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ORIGINAL ARTICLE
Frontline autologous stem cell transplantation in high-risk peripheral T-cell lymphoma: a prospective study from The Gel-Tamo Study Group
José Rodríguez 1 , Eulogio Conde 2 , Antonio Gutiérrez 1 , Reyes Arranz 3 , Ángel León 4 , Julián Marín 5 , Maurizio Bendandi 6 , Carmen Albo 7 , María Dolores Caballero 8 , On behalf of the 'Grupo Español de Linfomas/Trasplante Autólogo de Médula Ósea' (GEL-TAMO)
  1 Hospital Universitario Son Dureta, Palma, Spain ;   2 Hospital de Valdecilla, Santander, Spain   3 Hospital La Princesa, Madrid, Spain ;   4 Hospital de Jerez de la Frontera, Cádiz; Santander, Spain ;   5 Hospital Nuestra Señora de Aránzazu, San Sebastián, Spain ;   6 Clínica Universitaria de Navarra, Pamplona, Spain ;   7 Hospital Xeral-Cies, Pontevedra, Spain ;   8 Hospital Clínico de Salamanca, Salamanca, Spain
Correspondence to J. Rodríguez, Service of Oncology, University Hospital Son Dureta, Avenue Andrea Doria 55, Palma de Mallorca 07014, Spain. Tel: +34 971 175000; Fax: +34 971 175500; e-mail: jrodriguez@hsd.es
Copyright 2007 The Authors Journal compilation 2007 Blackwell Munksgaard
KEYWORDS
peripheral T-cell lymphoma • autologous stem-cell transplantation • frontline • prospective

Abstract

AbstractPatients and methodsRESULTSDiscussionReferences

Objective: Retrospective data shows that peripheral T-cell lymphoma (PTCL) patients sensitive to conventional chemotherapy for aggressive lymphomas may respond better if this treatment is consolidated with frontline autologous stem cell transplantation (ASCT). Here, we present data from a prospective phase II trial of high-dose chemotherapy and ASCT as a frontline consolidation therapy for aggressive nodal PTCL.

Methods: This study involved 26 gallium-scan-positive patients with high-risk nodal PTCL [excluding anaplastic lymphoma kinase (ALK) positive]. Patients received three courses of MegaCHOP before they were evaluated, and those that were gallium-scan-negative at this stage then received another course of MegaCHOP and ASCT. Patients who remained gallium-scan-positive received two courses of an IFE regimen (ifosfamide 10 g/m2, etoposide 150 mg/m2/12 h on days 1-3) and if they at least achieved PR, they then received the transplant.

Results: Complete response (CR) was achieved by 12 patients (46%) after three courses of MegaCHOP and 12 patients received IFE as a salvage therapy. After the ASCT (n = 19), 89% of patients achieved CR. In contrast, six patients (23%) did not receive the transplant because of the progression of the disease (n = 5) or lethal toxicity (n = 1). One patient in first-line CR refused ASCT. After a median follow-up of 35 months, the overall survival (OS) and progression-free survival (PFS) at 3 yr was 73% and 53%, respectively. Moreover, the OS, PFS and disease-free survival (DFS) were 84%, 56% and 63%, respectively 2 yr after transplant in patients who received ASCT consolidation (n = 19).

Conclusions: Early salvage therapy for patients with high-risk aggressive nodal PTCL that do not achieve CR after three courses of chemotherapy and ASCT frontline consolidation for chemosensitive patients may improve treatment outcome.


Accepted for publication 4 March 2007

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1600-0609.2007.00856.x About DOI

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