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临床试验/NCT06262581
NCT06262581招募中2 期

Neoadjuvant Tisleizumab(BGB-A317) for dMMR/MSI-H Non-late Stage Colorectal Cancer Patients

Sun Yat-sen University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2023年9月23日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
40
试验地点
1
主要终点
pathological complete regression rate

研究概览

简要总结

According to the cancer statistics in 2020, colorectal cancer (CRC) remains a major public health issue worldwide, representing the third common cancer (10%) and second leading cause of death (9.4%) with 5-year survival rate approaching 65%. Meanwhile, 28.8% of the newly diagnosed cases and 30.3% of the CRC-related death occurs in China. Among all the CRC, stage I-III account for 75%. For the standard management for non-late stage(stage I-III) CRC patients, surgery including the primary site and local lymph nodes dissection has been the most important one. But for the high-risk stage II and locally-advanced stage III CRC, neoadjuvant or adjuvant therapy such as chemotherapy and radiotherapy plays a vital role in preventing the residual cancer cells to relapse and spread to distant sites after surgery. For the past decades, immunotherapy like anti-PD-1 and anti-CTLA4 checkpoint inhibitor achieves great process in solid tumor treatment especially for late-stage CRC. And Pembrolizumab and Nivolumab has been proved for dMMR/MSI-H late-stage-CRC by FDA. Combination of Ipilimumab and Nivolumab has achieved great success among the early-stage-CRC in NICHE study. The investigators here to carry out a phase II clinical trial to explore the safety and effect of single anti-PD-1 (Tisleizumab-BGB-A317 ) neoadjuvant treatment for non-late stage CRC patients.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Able to provide consents and agree to follow the trial requirement and assessment;
  • Age >=18
  • ECOG score: 0 or1
  • Biopsy pathological diagnosis as MSI-H/dMMR( both IHC and PCR method required)
  • Measurable and assessible primary tumor sites according to RECIST 1.1
  • Able to provide 22ml peripheral blood for assessment for ctDNA
  • With all organ function sufficient
  • No bowel obstruction or fistula
  • No previous chemotherapy, radiotherapy and immunotherapy accepted history
  • Distant metastasis excluded before surgery by CT scan
  • Contraception required for women for the whole enrollment time until 3 months after last dose of immunotherapy

排除标准

  • self-autoimmune diseases history such as SLE
  • People who using the immune suppressor
  • Severe allergy to other mono-clone antibody
  • Cerebral metastasis which hasn't be managed yet
  • Hypertension(SBP>140mmHg,DBP>90mmHg)
  • Uncontrolled diabetes(FBG>10mmol/L)
  • Accepted anti-PD-1 or anti-PD-L1 immunotherapy in the past
  • Uncontrolled heart diseases such as NYHA II heart failure, unstable angina , cardiac infarction in 1 year and arrhythmia
  • Systemic inflammation which needs whole body treatment
  • Urine routine: protein >=++ or 24hr urine protein>=1g
  • Innate or acquired immune deficiency like HIV and HBV
  • Enrolled in other clinical trial already
  • Confirmed as metastasis before the surgery
  • Other malignancies has been diagnosed before
  • Tuberculosis
  • Pregnancy

研究组 & 干预措施

dMMR/MSI-H stage I-III CRC patients

Experimental

Patients will accept 4 dose of Tisleizumab(BGB-A317) treatment after enrollment and the assessment of the therapeutic effect by clinicians would be finished after that. Once the patients has been qualified as cCR , they could be exempted for surgery and continued the watch and wait management. If the patient has been assessed as able to R0 surgery , then they would received surgery. Otherwise ,they would be excluded from the trial.

干预措施: Tisleizumab(BGB-A317) (Drug)

结局指标

主要结局

pathological complete regression rate

时间窗: From enrollment to 1 year after surgery

Patients without noninvasive or focal-invasive residues or involved lymph nodes should be considered as having achieved pCR. The rate is these patients over the whole group.

次要结局

  • CR rate(From enrollment to 1 year after surgery)
  • Major Pathological Response rate(From enrollment to 1 year after surgery)
  • Disease free survival(From enrollment to 1 year after surgery)

研究者

发起方
Sun Yat-sen University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Gong Chen

Professor

Sun Yat-sen University

研究点 (1)

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