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直肠癌患者接受全新辅助治疗后的器官保存。

Organ Preservation in Patients With Rectal Adenocarcinoma Treated With Total Neoadjuvant Therapy.

机构信息

Department of Surgery, Colorectal Service, Memorial Sloan Kettering Cancer Center, New York, NY.

Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY.

出版信息

J Clin Oncol. 2022 Aug 10;40(23):2546-2556. doi: 10.1200/JCO.22.00032. Epub 2022 Apr 28.


DOI:10.1200/JCO.22.00032
PMID:35483010
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9362876/
Abstract

PURPOSE: Prospective data on the efficacy of a watch-and-wait strategy to achieve organ preservation in patients with locally advanced rectal cancer treated with total neoadjuvant therapy are limited. METHODS: In this prospective, randomized phase II trial, we assessed the outcomes of 324 patients with stage II or III rectal adenocarcinoma treated with induction chemotherapy followed by chemoradiotherapy (INCT-CRT) or chemoradiotherapy followed by consolidation chemotherapy (CRT-CNCT) and either total mesorectal excision (TME) or watch-and-wait on the basis of tumor response. Patients in both groups received 4 months of infusional fluorouracil-leucovorin-oxaliplatin or capecitabine-oxaliplatin and 5,000 to 5,600 cGy of radiation combined with either continuous infusion fluorouracil or capecitabine during radiotherapy. The trial was designed as two stand-alone studies with disease-free survival (DFS) as the primary end point for both groups, with a comparison to a null hypothesis on the basis of historical data. The secondary end point was TME-free survival. RESULTS: Median follow-up was 3 years. Three-year DFS was 76% (95% CI, 69 to 84) for the INCT-CRT group and 76% (95% CI, 69 to 83) for the CRT-CNCT group, in line with the 3-year DFS rate (75%) observed historically. Three-year TME-free survival was 41% (95% CI, 33 to 50) in the INCT-CRT group and 53% (95% CI, 45 to 62) in the CRT-CNCT group. No differences were found between groups in local recurrence-free survival, distant metastasis-free survival, or overall survival. Patients who underwent TME after restaging and patients who underwent TME after regrowth had similar DFS rates. CONCLUSION: Organ preservation is achievable in half of the patients with rectal cancer treated with total neoadjuvant therapy, without an apparent detriment in survival, compared with historical controls treated with chemoradiotherapy, TME, and postoperative chemotherapy.

摘要

目的:采用全新辅助治疗治疗局部晚期直肠癌患者的观察等待策略实现器官保存的疗效的前瞻性数据有限。

方法:在这项前瞻性、随机的二期试验中,我们评估了 324 例接受诱导化疗加放化疗(INCT-CRT)或放化疗加巩固化疗(CRT-CNCT),以及肿瘤反应基础上的全直肠系膜切除术(TME)或观察等待的 II 期或 III 期直肠腺癌患者的结局。两组患者均接受氟尿嘧啶-亚叶酸-奥沙利铂或卡培他滨-奥沙利铂静脉输注 4 个月,同时接受 5000 至 5600cGy 放疗,并在放疗期间联合持续输注氟尿嘧啶或卡培他滨。该试验设计为两项独立研究,两组的主要终点均为无病生存(DFS),并基于历史数据假设了一个零假设。次要终点为 TME 无病生存。

结果:中位随访 3 年。INCT-CRT 组的 3 年 DFS 为 76%(95%CI,69 至 84),CRT-CNCT 组为 76%(95%CI,69 至 83),与历史上观察到的 3 年 DFS 率一致。INCT-CRT 组的 3 年 TME 无病生存率为 41%(95%CI,33 至 50),CRT-CNCT 组为 53%(95%CI,45 至 62)。两组间局部无复发生存率、远处无转移生存率或总生存率无差异。重新分期后行 TME 和肿瘤复发生长后行 TME 的患者的 DFS 率相似。

结论:与历史上接受放化疗、TME 和术后化疗的对照相比,采用全新辅助治疗治疗的直肠癌患者有一半可以实现器官保存,且生存无明显受损。

相似文献

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Organ Preservation in Patients With Rectal Adenocarcinoma Treated With Total Neoadjuvant Therapy.

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[2]
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[3]
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[4]
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[5]
Organ Preservation in Rectal Adenocarcinoma: a phase II randomized controlled trial evaluating 3-year disease-free survival in patients with locally advanced rectal cancer treated with chemoradiation plus induction or consolidation chemotherapy, and total mesorectal excision or nonoperative management.

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[6]
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[7]
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[8]
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[9]
[Comparison of long-term efficacy between watch and wait strategy and total mesorectal excision in locally advanced rectal cancer patients with clinical complete response after neoadjuvant therapy].

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[10]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Chemoradiotherapy Plus Induction or Consolidation Chemotherapy as Total Neoadjuvant Therapy for Patients With Locally Advanced Rectal Cancer: Long-term Results of the CAO/ARO/AIO-12 Randomized Clinical Trial.

JAMA Oncol. 2022-1-1

[2]
Quality of life after sphincter preservation surgery or abdominoperineal resection for low rectal cancer (ASPIRE): A long-term prospective, multicentre, cohort study.

Lancet Reg Health West Pac. 2020-12-28

[3]
Neoadjuvant chemotherapy with FOLFIRINOX and preoperative chemoradiotherapy for patients with locally advanced rectal cancer (UNICANCER-PRODIGE 23): a multicentre, randomised, open-label, phase 3 trial.

Lancet Oncol. 2021-5

[4]
Short-course radiotherapy followed by chemotherapy before total mesorectal excision (TME) versus preoperative chemoradiotherapy, TME, and optional adjuvant chemotherapy in locally advanced rectal cancer (RAPIDO): a randomised, open-label, phase 3 trial.

Lancet Oncol. 2021-1

[5]
NCCN Guidelines Insights: Rectal Cancer, Version 6.2020.

J Natl Compr Canc Netw. 2020-7

[6]
Randomized Phase II Trial of Chemoradiotherapy Plus Induction or Consolidation Chemotherapy as Total Neoadjuvant Therapy for Locally Advanced Rectal Cancer: CAO/ARO/AIO-12.

J Clin Oncol. 2019-5-31

[7]
Long-term outcomes of clinical complete responders after neoadjuvant treatment for rectal cancer in the International Watch & Wait Database (IWWD): an international multicentre registry study.

Lancet. 2018-6-23

[8]
Adoption of Total Neoadjuvant Therapy for Locally Advanced Rectal Cancer.

JAMA Oncol. 2018-6-14

[9]
Organ Preservation in Rectal Adenocarcinoma: a phase II randomized controlled trial evaluating 3-year disease-free survival in patients with locally advanced rectal cancer treated with chemoradiation plus induction or consolidation chemotherapy, and total mesorectal excision or nonoperative management.

BMC Cancer. 2015-10-23

[10]
Neoadjuvant 5-FU or Capecitabine Plus Radiation With or Without Oxaliplatin in Rectal Cancer Patients: A Phase III Randomized Clinical Trial.

J Natl Cancer Inst. 2015-9-14

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