Ibrutinib With Rituximab in First-Line Treatment of Older Patients With Mantle Cell Lymphoma.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
10 01 2022
Historique:
pubmed: 20 11 2021
medline: 22 2 2022
entrez: 19 11 2021
Statut: ppublish

Résumé

Most patients with mantle cell lymphoma (MCL) are older. In this study, we investigated the efficacy and safety of a chemotherapy-free combination with ibrutinib and rituximab (IR) in previously untreated older patients with MCL (age ≥ 65 years). We enrolled 50 patients with MCL in this single-institution, single-arm, phase II clinical trial (NCT01880567). Patients with Ki-67% ≥ 50% and blastoid morphology were excluded. Ibrutinib was administered with rituximab up to 2 years with continuation of ibrutinib alone. The primary objective was to assess the overall response rate and safety of IR. In evaluable samples, whole-exome sequencing and bulk RNA sequencing from baseline tissue samples were performed. The median age was 71 years (interquartile range 69-76 years). Sixteen percent of patients had high-risk simplified MCL international prognostic index. The Ki-67% was low (< 30%) in 38 (76%) and moderately high (≥ 30%-50%) in 12 (24%) patients. The best overall response rate was 96% (71% complete response). After a median follow-up of 45 months (interquartile range 24-56 months), 28 (56%) patients came off study for various reasons (including four progression, 21 toxicities, and three miscellaneous reasons). The median progression-free survival and overall survival were not reached, and 3-year survival was 87% and 94%, respectively. None of the patients died on study therapy. Notably, 11 (22%) patients had grade 3 atrial fibrillation. Grade 3-4 myelosuppression was seen in < 5% of patients. Differential overexpression of IR combination is effective in older patients with MCL. Baseline evaluation for cardiovascular risks is highly recommended. Randomized trial is needed for definitive conclusions.

Identifiants

pubmed: 34797699
doi: 10.1200/JCO.21.01797
pmc: PMC8718245
doi:

Substances chimiques

Biomarkers, Tumor 0
Piperidines 0
ibrutinib 1X70OSD4VX
Rituximab 4F4X42SYQ6
Adenine JAC85A2161

Banques de données

ClinicalTrials.gov
['NCT01880567', 'NCT02427620']

Types de publication

Clinical Trial, Phase II Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

202-212

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA210250
Pays : United States
Organisme : NIH HHS
ID : S10 OD024977
Pays : United States

Auteurs

Preetesh Jain (P)

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

Shuangtao Zhao (S)

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

Hun Ju Lee (HJ)

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

Holly A Hill (HA)

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

Chi Young Ok (CY)

Department of Hemato-pathology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Rashmi Kanagal-Shamanna (R)

Department of Hemato-pathology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Fredrick B Hagemeister (FB)

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

Nathan Fowler (N)

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

Luis Fayad (L)

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

Yixin Yao (Y)

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

Yang Liu (Y)

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

Omar B Moghrabi (OB)

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

Lucy Navsaria (L)

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

Lei Feng (L)

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

Graciela M Nogueras Gonzalez (GM)

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

Guofan Xu (G)

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

Selvi Thirumurthi (S)

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

David Santos (D)

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

Cezar Iliescu (C)

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

Guilin Tang (G)

Department of Hemato-pathology, The University of Texas MD Anderson Cancer Center, Houston, TX.

L Jeffrey Medeiros (LJ)

Department of Hemato-pathology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Francisco Vega (F)

Department of Hemato-pathology, The University of Texas MD Anderson Cancer Center, Houston, TX.

Michelle Avellaneda (M)

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

Maria Badillo (M)

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

Christopher R Flowers (CR)

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

Linghua Wang (L)

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

Michael L Wang (ML)

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

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