NCT07134101Not yet recruitingPhase 2
Neoadjuvant Therapy for Locally Advanced Low Rectal Cancer (SMARTi-RC01)
Neoadjuvant Chemoradiotherapy Combined With Serplulimab With or Without Bevacizumab for Locally Advanced Rectal Cancer: A Single-Center, Open-Label, Phase II Randomized Trial
Source: ClinicalTrials.gov · Last updated 29 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The goal of this clinical trial is to learn if combining serplulimab (PD-1 inhibitor) with bevacizumab and short-course total neoadjuvant therapy (TNT) works to treat locally advanced mid-to-low rectal cancer in adults. It will also learn about the safety of this combination. The main questions it aims to answer are: Does adding bevacizumab to serplulimab and TNT increase the complete remission rate (cCR + pCR) compared with serplulimab and TNT alone? What medical problems do participants have when receiving these treatments? Researchers will compare: Experimental group: serplulimab + bevacizumab + chemotherapy + short-course radiotherapy Control group: serplulimab + chemotherapy + short-course radiotherapy Participants will: Receive either the experimental or control regimen for about 4-5 months before surgery or a watch-and-wait approach if complete response is achieved Undergo treatment in cycles that include chemotherapy, immunotherapy (and bevacizumab if in the experimental group), and short-course radiotherapy Visit the clinic regularly for check-ups, blood tests, imaging, endoscopy, and to monitor side effects Be followed for up to 5 years after treatment to assess cancer control, organ preservation, and survival outcomes
- Status (registry)
- Not yet recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 138 (estimated)
- First submitted
- 11 Aug 2025
- Start date
- Sept 2025
- Primary completion date
- Aug 2028
- Lead sponsor
- The First Affiliated Hospital with Nanjing Medical University
- Diseases
- Colorectal cancer
- NCT number
- NCT07134101
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 138
- From Sept 2025 to the primary completion date, Aug 2028
- No sites listed in no 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.
Prior treatment
- Allergy: Known hypersensitivity to any component of the investigational drugs.
- Other Clinical Trial Participation: Currently enrolled in another interventional drug clinical trial.
Other illness
- Participants will be excluded if any of the following conditions apply:
- Molecular Subtype: Rectal cancer with deficient mismatch repair (dMMR) or microsatellite instability-high (MSI-H) status.
- Autoimmune Disease: Active, known, or suspected autoimmune disease.
- Immunodeficiency: Known history of primary immunodeficiency.
- Transplant History: History of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation.
- Urgent Surgical Indications: Intestinal perforation, gastrointestinal bleeding, or other conditions requiring emergency surgery.
- Other Conditions: Any other condition judged by the investigator to make the patient unsuitable for the study.
Lab values
- Uncontrolled Comorbidities, including but not limited to:
- HIV infection (HIV antibody positive) Active or poorly controlled severe infection Active hepatitis Severe or uncontrolled systemic diseases (e.g., severe psychiatric or neurological disorders, epilepsy, dementia, unstable or decompensated respiratory, cardiovascular, hepatic, or renal disease, uncontrolled hypertension ≥ CTCAE Grade 2 despite medication) Active bleeding or recent thrombotic disease requiring therapeutic anticoagulation, or bleeding tendency, or coagulation abnormalities (INR \> 1.5 × ULN, APTT \> 1.5 × ULN)
- Laboratory Abnormalities at Baseline:
- Hemoglobin \< 80 g/L Absolute neutrophil count (ANC) \< 1.5 × 10⁹/L Platelets \< 80 × 10⁹/L ALT or AST \> 2.5 × ULN ALP \> 2.5 × ULN Total bilirubin ≥ 1.5 × ULN Serum creatinine ≥ 1 × ULN
Other
- Pregnancy or Lactation: Pregnant or breastfeeding women.
Who the study is looking for
- Participants must meet all of the following criteria to be eligible for the study:
- Age: 18 to 75 years old.
- Diagnosis: Pathologically confirmed rectal adenocarcinoma with proficient mismatch repair (pMMR) / microsatellite stable (MSS) status, based on biopsy of the primary tumor.
- Disease Stage: Untreated, preoperative clinical stage cT2-T4 and/or N+, M0 (AJCC 8th edition), unsuitable for initial local excision to achieve radical cure.
- Tumor Location: Tumor within 8 cm from the anal verge, or assessed by surgeons as not suitable for immediate sphincter-preserving surgery.
- Organ Preservation Intent: Strong desire for sphincter preservation and willingness to accept close surveillance for at least 2 years after chemoradiotherapy.
- Surgical Candidacy: Agrees to undergo radical surgery and judged by surgeon to have no contraindication to surgery.
- Cancer History: No concurrent multiple primary malignancies.
- Measurable Lesions: At least one measurable or evaluable lesion according to RECIST v1.1 criteria.
- Life Expectancy: ≥ 3 months.
- Performance Status: ECOG performance status score of 0-1.
- Compliance: Good compliance and willingness to sign written informed consent.
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.