早期局部晚期直肠癌患者的病理完全反应率更高

J. Suarez , M. Alsina , N. Castro , G. Marin , C. Llanos , B. Oronoz , E. Mata , R. Aznárez , G. Jiménez , M.I. Martínez , R. Vera
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引用次数: 0

摘要

背景过去几十年来,结直肠癌的发病率和死亡率逐渐下降,但早发直肠癌(EORC;50 岁以下)的发病率却在惊人地上升。早发性直肠癌通常在晚期才被诊断出来,并呈现内在的分子改变。有必要采取新策略来提高早期诊断率并改善治疗管理。材料与方法回顾性分析了被诊断为局部晚期直肠癌(LARC)并在化放疗新辅助治疗(NAT)后接受根治性手术治疗的患者,比较了EORC与晚期直肠癌(LORC)之间的差异。结果 多达 1140 名患者被诊断为直肠癌并接受了根治性手术。其中,399 名直肠癌患者在手术前接受了 NAT 治疗,其中 9% 的患者(36 人)患有 EORC。局部晚期 EORC 的发病率从 6.6% 上升至 12.7%(2001-2020 年)。在诊断变量方面,早发和晚发组群之间没有发现差异,但在 EORC 组群中发现了略多的缺乏错配修复的肿瘤。平均无病生存期和平均癌症特异性生存期相似。尽管如此,与 LARC 相比,EORC 患者的病理完全缓解率(pCRs)更高(36.3% 对 12.4%;P = 0.000)。EORC患者的pCR率更高,这表明应进一步研究器官保存策略在这一特殊人群中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Higher rate of pathologic complete response in patients with early-onset locally advanced rectal cancer

Background

Although incidence and mortality rates of colorectal cancer have progressively decreased during the past decades, early-onset rectal cancer (EORC; <50 years old) is rising alarmingly. EORC is often diagnosed at advanced stages and presents intrinsic molecular alterations. New strategies are necessary to increase early diagnosis and to improve therapeutic management. We present the analysis of our locally advanced EORC patients evaluating their specific response to chemoradiotherapy.

Materials and methods

Patients diagnosed with locally advanced rectal cancer (LARC) and treated with curative surgery after neoadjuvant treatment (NAT) with chemoradiotherapy were retrospectively analysed, comparing differences between EORC and late-onset rectal cancer (LORC). Incidence rates between 2001 and 2020, as well as diagnostic and treatment response variables, were compared.

Results

Up to 1140 patients were diagnosed with rectal cancer and underwent curative surgery. From them, there were 399 patients with LARC who received NAT before surgery, and 9% of them had EORC (36 patients). The incidence of locally advanced EORC increased from 6.6% to 12.7% (2001-2020). No differences were found considering diagnostic variables between the early- and late-onset cohorts, although slightly more deficient mismatch repair tumours were found within the EORC cohort. Mean disease-free survival and mean cancer-specific survival were similar. Notwithstanding, EORC patients achieve higher rates of pathological complete responses (pCRs), compared with LARC (36.3% versus12.4%; P = 0.000).

Conclusions

Our analyses confirm the increase in incidence of EORC from 2001 to 2020 in Navarra. EORC patients achieved a higher pCR rate, thus suggesting that the role of organ preservation strategies should be further investigated in this unique population.

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