AI model may predict who can skip surgery for rectal cancer
NCT ID NCT06364371
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This observational study is developing a model that combines MRI scans, blood tests, and tissue samples to predict whether rectal cancer patients achieve a complete response after neoadjuvant therapy. Researchers will enroll 106 patients with locally advanced rectal cancer and collect data before, during, and after treatment. The goal is to improve selection for a watch-and-wait approach, potentially sparing some patients from surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this model could help doctors identify which rectal cancer patients can safely avoid surgery after neoadjuvant therapy, improving quality of life.
- What could go wrong
- This is an early observational study with only 106 participants, so the model may not be accurate enough for widespread use. It is not a treatment trial.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
About 106 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Jun 2024
- Expected to finish
-
Jun 2028
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients are pathological confirmed as rectal adenocarcinoma, clinical stage T3-4NxM0, and underwent the neoadjuvant therapy before surgical treatment.
- Ages
-
18 to 80 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Histologically confirmed rectal adenocarcinoma; 2. Clinical stage T3-4NxM0, with or without positive Mesorectum Fascia(MRF), and with or without positive Extra-Mural Venous Invasion(EMVI); 3. Preoperative staging method: All patients undergo preoperative staging with enhanced CT. Criteria for mesorectal lymph node metastasis: Short axis ≥ 10mm lymph nodes or lymph node morphology and CT characteristics consistent with typical lymph node metastasis. Preoperative chest, abdominal CT, and pelvic MRI exclude distant metastases; 4. Absence of signs of intestinal obstruction; or relief of obstruction after proximal colon diversion surgery; 5. No history of previous colorectal surgery; 6. No history of previous chemotherapy or radiotherapy; 7. No history of previous biological therapy (such as monoclonal antibodies), immunotherapy \[such as anti-programmed cell death protein 1(PD-1) antibodies, anti-PD-L1 antibodies, anti-PD-L2 antibodies, or anti-Cytotoxic T Lymphocyte-Associated Antigen-4(CTLA-4)\], or other investigational drug therapy; 8. No history of previous hormonal therapy: no restrictions; 9. Signed informed consent form. Exclusion Criteria: 1. Patients requiring antiarrhythmic therapy (excluding β-blockers or digoxin), symptomatic coronary artery disease, recent myocardial infarction within the past 6 months, or congestive heart failure exceeding New York Heart Association(NYHA) class II; 2. Poorly controlled severe hypertension; 3. History of HIV infection or active chronic hepatitis B or C (high viral DNA load); 4. Active pulmonary tuberculosis (TB) or receiving anti-TB treatment, or having received anti-TB treatment within the past year; 5. Other active clinically severe infections ; 6. Evidence of distant metastases outside the pelvis preoperatively; 7. Cachexia, organ decompensation; 8. History of pelvic or abdominal radiotherapy; 9. Multifocal colorectal cancer; 10. Patients requiring management for epileptic seizures (e.g., with steroids or antiepileptic therapy); 11. History of other malignant tumors within the past 5 years, excluding cured carcinoma in situ of the cervix or basal cell carcinoma of the skin; 12. Substance abuse or medical, psychological, or social conditions that may interfere with patient participation in the study or assessment of study results; 13. Presence of any active autoimmune disease or history of autoimmune disease (including but not limited to: interstitial pneumonia, uveitis, enteritis, hepatitis, pituitary inflammation, nephritis, hyperthyroidism, hypothyroidism; patients with vitiligo or childhood asthma that has completely resolved and does not require any intervention in adulthood may be included; patients with asthma requiring bronchodilators for medical intervention cannot be included); 14. Vaccination with any anti-infective vaccine (e.g., influenza vaccine, varicella vaccine, etc.) within 4 weeks before enrollment; 15. Complications requiring long-term use of immunosuppressive drugs or systemic or local administration of corticosteroids with immunosuppressive effects (dose \> 10mg/day of prednisone or equivalent corticosteroids); 16. Known or suspected allergy to the investigational drug or any medication administered related to this trial; 17. Any unstable condition or situation that may jeopardize patient safety and compliance; 18. Pregnancy or lactation in women of childbearing potential who have not taken adequate contraceptive measures; 19. Refusal to sign the informed consent form.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Locally advanced rectal adenocarcinoma are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
The Sixth Affiliated Hospital, Sun Yatsen University
RECRUITINGGuangzhou, Guangdong, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can immunotherapy plus chemo melt colorectal tumors before surgery?
- Can drug cocktail spare rectal cancer patients from surgery?
- Can two immunotherapy drugs help rectal cancer patients skip pelvic radiation?
- Can a Butter-Derived supplement protect the gut during cancer radiation?
- Can an immunotherapy cocktail make rectal tumors disappear before surgery?
- MRI and microbes: a new way to predict rectal cancer outcomes?