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

Author:

Bond David A.1ORCID,Switchenko Jeffrey M.2ORCID,Villa Diego34ORCID,Maddocks Kami1,Churnetski Michael5,Gerrie Alina S.34ORCID,Goyal Subir2,Shanmugasundaram Krithika5,Calzada Oscar5,Kolla Bhaskar6ORCID,Bachanova Veronika6,Gerson James N.78,Barta Stefan K.78,Hill Brian T.9,Sawalha Yazeed19,Martin Peter10,Maldonado Edward11ORCID,Gordon Max1112ORCID,Danilov Alexey V.1113,Grover Natalie S.14ORCID,Mathews Stephanie14,Burkart Madelyn15ORCID,Karmali Reem15ORCID,Ghosh Nilanjan16,Park Steven I.16,Epperla Narendranath1ORCID,Badar Talha17ORCID,Guo Jin10,Hamadani Mehdi17ORCID,Fenske Timothy S.17,Malecek Mary-Kate18ORCID,Kahl Brad S.18ORCID,Flowers Christopher R.512,Blum Kristie A.5,Cohen Jonathon B.5ORCID

Affiliation:

1. Division of Hematology, The Ohio State University, Columbus, OH;

2. Winship Cancer Institute, Biostatistics and Bioinformatics, Emory University, Atlanta, GA;

3. Centre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada;

4. Division of Medical Oncology, University of British Columbia, Vancouver, BC, Canada;

5. Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA;

6. Division of Hematology Oncology and Transplantation, University of Minnesota, Minneapolis, MN;

7. Division of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, PA;

8. Division of Hematology-Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA;

9. Department of Hematology and Medical Oncology, Taussig Cancer Institute,Cleveland Clinic, Cleveland, OH;

10. Division of Hematology and Oncology, Weill Cornell Medical Center/New York Presbyterian Hospital, New York, NY;

11. Knight Cancer Institute, Oregon Health Sciences University, Portland, OR;

12. Department of Lymphoma and Myeloma, MD Anderson Cancer Center, Houston, TX;

13. Department of Hematology and Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, CA;

14. Division of Hematology, University of North Carolina, Chapel Hill, NC;

15. Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Division of Hematology, Northwestern University, Chicago, IL;

16. Levine Cancer Institute, Atrium Health, Charlotte, NC;

17. BMT Cellular Therapy Program, Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, WI; and

18. Department of Medicine, Washington University, St Louis, MO

Abstract

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.

Publisher

American Society of Hematology

Subject

Hematology

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