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Treatment Outcomes with CHOP Chemotherapy in Adult Patients with Hemophagocytic Lymphohistiocytosis
The objective of the current study was to investigate the treatment outcomes for the use of cyclophosphamide, adriamycin, vincristine, and prednisolone (CHOP) chemotherapy in adult patients with hemophagocytic lymphohistiocytosis (HLH). Seventeen HLH patients older than 18 yr of age were treated wit...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Korean Academy of Medical Sciences
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2526520/ https://www.ncbi.nlm.nih.gov/pubmed/18583880 http://dx.doi.org/10.3346/jkms.2008.23.3.439 |
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author | Shin, Ho-Jin Chung, Joo Seop Lee, Je-Jung Sohn, Sang Kyun Choi, Young Jin Kim, Yeo-Kyeoung Yang, Deok-Hwan Kim, Hyeoung-Joon Kim, Jong Gwang Joo, Young Don Lee, Won Sik Sohn, Chang-Hak Lee, Eun Yup Cho, Goon Jae |
author_facet | Shin, Ho-Jin Chung, Joo Seop Lee, Je-Jung Sohn, Sang Kyun Choi, Young Jin Kim, Yeo-Kyeoung Yang, Deok-Hwan Kim, Hyeoung-Joon Kim, Jong Gwang Joo, Young Don Lee, Won Sik Sohn, Chang-Hak Lee, Eun Yup Cho, Goon Jae |
author_sort | Shin, Ho-Jin |
collection | PubMed |
description | The objective of the current study was to investigate the treatment outcomes for the use of cyclophosphamide, adriamycin, vincristine, and prednisolone (CHOP) chemotherapy in adult patients with hemophagocytic lymphohistiocytosis (HLH). Seventeen HLH patients older than 18 yr of age were treated with CHOP chemotherapy. A response evaluation was conducted for every two cycles of chemotherapy. With CHOP chemotherapy, complete response was achieved for 7/17 patients (41.2%), a partial response for 3/17 patients (17.6%), and the overall response rate was 58.8%. The median response duration (RD) was not reached and the 2-yr RD rate was 68.6%, with a median follow-up of 100 weeks. Median overall survival (OS) was 18 weeks (95% CI, 6-30 weeks) and the 2-yr OS rate was 43.9%. Reported grade 3 or 4 non-hematological toxicities were increased serum liver enzyme levels and stomatitis. Grade 3 or 4 hematological toxicities were leukopenia (50.8%), anemia (20%), and thrombocytopenia (33.9%). Neutropenic fever was observed in 21.6% of patients (14/65 cycles), and most of the cases were resolved with supportive care including treatment with broad-spectrum antibiotics. CHOP chemotherapy seems to be effective in adult HLH patients and the toxicities are manageable. |
format | Text |
id | pubmed-2526520 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | The Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-25265202008-11-07 Treatment Outcomes with CHOP Chemotherapy in Adult Patients with Hemophagocytic Lymphohistiocytosis Shin, Ho-Jin Chung, Joo Seop Lee, Je-Jung Sohn, Sang Kyun Choi, Young Jin Kim, Yeo-Kyeoung Yang, Deok-Hwan Kim, Hyeoung-Joon Kim, Jong Gwang Joo, Young Don Lee, Won Sik Sohn, Chang-Hak Lee, Eun Yup Cho, Goon Jae J Korean Med Sci Original Article The objective of the current study was to investigate the treatment outcomes for the use of cyclophosphamide, adriamycin, vincristine, and prednisolone (CHOP) chemotherapy in adult patients with hemophagocytic lymphohistiocytosis (HLH). Seventeen HLH patients older than 18 yr of age were treated with CHOP chemotherapy. A response evaluation was conducted for every two cycles of chemotherapy. With CHOP chemotherapy, complete response was achieved for 7/17 patients (41.2%), a partial response for 3/17 patients (17.6%), and the overall response rate was 58.8%. The median response duration (RD) was not reached and the 2-yr RD rate was 68.6%, with a median follow-up of 100 weeks. Median overall survival (OS) was 18 weeks (95% CI, 6-30 weeks) and the 2-yr OS rate was 43.9%. Reported grade 3 or 4 non-hematological toxicities were increased serum liver enzyme levels and stomatitis. Grade 3 or 4 hematological toxicities were leukopenia (50.8%), anemia (20%), and thrombocytopenia (33.9%). Neutropenic fever was observed in 21.6% of patients (14/65 cycles), and most of the cases were resolved with supportive care including treatment with broad-spectrum antibiotics. CHOP chemotherapy seems to be effective in adult HLH patients and the toxicities are manageable. The Korean Academy of Medical Sciences 2008-06 2008-06-20 /pmc/articles/PMC2526520/ /pubmed/18583880 http://dx.doi.org/10.3346/jkms.2008.23.3.439 Text en Copyright © 2008 The Korean Academy of Medical Sciences 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 | Original Article Shin, Ho-Jin Chung, Joo Seop Lee, Je-Jung Sohn, Sang Kyun Choi, Young Jin Kim, Yeo-Kyeoung Yang, Deok-Hwan Kim, Hyeoung-Joon Kim, Jong Gwang Joo, Young Don Lee, Won Sik Sohn, Chang-Hak Lee, Eun Yup Cho, Goon Jae Treatment Outcomes with CHOP Chemotherapy in Adult Patients with Hemophagocytic Lymphohistiocytosis |
title | Treatment Outcomes with CHOP Chemotherapy in Adult Patients with Hemophagocytic Lymphohistiocytosis |
title_full | Treatment Outcomes with CHOP Chemotherapy in Adult Patients with Hemophagocytic Lymphohistiocytosis |
title_fullStr | Treatment Outcomes with CHOP Chemotherapy in Adult Patients with Hemophagocytic Lymphohistiocytosis |
title_full_unstemmed | Treatment Outcomes with CHOP Chemotherapy in Adult Patients with Hemophagocytic Lymphohistiocytosis |
title_short | Treatment Outcomes with CHOP Chemotherapy in Adult Patients with Hemophagocytic Lymphohistiocytosis |
title_sort | treatment outcomes with chop chemotherapy in adult patients with hemophagocytic lymphohistiocytosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2526520/ https://www.ncbi.nlm.nih.gov/pubmed/18583880 http://dx.doi.org/10.3346/jkms.2008.23.3.439 |
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