Autologous stem cell transplant in fit patients with refractory or early relapsed diffuse large B-cell lymphoma that responded to salvage chemotherapy
Aung M. Tun,
Yucai Wang,
Seth Maliske,
Ivana Micallef,
David J. Inwards,
Thomas M. Habermann,
Luis Porrata,
Jonas Paludo,
Jose Villasboas Bisneto,
Allison Rosenthal,
Mohamed A Kharfan-Dabaja,
Stephen M. Ansell,
Grzegorz S. Nowakowski,
Umar Farooq,
Patrick B. Johnston
Affiliations
Aung M. Tun
Division of Hematology, Mayo Clinic, Rochester, Minnesota; Division of Hematologic Malignancies and Cellular Therapeutics, The University of Kansas, Kansas City
Yucai Wang
Division of Hematology, Mayo Clinic, Rochester, Minnesota
Seth Maliske
Division of Hematology, Oncology, and Blood and Marrow Transplantation, University of Iowa, Iowa City, Iowa
Ivana Micallef
Division of Hematology, Mayo Clinic, Rochester, Minnesota
David J. Inwards
Division of Hematology, Mayo Clinic, Rochester, Minnesota
Thomas M. Habermann
Division of Hematology, Mayo Clinic, Rochester, Minnesota
Luis Porrata
Division of Hematology, Mayo Clinic, Rochester, Minnesota
Jonas Paludo
Division of Hematology, Mayo Clinic, Rochester, Minnesota
Jose Villasboas Bisneto
Division of Hematology, Mayo Clinic, Rochester, Minnesota
Allison Rosenthal
Internal Medicine, Division of Hematology/Oncology, Mayo Clinic Arizona, Scottsdale, Arizona
Mohamed A Kharfan-Dabaja
Division of Hematology-Oncology and Blood and Marrow Transplantation and Cellular Therapy Program, Mayo Clinic, Jacksonville, Florida
Stephen M. Ansell
Division of Hematology, Mayo Clinic, Rochester, Minnesota
Grzegorz S. Nowakowski
Division of Hematology, Mayo Clinic, Rochester, Minnesota
Umar Farooq
Division of Hematology, Oncology, and Blood and Marrow Transplantation, University of Iowa, Iowa City, Iowa
Patrick B. Johnston
Division of Hematology, Mayo Clinic, Rochester, Minnesota
Chimeric antigen receptor T-cell (CAR-T) therapy is the new standard of care in fit patients with refractory or early relapsed diffuse large B-cell lymphoma (DLBCL). However, there may still be a role for salvage chemotherapy (ST) and autologous stem cell transplant (ASCT) in certain circumstances (eg, lack of CAR-T resources, chemosensitive relapses, etc). We retrospectively studied 230 patients with refractory or early relapsed DLBCL who underwent ST and ASCT. Median line of ST was 1 (range 1-3). Best response before ASCT was complete response (CR) in 106 (46%) and partial response (PR) in 124 (54%) patients. Median follow-up after ASCT was 89.4 months. The median progression-free (PFS) and overall survival (OS) were 16.1 and 43.3 months, respectively. Patients relapsing between 6 to 12 months after frontline therapy had numerically better median PFS (29.6 months) and OS (88.5 months). Patients who required 1 line of ST, compared to those requiring >1 line, had better median PFS (37.9 vs 3.9 months; P = 0.0005) and OS (68.3 vs 12.0 months; P = 0.0005). Patients who achieved CR had better median PFS (71.1 vs 6.3 months; P