A novel comorbidity score for older adults with non-Hodgkin lymphoma: the 3-factor risk estimate scale

Author:

Gordon Max J.1,Duan Zhigang2,Zhao Hui2,Nastoupil Loretta3ORCID,Ferrajoli Alessandra4,Danilov Alexey V.5,Giordano Sharon H.2

Affiliation:

1. 1Department of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX

2. 2Department of Health Services Research, The University of Texas MD Anderson Cancer Center, Houston, TX

3. 3Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX

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

5. 5Department of Hematology & Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA

Abstract

Abstract For patients with non-Hodgkin lymphoma (NHL), formal comorbidity assessment is recommended but is rarely conducted in routine practice. A simple, validated measure of comorbidities that standardizes their assessment could improve adherence to guidelines. We previously constructed the 3-factor risk estimate scale (TRES) among patients with chronic lymphocytic leukemia (CLL). Here, we investigated TRES in multiple NHL subtypes. In the surveillance, epidemiology, and end results–Medicare database, patients with NHL diagnosed from 2008 to 2017 were included. Upper gastrointestinal, endocrine, and vascular comorbidities were identified using ICD-9/ICD-10 codes to assign TRES scores. Patient characteristic distributions were compared using χ2 or t test. Association of mortality and TRES score was assessed using Kaplan-Meier and multivariable Cox regression model for competing risk. A total of 40 486 patients were included in the study. Median age was 77 years (interquartile range [IQR], 71-83 years). The most frequent NHL subtypes were CLL (28.2%), diffuse large B-cell (27.6%), and follicular lymphoma (12.6%). Median follow-up was 33 months (IQR, 13-60 months). TRES was low, intermediate, and high in 40.8%, 37.0%, and 22.2% of patients, corresponding to median overall survival (OS) of 8.2, 5.3, and 2.9 years (P < .001), respectively. TRES was associated with OS in all NHL subtypes. In multivariable models, TRES was associated with inferior OS and NHL-specific survival. TRES is clinically translatable and associated with OS and lymphoma-specific survival in older adults with NHL.

Publisher

American Society of Hematology

Subject

Hematology

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