A Phase III Trial of Anus-preservation in Low Rectal Adenocarcinoma Based on MMR/MSI Status

Radiation Clinical Trial

Official title:

A Randomized, Controlled, Open-label, Multicenter, Phase III Trial of Anus-preservation in Low Rectal Adenocarcinoma Based on MMR/MSI Status(APRAM)

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05669092
• Other study ID #: CARTOnG 2201
• Status: Recruiting
• Phase: Phase 3
• Start date: November 1, 2022
• Est. completion date: December 31, 2025

Study information

• Verified date: December 2022
• Source: Zhejiang Cancer Hospital
• Contact: JI ZHU
• Phone: 13501978674
• Email: zhuji[@]zjcc.org.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

pMMR/MSS and 32 dMMR/MSI-H patientspatients were planned to be enrolled. Patients with dMMR/MSI-H will be randomly assigned to the immunotherapy arm or short-course radiotherapy sequential immunotherapy arm; pMMR/MSS patients will receive capecitabine-irinotecan based concurrent radiotherapy before being randomly assigned to the XELIRI or FOLFRINOX arm. The rate of complete response (sustained cCR for ≥ 1 year), long-term prognosis and adverse effects will be analyzed.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 174
• Est. completion date: December 31, 2025
• Est. primary completion date: December 31, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. pathological confirmed adenocarcinoma;

2. clinical stage T2-4 and/or N+,Not suitable for initial local excision to achieve radical treatment;

3. the distance from anal verge less than = 5cm,or surgical evaluation concludes that direct surgical anal preservation is not possible without distance metastases;

4. age 18-70 years old, female and male;

5. Strong desire for anal preservation and ability to be closely monitored for at least 2 years after chemoradiotherapywith good compliance;

6. without distant metastases;

7. ECOG Performance status 0-1;

8. Detection of UGT1A1*6 and *28 gene status (for pMMR patients);

9. Sufficient bone marrow reserve and physical capacity to receive consolidation chemotherapy after chemoradiotherapy (for pMMR patients);

10. with good compliance;

11. signed the inform consen.

Exclusion Criteria:

1. pregnant or breastfeeding women;

2. Persons with a history of uncontrolled epilepsy, central nervous system disorders, or psychiatric disorders whose clinical severity, as judged by the investigator, may prevent the signing of informed consent or affect the patient's compliance with oral medications;

3. Difficult to achieve complete remission at the available level of evidence, such as:

tumor largest diameter >10 cm; largest diameter of lateral lymph nodes >2 cm; baseline CEA >= 100; biopsy pathology with an indolent cell carcinoma component; tumor of circumferential narrowing type on anal finger examination, with inclusion decided by the judgment of the evaluation team if necessary;

4. Clinically significant (i.e., active) heart disease, such as symptomatic coronary artery disease, New York Heart Association (NYHA) class II or worse congestive heart failure or severe arrhythmias requiring pharmacological intervention, or a history of myocardial infarction within the last 12 months;

5. persons requiring immunosuppressive therapy for organ transplantation;

6. Persons with severe uncontrolled recurrent infections, or other severe uncontrolled concomitant diseases;

7. Subjects with baseline routine blood and biochemical indicators do not meet the following criteria: hemoglobin = 90g/L; absolute neutrophil count (ANC) = 1.5×109/L; platelets = 100×109/L; ALT, AST = 2.5 times the upper limit of normal; ALP = 2.5 times the upper limit of normal; serum total bilirubin < 1.5 times the upper limit of normal; serum creatinine < 1 times the upper limit of normal limit; serum albumin =30g/L;

8. Known to have dihydropyrimidine dehydrogenase (DPD) deficiency;

9. allergic to any investigational drug component.

Related Conditions & MeSH terms

• Adenocarcinoma
• Radiation
• Toripalimab

Intervention

Drug:
• Toripalimab
3mg/Kg iv d1q2w

Radiation:
• CRT
IMRT 50Gy/25fx 625mg/m2 bid d1-5 qw Irinotecan:1?Full wild (GG+6/6): 80mg/m2/week for 5 times 2?Single site mutation (GG+6/7 or GA+6/6): 65mg/m2/week for 5 times 3?Double locus mutation (GG+7/7 or AA+6/6 or GA+6/7): 50mg/m2/week for the 1st, 2nd, 4th and 5th week for 4 times
• SCRT
25Gy/5fx

Drug:
• XELIRI
Capecitabine: 1000mg/m2 bid d1-14 Irinotecan: 200mg/m2 ivgtt d1 q3w
• FOLFRINOX
Irinotecan: 150mg/m2 ivgtt d1 (double locus mutation downregulated to 120mg/m2) Oxaliplatin: 85mg/m2 ivgtt d1 5-FU: 2400mg/m2 ivgtt 46h q2w

Locations

Country	Name	City	State
China	Zhengjiang Cancer Hospital	Hangzhou	Zhejiang

Sponsors (1)

Lead Sponsor	Collaborator
Zhejiang Cancer Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	complete response (CR) rate.	cCR = 1 year.	The status of cCR will be evaluated after the completion of neoadjuvant therapy.
Secondary	adverse effects rate.	CTC 4.0 standard.	From date of randomization until the date of death from any cause, assessed up to 5 years ] Rate of chemotherapy, radiotherapy and immunotherapy related adverse events.
Secondary	QoL	Quality of life will be evaluated using EORTC QLQ-C30 score	From date of randomization until the date of death from any cause, assessed up to 10 years
Secondary	3 year local recurrence free survival rate	Rate of 3 year local recurrence free survival	From date of randomization until the date of first documented pelvic failure, assessed up to 36 months. ]
Secondary	3 year disease free survival rate	Rate of 3 year disease free survival	From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 36 months. ]
Secondary	3 year overall survival rate	Rate of 3 year overall survival	From date of randomization until the date of death from any cause, assessed up to 36 months.
Secondary	Organ preservation	TME-free survival	From date of randomization until the date of surgery