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Combination of acalabrutinib with lenalidomide and rituximab in relapsed/refractory aggressive B-cell non-Hodgkin lymphoma: a single-arm phase II trial

Author

Listed:
  • Changhee Park

    (Seoul National University Hospital)

  • Ho Sup Lee

    (Kosin University College of Medicine, Gospel Hospital)

  • Ka-Won Kang

    (Korea University College of Medicine, Anam Hospital)

  • Won-Sik Lee

    (Busan Paik Hospital)

  • Young Rok Do

    (Keimyung University Dongsan Medical Center)

  • Jae-Yong Kwak

    (Jeonbuk National University Medical School)

  • Ho-Jin Shin

    (Pusan National University)

  • Sung-Yong Kim

    (KonKuk University)

  • Jun Ho Yi

    (Chung-Ang University)

  • Sung-Nam Lim

    (Inje University Haeundae Paik Hospital)

  • Jeong-Ok Lee

    (Seoul National University Bundang Hospital)

  • Deok-Hwan Yang

    (Chonnam National University Hwasun Hospital)

  • Hun Jang

    (PROTEINA Co., Ltd)

  • Byoungsan Choi

    (PROTEINA Co., Ltd)

  • Jiwoo Lim

    (GenomeOpinion Inc.)

  • Choong Hyun Sun

    (GenomeOpinion Inc.)

  • Ja Min Byun

    (Seoul National University Hospital)

  • Sung-Soo Yoon

    (Seoul National University Hospital)

  • Youngil Koh

    (Seoul National University Hospital
    GenomeOpinion Inc.)

Abstract

Potential synergism between Bruton’s tyrosine kinase (BTK) inhibitor and lenalidomide in treating aggressive B-cell lymphoma has been suggested. Here, the authors report a single-arm phase II clinical trial of combination of acalabrutinib, lenalidomide and rituximab (R2A) in patients with aggressive relapsed/refractory aggressive (R/R) B-cell non-Hodgkin lymphoma (NHL). The primary endpoint of this study is objective response rate (ORR), and the secondary endpoints are complete remission (CR) rate, duration of response (DoR), progression-free survival (PFS) and overall survival (OS). A total of 66 patients are enrolled mostly with diffuse large B-cell lymphoma. The ORR is 54.5% and CR rate is 31.8% meeting the primary end point. The median DoR is 12.9 months, and 1-year PFS and OS rate is 33.1% and 67.5% respectively. Adverse events (AE) are manageable with the most frequent AE being neutropenia (31.8%). Patients with MYD88 mutations, subtypes known for NF-κB activation, and high BTK expression by immunohistochemistry respond well. Overall, these results show a significant efficacy of the R2A regimen in patients with aggressive R/R B-cell NHL, with exploratory biomarkers suggesting potential associations with response. (ClinicalTrials.gov 51 identifier: NCT04094142)

Suggested Citation

  • Changhee Park & Ho Sup Lee & Ka-Won Kang & Won-Sik Lee & Young Rok Do & Jae-Yong Kwak & Ho-Jin Shin & Sung-Yong Kim & Jun Ho Yi & Sung-Nam Lim & Jeong-Ok Lee & Deok-Hwan Yang & Hun Jang & Byoungsan Ch, 2024. "Combination of acalabrutinib with lenalidomide and rituximab in relapsed/refractory aggressive B-cell non-Hodgkin lymphoma: a single-arm phase II trial," Nature Communications, Nature, vol. 15(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-47198-4
    DOI: 10.1038/s41467-024-47198-4
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