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OpenTrials
Active, Not Recruiting

NCT Number: NCT04833387

PD-1 Antibody Following Preoperative Chemoradiotherapy for Locally Advanced pMMR/MSS Rectal Cancer

In this open-label phase II study, patients will be scheduled for neoadjuvant treatment with PD-1 antibody following preoperative Chemoradiotherapy with capecitabine for pMMR/MSS rectal cancer staged as locally advanced (cT3-T4N+/-M0 for rectal cancer). This treatment will be given during the window period until surgical resection of the tumor.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

651 Dongfeng Road East

Guangzhou, Guangdong, 510060, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients who personally provided written consent for participation in the study
  • Treatment-naive patients with rectal cancer, in whom the inferior margin of the tumor was at a distance of 12 cm or less from the AV before CRT
  • Primary rectal cancer histopathologically confirmed to be adenocarcinoma
  • Clinical stage of T3,and T4 ,N any,M0,before CRT
  • Macroscopic radical resection could be feasible, based on diagnostic imaging before CRT
  • Patients with the ECOG performance status of 0 or 1 at the time of enrollment
  • Patients without distant metastasis on the imaging test before CRT
  • Preoperative biopsy of tumor immunohistochemistry TPS>1% or CPS>1
  • Life expectancy of greater than 2 years
  • No signs of intestinal obstruction; or the obstruction has been relieved after the proximal colostomy operation
  • Hematology: WBC>4000/mm3; PLT>100000/mm3; Hb>10g/dL
  • Liver function: SGOT and SGPT are less than 1.5 times the normal value; bilirubin is less than 1.5mg/dL
  • Renal function: creatinine <1.8mg/dL Others: non-pregnant or breast-feeding women; no other malignant diseases (except for non-melanoma or cervical carcinoma in situ) within 5 years or during the same period; no mental illness that causes the inability to obtain informed consent; no other serious diseases that can shorten the survival time disease.
  • Have not received rectal surgery in the past;
  • Have not received chemotherapy or radiotherapy in the past;
  • Have not received biological treatment in the past;
  • Past endocrine therapy: unlimited.

Exclusion criteria

  • Rectal cancer with unstable microsatellite (MSI or dMMR);
  • Preoperative biopsy of tumor immunohistochemistry TPS≤1% or CPS≤1
  • Known history of human immunodeficiency virus (HIV) or chronic hepatitis B or C (high copy viral DNA);
  • Autoimmune diseases;
  • Other active clinical serious infections (>NCI-CTC version 3.0);
  • Patients in clinical phase I;
  • There is evidence that there is distant metastasis before surgery;
  • Cachexia, decompensation of organ function;
  • Have a history of pelvic or abdominal radiotherapy;
  • Multiple primary cancers;
  • Patients who need treatment for seizures (such as steroids or anti-epileptic treatment);
  • Have a known additional malignant tumors within 5 years. Exceptions include basal cell carcinoma of the skin that has undergone potentially curative therapy or in situ cervical cancer;
  • Chronic inflammatory bowel disease, intestinal obstruction;
  • Drug abuse and medical, psychological or social conditions may interfere with patients' participation in research or have an impact on the evaluation of research results;
  • Known or suspected to be allergic to the study drug or to any drug given in connection with this test;
  • Any unstable conditions or situations that may endanger patient safety and compliance

Treatment and study plan

PD-1 antibody

Drug

Capecitabine:Dose of 1650mg/m2,14days; Radiation:50Gy/25 fractions;IBI308: 200mg on day1 of each cycle, 3 cycles; Surgical therapy:The resection (LAR), intersphincteric resection (ISR), or abdominoperineal resection (APR)

Primary outcomes

  1. Pathological complete response

    Time frame: 1 year

    Pathological complete response will be evaluated with American Joint Committee on Cancer (AJCC) Cancer Staging

Secondary outcomes

  1. Relapse-free survival (RFS)

    Time frame: 3 years

  2. Overall survival (OS)

    Time frame: 3 years

  3. Clinical complete response (CCR)

    Time frame: 1 year

Sponsors and collaborators

Lead sponsor

Sun Yat-sen University

Other

Collaborators

  • Fudan University
  • Liaoning Cancer Hospital & Institute

Registry information

Official study title

PD-1 Antibody as a Sequential Therapy Following Preoperative Chemoradiotherapy for Locally Advanced pMMR/MSS Rectal Cancer: an Open, Multi-center, Phase II Clinical Trial

Important dates

Study start
2021
Primary completion
2024
Study completion
2026
First posted
Apr 6, 2021
Registry last updated
Jan 11, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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