Retrospective characterization of nodal marginal zone lymphoma

Author:

Stuver Robert1ORCID,Drill Esther2ORCID,Qualls David1,Okwali Michelle1,Lee Batlevi Connie1ORCID,Caron Philip C.1,Dogan Ahmet34ORCID,Epstein-Peterson Zachary D.14ORCID,Falchi Lorenzo14,Hamlin Paul A.14ORCID,Horwitz Steven M.145,Imber Brandon S.6ORCID,Intlekofer Andrew M.147,Johnson William T.145ORCID,Khan Niloufer14ORCID,Kumar Anita14ORCID,Lahoud Oscar B.1458,Lue Jennifer Kimberly14ORCID,Matasar Matthew J.14ORCID,Moskowitz Alison J.14,Noy Ariela14ORCID,Owens Colette N.1,Palomba M. Lia145,Schöder Heiko49ORCID,Vardhana Santosha A.147ORCID,Yahalom Joachim46,Zelenetz Andrew D.14ORCID,Salles Gilles14ORCID,Straus David J.14

Affiliation:

1. 1Department of Medicine, Lymphoma Service, Memorial Sloan Kettering Cancer Center, New York, NY

2. 2Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY

3. 3Department of Pathology and Laboratory Medicine, Hematopathology Service, Memorial Sloan Kettering Cancer Center, New York, NY

4. 4Department of Medicine, Weill Cornell Medical College, New York, NY

5. 5Department of Medicine, Cellular Therapy Service, Memorial Sloan Kettering Cancer Center, New York, NY

6. 6Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY

7. 7Human Oncology & Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY

8. 8Department of Medicine, Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, NY

9. 9Department of Radiology, Molecular Imaging and Therapy Service, Memorial Sloan Kettering Cancer Center, New York, NY

Abstract

Abstract Nodal marginal zone lymphoma (NMZL) is a rare non-Hodgkin B-cell lymphoma that has historically been difficult to define, though is now formally recognized by the World Health Organization Classification. To better characterize the clinical outcomes of patients with NMZL, we reviewed a sequential cohort of 187 patients with NMZL to describe baseline characteristics, survival outcomes, and time-to-event data. Initial management strategies were classified into five categories: observation, radiation, anti-CD20 monoclonal antibody therapy, chemoimmunotherapy, or other. Baseline Follicular Lymphoma International Prognostic Index scores were calculated to evaluate prognosis. A total of 187 patients were analyzed. The five-year overall survival was 91% (95% confidence interval [CI], 87-95), with a median follow-up time of 71 months (range, 8-253) among survivors. A total of 139 patients received active treatment at any point, with a median follow-up time of 56 months (range, 13-253) among survivors who were never treated. The probability of remaining untreated at five years was 25% (95% CI, 19-33). For those initially observed, the median time to active treatment was 72 months (95% CI, 49-not reached). For those who received at least one active treatment, the cumulative incidence of receiving a second active treatment at 60 months was 37%. Transformation to large B-cell lymphoma was rare, with a cumulative incidence of 15% at 10 years. In summary, our series is a large cohort of uniformly diagnosed NMZL with detailed analyses of survival and time to event analyses. We showed that NMZL commonly presents as an indolent lymphoma for which initial observation is often a reasonable strategy.

Publisher

American Society of Hematology

Subject

Hematology

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