Rectal CancerBARONCT04947020
DataBase for Analysis of Rectal Cancer Oncological Results
An observational study of Rectal Cancer and Metformin, run by Jagiellonian University at 1 site in Poland.
Trial summary
The data will be obtained from 10 tertiary centers located in Poland (Cracow - coordinating center, Warsaw - 3 centers, Sosnowiec, Szczecin, Bydgoszcz, Lublin, Gdansk, Poznan) and 5 foreign centers. The analyses will include patients with rectal cancer operated on between 2013-2019. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Rectal Cancer, Metformin, Overall Survival
- What is being tested?
- Metformin
- How many people
- 2,443 participants
- Where
- 1 sitePoland
- Study dates
- 1 Aug 2021to 31 Dec 2024
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Adult patients with primary rectal cancer operated on between 2013 and 2019.
Who may be able to join
- Primary rectal cancer confirmed histologically
- Age ≥ 18
Who cannot join
- Recurrent rectal cancer
- Oncological radicalization after previous local excision of rectal cancer
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Multicenter Retrospective Trial for Analysis of Oncological Results of Patients with Primary Rectal Cancer Operated on Between 2013-2019
The data will be obtained from 10 tertiary centers located in Poland (Cracow - coordinating center, Warsaw - 3 centers, Sosnowiec, Szczecin, Bydgoszcz, Lublin, Gdansk, Poznan) and 5 foreign centers.
The analyses will include patients with rectal cancer operated on between 2013-2019. A database in MS Excel is prepared that consists of following data:
Read more
- Type of neoadjuvant treatment (if any)
- Time-interval between the end of neoadjuvant treatment and surgery
- Type of surgery
- Staging of rectal cancer i.e. (y)pTNM
- Number of retrieved lymph nodes
- Number of lymph nodes with metastases
- R classification (R0, R1, R2)
- Preoperative medications (metformin, statins, NSAIDs, anticoagulants)
- Recurrence date and type (local, systemic, both diagnosed at the same time)
- Date of death or date of last follow-up visit
The aims of the study are following:
- Establishing whether neoadjuvant treatment (PSCR or chemoradiotherapy) influences number of retrieved lymph nodes in rectal cancer
- Establishing whether time-interval between the end of PSCR and surgery influences lymph node yield
- Establishing the prognostic value of lymph node ratio - validation of the previously calculated cutoff point at the level of 0.41
- Determining independent prognostic factors in rectal cancer - in particular related to medications taken before the operation, metformin and anti diabetic drugs in the first place
Read the detailed description
Previously published studies showed that preoperative treatment of rectal cancer is associated with a lower number of lymph nodes retrieved during resection that is often lower than the recommended number of 12 nodes necessary for proper establishing of ypN category. A few studies revealed that lymph node ratio (LNR) is a more precise prognostic factor than pN category. The analysis conducted at the 1st Department of Surgery (Jagiellonian University, Cracow, Poland) based on patients' data from 1999 - 2006 year indicated that the median number of harvested lymph nodes after preoperative short course radiotherapy 5x5 Gy (PSCR) was 16. Therefore, PSCR did not seem to influence the number of lymph nodes in the operative specimen. Time-interval between radiotherapy and surgery (7-10 days versus 4-5 weeks) was not associated with lymph node yield, either.
Medication taken by the patients before operation may influence the treatment results as well. In a couple of studies metformin was identified as inhibitor of carcinogenesis according to antiangiogenic and antimetabolic effects and as a potential radiosensitizer. The anticancer property of metformin is largely attributed to its capability in modulating signaling pathways involved in cellular proliferation, apoptosis, and metabolism. In the last decade, mounting evidence supports the use of metformin in the prevention and treatment of colorectal cancer. Moreover, the use of metformin as monotherapy or as an adjuvant in colorectal cancer patients has led to further dose reduction and increased radio-chemosensitivity which lead to minimal gastrointestinal side effects and reduced toxicity. The use of metformin was associated with improved survival among colorectal cancer patients with type 2 diabetes mellitus compared to sulfonylureas and insulin. The effect of metformin in nondiabetic patients has not been evaluated so far. Based on the aforementioned results, it seems well-grounded to establish the influence of other medications (statins, nonsteroidal anti-inflammatory drugs, anticoagulants) on the results of combined treatment of rectal cancer with the assessment whether they are independent prognostic factors in comparison with such parameters as (y)pT, (y)pN or LNR.
After study initiation, a template of MS Excel database with manual will be sent to the Principal Investigators in every participating center. After obtaining the filled sheets from all participating centers, a central database will be prepared. No personal data of the patients (name, surname, personal ID numbers) will be collected and data in the central database will be anonymized.
Number of harvested lymph nodes will be compared in patients who underwent neoadjuvant chemoradiotherapy, PSCR, or surgery alone. In addition, number of retrieved lymph nodes and lymph node ratio will be compared in patients operated on after different time-intervals between PSCR and surgery (< 7 days and > 4 weeks). Kaplan-Meier curves will be drawn to established influence of number and ratio of harvested lymph nodes on overall survival and disease-free survival. Local and systemic recurrence rate will be established and compared in analysed patients. Statistical analysis will be performed with SPSS 27 for Mac. Variables without normal distribution will be compared by means of Mann Whitney U and Chi-square tests. Cumulative proportions of surviving will be compared with the use of log-rank test. Univariate and multivariate Cox regression will be performed to establish prognostic factors in analysed population.
The study is academic and non-commercial. The participating centers will not have to cover any additional cost as the treatment options analysed constitute standard clinical practice. No financial support is granted for investigators nor study participants.
- Being tested
- Metformin
- Medical subject headings
- Rectal Neoplasms, Lymphatic Metastasis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
MetforminDrug
Also called Avamina, Etform, Formetic, Glucophage
Metformin use before operation due to previously diagnosed diabetes.
| Study group | Role | What they receive |
|---|---|---|
| Rectal cancer | Patients with primary rectal cancer operated on between 2013 and 2019. Receives: Drug: Metformin |
What is being measured
The primary outcome is the main question the study is designed to answer.
Overall survival
Overall survival of analysed patients
Measured: 3 years
Secondary outcomes (1)
Disease-free survival
Disease-free survival of analysed patients
Measured: 3 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted1 Jul 2021
- Study start1 Aug 2021
- Primary completion30 Dec 2022
- Study completion31 Dec 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Rectal CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Retrospective
- Enrolment
- 2,443 participants (actual)
Sponsor and investigators
- Lead sponsor
- Jagiellonian University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Radoslaw Pach, MD, PhD, Jagiellonian University
- Investigators
- Radoslaw Pach, PhD, Principal investigator, Jagiellonian UniversityAntoni Szczepanik, PhD, Study chair, Jagiellonian University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04947020
- Sponsor's protocol ID
- BARO Trial
- Acronym
- BARO
- Status last verified
- Feb 2025
- First submitted
- 24 Jun 2021
- Last updated
- 25 Feb 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Anonimized database will be shared only with researchers participating in the study.
Study at a glance
From the registry record, last updated by the sponsor on 25 Feb 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Multicenter Retrospective Trial for Analysis of Oncological Results of Patients with Primary Rectal Cancer Operated on Between 2013-2019
- ClinicalTrials.gov ID
- NCT04947020
- Acronym / sponsor ID
- BARO / BARO Trial
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 2,443 participants (actual)
- Lead sponsor
- Jagiellonian UniversityUniversity, hospital or other
- Study start
- 1 Aug 2021 (actual)
- Primary completion
- 30 Dec 2022 (actual)
- Study completion
- 31 Dec 2024 (actual)
- First posted
- 1 Jul 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The data will be obtained from 10 tertiary centers located in Poland (Cracow - coordinating center, Warsaw - 3 centers, Sosnowiec, Szczecin, Bydgoszcz, Lublin, Gdansk, Poznan) and 5 foreign centers.
The analyses will include patients with rectal cancer operated on between 2013-2019. A database in MS Excel is prepared that consists of following data:
- Type of neoadjuvant treatment (if any)
- Time-interval between the end of neoadjuvant treatment and surgery
- Type of surgery
- Staging of rectal cancer i.e. (y)pTNM
- Number of retrieved lymph nodes
- Number of lymph nodes with metastases
- R classification (R0, R1, R2)
- Preoperative medications (metformin, statins, NSAIDs, anticoagulants)
- Recurrence date and type (local, systemic, both diagnosed at the same time)
- Date of death or date of last follow-up visit
The aims of the study are following:
- Establishing whether neoadjuvant treatment (PSCR or chemoradiotherapy) influences number of retrieved lymph nodes in rectal cancer
- Establishing whether time-interval between the end of PSCR and surgery influences lymph node yield
- Establishing the prognostic value of lymph node ratio - validation of the previously calculated cutoff point at the level of 0.41
- Determining independent prognostic factors in rectal cancer - in particular related to medications taken before the operation, metformin and anti diabetic drugs in the first place
Detailed description
Previously published studies showed that preoperative treatment of rectal cancer is associated with a lower number of lymph nodes retrieved during resection that is often lower than the recommended number of 12 nodes necessary for proper establishing of ypN category. A few studies revealed that lymph node ratio (LNR) is a more precise prognostic factor than pN category. The analysis conducted at the 1st Department of Surgery (Jagiellonian University, Cracow, Poland) based on patients' data from 1999 - 2006 year indicated that the median number of harvested lymph nodes after preoperative short course radiotherapy 5x5 Gy (PSCR) was 16. Therefore, PSCR did not seem to influence the number of lymph nodes in the operative specimen. Time-interval between radiotherapy and surgery (7-10 days versus 4-5 weeks) was not associated with lymph node yield, either.
Medication taken by the patients before operation may influence the treatment results as well. In a couple of studies metformin was identified as inhibitor of carcinogenesis according to antiangiogenic and antimetabolic effects and as a potential radiosensitizer. The anticancer property of metformin is largely attributed to its capability in modulating signaling pathways involved in cellular proliferation, apoptosis, and metabolism. In the last decade, mounting evidence supports the use of metformin in the prevention and treatment of colorectal cancer. Moreover, the use of metformin as monotherapy or as an adjuvant in colorectal cancer patients has led to further dose reduction and increased radio-chemosensitivity which lead to minimal gastrointestinal side effects and reduced toxicity. The use of metformin was associated with improved survival among colorectal cancer patients with type 2 diabetes mellitus compared to sulfonylureas and insulin. The effect of metformin in nondiabetic patients has not been evaluated so far. Based on the aforementioned results, it seems well-grounded to establish the influence of other medications (statins, nonsteroidal anti-inflammatory drugs, anticoagulants) on the results of combined treatment of rectal cancer with the assessment whether they are independent prognostic factors in comparison with such parameters as (y)pT, (y)pN or LNR.
After study initiation, a template of MS Excel database with manual will be sent to the Principal Investigators in every participating center. After obtaining the filled sheets from all participating centers, a central database will be prepared. No personal data of the patients (name, surname, personal ID numbers) will be collected and data in the central database will be anonymized.
Number of harvested lymph nodes will be compared in patients who underwent neoadjuvant chemoradiotherapy, PSCR, or surgery alone. In addition, number of retrieved lymph nodes and lymph node ratio will be compared in patients operated on after different time-intervals between PSCR and surgery (< 7 days and > 4 weeks). Kaplan-Meier curves will be drawn to established influence of number and ratio of harvested lymph nodes on overall survival and disease-free survival. Local and systemic recurrence rate will be established and compared in analysed patients. Statistical analysis will be performed with SPSS 27 for Mac. Variables without normal distribution will be compared by means of Mann Whitney U and Chi-square tests. Cumulative proportions of surviving will be compared with the use of log-rank test. Univariate and multivariate Cox regression will be performed to establish prognostic factors in analysed population.
The study is academic and non-commercial. The participating centers will not have to cover any additional cost as the treatment options analysed constitute standard clinical practice. No financial support is granted for investigators nor study participants.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Rectal cancer | – | Drug: MetforminPatients with primary rectal cancer operated on between 2013 and 2019. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Adult patients with primary rectal cancer operated on between 2013 and 2019.
Key inclusion criteria (2 listed)
- Primary rectal cancer confirmed histologically
- Age ≥ 18
Key exclusion criteria (2 listed)
- Recurrent rectal cancer
- Oncological radicalization after previous local excision of rectal cancer
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| MetforminAlso: Avamina, Etform, Formetic, GlucophageMetformin use before operation due to previously diagnosed diabetes. | Drug | Rectal cancer |
Primary outcome
Overall survival
Time frame: 3 years
Overall survival of analysed patients
1 secondary outcome
Disease-free survival
Time frame: 3 years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Feb 2025.
- Individual participant dataSharing planned: No. Anonimized database will be shared only with researchers participating in the study.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Radoslaw Pach, PhD principal investigator
Jagiellonian University
Antoni Szczepanik, PhD study chair
Jagiellonian University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Rectal Cancer and Metformin, run by Jagiellonian University at 1 site in Poland.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 25 Feb 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Poland. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Overall survival (time frame: 3 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Feb 2025.