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NCT06455124RecruitingPhase 2

Short-course Radiotherapy Combined With CapeOx and PD-1 Inhibitor After Local Excision for High-risk Early Rectal Cancer (TORCH-LE)

Source: ClinicalTrials.gov · Last updated 13 Jun 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a single arm phase II study to explore the 3y LRFS and safety for high-risk early rectal cancer after local excision with short-course radiotherapy and chemo-immunotherapy.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
60 (estimated)
First submitted
6 Jun 2024
Start date
8 May 2024
Primary completion date
30 Jun 2026
Lead sponsor
Fudan University
NCT number
NCT06455124

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 60
  • From 8 May 2024 to the primary completion date, 30 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • history of other malignancies within 5 years
  • serious medical illness, such as severe mental disorders, cardiac disease, uncontrolled infection, etc.
  • immunodeficiency disease or long-term using of immunosuppressive agents
  • allergic to any component of the therapy

Lab values

  • baseline blood and biochemical indicators do not meet the following criteria: neutrophils≥1.5×10\^9/L, Hb≥90g/L, PLT≥100×10\^9/L, ALT/AST ≤2.5 ULN, Cr≤ 1 ULN

Other

  • pregnancy or breast-feeding women
  • pathological confirmed signet ring cell carcinoma
  • DPD deficiency

Who the study is looking for

  • age 18-75 years old, female and male
  • pathological confirmed adenocarcinoma
  • the distance from anal verge ≤ 7 cm
  • pT1 after local excision of the primary rectal cancer, with at least one of the high-risk features including margin positivity/very close margin (\<1mm) at time of local excision, depth of invasion \>1 mm or SM3 invasion (submucosal invasion to the lower third of the submucosal level), high grade or poorly differentiated, lymphovascular invasion, perineural invasion, tumour budding, or pT2 tumor.
  • refuse radical surgery
  • without pelvic or distance metastases
  • KPS \>=70
  • with good compliance
  • microsatellite repair status is MSS/pMMR
  • without previous anti-cancer therapy or immunotherapy
  • signed the inform consent

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Fudan University Shanghai Cancer Center
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.