Real-world outcomes and management strategies for venetoclax-treated chronic lymphocytic leukemia patients in the United States.


Journal Article

Venetoclax is a BCL2 inhibitor approved for 17p-deleted relapsed/refractory chronic lymphocytic leukemia with activity following kinase inhibitors. We conducted a multicenter retrospective cohort analysis of patients with chronic lymphocytic leukemia treated with venetoclax to describe outcomes, toxicities, and treatment selection following venetoclax discontinuation. A total of 141 chronic lymphocytic leukemia patients were included (98% relapsed/refractory). Median age at venetoclax initiation was 67 years (range 37-91), median prior therapies was 3 (0-11), 81% unmutated IGHV, 45% del(17p), and 26.8% complex karyotype (≥ 3 abnormalities). Prior to venetoclax initiation, 89% received a B-cell receptor antagonist. For tumor lysis syndrome prophylaxis, 93% received allopurinol, 92% normal saline, and 45% rasburicase. Dose escalation to the maximum recommended dose of 400 mg daily was achieved in 85% of patients. Adverse events of interest included neutropenia in 47.4%, thrombocytopenia in 36%, tumor lysis syndrome in 13.4%, neutropenic fever in 11.6%, and diarrhea in 7.3%. The overall response rate to venetoclax was 72% (19.4% complete remission). With a median follow up of 7 months, median progression free survival and overall survival for the entire cohort have not been reached. To date, 41 venetoclax treated patients have discontinued therapy and 24 have received a subsequent therapy, most commonly ibrutinib. In the largest clinical experience of venetoclax-treated chronic lymphocytic leukemia patients, the majority successfully completed and maintained a maximum recommended dose. Response rates and duration of response appear comparable to clinical trial data. Venetoclax was active in patients with mutations known to confer ibrutinib resistance. Optimal sequencing of newer chronic lymphocytic leukemia therapies requires further study.

Full Text

Duke Authors

Cited Authors

  • Mato, AR; Thompson, M; Allan, JN; Brander, DM; Pagel, JM; Ujjani, CS; Hill, BT; Lamanna, N; Lansigan, F; Jacobs, R; Shadman, M; Skarbnik, AP; Pu, JJ; Barr, PM; Sehgal, AR; Cheson, BD; Zent, CS; Tuncer, HH; Schuster, SJ; Pickens, PV; Shah, NN; Goy, A; Winter, AM; Garcia, C; Kennard, K; Isaac, K; Dorsey, C; Gashonia, LM; Singavi, AK; Roeker, LE; Zelenetz, A; Williams, A; Howlett, C; Weissbrot, H; Ali, N; Khajavian, S; Sitlinger, A; Tranchito, E; Rhodes, J; Felsenfeld, J; Bailey, N; Patel, B; Burns, TF; Yacur, M; Malhotra, M; Svoboda, J; Furman, RR; Nabhan, C

Published Date

  • September 2018

Published In

Volume / Issue

  • 103 / 9

Start / End Page

  • 1511 - 1517

PubMed ID

  • 29880613

Pubmed Central ID

  • 29880613

Electronic International Standard Serial Number (EISSN)

  • 1592-8721

Digital Object Identifier (DOI)

  • 10.3324/haematol.2018.193615


  • eng

Conference Location

  • Italy