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临床试验/NCT04241731
NCT04241731Unknown2 期

A Multicenter Phase II Clinical Study of Cetuximab Plus Raltitrexed for Maintenance Treatment in Advanced Colorectal Cancer

Jiangsu Cancer Institute & Hospital1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2019年11月28日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
发起方
入组人数
50
试验地点
1
主要终点
The time from the beginning of first-line treatment until the disease progresses.

研究概览

简要总结

Maintenance treatment can extend patient survival and improve patient quality of life. Bevacizumab alone or capecitabine combined with bevacizumab as a maintenance treatment have been widely used in clinical practice. In contrast, there are little datas of cetuximab as a maintenance treatment. The purpose of this study is to evaluate efficacy and safety of Raltitrexed plus Cetuximab as the maintenance treatment, and to provide a new choice for RAS wild-type colorectal cancer patients after advanced first-line chemotherapy.

详细描述

Maintenance treatment can prevent the toxicity and give patients a relative buffer period to alleviate the impact of follow-up treatment on the body without reducing efficacy. Bevacizumab alone or capecitabine combined with bevacizumab as a maintenance treatment have been widely used in clinical practice. There are little datas of cetuximab as a maintenance treatment ,some studies show that Cetuximab is effective in maintenance treatment, and some studies have reported adverse effects of Capecitabine combined with Cetuximab.So it is worthwhile to explore more suitable maintenance treatment options. Raltitrexed, a TS enzyme inhibitor, is an effective chemotherapy drug for colorectal cancer. We plan to evaluate efficacy and safety of Raltitrexed plus Cetuximab in maintenance treatment. Maybe we can provide a new choice for RAS wild-type colorectal cancer patients after advanced first-line chemotherapy.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18-75 years old, no gender restriction;
  • RAS wild-type
  • Unresectable metastatic colorectal cancer confirmed by histopathology and / or cytology;
  • Disease stable or improved while on first-line use of FOLFOX/FOLFIRI with cetuximab for 4-6 months;
  • At least one measurable objective tumor lesion by spiral CT scan,the longest diameter measured ≧ 10 mm,or by conventional CT scan,the diameter measured ≧ 20 mm.
  • Eastern Cooperative Oncology Group (ECOG) general status score is 0-2;
  • Life expectancy of at least 3 months;
  • Blood routine, liver and kidney function within the 7 days before screening meet the following criteria: Absolute neutrophil count ≥ 1.5x10^9 / L; hemoglobin ≥ 9.0 g / dl; platelet count ≥ 80 x10^9 / L; total bilirubin ≤ 1.5 times the upper limit of normal (ULN); alanine aminotransferase and aspartate aminotransferase ≤ 2.5 x ULN (≤5 x ULN in patients with liver metastases); ≤3 x ULN in patients with liver metastases (≤5 x ULN in patients with liver metastases); serum creatinine ≤1.5 x ULN;
  • Agree to sign informed consent.

排除标准

  • BRAF mutant
  • Symptomatic brain or meningeal metastases (unless patients receive treatment> 6 months, imaging results are negative within 4 weeks before joining the study, and tumor-related clinical symptoms are stable before joining the study);
  • Previous malignant disease within five years, with the exception of the cured primary cervical cancer or basal cell carcinoma of the skin;
  • Chronic intestinal disease, infectious intestinal disease, intestinal obstruction, active clinical severe infection and other diseases;
  • With ascites
  • Substance abuse and medical, psychological or social conditions that may interfere with the participation of patients in the study or influence the evaluation of the results of the study;
  • Unsuitable for the study or other chemotherapy determined by investigator.

研究组 & 干预措施

Raltitrexed Plus Cetuximab

Experimental

Raltitrexed Plus Cetuximab

干预措施: Raltitrexed (Drug)

Raltitrexed Plus Cetuximab

Experimental

Raltitrexed Plus Cetuximab

干预措施: Cetuximab (Drug)

结局指标

主要结局

The time from the beginning of first-line treatment until the disease progresses.

时间窗: 24 months

Progression Free Survival 1.

The time from the beginning of maintenance treatment until the disease progresses.

时间窗: 24 months

Progression Free Survival 2.

次要结局

  • Overall survival (OS)(24 months)
  • Incidence of Treatment-Emergent Adverse Events Based on NCI-CTC 4.0(24 months)
  • Quality of life score(24 months)

研究者

发起方
Jiangsu Cancer Institute & Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Liangjun Zhu M.M.

Ward Director of Internal Medicine

Jiangsu Cancer Institute & Hospital

研究点 (1)

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