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Pediatric adrenocortical carcinoma: clinical features and application of neoadjuvant chemotherapy
OBJECTIVE: To summarize the clinical characteristics of children with adrenocortical carcinoma (ACC) and preliminarily explore the indications for and efficacy of neoadjuvant chemotherapy in certain patients. METHODS: The data of 49 children with adrenocortical tumors (ACT) in the past 15 years were...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563212/ https://www.ncbi.nlm.nih.gov/pubmed/37814272 http://dx.doi.org/10.1186/s40001-023-01381-3 |
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author | Lin, Yu Yang, Shen Yang, Wei Cheng, Haiyan Chang, Xiaofeng Zhu, Zhiyun Feng, Jun Han, Jianyu Ren, Qinghua Chang, Saishuo Liu, Shan Yu, Tong Hou, Boren Li, Pengfei Meng, Deguang Zhang, Xianwei Qin, Hong Wang, Huanmin |
author_facet | Lin, Yu Yang, Shen Yang, Wei Cheng, Haiyan Chang, Xiaofeng Zhu, Zhiyun Feng, Jun Han, Jianyu Ren, Qinghua Chang, Saishuo Liu, Shan Yu, Tong Hou, Boren Li, Pengfei Meng, Deguang Zhang, Xianwei Qin, Hong Wang, Huanmin |
author_sort | Lin, Yu |
collection | PubMed |
description | OBJECTIVE: To summarize the clinical characteristics of children with adrenocortical carcinoma (ACC) and preliminarily explore the indications for and efficacy of neoadjuvant chemotherapy in certain patients. METHODS: The data of 49 children with adrenocortical tumors (ACT) in the past 15 years were retrospectively analyzed, and after pathology assessment using Weiss system grading, 40 children diagnosed with ACC were included. Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 and three-dimensional (3D) reconstruction of contrast-enhanced computed tomography data were used to evaluate the response to neoadjuvant chemotherapy. RESULTS: Forty patients (17 males, 23 females) with ACC were enrolled. Abnormal hormone levels were common in children with ACC (n = 31), and in terms of clinical presentation, sexual precocity was the most common (n = 14, 35.0%), followed by Cushing’s syndrome (n = 12, 30.0%). Seven of 40 children received neoadjuvant chemotherapy due to a maximum lesion diameter greater than 10 cm (n = 4), invasion of surrounding tissues (n = 2), intravenous tumor thrombus (n = 2), and/or distant metastasis (n = 2); 2 patients achieved partial response, and 5 had stable disease according to the RECIST 1.1 standard. Furthermore, 3D tumor volume reconstruction was performed in 5 children before and after neoadjuvant chemotherapy. Tumor volumes were significantly reduced in all 5 children, with a median volume reduction of 270 (interquartile range, IQR 83, 293) (range: 49–413) ml. After surgery with/without chemotherapy, the 5-year overall survival rate for all children was 90.0% (95% CI-confidence interval 80.0–100.0%), and the 5-year event-free survival rate was 81.5% (95% CI 68.0–97.7%). CONCLUSION: In the diagnosis and treatment of pediatric ACC, a comprehensive endocrine evaluation is necessary to facilitate early diagnosis. Surgery and chemotherapy are important components of ACC treatment, and neoadjuvant chemotherapy should be considered for children with ACC who meet certain criteria, such as a large tumor, distant metastases, or poor general condition. |
format | Online Article Text |
id | pubmed-10563212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-105632122023-10-11 Pediatric adrenocortical carcinoma: clinical features and application of neoadjuvant chemotherapy Lin, Yu Yang, Shen Yang, Wei Cheng, Haiyan Chang, Xiaofeng Zhu, Zhiyun Feng, Jun Han, Jianyu Ren, Qinghua Chang, Saishuo Liu, Shan Yu, Tong Hou, Boren Li, Pengfei Meng, Deguang Zhang, Xianwei Qin, Hong Wang, Huanmin Eur J Med Res Research OBJECTIVE: To summarize the clinical characteristics of children with adrenocortical carcinoma (ACC) and preliminarily explore the indications for and efficacy of neoadjuvant chemotherapy in certain patients. METHODS: The data of 49 children with adrenocortical tumors (ACT) in the past 15 years were retrospectively analyzed, and after pathology assessment using Weiss system grading, 40 children diagnosed with ACC were included. Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 and three-dimensional (3D) reconstruction of contrast-enhanced computed tomography data were used to evaluate the response to neoadjuvant chemotherapy. RESULTS: Forty patients (17 males, 23 females) with ACC were enrolled. Abnormal hormone levels were common in children with ACC (n = 31), and in terms of clinical presentation, sexual precocity was the most common (n = 14, 35.0%), followed by Cushing’s syndrome (n = 12, 30.0%). Seven of 40 children received neoadjuvant chemotherapy due to a maximum lesion diameter greater than 10 cm (n = 4), invasion of surrounding tissues (n = 2), intravenous tumor thrombus (n = 2), and/or distant metastasis (n = 2); 2 patients achieved partial response, and 5 had stable disease according to the RECIST 1.1 standard. Furthermore, 3D tumor volume reconstruction was performed in 5 children before and after neoadjuvant chemotherapy. Tumor volumes were significantly reduced in all 5 children, with a median volume reduction of 270 (interquartile range, IQR 83, 293) (range: 49–413) ml. After surgery with/without chemotherapy, the 5-year overall survival rate for all children was 90.0% (95% CI-confidence interval 80.0–100.0%), and the 5-year event-free survival rate was 81.5% (95% CI 68.0–97.7%). CONCLUSION: In the diagnosis and treatment of pediatric ACC, a comprehensive endocrine evaluation is necessary to facilitate early diagnosis. Surgery and chemotherapy are important components of ACC treatment, and neoadjuvant chemotherapy should be considered for children with ACC who meet certain criteria, such as a large tumor, distant metastases, or poor general condition. BioMed Central 2023-10-09 /pmc/articles/PMC10563212/ /pubmed/37814272 http://dx.doi.org/10.1186/s40001-023-01381-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Lin, Yu Yang, Shen Yang, Wei Cheng, Haiyan Chang, Xiaofeng Zhu, Zhiyun Feng, Jun Han, Jianyu Ren, Qinghua Chang, Saishuo Liu, Shan Yu, Tong Hou, Boren Li, Pengfei Meng, Deguang Zhang, Xianwei Qin, Hong Wang, Huanmin Pediatric adrenocortical carcinoma: clinical features and application of neoadjuvant chemotherapy |
title | Pediatric adrenocortical carcinoma: clinical features and application of neoadjuvant chemotherapy |
title_full | Pediatric adrenocortical carcinoma: clinical features and application of neoadjuvant chemotherapy |
title_fullStr | Pediatric adrenocortical carcinoma: clinical features and application of neoadjuvant chemotherapy |
title_full_unstemmed | Pediatric adrenocortical carcinoma: clinical features and application of neoadjuvant chemotherapy |
title_short | Pediatric adrenocortical carcinoma: clinical features and application of neoadjuvant chemotherapy |
title_sort | pediatric adrenocortical carcinoma: clinical features and application of neoadjuvant chemotherapy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10563212/ https://www.ncbi.nlm.nih.gov/pubmed/37814272 http://dx.doi.org/10.1186/s40001-023-01381-3 |
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