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NCT Number: NCT04916054

Time to Surgery and Survival Outcomes for Patients With Resected Colorectal Carcinoma: Multicenter Study (BIG RENAPE)

Colorectal cancer (CRC) is diagnosed in one million patients each year worldwide and is the 2nd leading cause of cancer death. Peritoneal metastasis (MP) is seen in 10% of CRC patients and is the metastatic site with the worst prognosis.

Complete cytoreduction surgery (CCS) is the only treatment that allows for prolonged survivals. Five-year overall survival (OS) after CCS ranges from 30% to 60% compared with 0 to 5% with exclusive medical treatment.

Chemotherapy (CT) with fluoropyrimidine and oxaliplatin and/or irinotecan 3 months pre-operatively and 3 months adjuvant is widely used. The benefits of perioperative CT have been demonstrated in another resectable metastatic site, the liver and has become by extension a therapeutic standard in France for CRC MPs. However, the impact of delay in the initiation of surgery and adjuvant or neoadjuvant CT is unknown for CRC MPs.

Several deleterious oncologic effects are related to a long period without treatment between

* Neoadjuvant chemotherapy and surgery: * Surgery and adjuvant chemotherapy.

Several meta-analyses have demonstrated, for at least 13 different cancers, a continuous association between delays in treatment (CT, radiotherapy, or surgery) and cancer mortality. For CRC, Hanna's meta-analysis showed that for every 4-week delay in adjuvant surgery or CT, the risk of cancer death increased by 6 and 13%, respectively.

These long delays between CT and excisional surgery also decrease survival in patients with liver metastases from colorectal origins and MPs from ovarian origins but this has never been evaluated in patients with MPs from colorectal origins.

Demonstrating an oncologic impact of therapeutic delays would have several strategic practical impacts such as:

* Promoting pre- and post-operative rehabilitation programs to facilitate recovery and reduce time to retreatment. * To use more easily techniques (protective stoma, multi-stage surgery) limiting the risk of complications and therefore the delays in treatment. * Propose clinical research protocols aimed at reducing these delays with knowledge of plausible statistical hypotheses.

A therapeutic strategy of shortening the time between each treatment therefore deserves to be evaluated in metastatic forms of colorectal cancer.

The investigators would like to evaluate the hypothesis that shortened time between treatments could have a prognostic impact on recurrence-free survival.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CHU LYON, Lyon, France

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About this study

This is a retrospective study including exhaustively all patients operated CC0-CC1 of peritoneal carcinosis between 2007 and 2019 meeting the inclusion criteria:

  • Patients from the Institut de cancérologie de l'Ouest and the CHU of Lyon for the study period 2007-2016
  • Patients included in the BIG-RENAPE network between 2016 and 2019

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age >18 years
  • Histological evidence of peritoneal metastases
  • Primary colorectal cancer
  • Surgical cytoreduction CC0 or CC1

Exclusion criteria

  • Patient who has not received at least 3 courses of pre and/or post cytoreduction chemotherapy
  • Primitive appendicitis
  • Unknown primitive
  • Patient with incomplete CC2 and/or palliative surgery
  • Patient opposed to the use of their data for research.
  • Isolated local pelvic recurrence.
  • Extraperitoneal metastases not resected or destroyed before or during cytoreduction.
  • Patient opposed to the use of his/her data for research purposes

Treatment and study plan

Primary outcomes

  1. to determine whether the time between each anti-tumor therapy has a prognostic impact on recurrence-free survival

    Time frame: 2 years

    recurrence-free survival

Secondary outcomes

  1. To evaluate the impact on overall survival

    Time frame: 2 years

    overall survival

Sponsors and collaborators

Lead sponsor

Institut Cancerologie de l'Ouest

Other

Collaborators

  • Hospices Civils de Lyon

Registry information

Acronym: DELARC

Important dates

Study start
2021
Primary completion
2021
Study completion
2022
First posted
Jun 7, 2021
Registry last updated
Feb 13, 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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