Updated results from the phase 3 HELIOS study of ibrutinib, bendamustine, and rituximab in relapsed chronic lymphocytic leukemia/small lymphocytic lymphoma.
G FraserP CramerF DemirkanR Santucci SilvaS GrosickiA PristupaA JanssensJ MayerN L BartlettM-S DilhuydyH PylypenkoJ LoscertalesA AvigdorSimon A RuleD VillaO SamoilovaP PanagiotidisA GoyM A PavlovskyC KarlssonM HallekM MahlerM SalmanS SunC PhelpsS BalasubramanianA HowesA Chanan-KhanPublished in: Leukemia (2018)
We report follow-up results from the randomized, placebo-controlled, phase 3 HELIOS trial of ibrutinib+bendamustine and rituximab (BR) for previously treated chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL) without deletion 17p. Overall, 578 patients were randomized 1:1 to either ibrutinib (420 mg daily) or placebo, in combination with 6 cycles of BR, followed by ibrutinib or placebo alone. Median follow-up was 34.8 months (range: 0.1-45.8). Investigator-assessed median progression-free survival (PFS) was not reached for ibrutinib+BR, versus 14.3 months for placebo+BR (hazard ratio [HR] [95% CI], 0.206 [0.159-0.265]; P < 0.0001); 36-month PFS rates were 68.0% versus 13.9%, respectively. The results are consistent with the primary analysis findings (HR = 0.203, as assessed by independent review committee, with 17-month median follow-up). Median overall survival was not reached in either arm; HR (95% CI) for ibrutinib+BR versus placebo: 0.652 (0.454-0.935; P = 0.019). Minimal residual disease (MRD)-negative response rates were 26.3% for ibrutinib+BR and 6.2% for placebo+BR (P < 0.0001). Incidence of treatment-emergent adverse events (including grades 3-4) were generally consistent with the initial HELIOS report. These long-term data support improved survival outcomes and deepening responses with ibrutinib+BR compared with BR in relapsed CLL/SLL.
Keyphrases
- chronic lymphocytic leukemia
- double blind
- placebo controlled
- phase iii
- clinical trial
- phase ii
- diffuse large b cell lymphoma
- open label
- free survival
- study protocol
- acute lymphoblastic leukemia
- acute myeloid leukemia
- randomized controlled trial
- multiple myeloma
- ejection fraction
- squamous cell carcinoma
- hodgkin lymphoma
- machine learning
- artificial intelligence
- patient reported outcomes
- big data
- data analysis
- patient reported