COVID-19 Deaths May Have Interfered With Results of CLL Trial

Venetoclax and hypomethylating agents appear to be more effective when used together.
Venetoclax and hypomethylating agents appear to be more effective when used together.
Researchers investigated whether adding venetoclax to ibrutinib and obinutuzumab would improve survival and allow for discontinuation of treatment in older patients with CLL.

It is unclear whether adding venetoclax to treatment with ibrutinib and obinutuzumab can improve outcomes in older patients with treatment-naïve chronic lymphocytic leukemia (CLL), according to a presentation at the ASCO Annual Meeting 2023.

Results from the phase 3 trial showed that adding venetoclax to ibrutinib and obinutuzumab did not improve progression-free survival (PFS). However, this result may have been influenced by an imbalance of COVID-19 deaths between the treatment arms, according to study presenter Jennifer Ann Woyach, MD, of The Ohio State University Comprehensive Cancer Center in Columbus.

The trial (ClinicalTrials.gov Identifier: NCT03737981) included 465 patients with previously untreated CLL who were 65 years of age or younger. The patients were randomly assigned to receive ibrutinib and obinutuzumab (IO; n=232) or venetoclax plus ibrutinib and obinutuzumab (IVO; n=233). Baseline characteristics were well balanced between the arms.

The rate of grade 3-5 hematologic adverse events was 48% in the IO arm and 61% in the IVO arm (P =.006). The rate of grade 3-5 non-hematologic adverse events was 66% and 67%, respectively (P =.743).

Grade 3 or higher COVID-19 was reported in 16 patients in the IO arm and 31 in the IVO arm. COVID-19 was fatal in 11 patients in the IO arm and 19 of those in the IVO arm.

At 18 months, the PFS rate was 87% in the IO arm and 85% in the IVO arm (hazard ratio [HR], 1.12; 95% CI, 0.70-1.79). When COVID-19 deaths were censored, the PFS rate was 92% in the IO arm and 94% in the IVO arm (HR, 0.82; 95% CI, 0.44-1.53).

At 18 months, the overall survival (OS) rate was 90% in the IO arm and 87% in the IVO arm (HR, 1.34; 95% CI, 0.80-2.25; P =.26). When COVID-19 deaths were censored, the OS rate was 95% in the IO arm and 96% in the IVO arm (HR, 0.97; 95% CI, 0.46-2.04; P =.93).

The complete response rate was 31.3% in the IO arm and 68.5% in the IVO arm. The rate of minimal residual disease negativity was 33.3% and 86.8%, respectively.

“In this trial, IVO is not superior to IO for the initial treatment of older patients with CLL,” Dr Woyach said. “However, COVID-19 may have significantly altered these results, with data suggesting a death imbalance for patients treated with IVO as compared with IO.”

Dr Woyach said long-term follow-up will be “critical” to determine if some patients benefit from IVO.  

Disclosures: This research was partly supported by Pharmacyclics, AbbVie, Genentech, and Abbott Molecular. Some study authors declared affiliations with biotech, pharmaceutical, and/or device companies. Please see the original reference for a full list of disclosures.

Reference

Woyach JA, Yin J, Brown JR, et al. Results of a phase 3 study of IVO vs IO for previously untreated older patients (pts) with chronic lymphocytic leukemia (CLL) and impact of COVID-19 (Alliance). ASCO 2023. June 2-6, 2023. Abstract 7500.

This article originally appeared on Hematology Advisor