Suppr超能文献

局部进展期直肠癌术前放化疗联合或不联合奥沙利铂及氟尿嘧啶诱导化疗:长期疗效分析。

Preoperative chemoradiation with or without induction oxaliplatin plus 5-fluorouracil in locally advanced rectal cancer. Long-term outcome analysis.

机构信息

Department of Oncology, Hospital General Universitario Gregorio Marañón, Ave. Doctor Esquerdo, 46, 28007, Madrid, Spain.

出版信息

Strahlenther Onkol. 2014 Feb;190(2):149-57. doi: 10.1007/s00066-013-0469-0. Epub 2013 Dec 6.

Abstract

BACKGROUND AND PURPOSE

It has been previously reported that a short FOLFOX-4 induction significantly improves pathologic complete response in locally advanced rectal cancer (LARC) patients treated with preoperative chemoradiation (CRT). In a larger and updated patient series, we analyzed FOLFOX-4 efficacy in terms of sphincter preservation and long-term outcomes.

PATIENTS AND METHODS

From January 1995 to December 2010, 335 LARC patients were treated with preoperative chemoradiation (4500-5040 cGy). Starting in May 2001, 207 consecutive patients additionally received induction FOLFOX-4. Surgery was performed 6 weeks (range 3-12 weeks) after chemoradiation.

RESULTS

Incidence of total tumor (63 vs. 54 %, p = 0.02) and nodal downstaging (60 vs. 43 %, p = 0.002) was significantly increased by induction FOLFOX-4. In an analysis of tumors located below 5 cm from the anal verge (n = 114, 34 %), sphincter preservation was feasible in 30 % in the FOLFOX-4 versus 13 % in the upfront CRT group (p = 0.04). Median follow-up time for the entire cohort of patients was 72.6 months (range 4-205 months). FOLFOX-4 was not associated with superior locoregional control (HR 0.88, p = 0.78), disease-free survival (HR 0.83, p = 0.55), distant metastases-free survival (HR 0.94, p = 0.81), or cancer-specific survival (HR 0.70, p = 0.15).

CONCLUSION

Short-intense induction FOLFOX-4 significantly improves downstaging and sphincter preservation in low rectal tumors. Long-term outcomes were not improved in the FOLFOX-4 group of patients.

摘要

背景与目的

先前有研究报道,术前放化疗(CRT)联合短程 FOLFOX-4 诱导化疗可显著提高局部进展期直肠癌(LARC)患者的病理完全缓解率。本研究在更大的更新的患者系列中,分析了 FOLFOX-4 在保留肛门括约肌和长期预后方面的疗效。

患者与方法

1995 年 1 月至 2010 年 12 月,335 例 LARC 患者接受术前 CRT(4500-5040cGy)治疗。自 2001 年 5 月起,207 例连续患者额外接受了 FOLFOX-4 诱导化疗。CRT 后 6 周(3-12 周)行手术。

结果

FOLFOX-4 诱导化疗可显著增加肿瘤(63% vs. 54%,p=0.02)和淋巴结降期(60% vs. 43%,p=0.002)的发生率。在分析肿瘤位于肛缘下 5cm 以内(n=114,34%)的患者中,FOLFOX-4 组可行保肛手术的比例为 30%,而 upfront CRT 组为 13%(p=0.04)。所有患者的中位随访时间为 72.6 个月(4-205 个月)。FOLFOX-4 并未改善局部区域控制(HR 0.88,p=0.78)、无疾病生存(HR 0.83,p=0.55)、无远处转移生存(HR 0.94,p=0.81)或癌症特异性生存(HR 0.70,p=0.15)。

结论

短程强化 FOLFOX-4 诱导化疗可显著提高低位直肠肿瘤的降期和保肛率。FOLFOX-4 组患者的长期预后并未改善。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验