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临床试验/NCT05427669
NCT05427669尚未招募3 期

Adjuvant Modified FOLFOXIRI Versus mFOLFOX6 in Patients With Postoperative MRD Positive Stage II-III Colorectal Cancer: A Multicenter, Open Lable Randomized Phase 3 Study (AFFORD)

Yanhong Deng0 个研究点目标入组 340 人开始时间: 2022年10月9日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
340
主要终点
3-year Disease-free Survival (DFS)

研究概览

简要总结

Surgery is the main treatment method for colon cancer. About 50% of patients can be cured with surgery alone. For colon cancer with high-risk stage II or III after surgery, the current guidelines recommend 3-6 months after surgery. adjuvant chemotherapy to reduce the risk of recurrence and metastasis. However, for this part of the population, the overall benefit of adjuvant chemotherapy is limited, and different high-risk factors have different weights; some patients will still experience recurrence and metastasis even after receiving adjuvant chemotherapy. A number of previous studies have shown that patients with a positive ctDNA test on postoperative liquid biopsy without postoperative adjuvant therapy have a recurrence risk of 70-80%. Even if they receive adjuvant chemotherapy, the recurrence risk is significantly higher than that of ctDNA-negative patients. ctDNA has received increasing attention as a predictor of postoperative recurrence risk.

This study intends to randomly assign 1:1 to mFOLFOXIRI regimen adjuvant chemotherapy for 6 months and mFOLFOX6 regimen for colon cancer patients with postoperative high-risk stage II-III and liquid biopsy results within 1 month after surgery. Adjuvant chemotherapy was performed for 6 months, ctDNA was dynamically monitored after 3 months of treatment and at the end of adjuvant therapy. During the follow-up period, CEA was reviewed every 3 months, and chest, abdomen, and pelvis CT and ctDNA were reviewed every 6 months; the primary endpoint of the study was 2 years RFS, secondary endpoints included 3-year DFS, OS, safety and tolerability. Through intensive postoperative adjuvant therapy, we hope to screen colon cancer patients with high recurrence risk to receive adjuvant chemotherapy and improve the survival prognosis of ctDNA-positive colon cancer patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18-70 years old
  • Histological or cytological documentation of adenocarcinoma of the colon or rectum. All other histological types are excluded.
  • ECOG performance status 0-1
  • Upfront surgery (R0 resection) and postoperative pathological stage II -III and the circulating tumor DNA (ctDNA) test results show that MRD was positive
  • Randomization must be within 8 weeks after surgery.
  • No distant metastasis after surgery
  • Appropriate organ function

排除标准

  • Postoperative CT scan showed distant meatstasis
  • Patients with postoperative obstruction or active bleeding
  • Other active malignant tumors in the past or at the same time (except for malignant tumors that have received curative treatment and have no disease for more than 5 years or carcinoma in situ that can be cured by adequate treatment)
  • The time from postoperative to start of adjuvant therapy has exceeded 8 weeks
  • Patients who have received neoadjuvant therapy
  • Active coronary artery disease, severe/unstable angina or newly diagnosed angina or myocardial infarction within 12 months prior to study participation
  • Thrombotic or embolic events within the past 6 months, such as cerebrovascular accident (including transient ischemic attack), pulmonary embolism, deep vein thrombosis
  • Unstable or any medical condition that affects patient safety and study compliance
  • Subjects with known allergy to the study drugs or to any of its excipients.

研究组 & 干预措施

mFOLFOXIRI

Experimental

Patients will receive mFOLFOXIRI chemotherapy once every two weeks for at the most 12 cycles as adjuvant therapy

干预措施: mFOLFOXIRI (Drug)

mFOLFOX6

Active Comparator

Patients will receive mFOLFOX6 chemotherapy once every two weeks for at the most 12 cycles as adjuvant therapy

干预措施: mFOLFOX6 (Drug)

结局指标

主要结局

3-year Disease-free Survival (DFS)

时间窗: 3 years

The DFS is defined as the time from the start of treatment to the date of first documented recurrence or metastais or death as a result of any cause, whichever occurred first.

次要结局

  • 3-year distant metastatic-free survival (DMFS)(3 year)
  • Overall survival(3 years)

研究者

发起方
Yanhong Deng
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Yanhong Deng

Professor

Sun Yat-sen University

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