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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03431428
Other study ID # 20171112
Secondary ID
Status Recruiting
Phase Phase 3
First received January 13, 2018
Last updated February 10, 2018
Start date January 1, 2018
Est. completion date December 31, 2022

Study information

Verified date December 2017
Source Liaoning Tumor Hospital & Institute
Contact rui zhang, doctor
Phone 8613898872185
Email zzzrrr1234@sina.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is evaluate the effect of two different surgical treatment on lower rectal cancer after almost clinical complete response(almost-cCR). All almost clinical complete response(almost-cCRs) were entered into two groups randomly. The estimated sample size of the minimal operation group was 221, and 221 in the Mile's group. Three years' progression-free survival(PFS) and overall survival(OS) were compared.


Description:

Patients with low rectal cancer were treated with neoadjuvant radiotherapy, and two cycles of XELOX at the interval. All almost-cCRs after neoadjuvant treatment were randomly divided into minimal operation group or Mile's group. All cCRs were treated with "watch and wait". Patients after local recurrence were randomly divided into minimal operation group or Mile's group. If pathological result was pathological staging 3 after neoadjuvant therapy(ypT3) in minimal operation group or local postoperative recurrence occurred, patients need supplement of abdominoperineal resection (APR). With 3 years follow-up,the main research goals are 3 years of progression-free survival(PFS) and overall survival(OS). Secondary endpoints are side effects of chemotherapy, assessment of quality of life, surgical complications, adverse prognostic factors and so on.


Recruitment information / eligibility

Status Recruiting
Enrollment 477
Est. completion date December 31, 2022
Est. primary completion date January 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

1. Histology is confirmed as rectal adenocarcinoma.

2. 18 to 75 years old.

3. Preoperative staging is lower than clinical stage primary tumor grade 3, regional lymph node grade 1, and metastasis was grade 0(cT3cN1M0).

4. The anus couldn't be retained after TME.

5. Almost-cCR or cCR recurrence during observation.

Exclusion Criteria:

1. Patients were unable to tolerate the operation.

2. Preoperative stage: T4b or progress during the treatment.

3. HIV infection stage or chronic hepatitis B.

4. Active clinical severe infections.

5. Evil liquid state or decompensation of organ function.

6. Other malignant tumor history in five years.

7. Other primary carcinoma.

8. Unstable condition and incompliance of the patient

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
transanal surgery
Transanal surgery could Preserve anus to reduce trauma and improve the quality of life
Miles surgery
Miles surgery cut off the anus, enlarge the trauma and reduce the quality of life.
Drug:
Preoperative chemoradiotherapy
After preoperative radiochemotherapy, two cycles of XELOX were given at the interval of waiting operation.

Locations

Country Name City State
China Liaoning cancer Hospital Shenyang Liaoning

Sponsors (1)

Lead Sponsor Collaborator
Zhang Rui

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary PFS The progression-free survival of 3 years three years
Primary OS 3 years of overall survival time three years
Secondary carcinoembryonic antigen(CEA) The level of carcinoembryonic antigen in blood every 3 months,for 2 years
Secondary carbohydrate antigen 19-9(CA-199) The level of carbohydrate antigen 19-9 in blood every 3 months,for 2 years
Secondary International Index of Erectile Function-15 Describe the function of Erectile ,only for male patients every 3 months ,for 2 years
Secondary International prostate symptom score Describe the function of prostate,only for male patients every 3 months ,for 2 years
Secondary Female sexual function index Describe the function of sexual for female patients every 3 months,for 2 years
Secondary Wexner incontinence score Describe the degree of Anus incontinence every 3 months,for 2 years
Secondary QOL Describe the quality of life for tumor patients every 3 months,for 2 years
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