DexaBEAM versus ICE salvage regimen prior to autologous transplantation for relapsed or refractory aggressive peripheral T cell lymphoma: a retrospective evaluation of parallel patient cohorts of one center
Autor: | Rolf M. Mesters, Angela Demant, Nils H. Thoennissen, Mareike Kuhlmann, Wolfgang E. Berdel, Carsten Müller-Tidow, Jan-Henrik Mikesch, Gabriela B. Thoennissen, Michael Mohr, Christoph Schliemann, Eva Schmidt, Georg Evers, Torsten Kessler, Michele Pohlen, Gabriele Köhler, Utz Krug, Johannes Wessling |
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Rok vydání: | 2012 |
Předmět: |
Melphalan
Adult Male Mucositis medicine.medical_specialty Adolescent medicine.medical_treatment Salvage therapy Kaplan-Meier Estimate Transplantation Autologous Dexamethasone Disease-Free Survival Carboplatin Young Adult Autologous stem-cell transplantation Antineoplastic Combined Chemotherapy Protocols Granulocyte Colony-Stimulating Factor Preoperative Care medicine Autologous transplantation Humans Ifosfamide Etoposide Aged Retrospective Studies Salvage Therapy Chemotherapy Peripheral Blood Stem Cell Transplantation business.industry Cytarabine Lymphoma T-Cell Peripheral Hematology General Medicine Middle Aged Carmustine Combined Modality Therapy Hematologic Diseases Hematopoietic Stem Cell Mobilization Surgery Transplantation Regimen Treatment Outcome Drug Evaluation Female business medicine.drug |
Zdroj: | Annals of hematology. 92(8) |
ISSN: | 1432-0584 |
Popis: | High-dose chemotherapy (HDT) followed by autologous stem cell transplantation (ASCT) is considered standard in the treatment of patients with relapsed or refractory aggressive peripheral T cell lymphoma (PTCL). However, the optimal salvage regimen before ASCT has not yet been established. We retrospectively analyzed 31 patients with relapsed or refractory aggressive PTCL after anthracycline-based first-line chemotherapy who received either DexaBEAM (dexamethasone, carmustine, etoposide, cytarabine, and melphalan; n = 16) or ICE (ifosfamide, carboplatin, and etoposide; n = 15) regimen as first salvage chemotherapy followed by HDT/ASCT. The overall response rate (OR) was significantly higher for patients treated with DexaBEAM (69 %; 95 % confidence interval 46.0–91.5 %) as compared to the ICE group (20 %; 95 % confidence interval −0.2–40.2 %; P = 0.01), with higher complete response (CR; 38 %; 95 % confidence interval 13.8–61.2 %; vs. 7 %; 95 % confidence interval −6.0–19.6 %) as well as partial response (PR; 31 vs. 13 %) rate. Changing regimen due to failure of first salvage therapy, 12 patients initially receiving ICE still achieved an OR of 58 % (33 % CR, 25 % PR) with DexaBEAM as second salvage therapy, whereas in three patients receiving ICE after DexaBEAM failure, only one achieved an OR (1 PR). Median progression-free survival was significantly higher in the DexaBEAM group (6.4 vs. 2 months; P = 0.01). Major adverse event in both groups was myelosuppression with higher but tolerable treatment-related toxicity for patients in the DexaBEAM group. For all patients proceeding to HDT/ASCT, a 3-year overall survival was 50 %. Together, considering the limitations of the retrospective design of the evaluation and the small sample size, our data suggest that DexaBEAM salvage chemotherapy is superior to ICE for patients with relapsed or refractory aggressive PTCL for remission induction prior to autologous transplantation, with higher but manageable treatment-related toxicity. |
Databáze: | OpenAIRE |
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