Transformed non‐Hodgkin lymphoma in the rituximab era: analysis of the <scp>NCCN</scp> outcomes database

Makiko Ban‐Hoefen(University of Rochester Medical Center), Ann Vanderplas(City of Hope), Allison Crosby‐Thompson(Dana-Farber Cancer Institute), Gregory A. Abel(Dana-Farber Cancer Institute), Myron S. Czuczman(Roswell Park Comprehensive Cancer Center), Leo I. Gordon(Northwestern University), Mark Kaminski(University of Michigan), Jennifer L. Kelly(University of Rochester), Michael Millenson(Fox Chase Cancer Center), Auayporn Nademanee(City of Hope), Maria Alma Rodriguez(The University of Texas MD Anderson Cancer Center), Andrew D. Zelenetz(Memorial Sloan Kettering Cancer Center), Joyce C. Niland(City of Hope), Ann S. LaCasce(Dana-Farber Cancer Institute), Jonathan W. Friedberg(University of Rochester)
British Journal of Haematology
September 20, 2013
Cited by 74Open Access
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Abstract

Histological transformation (HT) is a major cause of morbidity and mortality in patients with indolent non-Hodgkin lymphoma (NHL). The multicentre National Cancer Comprehensive Network database for NHL provides a unique opportunity to investigate the natural history of HT in the rituximab era. 118 patients with biopsy-confirmed indolent lymphoma and subsequent biopsy-confirmed HT were identified. Treatments for HT included autologous stem-cell transplant (auto-SCT) (n = 50), allogeneic SCT (allo-SCT) (n = 18), and treatment without transplant (n = 50). The 2-year overall survival (OS) for the entire cohort was 68%. For auto-SCT patients aged ≤ 60 years (n = 24), the 2-year OS was 74%. For non-transplanted patients aged ≤ 60 years (n = 19), the 2-year OS was 59%. The 2-year OS of patients naïve to chemotherapy prior to HT was superior to patients who were exposed to chemotherapy prior to HT (100% vs. 35%, P = 0.03). In this largest prospective cohort of patients of strictly defined HT in the rituximab era, the natural history of HT appears more favourable than historical studies. Younger patients who were not exposed to chemotherapy prior to HT experienced a prolonged survival even without transplantation. This study serves as a benchmark for future trials of novel approaches for HT in the Rituximab era.


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