Long-term disease-free survival in patients with angioimmunoblastic T-cell lymphoma after high-dose chemotherapy and autologous stem cell transplantation

Schetelig, Johannes and Fetscher, Sebastian and Reichle, Albert and Berdel, Wolfgang E. and Beguin, Yves and Brunet, Salut and Caballero, Dolores and Majolino, Ignazio and Hagberg, Hans and Johnsen, Hans E. and Kimby, Eva and Montserrat, Emilio and Stewart, Douglas and Copplestone, Adrian and Roesler, Wolf and Pavel, Jindra and Kingreen, Dorothea and Siegert, Wolfgang (2003) Long-term disease-free survival in patients with angioimmunoblastic T-cell lymphoma after high-dose chemotherapy and autologous stem cell transplantation. HAEMATOLOGICA, 88 (11). pp. 1272-1278. ISSN 0390-6078

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Abstract

Background and Objectives, Patients with angioimmunoblastic T-cell lymphoma (AIL) have a poor prognosis with conventional treatment. Design and Methods. We initiated an EBMT-based survey studying the impact of high-dose chemotherapy (HDCT) and autologous hematopoietic stem cell transplantation in patients with AIL. Data on 29 patients, who were transplanted between 1992 and 1998 in 16 transplant centers, were collected on standardized documentation forms. Results. The median age at transplantation was 53 years. HDCT was given as part of 1st-line therapy (N=14; 48%) or 2nd/3rd-line therapy (N=15; 52%). Regimens for the mobilization of peripheral blood stem cells (PBSC) included VIPE (N=7; 26%), DexaBEAM (N=6; 22%), CHOP-like regimens (N=6; 22%), other regimens (N=5; 19%) or alternatively growth factor alone (N=3; 11%). The median yield of PBSC was 3.8 x 10(6) CD34(+) cells/kg. Two patients received autologous bone marrow. The HDCT consisted of BEAM-type regimens in 16 patients, ICE-type regimens in 7, and other regimens in 6 patients. There was one treatment- related death. The rate of complete remissions increased from 45% before HDCT to 76% after HDCT. As of January 2003, after a median observation time of living patients of 5 years (range 2.5 to 10 years), 14 patients have died (13 from progressive disease), and 15 patients are alive. The probability of 5-year overall and event-free survival was 44% (95% Cl, 22% to 66%) and 37% (95% Cl, 17% to 57%), respectively. Long-term disease-free survival was observed in patients transplanted during 1st-line treatment as well as in the context of 2nd/3rd-line therapy. Interpretation and Conclusions. There is evidence that AIL is susceptible to high-dose chemotherapy. HDCT and autologous stem cell transplantation should be considered in selected patients with AIL.

Item Type: Article
Uncontrolled Keywords: NON-HODGKINS-LYMPHOMA; REAL CLASSIFICATION; FOLLOW-UP; LYMPHADENOPATHY; REGIMEN; IFOSFAMIDE; COMMITTEE; CISPLATIN; THERAPY; IMPACT; angioimmunoblastic T-cell lymphoma; high-dose chemotherapy; autologous stem cell transplantation
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Innere Medizin I
Depositing User: Dr. Gernot Deinzer
Date Deposited: 30 Aug 2021 05:51
Last Modified: 30 Aug 2021 05:51
URI: https://pred.uni-regensburg.de/id/eprint/38446

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