Risk of infectious adverse events of venetoclax therapy for hematologic malignancies: a systematic review and meta-analysis of RCTs.
Connor ProstyKhaled KatergiAlex NguyenOwen Dan LuoMark SorinVladimir CherniakMichael SebagKoray DemirEmily Gibson McDonaldTodd C LeeMatthew P ChengPublished in: Blood advances (2024)
Venetoclax is a small molecule inhibitor of BCL-2 used in the treatment of acute myelogenous leukemia (AML) and chronic lymphocytic leukemia (CLL). Recent postmarketing studies of ibrutinib, another small molecule inhibitor, suggested that these agents may predispose to opportunistic infections. We sought to systematically review the randomized controlled trial (RCT) evidence of venetoclax to assess whether it predisposes patients to infectious adverse events (IAEs) and neutropenia. We systematically reviewed RCTs comparing venetoclax therapy with active or placebo controls for patients with hematologic malignancies. Data on IAEs and neutropenia were pooled by Bayesian meta-analysis, and we computed the probability of any increased risk (P[risk ratio (RR) > 1]) of IAEs or neutropenic complications. Seven RCTs were included, comprising 2067 patients. In CLL (n = 1032), there was a low probability of increased risk of high-grade (P[RR > 1] = 71.2%) and fatal IAEs (P[RR > 1] = 64.5%) and high-grade neutropenia (P[RR > 1] = 63.4%). There were insufficient data to perform a meta-analysis of IAEs in AML; however, 1 trial suggested an increased risk of IAEs with venetoclax. Furthermore, in AML (n = 642), venetoclax was associated with a high probability of increased risk of high-grade neutropenia (P[RR > 1] = 94.6%) and febrile neutropenia (P[RR > 1] = 90.6%). Our results suggest that venetoclax has a low probability of increased risk of IAEs or neutropenia in CLL. By contrast, there is likely increased risk of high-grade neutropenia and febrile neutropenia in AML. Importantly, our analyses did not identify any specific IAEs that would benefit from routine antimicrobial prophylaxis or pre-emptive testing.
Keyphrases
- chronic lymphocytic leukemia
- high grade
- chemotherapy induced
- small molecule
- acute myeloid leukemia
- low grade
- end stage renal disease
- randomized controlled trial
- systematic review
- newly diagnosed
- ejection fraction
- chronic kidney disease
- peritoneal dialysis
- study protocol
- prognostic factors
- stem cells
- electronic health record
- clinical trial
- magnetic resonance imaging
- machine learning
- phase iii
- big data
- liver failure
- risk factors
- patient reported outcomes
- contrast enhanced
- patient reported
- acute respiratory distress syndrome
- urinary tract infection
- clinical practice
- open label
- protein protein
- acute lymphoblastic leukemia
- smoking cessation
- placebo controlled