| Literature DB >> 33593877 |
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.Entities:
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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