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TerminatedNCT02052921Updated May 11, 2020

Observation Versus Surgical Resection in Patients With Rectal Cancer Who Achieved Complete Clinical Response After Neoadjuvant Chemoradiotherapy

An interventional study of Rectal resection and Observation in Rectal Cancer, sponsored by Instituto do Cancer do Estado de São Paulo. Terminated at 1 site in Brazil. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2020-05-11.

Sponsored by Instituto do Cancer do Estado de São Paulo · Not applicable, Interventional, and Treatment

Why this study was terminated
During the execution time foreseen in the project, the expected number of patients was not reached.

From the registry’s dates

  • Registered 2 years 2 months after the study started (first participant enrolled Nov 2011, registered Jan 2014).
Phase
Not applicable
Study type
Interventional
Enrollment
13
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
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Study summary

With the possibility of pathological complete response in surgical specimens, some authors have proposed non-operative management of the patient group, when re-staged after neoadjuvant treatment, have complete clinical response. So far, this approach remains discussed in the literature, and there are still many uncertainties that patients with clinical complete response after chemoradiotherapy in fact no detectable viable tumor and may be omitted of radical surgical treatment. It is a still investigational approach and actually gained space even for patients with very high or who refuse surgery after all clarifications surgical risk.

Hypothesis: The preservation of the rectum in patients with adenocarcinoma of the middle and distal rectum (up to 10 cm) reaching clinical complete response after neoadjuvant chemoradiotherapy have similar rate of the rectal cancer recurrence than patients who underwent surgical rectal resection.

This will be a prospective, randomized, open label phase II of surgical resection versus conservative treatment (observation) in patients with mid and distal rectal cancer who achieved complete after neoadjuvant chemoradiotherapy combined with clinical response.

The main objective of this study is to assess whether conservative approach is similar to rectosigmoidectomy with complete mesorectal excision or amputation abdminoperineal the rectum in patients with complete clinical response after neoadjuvant therapy combined chemoradiotherapy.

Patient Selection: To be eligible patients who have neoadjuvant prior histologic diagnosis of rectal adenocarcinoma, tumors located within 10 cm from the anal verge, a complete clinical response after treatment with chemoradiotherapy for rectal tumors staged clinical and radiological T3-4 N0 M0 or T (any) N + M0, absence of colorectal synchronous tumors.

Treatment: Eligible patients will be randomized 1:1 to resection of the rectum or notice. The period for randomization of patients will be 12 weeks after the last dose of radiotherapy / chemotherapy, so that we can properly assess the antitumor response as described above. After randomization, patients in the surgical group will undergo resection of the rectum with complete excision of mesorectal within 2 weeks after randomization.

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Conditions studied

  • Rectal Cancer

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Keywords

  • Observation
  • Rectal Resection
  • complete clinical response
  • neoadjuvant chemoradiotherapy.
03

In context

Rectal Neoplasms

1,762 studies on the registry are indexed under Rectal Neoplasms; 518 are open to participants now.

This study's enrollment of 13 is below the median of 65 across 1,298 interventional studies indexed under Rectal Neoplasms.

Browse Rectal Neoplasms studies →

Lead sponsor

Instituto do Cancer do Estado de São Paulo is the lead sponsor of 90 studies on the registry; 23 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Histological diagnosis of rectal adenocarcinoma
  • tumors located within 10 cm from the anal verge by rigid proctoscopy measurement
  • Complete clinical response after neoadjuvant treatment with chemoradiotherapy for rectal tumors clinical and radiologically staged as T3-4 N0 M0 or T (any) N + M0
  • Absence of colorectal synchronous tumors
  • Age between 18 and 75 years
  • ECOG performance scale ≤ 2,
  • last dose of chemotherapy / radiation therapy in up to 12 weeks
  • Good organic function
  • Absence of serious comorbidities defined by the doctor to prevent surgical resection of the rectum and / or neoadjuvant therapy.

Exclusion criteria

Exclusion Criteria:

  • Comorbidities clinically significant where surgical resection and / or neoadjuvant therapy is impossible, according to medical assessment.
  • Prior antineoplastic therapy different from neoadjuvant therapy.
  • History of Crohn's disease or ulcerative colitis.
  • Confirmation or strongly suspected inherited polyp syndrome.
  • Pregnant women or during lactation (women of childbearing age should have a negative pregnancy test).
  • Concurrent participation in another research protocol involving therapeutic intervention.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
13 participants (actual)

Study arms

  • Active comparator
    Rectal resection

    Surgical rectal resection

    Procedure: Rectal resection

  • Experimental
    Observation

    Conservative approach

    Other: Observation

Interventions

  • ProcedureRectal resection

    Surgical rectal resection

  • OtherObservation
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What researchers measure

Primary outcomes

  1. Disease-free survival (DFS)

    Time frame: 3 years

Secondary outcomes

  1. Operative complication rate

    Time frame: 30 days

Other outcomes

  1. Presence of viable tumor in the surgical specimen

    Time frame: 3 years

  2. Pattern of recurrence

    Time frame: 3 years

  3. Overall survival (OS)

    Time frame: 5 years

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Study locations

1 site
  • Instituto Do Câncer Do Estado de São Paulo
    Sao Paulo, 01246-000, Brazil
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 11, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02052921
Lead sponsor
Instituto do Cancer do Estado de São Paulo
Responsible party
Sponsor
First posted
Feb 3, 2014
Start date
Nov 2011
Primary completion
Dec 2016
Completion
Apr 23, 2020
Last update
May 11, 2020

Study contacts

Ivan Cecconello, MD
principal investigator · Faculdade de Medicina da USP
Ulysses Ribeiro, MD
study director · Instituto do Câncer do Estado de São Paulo

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is terminated, as verified in May 2020. You cannot join it, but the record below documents what was studied.

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