Smart Start: Rituximab, Lenalidomide, and Ibrutinib in Patients With Newly Diagnosed Large B-Cell Lymphoma

Author:

Westin Jason1ORCID,Davis R. Eric1,Feng Lei2,Hagemeister Fredrick1ORCID,Steiner Raphael1,Lee Hun Ju1ORCID,Fayad Luis1,Nastoupil Loretta1ORCID,Ahmed Sairah1,Rodriguez Alma1ORCID,Fanale Michelle13,Samaniego Felipe1,Iyer Swaminathan P.1ORCID,Nair Ranjit1,Oki Yasuhiro1,Fowler Nathan1,Wang Michael1ORCID,Ma Man Chun John1ORCID,Vega Francisco4ORCID,McDonnell Timothy4,Pinnix Chelsea5,Griffith Donna1,Lu Yang6ORCID,Tewari Sanjit6ORCID,Sun Ryan2,Scott David W.7ORCID,Flowers Christopher R.1ORCID,Neelapu Sattva1ORCID,Green Michael R.18ORCID

Affiliation:

1. Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX

2. Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX

3. Seagen, Bothell, WA

4. Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX

5. Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX

6. Department of Nuclear Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX

7. British Columbia Cancer Centre for Lymphoid Cancer, Vancouver, British Columbia, Canada

8. Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX

Abstract

PURPOSE Chemoimmunotherapy for patients with newly diagnosed diffuse large B-cell lymphoma (DLBCL) is largely unchanged for decades. Both preclinical models and clinical data suggest the combination of lenalidomide and ibrutinib may have synergy in DLBCL, particularly in the non–germinal center B-cell-like subset. METHODS We enrolled 60 patients with newly diagnosed non–germinal center B-cell-like DLBCL in this investigator-initiated, single-arm phase II trial of rituximab, lenalidomide, and ibrutinib (RLI) with the sequential addition of chemotherapy (ClinicalTrials.gov identifier: NCT02636322 ). Patients were treated with rituximab 375 mg/m2 intravenous once on day 1, lenalidomide 25 mg once per day on days 1-10, and ibrutinib 560 mg once daily continuously of each 21-day cycle (RLI). After two cycles, standard chemotherapy was added to RLI for six additional cycles. The primary end points were overall response rate (ORR) after two cycles of RLI alone and complete response rate after completion of RLI with chemotherapy. In evaluable samples, circulating tumor DNA and DLBCL90 assays were performed. RESULTS The median age was 63.5 years (range, 29-83 years) with 28% age 70 years or older. The revised international prognostic index identified 42% as high risk, and 62% were double expressor of MYC and BCL2 protein. The ORR after two cycles of RLI was 86.2%, and the complete response rate at the end of RLI-chemotherapy was 94.5%. With a median follow-up of 31 months, the progression-free survival and overall survival were at 91.3% and 96.6% at 2 years, respectively. CONCLUSION Smart Start is the first study, to our knowledge, to treat newly diagnosed DLBCL with a targeted therapy combination before chemotherapy. RLI produced a high ORR, and RLI with chemotherapy resulted in durable responses. This establishes the potential for developing biologically driven and noncytotoxic first-line therapies for DLBCL.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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