TY - JOUR
T1 - Defining primary refractory large B-cell lymphoma
AU - Bock, Allison M.
AU - Mwangi, Raphael
AU - Wang, Yucai
AU - Khurana, Arushi
AU - Maurer, Matthew
AU - Ayers, Amy
AU - Kahl, Brad S.
AU - Martin, Peter
AU - Cohen, Jonathon B.
AU - Casulo, Carla
AU - Lossos, Izidore S.
AU - Farooq, Umar
AU - Ayyappan, Sabarish
AU - Reicks, Tanner
AU - Habermann, Thomas M.
AU - Witzig, Thomas E.
AU - Flowers, Christopher R.
AU - Cerhan, James R.
AU - Nastoupil, Loretta J.
AU - Nowakowski, Grzegorz S.
N1 - Publisher Copyright:
© 2024 by The American Society of Hematology.
PY - 2024/7/9
Y1 - 2024/7/9
N2 - Patients with large B-cell lymphoma (LBCL) that fail to achieve a complete response (CR) or who relapse early after anthracycline-containing immunochemotherapy (IC) have a poor prognosis and are commonly considered to have "primary refractory disease."However, different definitions of primary refractory disease are used in the literature and clinical practice. In this study, we examined variation in the time to relapse used to define refractory status and association with survival outcomes in patients with primary refractory LBCL in a single-center prospective cohort with validation in an independent multicenter cohort. Patients with newly diagnosed LBCL were enrolled in the Molecular Epidemiological Resource cohort (MER; N = 949) or the Lymphoma Epidemiology of Outcomes cohort (LEO; N = 2755) from September 2002 to May 2021. Primary refractory LBCL was defined as no response (stable disease [SD]) or progressive disease (PD) during, or by the end of, frontline (1L) IC (primary PD; PPD); partial response at end of treatment (EOT PR); or relapse within 3 to 12 months after achieving CR at EOT to 1L IC (early relapse). In the MER cohort, patients with PPD had inferior overall survival (OS; 2-year OS rate: 15% MER, 31% LEO) when compared with other subgroups considered in defining primary refractory disease, EOT PR (2-year OS rate: 38% MER, 50% LEO) and early relapse (2-year OS rate: 44% MER, 58% LEO). Among patients receiving 1L IC with curative intent, we identified that patients with PPD are the key subgroup with poor outcomes. We propose a definition of primary refractory LBCL as SD or PD during, or by the end of, 1L treatment.
AB - Patients with large B-cell lymphoma (LBCL) that fail to achieve a complete response (CR) or who relapse early after anthracycline-containing immunochemotherapy (IC) have a poor prognosis and are commonly considered to have "primary refractory disease."However, different definitions of primary refractory disease are used in the literature and clinical practice. In this study, we examined variation in the time to relapse used to define refractory status and association with survival outcomes in patients with primary refractory LBCL in a single-center prospective cohort with validation in an independent multicenter cohort. Patients with newly diagnosed LBCL were enrolled in the Molecular Epidemiological Resource cohort (MER; N = 949) or the Lymphoma Epidemiology of Outcomes cohort (LEO; N = 2755) from September 2002 to May 2021. Primary refractory LBCL was defined as no response (stable disease [SD]) or progressive disease (PD) during, or by the end of, frontline (1L) IC (primary PD; PPD); partial response at end of treatment (EOT PR); or relapse within 3 to 12 months after achieving CR at EOT to 1L IC (early relapse). In the MER cohort, patients with PPD had inferior overall survival (OS; 2-year OS rate: 15% MER, 31% LEO) when compared with other subgroups considered in defining primary refractory disease, EOT PR (2-year OS rate: 38% MER, 50% LEO) and early relapse (2-year OS rate: 44% MER, 58% LEO). Among patients receiving 1L IC with curative intent, we identified that patients with PPD are the key subgroup with poor outcomes. We propose a definition of primary refractory LBCL as SD or PD during, or by the end of, 1L treatment.
UR - http://www.scopus.com/inward/record.url?scp=85198263895&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85198263895&partnerID=8YFLogxK
U2 - 10.1182/bloodadvances.2024012760
DO - 10.1182/bloodadvances.2024012760
M3 - Article
C2 - 38669353
AN - SCOPUS:85198263895
SN - 2473-9529
VL - 8
SP - 3402
EP - 3415
JO - Blood Advances
JF - Blood Advances
IS - 13
ER -