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Favorable Event Free-Survival of High-Dose Chemotherapy Followed by Autologous Hematopoietic Stem Cell Transplantation for Higher Risk Diffuse Large B-Cell Lymphoma in First Complete Remission
High-dose chemotherapy followed by autologous stem cell transplantation (ASCT) has been applied to patients with diffuse large Bcell lymphoma (DLBCL); it is well established that ASCT shows significant survival benefits for chemosensitive relapse. However, half of relapsed patients are resistant to...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications, Pavia, Italy
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508550/ https://www.ncbi.nlm.nih.gov/pubmed/26330999 http://dx.doi.org/10.4081/hr.2015.5812 |
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author | Kaneko, Hiroto Tsutsumi, Yasuhiko Fujino, Takahiro Kuwahara, Saeko Ohshiro, Muneo Iwai, Toshiki Kuroda, Junya Yokota, Shouhei Horiike, Shigeo Taniwaki, Masafumi |
author_facet | Kaneko, Hiroto Tsutsumi, Yasuhiko Fujino, Takahiro Kuwahara, Saeko Ohshiro, Muneo Iwai, Toshiki Kuroda, Junya Yokota, Shouhei Horiike, Shigeo Taniwaki, Masafumi |
author_sort | Kaneko, Hiroto |
collection | PubMed |
description | High-dose chemotherapy followed by autologous stem cell transplantation (ASCT) has been applied to patients with diffuse large Bcell lymphoma (DLBCL); it is well established that ASCT shows significant survival benefits for chemosensitive relapse. However, half of relapsed patients are resistant to salvage chemotherapy, indicating that they are not suitable for ASCT. We retrospectively analyzed the clinical records of 47 patients with DLBCL classified as high or high-intermediate (higher) risk, according to the International Prognostic Index, who underwent upfront ASCT in first complete remission (CR1). Compared with 10 patients with similar characteristics who did not receive ASCT, event free survival at 5-year was significantly superior in ASCT group. Toxicity of ASCT was acceptable and therapy-related death was not observed. We therefore propose that upfront ASCT for higher risk DLBCL in CR1 might provide survival benefit, probably because the high-dose therapy removes minimally resided tumor. |
format | Online Article Text |
id | pubmed-4508550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | PAGEPress Publications, Pavia, Italy |
record_format | MEDLINE/PubMed |
spelling | pubmed-45085502015-09-01 Favorable Event Free-Survival of High-Dose Chemotherapy Followed by Autologous Hematopoietic Stem Cell Transplantation for Higher Risk Diffuse Large B-Cell Lymphoma in First Complete Remission Kaneko, Hiroto Tsutsumi, Yasuhiko Fujino, Takahiro Kuwahara, Saeko Ohshiro, Muneo Iwai, Toshiki Kuroda, Junya Yokota, Shouhei Horiike, Shigeo Taniwaki, Masafumi Hematol Rep Article High-dose chemotherapy followed by autologous stem cell transplantation (ASCT) has been applied to patients with diffuse large Bcell lymphoma (DLBCL); it is well established that ASCT shows significant survival benefits for chemosensitive relapse. However, half of relapsed patients are resistant to salvage chemotherapy, indicating that they are not suitable for ASCT. We retrospectively analyzed the clinical records of 47 patients with DLBCL classified as high or high-intermediate (higher) risk, according to the International Prognostic Index, who underwent upfront ASCT in first complete remission (CR1). Compared with 10 patients with similar characteristics who did not receive ASCT, event free survival at 5-year was significantly superior in ASCT group. Toxicity of ASCT was acceptable and therapy-related death was not observed. We therefore propose that upfront ASCT for higher risk DLBCL in CR1 might provide survival benefit, probably because the high-dose therapy removes minimally resided tumor. PAGEPress Publications, Pavia, Italy 2015-06-08 /pmc/articles/PMC4508550/ /pubmed/26330999 http://dx.doi.org/10.4081/hr.2015.5812 Text en ©Copyright H. Kaneko et al. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Kaneko, Hiroto Tsutsumi, Yasuhiko Fujino, Takahiro Kuwahara, Saeko Ohshiro, Muneo Iwai, Toshiki Kuroda, Junya Yokota, Shouhei Horiike, Shigeo Taniwaki, Masafumi Favorable Event Free-Survival of High-Dose Chemotherapy Followed by Autologous Hematopoietic Stem Cell Transplantation for Higher Risk Diffuse Large B-Cell Lymphoma in First Complete Remission |
title | Favorable Event Free-Survival of High-Dose Chemotherapy Followed by Autologous Hematopoietic Stem Cell Transplantation for Higher Risk Diffuse Large B-Cell Lymphoma in First Complete Remission |
title_full | Favorable Event Free-Survival of High-Dose Chemotherapy Followed by Autologous Hematopoietic Stem Cell Transplantation for Higher Risk Diffuse Large B-Cell Lymphoma in First Complete Remission |
title_fullStr | Favorable Event Free-Survival of High-Dose Chemotherapy Followed by Autologous Hematopoietic Stem Cell Transplantation for Higher Risk Diffuse Large B-Cell Lymphoma in First Complete Remission |
title_full_unstemmed | Favorable Event Free-Survival of High-Dose Chemotherapy Followed by Autologous Hematopoietic Stem Cell Transplantation for Higher Risk Diffuse Large B-Cell Lymphoma in First Complete Remission |
title_short | Favorable Event Free-Survival of High-Dose Chemotherapy Followed by Autologous Hematopoietic Stem Cell Transplantation for Higher Risk Diffuse Large B-Cell Lymphoma in First Complete Remission |
title_sort | favorable event free-survival of high-dose chemotherapy followed by autologous hematopoietic stem cell transplantation for higher risk diffuse large b-cell lymphoma in first complete remission |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508550/ https://www.ncbi.nlm.nih.gov/pubmed/26330999 http://dx.doi.org/10.4081/hr.2015.5812 |
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