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Myeloablative Chemotherapy for T-Cell Lymphoma: a Case for Autologous Stem Cell Transplantatin (Auto) in First Remission

In order to determine the long-term impact of AUTO in patients (pts) with T-cell lymphoma, we examined the outcome of 79 pts transplanted at the MD Anderson Cancer Center, in first partial or complete remission (CR) (AUTO1, n=20) or for relapsed / refractory disease (AUTO2, n=59) between 06/91 and 0...

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Bibliographic Details
Published in:Blood 2008-11, Vol.112 (11), p.1141-1141
Main Authors: Khouri, Issa F, Lopez, Adriana, Okoroji, Grace-Julia, Korbling, Martin, McCormick, Gloria, Hsu, Yvonne, de Padua, Leandro, Alousi, Amin M., Hosing, Chitra M., Kebriaei, Partow, Rondon, Gabriela, Giralt, Sergio A, de Lima, Marcos J., Anderlini, Paolo, Popat, Uday R, Qazilbash, Muzaffar H., Champlin, Richard E., Pro, Barbara
Format: Article
Language:English
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Summary:In order to determine the long-term impact of AUTO in patients (pts) with T-cell lymphoma, we examined the outcome of 79 pts transplanted at the MD Anderson Cancer Center, in first partial or complete remission (CR) (AUTO1, n=20) or for relapsed / refractory disease (AUTO2, n=59) between 06/91 and 05/08. > Median age (range) at transplantation was 49 (22–65) and 51 (16–77) for the AUTO1 and AUTO2 groups respectively (p=0.35); other baseline characteristics including gender, stage, B-symptoms, LDH, IPI, PET/Gallium status, history of marrow involvement, and performance status at transplantation were similar. There was a statistically significant difference between AUTO1 and AUTO2 with respect to histology {peripheral t-cell, angioimmunoblatic, and anaplastic/large cell were present in 80%, 5%, 15%, respectively in AUTO1, and 42%, 10%, and 45%, respectively in AUTO2 (p=0.02); one pt in AUTO2 had small lymphocytic and one had hepatosplenic T cell lymphoma}. Statistically significant differences were also noted with respect to B2-microglobulin (P=0.02; favoring AUTO1), number of prior chemotherapy regimens received {median 1 vs 3 for AUTO1 and AUTO2, respectively (p
ISSN:0006-4971
1528-0020
DOI:10.1182/blood.V112.11.1141.1141