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Active, not recruitingNCT06688786FIRMUpdated Jan 27, 2026

A Pospective, Single-arm, Multicenter Clinical Trial Evaluating Preoperative Neoadjuvant mFOLFOX6 Chemotherapy in Combination With PD1 Monoclonal Antibody in MSS/pMMR Locally Advanced Rectal Cancer

An interventional study of neoadjuvant mFOLFOX6 chemotherapy combined with PD-1 inhibitor therapy in Locally Advanced Rectal Cancer (LARC), sponsored by Xinhua Hospital, Shanghai Jiao Tong University School of Medicine. Active, not recruiting at 1 site in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-01-27.

Sponsored by Xinhua Hospital, Shanghai Jiao Tong University School of Medicine · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Not applicable
Ages
18 Years to 75 Years
Sex
All
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Study summary

Preoperative neoadjuvant chemoradiotherapy can induce tumor regression and reduce the risk of postoperative recurrence, serving as the standard treatment for locally advanced rectal cancer. However, neoadjuvant radiotherapy may increase the risk of postoperative complications, proctitis, enteritis, and reduced anal function. Exploring radiation-free approaches to prevent the effects of radiotherapy toxicity on postoperative complications and quality of life is now a significant research focus. Neoadjuvant chemotherapy represents a promising approach in the neoadjuvant treatment of rectal cancer. Neoadjuvant chemotherapy avoids the impact of radiotherapy on organ function, reduces the incidence of postoperative anastomotic leakage, and is beneficial for long-term anal function preservation. However, its low tumor regression rate limits its application in the neoadjuvant treatment of rectal cancer. For patients with locally advanced rectal cancer, there is an urgent need for a new neoadjuvant treatment strategy that can both significantly improve tumor regression rates and reduce the risk of postoperative anastomotic leakage, and protect long-term anal function. PD-1 inhibitors are highly effective in treating microsatellite instability-high (MSI-H) colorectal cancer patients, but show poor efficacy in the 95% of patients with microsatellite stable (MSS) tumors. The challenge now is to find combination therapies that can convert tumors into an "immune-activated tumor," thereby enhancing the effectiveness of immunotherapy in MSS patients. Oxaliplatin and 5-fluorouracil have roles in releasing tumor antigen epitopes, activating CD8+ cells, and reshaping the immune microenvironment. Multiple clinical studies and animal experiments have shown that combining PD-1 antibodies with FOLFOX generates a synergistic effect, showing strong antitumor activity. This study evaluates the efficacy, safety, and impact on postoperative anal function of preoperative neoadjuvant treatment with FOLFOX chemotherapy combined with PD-1 inhibitors in patients with MSS-type advanced rectal cancer. The radiotherapy-free approach aims to avoid radiotherapy-related toxicity, offering significant potential to enhance the efficacy of neoadjuvant chemotherapy, improve long-term survival, and protect anal function.

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Conditions studied

  • Locally Advanced Rectal Cancer (LARC)

Keywords

  • rectcal cancer
  • microsatellite stable
  • FOLFOX
  • neoadjuvant chemotherapy
  • PD-1 antibodies
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In context

Lead sponsor

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine is the lead sponsor of 222 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Advanced (cT3-4NxM0 or cTxN+M0) rectal cancer with the lower tumor margin within 15 cm of the anal verge
  2. Histopathology confirmed adenocarcinoma with an pMMR/MSS genetic profile.
  3. Absence of bowel obstruction, or bowel obstruction relieved by proximal colostomy.
  4. Age: 18-75
  5. ECOG: 0-1
  6. No prior chemotherapy, radiotherapy, targeted therapy, or immunotherapy received.
  7. Female participants must be non-lactating, with a negative pregnancy test result.

Exclusion criteria

Exclusion Criteria:

  1. Patients with distant metastasis
  2. History of receiving chemotherapy, radiotherapy, targeted therapy, or immunotherapy.
  3. Active autoimmune disease requiring systemic treatment within the 2 years prior to enrollment.
  4. History of other malignancies within the past 5 years, excluding cured cervical carcinoma in situ or basal cell carcinoma of the skin.
  5. History of HIV infection, or active chronic hepatitis B or C with high viral DNA copy numbers.
  6. Patients with active tuberculosis currently receiving anti-tuberculosis treatment or treated with anti-tuberculosis therapy within the past year prior to screening.
  7. Known or suspected allergy to the study drug or any study-related medications administered.
  8. Presence of severe cardiovascular or cerebrovascular disease.
  9. Within 14 days prior to the first dose, presence of a severe active or uncontrolled infection requiring systemic therapy, or unexplained fever >38.5°C.
  10. Receiving systemic corticosteroid treatment or other immunosuppressive agents within 14 days prior to the first dose, or immunostimulants within 4 weeks.
  11. History of confirmed neurological or psychiatric disorders, including epilepsy or dementia.
  12. The participant may be unable to complete the study due to other reasons, or the investigator considers them unsuitable for inclusion.
  13. Refusal to sign the informed consent form.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Combinational treatment group

    neoadjuvant mFOLFOX6 chemotherapy combined with PD-1 inhibitor therapy

    Drug: neoadjuvant mFOLFOX6 chemotherapy combined with PD-1 inhibitor therapy

Interventions

  • Drugneoadjuvant mFOLFOX6 chemotherapy combined with PD-1 inhibitor therapy

    Preoperative treatment with 4-6 cycles of mFOLFOX6 regimen combined with serplulimab

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What researchers measure

Primary outcomes

  1. Pathological complete response

    Time frame: Day 7 after surgery

  2. Major Pathological Response

    Time frame: Day 7 after surgery

Secondary outcomes

  1. Tumor regression grade

    Time frame: Day 7 after surgery

  2. Radiologic Response

    Time frame: Preoperative evaluation

  3. Neoadjuvant rectal score

    The Neoadjuvant rectal score ranges from 0 to 100, with higher scores indicating poorer response to neoadjuvant therapy.

    Time frame: Day 7 after surgery

  4. Postoperative complication

    Time frame: Within 2 weeks post-surgery

  5. Disease free survival

    Time frame: Three years after surgery

  6. Relapse free survival

    Time frame: Three years after surgery

  7. Wexner fecal incontinence scale

    Utilized to evaluate anal function, with higher scores indicating poorer anal function.

    Time frame: evaluated every 3 months for 3 years after surgery

  8. overall survival

    Time frame: Three years after surgery

  9. Adverse events

    Time frame: Prior to surgery, adverse events are evaluated the day before each chemotherapy cycle. After surgery, adverse events are evaluated at months 3, 6, 9, and 12.

07

Study locations

1 site
  • Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
    Shanghai, Shanghai Municipality 200092, China
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References and documents

Individual participant data

Plan to share: Yes — In this study personal information and data such as patient history, physical examination results, surgical records, and study questionnaire data will be collected. These data will be used to evaluate the efficacy and safety of the therapeutic regimen and for academic publication. The researcher will treat the personal data of patients confidentially and anonymize the data and information in any public release of the results of the study.

Supporting information: Study protocol, Sap, Csr

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06688786
Lead sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Responsible party
Tingyu Wu (Principal Investigator, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine) — Principal investigator
First posted
Nov 14, 2024
Start date
Nov 1, 2024
Primary completion
Jul 31, 2025
Completion
Dec 31, 2027 (estimated)
Last update
Jan 27, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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