Autologous stem cell transplantation for HIV-associated lymphoma in the antiretroviral and rituximab era: a retrospective study by the EBMT Lymphoma Working Party

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作者
Kai Hübel
Alessandro Re
Ariane Boumendil
Herve Finel
Marcus Hentrich
Stephen Robinson
Christoph Wyen
Mariagrazia Michieli
Edward Kanfer
Jose Luis Diez-Martin
Pascual Balsalobre
Laure Vincent
Wilfried Schroyens
Josep Maria Ribera Santasusana
Nicolaus Kröger
Xaver Schiel
Kate Cwynarski
Albert Esquirol
Aida Botelho Sousa
Chiara Cattaneo
Silvia Montoto
Peter Dreger
机构
[1] University Hospital of Cologne,St. Bartholomew’s Hospital
[2] Hematology,undefined
[3] Spedali Civili di Brescia,undefined
[4] EBMT Paris Study Office/CEREST-TC,undefined
[5] Hopital Saint-Antoine,undefined
[6] EBMT Paris Study Office,undefined
[7] Rotkreuzklinikum München,undefined
[8] University Hospital’s Bristol NHS Foundation Trust,undefined
[9] Praxis am Ebertplatz,undefined
[10] Centro di Riferimento Oncologico,undefined
[11] Hammersmith Hospital London,undefined
[12] Hospital General Universitario Gregorio Maranon,undefined
[13] Hospital Center University,undefined
[14] University Hospital Antwerpen,undefined
[15] Hospital Universitaria Germans Trias i Pujol,undefined
[16] University Hospital Eppendorf,undefined
[17] Klinikum Harlaching,undefined
[18] University College Hospital,undefined
[19] Hospital de la Santa Creu i Santpau,undefined
[20] Hospital dos Capuchos,undefined
[21] Barts Health NHS Trust,undefined
[22] University Hospital of Heidelberg,undefined
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The present study aimed at describing the outcome of patients with HIV-associated lymphomas following autologous hematopoietic stem cell transplantation (autoHCT) in the rituximab and combined antiretroviral therapy (cART) era. Eligible for this retrospective study were HIV-positive patients with lymphoma who received autoHCT between 2007 and 2013. A total of 118 patients were included with a median age of 45 years (range 24–66). Underlying diagnoses were diffuse large B cell lymphoma in 47%, Hodgkin lymphoma in 24%, Burkitt lymphoma in 18%, and plasmablastic lymphoma in 7% of patients. Disease status at autoHCT was complete remission in 44%, partial remission (PR) in 38%, and less than PR in 18% of the patients. With a median follow-up of 4 years, 3-year non-relapse mortality, incidence of relapse, progression-free survival (PFS) and overall survival (OS) were 10%, 27%, 63% and 66%, respectively. By multivariate analysis, disease status less than PR but not CD4+ cell count at the time of autoHCT was a significant predictor of unfavorable PFS and OS. In conclusion, in the era of cART and chemoimmunotherapy, the outcome of autoHCT for HIV-related lymphoma is driven by lymphoma-dependent risk factors rather than by characteristics of the HIV infection.
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页码:1625 / 1631
页数:6
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