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Effects of COVID-19 Pandemic on the Outcomes of Colorectal Cancer

Effects of the COVID-19 Pandemic on the Diagnosis, Treatment and Outcomes of Patients Affected by Colorectal Cancer Requiring Surgery: Results From a National Multicentre Cohort Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04712292
Acronym
COVID-CRC
Enrollment
15000
Registered
2021-01-15
Start date
2020-09-08
Completion date
2022-04-01
Last updated
2022-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Neoplasms Malignant

Keywords

colorectal cancer, diagnosis, screening, COVID-19, surgery, outcomes

Brief summary

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has been identified as the cause of the Coronavirus disease 19 (COVID-19), which was initially reported in December 2019 in China and has since rapidly spread worldwide. Since then, the COVID-19 pandemic has caused a detrimental effect of the national health care system, causing a drastic reduction of the screening programs for colorectal cancer and requiring the redistribution of the hospital resources from elective surgery to the care of patients with SARS-Cov\_2 infection requiring admission.

Detailed description

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has been identified as the cause of the Coronavirus disease 19 (COVID-19), which was initially reported in December 2019 in China and has since rapidly spread worldwide. Italy witnessed a rapid and uncontrolled spread of the infection after March 2020, and a worrisome increasing number of related deaths. The need for increased capacity for COVID-19 patients required elective activities to be drastically reduced or canceled. The unprecedented stress on the healthcare system has caused the reduction of the elective surgery and the cancer screening programs during the last 2 years. Studies predicting harmful impact of the COVID-19 pandemic on cancer care have been already published. However, it has not been proved whether the potential delay of screening, diagnosis and treatment could have a measurable effect on patients undergoing surgery for colorectal cancer in the COVID-19 era. The aim of the study is therefore to compare the 30-day perioperative and oncologic outcomes between patients undergoing surgery for cancer of the colon and rectum between January 2020 and December 2021 (study group) and those who had surgery for colorectal cancer between January 2018 and December 2019 (Control Group), in order to identify: * any change in the distribution of the histological stage (primary aim) * any change in the rate of palliative surgery (primary aim) * any change in the rate of non-radical surgery (R1 or R2 resection) ( primary aim) * any change in the rate of 30-day postoperative complications (secondary outcome) Anonimyzed data will be retrospectively collected on a RedCap platform hosted on the servers of the Alma Mater Studiorum University of Bologna. The variables included demographic characteristics, comorbidities, details of the disease at the diagnosis, details of the neoadjuvant therapy, perioperative variables and 30-day postoperative follow-up variables.

Interventions

PROCEDURESurgical procedure for confirmed or suspected colorectal cancer

Surgical procedure for cancer may include: * any radical surgery (right or left hemicolectomy, rectal resection, abdomino-perineal resection, total colectomy, proctocolectomy, and others depending on the tumor site and other tumor characteristics), * surgery for radicalization of cancer polyps previously removed endoscopically * surgery for excision of large polyps which are not removable endoscopically * staging surgery (laparoscopy or laparotomy), in case of advanced-non operable cancer * palliative surgery (defined as any surgery with no curative intent)

Sponsors

University of Bologna
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Any patient undergoing radical surgery for histologically confirmed diagnosis of cancer located in the colon, the rectum or the anus; or * any patient undergoing surgery with oncologic intents, for instance: radicalization of endoscopically removed cancerous polyp; radical surgery to remove large, at-risk polyp which are not removable by endoscopy; or * any patient undergoing planned or unpredicted palliative surgery for a primary cancer localized in the colon, rectum or anus; or * any patient undergoing a staging procedure (i.e. staging laparoscopy, surgical exploration), which did not result in any radical surgery due to advanced disease, metastasis, etc. and * age \> 18 years * elective or urgent surgery

Exclusion criteria

* Colorectal cancer recurring after previous surgery; * Cancer originating from other organs than the colon, the rectum and the anus; * Lack of significant histological details (expect when the cancer was not removed) * lack of 30-day follow-up

Design outcomes

Primary

MeasureTime frameDescription
Oncologic stage30 days from the surgeryThe stage will be reported at the histological examination according to TNM classification
Palliative surgeryat time 0 (surgery)Rate of palliative surgery (defined as any procedure which did not have the aim of radically removing the primary cancer, either planned preoperatively in order to reduce the symptoms, or which became necessary during surgery due to unexpected findings
Rate of radical surgery30 days from surgerySurgery is defined radical according to the absence of cancer (R0) at the surgical margins on the histological specimen

Secondary

MeasureTime frameDescription
Lung metastasesAt the preoperative staging or at surgery (time 0)Rate of single/multiple lung metastases
Associated symptomsBefore surgeryRate of patients who had a diagnosis of cancer without any associated symptoms - as sign of effectiveness of the screening
Aggressive cancer biology30 days from the surgeryBiology was considered aggressive if any of the following characteristics were found at the histological examination: signet ring cells, mucinous tumor, tumor budding, lymphovascular invasion, perineurial invasion, lymphangitis.
Postoperative complications30 days from surgeryRate of 30-day complications graded according to the Clavien-Dindo Classification
Mortality30 days from surgeryRate of 30-day deaths
Emergency surgerysurgery (time 0)rate of operations requiring surgery within 48 hours from the unpredicted admission to hospital
Rate of clinical T4 cancer at the preoperative stagingAt time 0 (surgery)Clinical T4 cancer are defined as those with high suspicious of local invasion of adjacent organs or structures, not necessary confirmed as T4 at the histological examination
Liver metastasesAt the preoperative staging or at surgery (time 0)Rate of single/multiple liver metastases

Countries

Italy

Contacts

Primary ContactMatteo Rottoli, MD, PhD
matteo.rottoli2@unibo.it+390512145262

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026