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Prospective Study of Short Course Radiation Therapy Followed by Neoadjuvant Chemotherapy and Surgery in Locally Advanced Rectal Cancer

N

National Cancer Institute, Egypt

Status and phase

Completed
Phase 2

Conditions

Locally Advanced Rectal Carcinoma

Treatments

Radiation: short course radiation therapy followed by 6 cycles of CAPOX then surgery

Study type

Interventional

Funder types

Other

Identifiers

NCT05622357
201617097

Details and patient eligibility

About

The goal of this clinical trial is to investigate total neoadjuvant therapy (TNT) using short course radiation therapy (SCRT) followed by full course of chemotherapy then surgery in locally advanced rectal cancer. The main questions it aims to answer are:

  • Is total neoadjuvant treatment in this design safe & tolerable?
  • Impact of this design on treatment related outcomes in terms of pathological and clinical responses.

Full description

Patients will be assigned to an experimental arm in which preoperative short course 5 x 5 Gy radiation therapy is followed by six cycles of combination chemotherapy (capecitabine and oxaliplatin) and surgery within 4-6 weeks

Enrollment

51 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Histopathological proof of rectal adenocarcinoma.
  • Tumors located within 15 cm and not less than 4 cm from anal verge.
  • Age: ≥ 18 years.
  • Locally advanced resectable rectal cancer (cT3/4 N0- Any T N+ve).
  • ECOG Performance Status: 0-2.

Exclusion criteria

  • Non-epithelial rectal malignancy such as sarcoma or lymphoma.
  • Unresectable tumors in which surgery will never be possible even if substantial tumor downsizing is seen.
  • Recurrent rectal cancer.
  • Previous history of malignancy within the last 5 years.
  • Previous pelvic irradiation.
  • Psychiatric or addictive disorder that would preclude study therapy.
  • Concurrent uncontrolled medical conditions.
  • Pregnancy or breast feeding.
  • Any contraindication to surgery.
  • Extensive peripheral neuropathy.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

51 participants in 1 patient group

Short course RT followed by full course of chemotherapy then surgery
Experimental group
Description:
Short course radiation therapy ( 25 Gy/ 5 fractions/ 1 week) , followed by 6 cycles of chemotherapy CAPOX, followed 4-6 weeks by surgery.
Treatment:
Radiation: short course radiation therapy followed by 6 cycles of CAPOX then surgery

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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