Clinical trial · Interventional
Radical vs Local Excision for Rectal Cancer With Clinically Complete Remission
Comparing the Oncologic Efficacy of Radical Versus Local Excision for Rectal Cancer With Clinically Complete Remission to Neoadjuvant Chemoradiation Therapy: A Randomized Controlled Clinical Trial
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
In the present project, the investigators plan to more accurately select the rectal cancer patients with pathological complete response (pCR) to preoperative concomitant chemoradiation therapy (CCRT), taking advantage of quantification of circulating tumor DNA (ctDNA) in addition to the current available diagnostic modalities, including CT, MRI, PET and colonoscopy. The patients with suspected pCR to CCRT will be randomized to radical surgery and local excision groups, followed by the comparison of the oncologic outcomes between two treatment methods. The investigators hypothesized that if the pCR for patients with rectal cancer after CCRT can be more accurately predicted, such patients can be safely treated with limited surgery to enhance the post-treatment life quality, in comparison with patients undergoing radical surgery.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Rectal Cancer | Malignant Rectal Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Surgery | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Watch and wait group
- description
- In this group, the patients with clinically complete response will undergo non-surgical treatment (watch-and-wait group)
- interventionNames
- Procedure: Surgery
- type
- ACTIVE_COMPARATOR
- label
- Surgical group
- description
- In this group, the patients with clinically complete response will undergo surgical treatment (LAR with anal preservation or APR)
- interventionNames
- Procedure: Surgery
Primary outcomes (1)
- measure
- Overall disease-free survival
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. rectal adenocarcinoma completed nCRT and the imaging studies showed no residual malignancy; 2. physical status is within American Society of Anesthesiology(ASA)class Ⅰ to Ⅲ; 3. the lesion side can be reached by the transanal local excision, generally within 6 cm above anal verge; 4. age is 18-75 years. Exclusion Criteria: 1. Quantification of ct DNA shows residual malignancy; 2. Body mass index(BMI)\>40 kg/m2; 3. Previous abdominal or pelvic surgery; 4. abnormal hepatologic (Bil\>2.0 mg/dl), renal (Cre≧2.0) and hematologic(WBC\<3000, HB\<8.0, platelet\<50000) profiles after CCRT.
References
Publications (0)
Data not yet available