腹腔镜结肠癌右半结肠切除术的肿瘤学结果:三年随访结果

Jung Hoon Cho, Dae Ro Lim, Hyuk Hur, Byung Soh Min, Seung Hyuk Baik, Kang Young Lee, Nam Kyu Kim
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摘要

目的:该研究旨在评估腹腔镜辅助右半结肠切除术治疗结肠癌的肿瘤学效果,并将结果与之前的随机试验结果进行比较:方法:从 2006 年 6 月到 2008 年 12 月,对 156 名连续接受腹腔镜右半结肠切除术的结肠癌患者进行了评估。结果:84 名男性患者和 72 名女性患者接受了腹腔镜右半结肠切除术:结果:84 名男性患者和 72 名女性患者接受了手术。平均住院时间为 7.0 ± 1.5 天(4 至 12 天不等)。转换率为 3.2%。并发症总数为 30 例(19.2%)。未发现吻合口漏。30 天内无死亡病例。所有阶段的 3 年总存活率为 93.3%。各期的 3 年总生存率分别为:I 期 100%,II 期 97.3%,III 期 84.8%。所有分期的 3 年无病生存率为 86.1%。各期的 3 年无病生存率分别为:I 期 96.2%,II 期 90.3%,III 期 75.6%。平均随访时间为36.3(3至60)个月:结论:腹腔镜右半结肠切除术治疗结肠癌在技术上是可行的,在肿瘤结果方面也是安全的。目前的数据支持之前报道的随机试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Oncologic Outcomes of a Laparoscopic Right Hemicolectomy for Colon Cancer: Results of a 3-Year Follow-up.

Purpose: The purpose of the study is to evaluate the oncologic outcomes of a laparoscopic-assisted right hemicolectomy for the treatment of colon cancer and compare the results with those of previous randomized trials.

Methods: From June 2006, to December 2008, 156 consecutive patients who underwent a laparoscopic right hemicolectomy with a curative intent for colon cancer were evaluated. The clinicopatholgic outcomes and the oncologic outcomes were evaluated retrospectively by using electronic medical records.

Results: There were 84 male patients and 72 female patients. The mean possible length of stay was 7.0 ± 1.5 days (range, 4 to 12 days). The conversion rate was 3.2%. The total number of complications was 30 (19.2%). Anastomotic leakage was not noted. There was no mortality within 30 days. The 3-year overall survival rate of all stages was 93.3%. The 3-year overall survival rates according to stages were 100% in stage I, 97.3% in stage II, and 84.8% in stage III. The 3-year disease-free survival rate of all stages was 86.1%. The 3-year disease-free survival rates according to stage were 96.2% in stage I, 90.3% in stage II, and 75.6% in stage III. The mean follow-up period was 36.3 (3 to 60) months.

Conclusion: A laparoscopic right hemicolectomy for the treatment of colon cancer is technically feasible and safe to perform in terms of oncologic outcomes. The present data support previously reported randomized trials.

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