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Analysis of treatment outcomes for primary tonsillar lymphoma
PURPOSE: Although each Waldeyer’s ring sub-site is considered an independent prognostic factor, few studies have assessed the prognosis and treatment of tonsillar lymphoma. Treatment outcomes were analyzed in patients with primary tonsillar lymphoma who were treated with chemotherapy and radiotherap...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Radiation Oncology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5207373/ https://www.ncbi.nlm.nih.gov/pubmed/28030899 http://dx.doi.org/10.3857/roj.2016.01781 |
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author | Lee, Yun Hee Cho, Seok Goo Jung, Seung Eun Kim, Sung Hoon O, Joo Hyun Park, Gyeong Sin Yang, Suk Woo Lee, In Seok Rhee, Chin Kook Choi, Byung Ock |
author_facet | Lee, Yun Hee Cho, Seok Goo Jung, Seung Eun Kim, Sung Hoon O, Joo Hyun Park, Gyeong Sin Yang, Suk Woo Lee, In Seok Rhee, Chin Kook Choi, Byung Ock |
author_sort | Lee, Yun Hee |
collection | PubMed |
description | PURPOSE: Although each Waldeyer’s ring sub-site is considered an independent prognostic factor, few studies have assessed the prognosis and treatment of tonsillar lymphoma. Treatment outcomes were analyzed in patients with primary tonsillar lymphoma who were treated with chemotherapy and radiotherapy (RT). MATERIALS AND METHODS: Nineteen patients with diffuse large B-cell lymphoma were evaluated, with a median follow-up of 53 months. Age, sex, and histology, amongst other factors, were reviewed. Progression-free survival (PFS) and overall survival (OS) rates were analyzed. RESULTS: Most patients had Ann Arbor stage I-II (94.7%), IPI score of 0 (89.5%), and complete remission after chemotherapy (89.5%). The 5-year PFS and OS rates were 74.6% and 80%, respectively. In univariate analysis, the rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) regimen resulted in a better PFS than the cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) regimen (88.9% vs. 50.0%; p = 0.053). RT dose was related to the survival outcome (p = 0.010 for PFS, p = 0.044 for OS). Patients were classified into the CHOP + RT (>40 Gy) group and R-CHOP + RT (≤40 Gy) group. The 5-year PFS rates were 50% in the CHOP + RT group, and 100 % in the R-CHOP + RT group (p = 0.018). The 5-year OS rates were 66.7% and 100%, respectively (p = 0.087). CONCLUSION: Primary tonsillar lymphoma patients typically have favorable outcomes. Chemotherapy (R-CHOP) combined with relatively lower dose consolidative RT may be safe and effective for primary tonsillar lymphoma. |
format | Online Article Text |
id | pubmed-5207373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Society for Radiation Oncology |
record_format | MEDLINE/PubMed |
spelling | pubmed-52073732017-01-04 Analysis of treatment outcomes for primary tonsillar lymphoma Lee, Yun Hee Cho, Seok Goo Jung, Seung Eun Kim, Sung Hoon O, Joo Hyun Park, Gyeong Sin Yang, Suk Woo Lee, In Seok Rhee, Chin Kook Choi, Byung Ock Radiat Oncol J Original Article PURPOSE: Although each Waldeyer’s ring sub-site is considered an independent prognostic factor, few studies have assessed the prognosis and treatment of tonsillar lymphoma. Treatment outcomes were analyzed in patients with primary tonsillar lymphoma who were treated with chemotherapy and radiotherapy (RT). MATERIALS AND METHODS: Nineteen patients with diffuse large B-cell lymphoma were evaluated, with a median follow-up of 53 months. Age, sex, and histology, amongst other factors, were reviewed. Progression-free survival (PFS) and overall survival (OS) rates were analyzed. RESULTS: Most patients had Ann Arbor stage I-II (94.7%), IPI score of 0 (89.5%), and complete remission after chemotherapy (89.5%). The 5-year PFS and OS rates were 74.6% and 80%, respectively. In univariate analysis, the rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) regimen resulted in a better PFS than the cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) regimen (88.9% vs. 50.0%; p = 0.053). RT dose was related to the survival outcome (p = 0.010 for PFS, p = 0.044 for OS). Patients were classified into the CHOP + RT (>40 Gy) group and R-CHOP + RT (≤40 Gy) group. The 5-year PFS rates were 50% in the CHOP + RT group, and 100 % in the R-CHOP + RT group (p = 0.018). The 5-year OS rates were 66.7% and 100%, respectively (p = 0.087). CONCLUSION: Primary tonsillar lymphoma patients typically have favorable outcomes. Chemotherapy (R-CHOP) combined with relatively lower dose consolidative RT may be safe and effective for primary tonsillar lymphoma. The Korean Society for Radiation Oncology 2016-12 2016-10-31 /pmc/articles/PMC5207373/ /pubmed/28030899 http://dx.doi.org/10.3857/roj.2016.01781 Text en Copyright © 2016 The Korean Society for Radiation Oncology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (http://creativecommons.org/licenses/by-nc/4.0) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Yun Hee Cho, Seok Goo Jung, Seung Eun Kim, Sung Hoon O, Joo Hyun Park, Gyeong Sin Yang, Suk Woo Lee, In Seok Rhee, Chin Kook Choi, Byung Ock Analysis of treatment outcomes for primary tonsillar lymphoma |
title | Analysis of treatment outcomes for primary tonsillar lymphoma |
title_full | Analysis of treatment outcomes for primary tonsillar lymphoma |
title_fullStr | Analysis of treatment outcomes for primary tonsillar lymphoma |
title_full_unstemmed | Analysis of treatment outcomes for primary tonsillar lymphoma |
title_short | Analysis of treatment outcomes for primary tonsillar lymphoma |
title_sort | analysis of treatment outcomes for primary tonsillar lymphoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5207373/ https://www.ncbi.nlm.nih.gov/pubmed/28030899 http://dx.doi.org/10.3857/roj.2016.01781 |
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