Status:

UNKNOWN

Neoadjuvant Chemotherapy in Patients With Moderate Risk Mid Rectal Cancer

Lead Sponsor:

Blokhin's Russian Cancer Research Center

Conditions:

Rectal Neoplasms Malignant

Rectum Carcinoma

Eligibility:

All Genders

18-75 years

Phase:

PHASE3

Brief Summary

The purpose of this study is to determine whether 3 months of neoadjuvant CapOx is non-inferior to neoadjuvant radiotherapy in patients with moderate risk CRM"-" mid rectal cancer.

Detailed Description

This trial aims to investigate the efficacy of neoadjuvant chemotherapy compared to 5x5 Gy neoadjuvant radiotherapy in moderate risk CRM-negative rectal cancer patients. This is a prospective multicen...

Eligibility Criteria

Inclusion

  • Informed consent
  • Histologically verified colon rectal adenocarcinoma
  • сT3c-T3dN0-1M0, cT1-T3dN2M0. cancer of the middle rectum (based on pelvic MRI)
  • Tumor more than 2 mm from mesorectal fascia (based on pelvic MRI)
  • Eastern Cooperative Oncology Group (ECOG) status 0-2
  • Haemoglobin (HGB) \> 90 g/L
  • Platelet Count (PLT) \> 120x10\*9/L
  • Serum creatinine \< 150 µmol/L
  • Total bilirubin \< 25 µmol/L

Exclusion

  • inability to obtain informed consent
  • distant metastases
  • synchronous or metachronous tumors
  • previous chemotherapy or radiotherapy
  • clinically significant cardiovascular disorders (myocardial infarction \< 6 months before visit, stroke \< \< 6 months before visit, instable angina \< 3 months before visit, arrhythmia, uncontrolled hypertension \> 160/100 mm hg
  • clinically significant neurological disorders
  • previous neuropathy 2 or higher
  • current infection or heavy systemic disease
  • pregnancy, breastfeeding
  • ulcerative colitis
  • individual intolerance to treatment components
  • proven dihydropyrimidine dehydrogenase (DPD) deficiency
  • participation in other clinical trials
  • psychiatric disorders, which render patient unable to follow instructions or understand his/her condition
  • technical inability to perform pelvic MRI
  • inability of long-term followup of the patient
  • HIV

Key Trial Info

Start Date :

October 14 2019

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

October 1 2024

Estimated Enrollment :

316 Patients enrolled

Trial Details

Trial ID

NCT04134897

Start Date

October 14 2019

End Date

October 1 2024

Last Update

February 9 2021

Active Locations (1)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (1 locations)

1

N.N.Blokhin Russian Cancer Research Center

Moscow, Russia, 115478