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Irinotecan plus temozolomide in relapsed Ewing sarcoma: an integrated analysis of retrospective studies
BACKGROUND: The prognosis of patients with relapsed Ewing sarcoma is poor. In this study, we aimed to pooled-analyze the efficacy and safety of the combination of irinotecan and temozolomide in treating patients with relapsed Ewing sarcoma. METHODS: PubMed, Cochrane CENTRAL, Web of Science, and EMBA...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969362/ https://www.ncbi.nlm.nih.gov/pubmed/35361149 http://dx.doi.org/10.1186/s12885-022-09469-5 |
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author | Wang, Bi-Cheng Xiao, Bo-Ya Lin, Guo-He |
author_facet | Wang, Bi-Cheng Xiao, Bo-Ya Lin, Guo-He |
author_sort | Wang, Bi-Cheng |
collection | PubMed |
description | BACKGROUND: The prognosis of patients with relapsed Ewing sarcoma is poor. In this study, we aimed to pooled-analyze the efficacy and safety of the combination of irinotecan and temozolomide in treating patients with relapsed Ewing sarcoma. METHODS: PubMed, Cochrane CENTRAL, Web of Science, and EMBASE were systematically searched on September 27, 2021. The primary outcomes were rates of objective response and disease control, and the secondary outcomes were toxicities. RESULTS: Six retrospective studies with 184 patients were enrolled in the analysis. The median age ranged from 14 to 21. The integrated rates were 44% (95% confidence interval [CI] 31–58) for objective response and 66% (55–77) for disease control. Grade 3–4 neutropenia, thrombocytopenia, and diarrhea occurred in 8% (3–16), 7% (3–11), and 8% (5–10) of chemotherapeutic cycles, respectively. 18% (7–32) and 6% (2–11) of patients suffered grade 3–4 neutropenia and thrombocytopenia after irinotecan plus temozolomide treatment. CONCLUSION: Irinotecan plus temozolomide combination chemotherapy showed antitumor activity and an acceptable safety profile in patients with relapsed Ewing sarcoma. More future prospective studies are needed to confirm the retrospective results. |
format | Online Article Text |
id | pubmed-8969362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-89693622022-04-01 Irinotecan plus temozolomide in relapsed Ewing sarcoma: an integrated analysis of retrospective studies Wang, Bi-Cheng Xiao, Bo-Ya Lin, Guo-He BMC Cancer Research BACKGROUND: The prognosis of patients with relapsed Ewing sarcoma is poor. In this study, we aimed to pooled-analyze the efficacy and safety of the combination of irinotecan and temozolomide in treating patients with relapsed Ewing sarcoma. METHODS: PubMed, Cochrane CENTRAL, Web of Science, and EMBASE were systematically searched on September 27, 2021. The primary outcomes were rates of objective response and disease control, and the secondary outcomes were toxicities. RESULTS: Six retrospective studies with 184 patients were enrolled in the analysis. The median age ranged from 14 to 21. The integrated rates were 44% (95% confidence interval [CI] 31–58) for objective response and 66% (55–77) for disease control. Grade 3–4 neutropenia, thrombocytopenia, and diarrhea occurred in 8% (3–16), 7% (3–11), and 8% (5–10) of chemotherapeutic cycles, respectively. 18% (7–32) and 6% (2–11) of patients suffered grade 3–4 neutropenia and thrombocytopenia after irinotecan plus temozolomide treatment. CONCLUSION: Irinotecan plus temozolomide combination chemotherapy showed antitumor activity and an acceptable safety profile in patients with relapsed Ewing sarcoma. More future prospective studies are needed to confirm the retrospective results. BioMed Central 2022-03-31 /pmc/articles/PMC8969362/ /pubmed/35361149 http://dx.doi.org/10.1186/s12885-022-09469-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Wang, Bi-Cheng Xiao, Bo-Ya Lin, Guo-He Irinotecan plus temozolomide in relapsed Ewing sarcoma: an integrated analysis of retrospective studies |
title | Irinotecan plus temozolomide in relapsed Ewing sarcoma: an integrated analysis of retrospective studies |
title_full | Irinotecan plus temozolomide in relapsed Ewing sarcoma: an integrated analysis of retrospective studies |
title_fullStr | Irinotecan plus temozolomide in relapsed Ewing sarcoma: an integrated analysis of retrospective studies |
title_full_unstemmed | Irinotecan plus temozolomide in relapsed Ewing sarcoma: an integrated analysis of retrospective studies |
title_short | Irinotecan plus temozolomide in relapsed Ewing sarcoma: an integrated analysis of retrospective studies |
title_sort | irinotecan plus temozolomide in relapsed ewing sarcoma: an integrated analysis of retrospective studies |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8969362/ https://www.ncbi.nlm.nih.gov/pubmed/35361149 http://dx.doi.org/10.1186/s12885-022-09469-5 |
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