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Completed

NCT Number: NCT04864067

No Operation After Short Course Radiotherapy Followed By Consolidation Chemotherapy In Locally Advanced Rectal Cancer

This study is designed to explore the hypothesis that in patients with a Locally advanced rectal cancer (LARC) treated with a Total neoadjuvant therapy (TNT) strategy based on short course radiotherapy (5x5Gy) followed by neoadjuvant consolidation chemotherapy is associated with a higher rate of pathological clinical response and sustained (>1year) complete clinical response when compared to an historical cohort treated with long course chemoradiation therapy (CRT), total mesorectal excision (TME) and adjuvant chemotherapy (ACT).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Complejo Asistencial Doctor Sótero del Rio, Santiago, RM, Chile

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About this study

Non-operative management with a Watch and Wait (W&W) strategy has been advocated for selected patients with a locally advanced rectal cancer (LARC) and a complete clinical response (cCR) after neoajuvant (NA) treatment.

In this context, total neoadjuvant therapy (TNT), i.e the use of radiotherapy and full dose of post-operative chemotherapy as part of NA treatment, has emerged as a strategy to enhance treatment response.

Currently, TNT has reported higher rates of pCR and organ preservation when compared to current standard of care. However, the best TNT strategy is still unknown. We therefore hypothesize that in LARC patients, the use of a TNT strategy based on short course RT followed by consolidation chemotherapy is associated with a higher rate of pCR and sustained (>1year) cCR when compared to an historic cohort.

The main aim of the present proposal is to assess the effects of a standardized TNT model in LARC patients as a strategy for enhanced pCR/sustained cCR. For this purpose, we propose the following experimental model: In primary Aim 1 we will study if the effects of a TNT strategy over patients with a LARC enhance the rate of pCR/sustained cCR by (1) evaluating the compliance and toxicity of a TNT strategy as a proof of concept of its applicability, (2) assessing the rate of cCR at the end of TNT and (3) assessing the rate of pCR in the surgically managed subgroup and sustained cCR (>1year) in the W&W subgroup. Additionally, in primary Aim 2, we will determine if patients with a W&W strategy have better functional outcomes and quality of life (QoL) than patients treated with TME after TNT by (1) using validated questionnaires for the evaluation of bowel, sexual and urinary function for W&W and TME patients and (2) by evaluating the QoL using a widely-used standardized questionnaire.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histologically confirmed diagnosis of adenocarcinoma of the rectum
  • Clinical Stage II (T3-4, N-) or Stage III (any T, N+) based on Magnetic Resonance Imaging (MRI)
  • Tumors < 7cm from anal verge (palpable)
  • No prior history of rectal cancer

Exclusion criteria

  • Patients with tumors >7cm from anal verge
  • ECOG >1,
  • Contraindication for chemotherapy: Hemoglobin <8, White Blood Count <4000, Platelets <100,000, Creatinine Clearance <50ml/min, Total Bilirubin <5mg/dl,
  • Stage IV at diagnosis
  • Coronary artery disease, either no treated or recent acute coronary syndrome in the last 12 months.
  • Congestive heart failure
  • Peripheral neuropathy
  • Previous pelvic radiotherapy
  • Prior rectal cancer treatment
  • Pregnancy or nursery
  • Any contraindications to MRI (e.g. patients with pacemakers)
  • Indication of pelvic exenteration
  • Impossibility to consent.

Treatment and study plan

Oxaliplatin

Drug

Consolidation Chemotherapy

Other names: All Brands

5-Fluoracil

Drug

Consolidation Chemotherapy

Other names: All Brands

Leucovorin

Drug

Consolidation Chemotherapy

Other names: All Brands

Capecitabine

Drug

Consolidation Chemotherapy

Other names: All Brands

5x5 Gy

Radiation

Neoadjuvant Radiotherapy

Quality of life questionnaires

Behavioral

Quality of Life Evaluation (LARS Score, IIEF, FSFI, I-PSS and EORTC QLQ-C30)

DRE/ Endoscopy

Procedure

Flexible Sigmoidoscopy and Digital Rectal Exam

Primary outcomes

  1. Rate of pathological and sustained clinical response

    Time frame: 3 years

    Combined number of patients with pathological response in the surgical specimen and patients in a Watch and Wait protocol with a sustained clinical response longer than a year.

  2. Quality of Life and Funcional Outcomes

    Time frame: 3 years

    Standardized evaluation using validated questionnaires comparing patients undergoing TME versus WW patients in the cohort

Secondary outcomes

  1. Adverse events

    Time frame: 3 years

    Adverse events will be graded using the NCI Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0.

Sponsors and collaborators

Lead sponsor

Servicio de Salud Metropolitano Sur Oriente

Other Gov

Registry information

Official study title

No Operation After Short Course Equivalent Dose (Ht) Radiation Therapy Followed By Consolidation Chemotherapy In Locally Advanced Rectal Cancer: The Prospective, Single Arm NOAHS-ARC Trial

Acronym: NOAHS-ARC

Important dates

Study start
2021
Primary completion
2026
Study completion
2026
First posted
Apr 28, 2021
Registry last updated
May 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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