| Literature DB >> 30768675 |
Toby A Eyre1, Amy A Kirkwood2, Sat Gohill3, George Follows4, Renata Walewska5, Harriet Walter6, Matthew Cross7, Francesco Forconi8, Nimish Shah9, Richard Chasty10, Alistair Hart11, Angus Broom12, Helen Marr13, Piers E M Patten14, Andy Dann15, Arvind Arumainathan16, Tal Munir17, Paneesha Shankara18, Adrian Bloor19, Rosalynd Johnston20, Kim Orchard21, Anna H Schuh1,22, Christopher P Fox23.
Abstract
Venetoclax is a BCL2 inhibitor with activity in relapsed/refractory (R/R) chronic lymphocytic leukaemia (CLL). We conducted a multi-centre retrospective analysis of 105 R/R CLL patients who received venetoclax pre-National Health Service commissioning. The median age was 67 years and median prior lines was 3 (range: 1-15). 48% had TP53 disruption. At ≥2 lines, 60% received a Bruton Tyrosine Kinase inhibitor (BTKi) and no prior phosphoinositide 3-kinase inhibitor (Pi3Ki), 25% received a Pi3Ki and no prior BTKi, and 10% received both. Patients discontinued B cell receptor inhibitor (BCRi) because of toxicity in 44% and progression in 54%. Tumour lysis syndrome risk was low, intermediate or high in 27%, 25%, and 48% respectively. Overall response was 88% (30% complete response [CR]). The overall response rate was 85% (CR 23%) in BTKi-exposed patients, 92% (CR 38%) in Pi3Ki-exposed patients and 80% (CR 20%) in both (P = 0·59). With a median follow-up of 15·6 months, 1-year progression-free survival was 65·0% and 1-year overall survival was 75·1%. Dose reduction or temporary interruption did not result in an inferior progression-free or discontinuation-free survival. Risk of progression or death after stopping a prior BCRi for progression was double compared to those stopping for other reasons (predominantly toxicity) (Hazard Ratio 2·01 P = 0·05). Venetoclax is active and well tolerated in R/R CLL post ≥1 BCRi. Reason(s) for stopping BCRi influences venetoclax outcomes.Entities:
Keywords: B cell receptor inhibitor, ibrutinib, idelalisib, p53 venetoclax; BCL2; chronic lymphocytic leukaemia
Year: 2019 PMID: 30768675 DOI: 10.1111/bjh.15802
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998