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NCT Number: NCT04443543

An Adaptive-design Prospective Cohort Study of Watch and Wait Strategy in Patients With Locally Advanced Rectal Cancer

The study is designed to test the hypothesis that the clinical complete response (CCR) rate of patients with locally advanced rectal cancer (LARC) treated with neoadjuvant chemoradiotherapy will increase after an adaptive-design paradigm, as well as the rate of 2-year organ preservation, recurrence, quality of life, DFS and OS.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Fudan University Shanghai Cancer Cencer

Shanghai, Shanghai Municipality, 200032, China

About this study

  • Primary objective:

Evaluate the CCR rate of low rectal cancer using adaptive and optimized chemotherapy and radiotherapy strategies (all population and dMMR/MSI-H subgroup)

  • Secondary objectives:

2.1 Evaluate the 2-year anal preservation rate, recurrence rate, quality of life, DFS and OS 2.2 Explore the subgroup of patients suitable for observation.

  • Outline:

Patients after long-course chemoradiation are grouped based on their MSI-H/dMMR status. For patients with MSI-H/dMMR, consolidation immunotherapy of Tislelizumab (BGB-A317) will be assigned. For patients with MSS/pMMR, consolidation chemotherapy will be given according to their tumor response. After completion of consolidation therapy, those who reach clinical complete response will receive organ preservation (watch and wait) strategy in place of radical surgery. During treatment, once local regrowth occurs or poor tumor response, total mesorectal excision (TME) surgery will be performed.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • pathological confirmed adenocarcinoma
  • clinical stage T2-4 and/or N+, inappropriate for local excision
  • the distance from anal verge less than 5 cm, or considered inappropriate for anal preservation by surgeons.
  • Strong desire to preserve the anus, able to receive close surveillance for at least 2 years after chemoradiotherapy.
  • without distance metastases
  • aged between 18 to 75 years old.
  • performance status score: 0~1
  • UGT1A1*28 6/6 or 6/7
  • sign the inform consent

Exclusion criteria

  • pregnancy or breast-feeding women
  • serious medical illness
  • difficult to achieve complete response assessed by current evidence: the maximal diameter of tumor >10cm; the maximal diameter of lateral lymph node >2cm; baseline CEA>=100; biopsy pathology confirmed signet ring cell carcinoma components; digital rectal examination found that the tumor is peri-narrowed.
  • baseline blood and biochemical indicators do not meet the following criteria: neutrophils≥1.5×10^9/L, Hb≥90g/L, PLT≥100×10^9/L, ALT/AST ≤2.5 ULN, Cr≤ 1 ULN
  • DPD deficiency
  • UGT1A1*28 7/7

Treatment and study plan

Capecitabine (Xeloda) Pharmacogenetic Test Reagents

Drug

CRT: 625mg/m2 bid Monday-Friday per week XELIRI: 1000mg/m2 bid d1-14

Irinotecan

Drug

CRT:80mg/m2 (UGT1A1*28 6/6) or 65mg/m2 (UGT1A1*28 6/7) XELIRI: 200mg/m2 bid d1 FOLFIRINOX: 150mg/m2 d1

IMRT

Radiation

Pelvic Radiation: 50Gy/25Fx

Oxaliplatin

Drug

FOLFIRINOX: 85mg/m2 d1

5Fluorouracil

Drug

FOLFIRINOX: 400mg/m2 iv d1bolus, 2400mg/m2 ivgtt 46h

Tislelizumab

Drug

200mg iv

Primary outcomes

  1. clinical complete response rate

    Time frame: two weeks after completion of CRT or consolidation chemotherapy.

    After nCRT, the lesions of rectal completely respond. Tumor residue cannot be found by digital rectal examination, endoscopic biopsy and radiology.

Secondary outcomes

  1. 2y-anal preservation rate

    Time frame: 2 years

    2-year anal preservation rate will be defined as the percentage of patients alive without receiving abdominoperineal resection at 2 years measured from the date of completion of CRT.

  2. 2y-local recurrence rate

    Time frame: 2 years

    2-year local recurrence rate will be defined as the percentage of patients alive developing local recurrence at 2 years measured from the date of completion of CRT.

  3. Impact of participants' quality of life

    Time frame: 2 years

    quality of life is evaluated according to EORTC C-30 questionnare.

  4. overall survival

    Time frame: 3 years

    3-year OS will be defined as the percentage of patients alive at 3 years measured from the date of completion of CRT.

Study contacts

Contact information is provided by the study sponsor or research team.

Ji Zhu

CONTACT

[email protected]

+86-2164175590 ext. 81607

Sponsors and collaborators

Lead sponsor

Fudan University

Other

Registry information

Official study title

Watch and Wait Strategy in Patients With Locally Advanced Rectal Cancer After Neoadjuvant Chemoradiotherapy: A Multi-centre, Adaptive-design, Phase II Prospective Cohort Study

Important dates

Study start
2020
Primary completion
2026
Study completion
2026
First posted
Jun 23, 2020
Registry last updated
Jun 30, 2020

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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