Early relapse identifies MCL patients with inferior survival after intensive or less intensive frontline therapy

Blood Advances - Tập 5 - Trang 5179-5189 - 2021
David A. Bond1, Jeffrey M. Switchenko2, Diego Villa3,4, Kami Maddocks1, Michael Churnetski5, Alina S. Gerrie3,4, Subir Goyal2, Krithika Shanmugasundaram5, Oscar Calzada5, Bhaskar Kolla6, Veronika Bachanova6, James N. Gerson7,8, Stefan K. Barta7,8, Brian T. Hill9, Yazeed Sawalha1,9, Peter Martin10, Edward Maldonado11, Max Gordon11,12, Alexey V. Danilov11,13, Natalie S. Grover14
1Division of Hematology, The Ohio State University, Columbus, OH
2Winship Cancer Institute, Biostatistics and Bioinformatics, Emory University, Atlanta, GA
3Centre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada
4Division of Medical Oncology, University of British Columbia, Vancouver, BC, Canada
5Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA
6Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, MN
7Division of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA
8Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA
9Department of Hematology and Medical Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, OH
10Division of Hematology and Oncology, Weill Cornell Medical Center/New York Presbyterian Hospital, New York, NY
11Knight Cancer Institute, Oregon Health Sciences University, Portland, OR
12Department of Lymphoma and Myeloma, MD Anderson Cancer Center, Houston, TX
13Department of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, CA
14Division of Hematology, University of North Carolina, Chapel Hill, NC

Tóm tắt

Abstract Although an expanding array of effective treatments has resulted in recent improvement in survival of patients with mantle cell lymphoma (MCL), outcomes remain heterogeneous, and identification of prognostic factors remains a priority. We assessed the prognostic impact of time to progression of disease (POD) after first-line therapy among 455 patients with relapsed MCL. Patients were categorized by duration of first remission as PRF/POD6, defined as progressive disease during induction or POD within 6 months of diagnosis (n = 65; 14%); POD6-24, defined as POD between 6 and 24 months after diagnosis (n = 153; 34%); and POD>24, defined as POD >24 months after diagnosis (n = 237; 53%). The median overall survival from POD (OS2) was 1.3 years (95% confidence interval [CI], 0.9-2.4) for patients with PRF/POD6, 3 years (95% CI, 2-6.8) for those with POD6-24, and 8 years (95% CI, 6.2-NR) for those with POD>24. Median OS2 was inferior in patients with early POD (defined as PRF/POD6 or POD6-24) after both intensive and less intensive frontline treatment. The prognostic performance of time until POD was replicated in an independent cohort of 245 patients with relapsed MCL, with median OS2 of 0.3 years (95% CI, 0.1-0.5) for PRF/POD6, 0.8 years (95% CI, 0.6-0.9) for POD6-24, and 2.4 years (95% CI 2.1-2.7) for POD>24. Early POD is associated with inferior OS2 in patients with relapsed MCL, identifying a high-risk population for future prospective studies.

Tài liệu tham khảo

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