Up-Front Autologous Stem-Cell Transplantation in Peripheral T-Cell Lymphoma: NLG-T-01

Author:

d'Amore Francesco1,Relander Thomas1,Lauritzsen Grete F.1,Jantunen Esa1,Hagberg Hans1,Anderson Harald1,Holte Harald1,Österborg Anders1,Merup Mats1,Brown Peter1,Kuittinen Outi1,Erlanson Martin1,Østenstad Bjørn1,Fagerli Unn-Merete1,Gadeberg Ole V.1,Sundström Christer1,Delabie Jan1,Ralfkiaer Elisabeth1,Vornanen Martine1,Toldbod Helle E.1

Affiliation:

1. Francesco d'Amore and Helle Erbs Toldbod, Aarhus University Hospital, Aarhus; Peter de Nully Brown and Elisabeth Ralfkiaer, Copenhagen University Hospital, Copenhagen; Ole Vestergaard Gadeberg, Vejle Hospital, Vejle, Denmark; Thomas Relander, Skåne University Hospital; Harald Anderson, Lund University, Lund; Hans Hagberg and Christer Sundström, Uppsala University Hospital, Uppsala; Anders Österborg and Mats Merup, Karolinska University Hospital, Stockholm; Martin Erlanson, Umeå University Hospital, Umeå,...

Abstract

Purpose Systemic peripheral T-cell lymphomas (PTCLs) respond poorly to conventional therapy. To evaluate the efficacy of a dose-dense approach consolidated by up-front high-dose chemotherapy (HDT) and autologous stem-cell transplantation (ASCT) in PTCL, the Nordic Lymphoma Group (NLG) conducted a large prospective phase II study in untreated systemic PTCL. This is the final report, with a 5-year median follow-up, of the NLG-T-01 study. Patients and Methods Treatment-naive patients with PTCL age 18 to 67 years (median, 57 years) were included. Anaplastic lymphoma kinase (ALK) –positive anaplastic large-cell lymphoma (ALCL) was excluded. An induction regimen of six cycles of biweekly CHOEP (cyclophosphamide, doxorubicin, vincristine, etoposide, and prednisone) was administered (in patients age > 60 years, etoposide was omitted). If in complete or partial remission, patients proceeded to consolidation with HDT/ASCT. Results Of 166 enrolled patients, 160 had histopathologically confirmed PTCL. The majority presented with advanced-stage disease, B symptoms, and elevated serum lactate dehydrogenase. A total of 115 underwent HDT/ASCT, with 90 in complete remission at 3 months post-transplantation. Early failures occurred in 26%. Treatment-related mortality was 4%. At 60.5 months of median follow-up, 83 patients were alive. Consolidated 5-year overall and progression-free survival (PFS) were 51% (95% CI, 43% to 59%) and 44% (95% CI, 36% to 52%), respectively. Best results were obtained in ALK-negative ALCL. Conclusion Dose-dense induction followed by HDT/ASCT was well tolerated and led to long-term PFS in 44% of treatment-naive patients with PTCL. This represents an encouraging outcome, particularly considering the high median age and adverse risk profile of the study population. Therefore, dose-dense induction and HDT/ASCT are a rational up-front strategy in transplantation-eligible patients with PTCL.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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