Clinical Characteristics and Outcomes in Patients with Early-Onset Locally Advanced Rectal Cancer.
JOURNAL OF CLINICAL ONCOLOGY(2024)
摘要
70 Background: Despite a reduction in both the incidence and mortality of CRC in the elderly population, recent studies have highlighted an increase in the incidence of early-onset CRC (EO-CRC). Clinical and prognostic data in this context are limited and conflicting. The aim of our study was to evaluate the clinical differences and outcomes of patients with early onset locally advanced rectal cancer. Methods: We retrospectively collected data from 305 patients affected by LARC treated in Italy at the Medical Oncology Units of the University Hospital of Cagliari, Istituto Nazionale dei Tumori Milan, and AOU Ospedali Riuniti Ancona. All patients underwent neoadjuvant chemoradiotherapy. The primary objective was overall survival (OS) while while secondary objectives were overall response rate (ORR) and major TRG. Results: Twenty five (8,2%) pts were EO-RC and 280 (91,8%) were LO-RC. In EO-RC the locations were distributed as follows: 9 (36%) lower rectum, 13 (52%) medium rectum, and 3 (12%) upper rectum. Pathologic responses were as follows: 3 (12%) TRG-0, 6 (24%) TRG-1, 10 (40%) TRG-2, and 6 (24%) TRG-3. While the radiological responses were as follows: 2 (8%) CR, 15 (60%) PR, 7 (28%) SD, and 1 (4%) PD. In LO-RC the locations were: 78 (27,8%) lower rectum, 153 (54,6%) medium rectum, and 49 (17,6%) upper rectum. Pathologic responses were as follows: 29 (10,4%) TRG-0, 60 (21,4%) TRG-1, 159 (56,8%) TRG-2, and 32 (11,4%) TRG-3. Radiological responses were as follows: 25 (8,9%) CR, 155 (61,4%) PR, 64 (22,9%) SD, and 19 (6,8%) PD. The 10 year overall survival was significantly higher in LO-RC patients compared to EO-CRC patients: 92.54% versus 70.83% (p = 0.0005). Conclusions: Compared to LO-RCs, EO-RC patients had more frequent low rectal tumors and higher rates of major pathological responses. Despite this, 10-year OS was found to be inferior in EO-RC. Further studies and insights will be necessary to better understand the biological and clinical characteristics of early-onset tumors.
更多查看译文
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
数据免责声明
页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果,我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问,可以通过电子邮件方式联系我们:report@aminer.cn