辅助放射治疗肾上腺皮质癌的治疗结果-三级护理中心13年的经验。

IF 0.9 Q4 ONCOLOGY
Divya Khosla, Rakesh Kapoor, Aditya K Singla, Kannan Periasamy, Shikha Goyal, Renu Madan, Narendra Kumar, Arunanshu Behera, Shrawan K Singh, Sanjay K Bhadada, Rama Walia
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引用次数: 1

摘要

目的:肾上腺皮质癌(ACC)是一种罕见的高侵袭性恶性肿瘤,通常在晚期诊断。辅助放疗的作用和疗效尚未明确。本研究的目的是描述影响ACC生存的各种临床特征和预后因素,以及放疗对总生存和无复发生存的作用。方法:对2007 - 2019年登记的30例患者进行回顾性分析。对包含临床和治疗细节的病历进行分析。数据采用SPSS 25.0进行分析。生存曲线采用Kaplan-Meier法计算。进行单因素和多因素分析,分析影响预后的因素。p值小于0.05认为有统计学意义。结果:患者中位年龄为37.5岁(范围5-72岁)。女性20例。26例为晚期(III/IV),仅有4例为早期。26例患者行全肾上腺切除术。83%的患者接受了辅助放射治疗。中位随访时间为35.5个月(范围7 -132个月)。估计3年和5年总生存率(OS)分别为67.2%和23.3%。囊膜浸润和阳性切缘是影响OS和无复发生存期(RFS)的独立预后因素。在接受辅助放疗的25例患者中,只有3例患者局部复发。结论:ACC是一种罕见的侵袭性肿瘤,以晚期肿瘤居多。手术切除阴性切缘仍然是主要的治疗方法。囊膜浸润和阳性切缘是独立的预后因素。辅助放疗降低了局部复发的风险,并且耐受性良好。在ACC的辅助治疗和姑息治疗中,放疗可以有效地应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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 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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Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
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审稿时长
15 weeks
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