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Treatment outcomes of adjuvant radiotherapy in adrenocortical carcinoma – A 13-years experience from a tertiary care centre

PURPOSE: Adrenocortical carcinoma (ACC) is a rare and highly aggressive malignant neoplasm, usually diagnosed in advanced stage. Role and efficacy of adjuvant radiotherapy has not been well defined. The objective of this study is to describe the various clinical characteristics and prognostic factor...

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Autores principales: Khosla, Divya, Kapoor, Rakesh, Singla, Aditya K, Periasamy, Kannan, Goyal, Shikha, Madan, Renu, Kumar, Narendra, Behera, Arunanshu, Singh, Shrawan K, Bhadada, Sanjay K, Walia, Rama
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969472/
https://www.ncbi.nlm.nih.gov/pubmed/36860827
http://dx.doi.org/10.1177/20363613231160699
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author Khosla, Divya
Kapoor, Rakesh
Singla, Aditya K
Periasamy, Kannan
Goyal, Shikha
Madan, Renu
Kumar, Narendra
Behera, Arunanshu
Singh, Shrawan K
Bhadada, Sanjay K
Walia, Rama
author_facet Khosla, Divya
Kapoor, Rakesh
Singla, Aditya K
Periasamy, Kannan
Goyal, Shikha
Madan, Renu
Kumar, Narendra
Behera, Arunanshu
Singh, Shrawan K
Bhadada, Sanjay K
Walia, Rama
author_sort Khosla, Divya
collection PubMed
description PURPOSE: Adrenocortical carcinoma (ACC) is a rare and highly aggressive malignant neoplasm, usually diagnosed in advanced stage. Role and efficacy of adjuvant radiotherapy has not been well defined. The objective of this study is to describe the various clinical characteristics and prognostic factors affecting the survival of ACC along with the role radiotherapy on overall survival and relapse free survival. METHODS: A retrospective analysis of 30 patients registered between 2007 and 2019 was carried out. The medical records containing clinical and treatment details were analysed. Data was analysed using SPSS 25.0. Survival curves were computed using Kaplan-Meier method. Univariate and multivariate analyses were performed to analyze the prognostic factors affecting the outcome. A p value of less than 0.05 was considered to be statistically significant. RESULTS: The median age of patients was 37.5 years (range, 5–72 years). 20 patients were females. Twenty-six patients had advanced stage (III/IV) disease while only four patients presented in early stage. Twenty-six patients underwent total adrenalectomy. Eighty three percent patients received adjuvant radiation therapy. The median follow up was 35.5 months (range, 7 monthss-132months). The estimated three- and 5-years overall survival (OS) was 67.2% and 23.3%, respectively. Capsular invasion and positive margins were the independent prognostic factors influencing both OS and relapse free survival (RFS). Out of 25 patients who received adjuvant radiation, only three patients had local relapse. CONCLUSION: ACC is a rare and aggressive neoplasm with majority of patients presenting in advanced stage. Surgical resection with negative margins remains the mainstay of treatment. Capsular invasion and positive margins are independent prognostic factors for survival. Adjuvant radiation reduces the risk of local relapse and is well tolerated. Radiation can be used effectively in adjuvant and palliative settings in ACC.
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spelling pubmed-99694722023-02-28 Treatment outcomes of adjuvant radiotherapy in adrenocortical carcinoma – A 13-years experience from a tertiary care centre Khosla, Divya Kapoor, Rakesh Singla, Aditya K Periasamy, Kannan Goyal, Shikha Madan, Renu Kumar, Narendra Behera, Arunanshu Singh, Shrawan K Bhadada, Sanjay K Walia, Rama Rare Tumors Original Article PURPOSE: Adrenocortical carcinoma (ACC) is a rare and highly aggressive malignant neoplasm, usually diagnosed in advanced stage. Role and efficacy of adjuvant radiotherapy has not been well defined. The objective of this study is to describe the various clinical characteristics and prognostic factors affecting the survival of ACC along with the role radiotherapy on overall survival and relapse free survival. METHODS: A retrospective analysis of 30 patients registered between 2007 and 2019 was carried out. The medical records containing clinical and treatment details were analysed. Data was analysed using SPSS 25.0. Survival curves were computed using Kaplan-Meier method. Univariate and multivariate analyses were performed to analyze the prognostic factors affecting the outcome. A p value of less than 0.05 was considered to be statistically significant. RESULTS: The median age of patients was 37.5 years (range, 5–72 years). 20 patients were females. Twenty-six patients had advanced stage (III/IV) disease while only four patients presented in early stage. Twenty-six patients underwent total adrenalectomy. Eighty three percent patients received adjuvant radiation therapy. The median follow up was 35.5 months (range, 7 monthss-132months). The estimated three- and 5-years overall survival (OS) was 67.2% and 23.3%, respectively. Capsular invasion and positive margins were the independent prognostic factors influencing both OS and relapse free survival (RFS). Out of 25 patients who received adjuvant radiation, only three patients had local relapse. CONCLUSION: ACC is a rare and aggressive neoplasm with majority of patients presenting in advanced stage. Surgical resection with negative margins remains the mainstay of treatment. Capsular invasion and positive margins are independent prognostic factors for survival. Adjuvant radiation reduces the risk of local relapse and is well tolerated. Radiation can be used effectively in adjuvant and palliative settings in ACC. SAGE Publications 2023-02-23 /pmc/articles/PMC9969472/ /pubmed/36860827 http://dx.doi.org/10.1177/20363613231160699 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Khosla, Divya
Kapoor, Rakesh
Singla, Aditya K
Periasamy, Kannan
Goyal, Shikha
Madan, Renu
Kumar, Narendra
Behera, Arunanshu
Singh, Shrawan K
Bhadada, Sanjay K
Walia, Rama
Treatment outcomes of adjuvant radiotherapy in adrenocortical carcinoma – A 13-years experience from a tertiary care centre
title Treatment outcomes of adjuvant radiotherapy in adrenocortical carcinoma – A 13-years experience from a tertiary care centre
title_full Treatment outcomes of adjuvant radiotherapy in adrenocortical carcinoma – A 13-years experience from a tertiary care centre
title_fullStr Treatment outcomes of adjuvant radiotherapy in adrenocortical carcinoma – A 13-years experience from a tertiary care centre
title_full_unstemmed Treatment outcomes of adjuvant radiotherapy in adrenocortical carcinoma – A 13-years experience from a tertiary care centre
title_short Treatment outcomes of adjuvant radiotherapy in adrenocortical carcinoma – A 13-years experience from a tertiary care centre
title_sort treatment outcomes of adjuvant radiotherapy in adrenocortical carcinoma – a 13-years experience from a tertiary care centre
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969472/
https://www.ncbi.nlm.nih.gov/pubmed/36860827
http://dx.doi.org/10.1177/20363613231160699
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