The Outcome of HyperCVAD Combined with Alemtuzumab for the Treatment of Aggressive T-Cell and NK-Cell Neoplasms.

We report our experience in using six cycles of hyperCVAD in combination with alemtuzumab for the treatment of aggressive T-cell and NK/T-cell neoplasms. Seven females and six males with the median age of 41 (range 18–60) diagnosed with T-cell acute lymphoblastic lymphoma and peripheral T-cell...

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Main Authors: Kuan, Jew-Win, Chang, Kian-Meng, Lau, Ngee Siang, Visalachy, Purushothaman, Tan, Sen Mui, Ong, Tee Chuan, Su, Anselm-Ting
Format: Article
Language:English
Published: Elsevier Ltd. 2011
Subjects:
Online Access:http://ir.unimas.my/id/eprint/12281/
http://ir.unimas.my/id/eprint/12281/7/A%20randomized%20double%20blind%20control%20trial%20comparing%20filgrastim%20%28abstract%29.pdf
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author Kuan, Jew-Win
Chang, Kian-Meng
Lau, Ngee Siang
Visalachy, Purushothaman
Tan, Sen Mui
Ong, Tee Chuan
Su, Anselm-Ting
author_facet Kuan, Jew-Win
Chang, Kian-Meng
Lau, Ngee Siang
Visalachy, Purushothaman
Tan, Sen Mui
Ong, Tee Chuan
Su, Anselm-Ting
author_sort Kuan, Jew-Win
building UNIMAS Institutional Repository
collection Online Access
description We report our experience in using six cycles of hyperCVAD in combination with alemtuzumab for the treatment of aggressive T-cell and NK/T-cell neoplasms. Seven females and six males with the median age of 41 (range 18–60) diagnosed with T-cell acute lymphoblastic lymphoma and peripheral T-cell and NK/T-cell neoplasms (nPTCL = 6, nT-cell ALL = 3, nNK/T-cell neoplasms = 4) from 2006 to 2008 were treated with alemtuzumab–hyperCVAD regimen. A total of nine patients (69%) responded to the regimen, with seven achieved complete remission and two achieved partial remission. The median progression free survival and overall survival duration among the responders with complete remission were 12.9 and 24.9 months respectively. The incidence of relapse among the responders was 44% and the overall survival rate was 23%. Only four (31%) patients completed the six cycles of alemtuzumab– hyperCVAD. Others were stopped earlier due to progressive disease (n = 2), cytomegalovirus (CMV) reactivation and/or disease (n = 3), death not due to disease (n = 2), and patient’s refusal to continue alemtuzumab (n = 2). The incidence of death not due to disease, CMV reactivation and recurrent CMV reactivation were 50, 50 and 17%, respectively. This study shows that alemtuzumab in combination with hyperCVAD regimen is a feasible regimen but with high toxicity. The toxicity might be reduced with the incorporation of filgrastim and use of valganciclovir as CMV prophylaxis.
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spelling unimas-122812016-06-10T07:46:58Z http://ir.unimas.my/id/eprint/12281/ The Outcome of HyperCVAD Combined with Alemtuzumab for the Treatment of Aggressive T-Cell and NK-Cell Neoplasms. Kuan, Jew-Win Chang, Kian-Meng Lau, Ngee Siang Visalachy, Purushothaman Tan, Sen Mui Ong, Tee Chuan Su, Anselm-Ting RZ Other systems of medicine We report our experience in using six cycles of hyperCVAD in combination with alemtuzumab for the treatment of aggressive T-cell and NK/T-cell neoplasms. Seven females and six males with the median age of 41 (range 18–60) diagnosed with T-cell acute lymphoblastic lymphoma and peripheral T-cell and NK/T-cell neoplasms (nPTCL = 6, nT-cell ALL = 3, nNK/T-cell neoplasms = 4) from 2006 to 2008 were treated with alemtuzumab–hyperCVAD regimen. A total of nine patients (69%) responded to the regimen, with seven achieved complete remission and two achieved partial remission. The median progression free survival and overall survival duration among the responders with complete remission were 12.9 and 24.9 months respectively. The incidence of relapse among the responders was 44% and the overall survival rate was 23%. Only four (31%) patients completed the six cycles of alemtuzumab– hyperCVAD. Others were stopped earlier due to progressive disease (n = 2), cytomegalovirus (CMV) reactivation and/or disease (n = 3), death not due to disease (n = 2), and patient’s refusal to continue alemtuzumab (n = 2). The incidence of death not due to disease, CMV reactivation and recurrent CMV reactivation were 50, 50 and 17%, respectively. This study shows that alemtuzumab in combination with hyperCVAD regimen is a feasible regimen but with high toxicity. The toxicity might be reduced with the incorporation of filgrastim and use of valganciclovir as CMV prophylaxis. Elsevier Ltd. 2011 Article PeerReviewed text en http://ir.unimas.my/id/eprint/12281/7/A%20randomized%20double%20blind%20control%20trial%20comparing%20filgrastim%20%28abstract%29.pdf Kuan, Jew-Win and Chang, Kian-Meng and Lau, Ngee Siang and Visalachy, Purushothaman and Tan, Sen Mui and Ong, Tee Chuan and Su, Anselm-Ting (2011) The Outcome of HyperCVAD Combined with Alemtuzumab for the Treatment of Aggressive T-Cell and NK-Cell Neoplasms. Indian journal of hematology & blood transfusion, 27 (3). pp. 136-145. ISSN 1473-0502 http://dx.doi.org/10.1016/j.transci.2015.03.017
spellingShingle RZ Other systems of medicine
Kuan, Jew-Win
Chang, Kian-Meng
Lau, Ngee Siang
Visalachy, Purushothaman
Tan, Sen Mui
Ong, Tee Chuan
Su, Anselm-Ting
The Outcome of HyperCVAD Combined with Alemtuzumab for the Treatment of Aggressive T-Cell and NK-Cell Neoplasms.
title The Outcome of HyperCVAD Combined with Alemtuzumab for the Treatment of Aggressive T-Cell and NK-Cell Neoplasms.
title_full The Outcome of HyperCVAD Combined with Alemtuzumab for the Treatment of Aggressive T-Cell and NK-Cell Neoplasms.
title_fullStr The Outcome of HyperCVAD Combined with Alemtuzumab for the Treatment of Aggressive T-Cell and NK-Cell Neoplasms.
title_full_unstemmed The Outcome of HyperCVAD Combined with Alemtuzumab for the Treatment of Aggressive T-Cell and NK-Cell Neoplasms.
title_short The Outcome of HyperCVAD Combined with Alemtuzumab for the Treatment of Aggressive T-Cell and NK-Cell Neoplasms.
title_sort outcome of hypercvad combined with alemtuzumab for the treatment of aggressive t-cell and nk-cell neoplasms.
topic RZ Other systems of medicine
url http://ir.unimas.my/id/eprint/12281/
http://ir.unimas.my/id/eprint/12281/
http://ir.unimas.my/id/eprint/12281/7/A%20randomized%20double%20blind%20control%20trial%20comparing%20filgrastim%20%28abstract%29.pdf