放疗、化疗和放化疗对胆囊癌患者生存结局的影响:一项真正基于人群的研究。

IF 1.5 4区 医学 Q4 ONCOLOGY
Translational cancer research Pub Date : 2025-06-30 Epub Date: 2025-06-25 DOI:10.21037/tcr-2024-2543
Feng Liu, Yanchao Qin, Linjie Li, Baoping Jiao
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引用次数: 0

摘要

背景:放疗或化疗在胆囊癌(GBC)中的临床价值仍有争议,特别是对不同分期的胆囊癌。因此,本研究基于监测、流行病学和最终结果(SEER)数据库的数据,分析了放疗、化疗和同步放化疗对不同分期GBC患者总生存期(OS)和癌症特异性生存期(CSS)的影响。方法:从SEER数据库中收集2010年1月1日至2017年12月31日诊断为GBC的患者资料,根据患者的治疗方案分为:非治疗组、单独放疗组、单独化疗组和同步放化疗组。在调整了人口统计学、肿瘤和手术相关因素后,采用Cox回归分析放疗、化疗和放化疗对OS的影响。使用竞争风险模型评估这三种疗法与CSS之间的关系。结果:本研究纳入6275例GBC患者,其中未治疗3444例,单独放疗152例,单独化疗1913例,放化疗766例。其中全因死亡4886例(77.86%),肿瘤特异性死亡4379例(69.78%)。多因素分析显示,放疗[风险比(HR) =0.700, 95%可信区间(CI): 0.581, 0.844]、化疗(HR =0.500, 95% CI: 0.465, 0.538)、放化疗(HR =0.486, 95% CI: 0.439, 0.538)显著改善了所有患者的OS(均p)。结论:我们的研究表明,晚期胆囊癌患者接受放疗、化疗或放化疗可显著改善其OS和CSS。因此,建议晚期患者在综合治疗中常规纳入放疗、化疗或放化疗,以提高生存率。然而,对于早期胆囊癌,放疗、化疗或放化疗对OS和CSS的改善作用有限,应根据患者的具体情况,如肿瘤的病理类型、分级、淋巴结转移等,个性化决定是否进行放疗或化疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of radiotherapy, chemotherapy, and chemoradiotherapy on survival outcomes in patients with gallbladder carcinoma: a real population-based study.

Background: The clinical value of radiotherapy or chemotherapy in gallbladder carcinoma (GBC) remains controversial, especially for GBCs at different stages. Therefore, this study analyzed the effects of radiotherapy, chemotherapy, and concurrent chemoradiotherapy on overall survival (OS) and cancer-specific survival (CSS) in patients with different stages of GBC based on data from the Surveillance, Epidemiology, and End Results (SEER) database.

Methods: Data on patients diagnosed with GBC from January 1, 2010 to December 31, 2017 were collected from the SEER database, and those involved patients were divided into the following groups according to their treatment regimens: non-therapy group, radiotherapy alone group, chemotherapy alone group, and concurrent chemoradiotherapy group. After adjusting for factors related to demographics, the tumor, and the procedure, Cox regression was performed to analyze the effect of radiotherapy, chemotherapy, and chemoradiotherapy on OS. The relationships between these three therapies and CSS were assessed using the competing risk model.

Results: This study included 6,275 GBC patients, among whom 3,444 received no therapy, 152 received radiotherapy alone, 1,913 received chemotherapy alone, and 766 received chemoradiotherapy. Of these patients, there were 4,886 (77.86%) all-cause death cases and 4,379 (69.78%) cancer-specific death cases. The multivariate analysis showed that radiotherapy [hazard ratio (HR) =0.700, 95% confidence interval (CI): 0.581, 0.844], chemotherapy (HR =0.500, 95% CI: 0.465, 0.538), and chemoradiotherapy (HR =0.486, 95% CI: 0.439, 0.538) significantly improved OS in all patients (all P<0.001); for stage III and IV GBC patients, radiotherapy, chemotherapy, and chemoradiotherapy significantly improved OS (all P<0.001). Regarding CSS, the competing risk model showed that chemotherapy (HR =0.589, 95% CI: 0.540, 0.635] and chemoradiotherapy (HR =0.577, 95% CI: 0.523, 0.636) improved CSS in all patients (both P<0.001); for patients with stage III GBC, radiotherapy, chemotherapy, and chemoradiotherapy significantly improved CSS (P=0.02, <0.001, <0.001, respectively); and for patients with stage IV GBC, chemotherapy and chemoradiotherapy significantly improved CSS (both P<0.001). The subgroup analyses based on different pathological types showed similar patterns in the effects of radiotherapy, chemotherapy, and chemoradiotherapy on OS and CSS.

Conclusions: Our study shows that advanced gallbladder cancer patients receiving radiotherapy, chemotherapy, or chemoradiotherapy can significantly improve their OS and CSS. Therefore, it is recommended that advanced patients routinely include radiotherapy, chemotherapy, or chemoradiotherapy in comprehensive treatment to improve survival rates. However, for early-stage gallbladder cancer, the improvement effects of radiotherapy, chemotherapy, or chemoradiotherapy on OS and CSS are limited, and the decision to perform radiotherapy or chemotherapy should be individualized based on the patient's specific conditions, such as the pathological type, grade, and lymph node metastasis of the tumor.

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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
252
期刊介绍: Translational Cancer Research (Transl Cancer Res TCR; Print ISSN: 2218-676X; Online ISSN 2219-6803; http://tcr.amegroups.com/) is an Open Access, peer-reviewed journal, indexed in Science Citation Index Expanded (SCIE). TCR publishes laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer; results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of cancer patients. The focus of TCR is original, peer-reviewed, science-based research that successfully advances clinical medicine toward the goal of improving patients'' quality of life. The editors and an international advisory group of scientists and clinician-scientists as well as other experts will hold TCR articles to the high-quality standards. We accept Original Articles as well as Review Articles, Editorials and Brief Articles.
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