisms and Therapeutic Perspectives.

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6.  Relapsed acute lymphoblastic leukaemia after allogeneic stem cell transplantation: a therapeutic dilemma challenging the armamentarium of immunotherapies currently available (case reports).

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9.  Safety and efficacy of navitoclax, a BCL-2 and BCL-XL inhibitor, in patients with relapsed or refractory lymphoid malignancies: results from a phase 2a study.

Authors:  Sven de Vos; John P Leonard; Jonathan W Friedberg; Jasmine Zain; Kieron Dunleavy; Rod Humerickhouse; John Hayslip; John Pesko; Wyndham H Wilson
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