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临床试验/NCT04643041
NCT04643041招募中不适用

Watch and Wait in Patients With dMMR/MSI-H Distal Rectal Cancer Accessed Pathological Complete Response After PD-1 Monoclonal Antibody Therapy-an Open Label, Multicenter, Prospective Study (BASKET)

Sixth Affiliated Hospital, Sun Yat-sen University1 个研究点 分布在 1 个国家目标入组 47 人开始时间: 2021年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
47
试验地点
1
主要终点
1 year DFS rate

研究概览

简要总结

Immunotherapy has achieved significant therapeutic effect in DNA mismatch repair-deficient or microsatellite instability-high (dMMR/MSI-H) colorectal cancer (CRC) , more than fifty percent of dMMR/MSI-H CRC patients might get pathological complete response(pCR) after PD-1 monoclonal antibody treatment. For distant rectal cancer(RC), radical resection and neoadjuvant chemotherapy or chemoradiotherapy might cause lots of treatment cost,damage to defecation and sexual function, acute toxicity, chronic dysfunction, even loss of anus and psychological disorder. This study aims to evaluate the effect and safety of watch and wait in patients with dMMR/MSI-H distal RC accessed pCR after PD-1 monoclonal antibody therapy.

详细描述

Immunotherapy has achieved significant therapeutic effect in DNA mismatch repair-deficient or microsatellite instability-high (dMMR/MSI-H) colorectal cancer (CRC). MMR expression and MSS status are the important effective factors of immunotherapy. PD-1monocolnal antibody therapy has accessed excellent treatment effect in advanced dMMR/MSI-H CRC and neoadjuvant therapeutic effect in early colon cancer, more than fifty percent of dMMR/MSI-H CRC patients might get pathological complete response(pCR) after PD-1 monoclonal antibody treatment. The treatments had been proved to be safe and the toxicities were controllable. Rectal cancer(RC) is one of the most common malignant tumors in China. So far, radical resection with or without neoadjuvant chemotherapy of chemoradiotherapy are still standard comprehensive treatments recommended to distal RC by NCCN, ESMO and CSCO. For distant RC, radical resection and neoadjuvant chemotherapy or chemoradiotherapy might cause lots of treatment cost,damage to defecation and sexual function, acute toxicity, chronic dysfunction, even loss of anus and psychological disorder. So far, whether watch and wait could be performed in patients with dMMR/MSI-H distal RC accessed pCR after PD-1 monoclonal antibody therapy or not is still not clear. Thus, this study aims to evaluate the effect and safety of watch and wait in patients with dMMR/MSI-H distal RC accessed pCR after PD-1 monoclonal antibody therapy.

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 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Preliminary inclusion criteria:
  • Histological identified rectal adenocarcinoma,
  • Tumor biopsy immunohistochemical (IHC) identified dMMR, including one or more deficient of the MSH1,MSH2,MSH6 and PMS2 protein expression and diagnosed as deficient mismatch repair(dMMR), or next generation sequencing identified (MSI-H); MRI identified tumor inferior margin lower than peritoneal reflection,
  • Clinical staging TxNxM0, with or without positive MRF, with or without positive EMVI,
  • Staging method:all patients undergo rectal palpation, high resolution MRI ± transrectal Ultrasound examination,positive perienteric lymph node(LN): short diameter ≥10mm LN or LN with typical metastatic shape and MRI character, clinical data should be re-evaluated and judged by center evaluation group when there are contradictory stagings,distant metastasis were excluded by chest and abdominal enhanced CT and pelvic enhanced MRI,
  • No intestinal obstruction symptom,or obstruction relieved after proximal colostomy,
  • No rectal surgery history,
  • No chemotherapy or radiotherapy history,
  • No biopharmaceutical treatment history(such as monoclonal antibody), immunotherapy(such as anti PD-1antibody, anti PD-L1 antibody, anti PD-L2 antibody or anti CTLA-4), or other research drug treatment,
  • Endocrinotherapy history restriction:No
  • Informed consent assigned, Final inclusion criteria:
  • Clinical complete response (cCR)(Chest,abdominal and pelvic enhanced CT or pelvic enhanced MRI or transrectal ultrasound proved)
  • Transrectal ultrasound biopsy or endoscopic biopsy proved pathologically complete response (pCR)

排除标准

  • Arrhythmia need anti-arrhythmia treatment(except β-blocking agent or Digoxin),symptomatic coronary heart disease or myocardial ischemia(myocardial infarction within 6 months) or congestive heart-failure (CHF) > NYHA grade II,
  • Severe hypertension not well controlled by drugs,
  • HIV infection history or active phase of chronic Hepatitis B or C(high copies of virus DNA),
  • Active tuberculosis(TB),accepting anti-TB treatment or anti-TB treatment within 1 year before trial screen,
  • Other active clinical severe infection(NCI-CTC V5.0),
  • Outside pelvic distant metastasis evidences,
  • Dyscrasia, organ dysfunction,
  • Pelvic or abdominal radiotherapy history,
  • Multiple CRC or Multi-primary tumors;
  • Epilepsy need treatments(Steroid or anti-epilepsy therapy),
  • Other malignant tumor history within 5 years,
  • Over abuse of drugs, medical and psychological or social conditions that might interfere patients or evaluation of the study results,
  • Any active autoimmune disease or autoimmune disease history (including but not restricted:interstitial pneumonia, uveitis,enteritis, hepatitis,hypophysitis, nephritis, hyperthyroidism, hypothyroidism, asthma need bronchodilators),
  • Any anti-infection vaccine injection 4 weeks before inclusion ,
  • Long-term exposure to immune-suppressor, combination of systemic or topical use of corticosteroids (dose>10mg/day prednisolone or equivalent hormone);
  • Known or suspicious allergy to any study related drugs,
  • Any unstable state might cause damage to the safety and compliance of patients,
  • Pregnant or breast feeding women who has ability to have children while without contraception,
  • Refuse to sign informed consent

研究组 & 干预措施

watch and wait

Experimental

patients with DNA mismatch repair-deficient or microsatellite instability-high distal rectal cancer accessed pathological complete response after 6 courses of PD-1 monoclonal antibody (200mg/Course/Q3W) therapy and start watch and wait.

干预措施: watch and wait (Behavioral)

结局指标

主要结局

1 year DFS rate

时间窗: 1 year

1 year Disease Free Survival Rate

次要结局

  • distant metastasis rate(3 years)
  • 3 years DFS Rate(3 years)
  • 3 years OS rate(3 years)
  • local recurrent rate(3 years)
  • Incidence rate of Grade ≥3 PD-1monoclonal antibody-related adverse events(1 year)

研究者

发起方
Sixth Affiliated Hospital, Sun Yat-sen University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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