Colitis-associated Colorectal Cancer (CAC)NCT06833021
Screening for Hepatitis Virus B Protein X (HBx) in Colitis-associated Cancer (CAC)
An observational study of Colitis-associated Colorectal Cancer (CAC), run by IRCCS San Raffaele at 1 site in Italy.
Trial summary
It was recently discovered that a protein from the Hepatitis B Virus (HBV), called HBx, is highly present in patients who were recently diagnosed with Ulcerative Colitis (UC). This was more common in UC patients than in healthy individuals or those with Crohn's Disease. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Colitis-associated Colorectal Cancer (CAC)
- What is being tested?
- Transcriptomic Analysis
- How many people
- 66 participants
- Where
- 1 siteItaly
- Study dates
- 1 Apr 2025to 1 Apr 2026
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
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: 66 total patients, of which 33 diagnosed with CAC and 33 representing the control group composed of CRC without colitis, diverticulitis, and CD without cancer. 20 patients will be enrolled at our center, and the remaining 40 will be equally distributed among the participating units: IRCCS Casa Sollievo della Sofferenza Hospital (San Giovanni Rotondo (FG), Italy) and Western University (London, Ontario, Canada).
Who may be able to join
- adult patients (age ≥18 years), both male and female, diagnosed with CAC, CRC, diverticulitis, IC or CD who had previously undergone endoscopic biopsy or surgical resection, according to standard clinical practice (from 2021 to 2024);
- patients with no documented history of HBV infection;
- patients who had already signed the informed consent authorizing the use of their clinical data for future scientific research.
Who cannot join
- patients under 18 years of age;
- adult patients (age ≥18 years), both male and female diagnosed with CAC, CRC, diverticulitis, IC or CD with a documented history of HBV infection;
- patients who have not signed the informed consent authorizing the use of their clinical data for future scientific research.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Italy1 site
IRCCS San Raffaele
Milan, Italy, 20132
Federica Ungaro, PhD., +39 0226437864, ungaro.federica@hsr.it
Francesco Fiorio, Biologist, +39 0226437159, fiorio.francesco@hsr.it
About this study
Official title: Multicenter Retrospective Study on Hepatitis B Virus Protein X (HBx) Screening in Patients With Colitis-associated Cancer (CAC)
It was recently discovered that a protein from the Hepatitis B Virus (HBV), called HBx, is highly present in patients who were recently diagnosed with Ulcerative Colitis (UC). This was more common in UC patients than in healthy individuals or those with Crohn's Disease. About 45% of the UC patients studied had this protein, possibly due to a virus jumping from animals to humans.
In experiments with mice, it was found that HBx alone can cause colitis (inflammation of the colon) by disrupting the normal function of the gut lining. This disruption leads to inflammation and immune system problems in the colon, even without other bacteria being involved. Mice treated with HBx showed fewer immune cells, which are crucial for resolving inflammation and fighting infections. This aligns with current theories about how UC develops.
Read more
Additionally, HBx affects the genes in the gut lining, promoting cell growth and changes that could lead to cancer. In human colon tissue samples, HBx activated processes linked to the Wnt pathway, which is known to be involved in colorectal cancer. This is similar to how HBx behaves in liver cells infected with HBV, where it prevents DNA repair and leads to cancer.
Based on these findings, it is believed that HBx disrupts the balance in the gut, causing chronic inflammation that could progress to cancer. To explore this further, a study is being conducted to detect HBx in tissue samples from patients with colitis-associated cancer (CAC). Advanced techniques will be used to analyze these samples and compare them with samples from patients with other conditions like diverticulitis, indeterminate colitis, and Crohn's disease without cancer
Read the detailed description
The human microbiota is a rich community of bacteria, viruses, fungi, protists, and archaea, and is an integral part of the body influencing its overall homeostasis. It colonizes all mucosal surfaces, with the gastrointestinal (GI) tract being the most densely populated. Although the most investigated gut colonizers are bacteria, emerging evidence highlights dysbiosis of the gut virome, made of both bacteriophages and eukaryotic targeting viruses, as responsible for influencing the overall intestinal microbiota composition and mucosal homeostasis by directly interacting with the other commensals, such as bacteria, or with the host, as for the eukaryotic-targeting viruses.
Eukaryotic viruses colonizing the mucosal surfaces may infect the host's cells without symptoms, and, even if asymptomatic, a virus-carrying host may hold a persistent immune response with a "continuum" of inflammatory mediators that might increase host susceptibility to disease. In parallel, eukaryotic viruses have been well-described as inducers of multiple mutational events, among which insertional mutagenesis, so viral infections are known to be responsible for about 20% of the global cancer burden. As an example, one of the most frequent infection-related cancers is hepatocarcinoma, mainly caused by the Hepatitis B virus (HBV).
Eukaryotic-targeting viruses have recently attracted considerable interest in gastrointestinal diseases such as ulcerative colitis (UC), a chronic inflammatory condition of the colonic tract, and colorectal cancer (CRC), the third most diagnosed malignancy and the fourth leading cause of cancer death in the world. UC and cancer share several factors influencing their etiogenesis, including intestinal dysbiosis. Of note, UC is a risk factor in developing colitis-associated colorectal cancer (CAC). Indeed, patients with UC have a risk of developing cancer approximately 2- to 3-fold more than the general population with poor prognosis. Dysplasia in CAC develops with different mechanisms in comparison to sporadic colorectal cancer. Patients affected by UC and CAC share a pro-inflammatory microenvironment within their mucosal tissues. Nevertheless, the mechanistic link between these two diseases is still missing.
It was recently reported that a factor derived from the Orthohepadnavirus genus, namely the Hepatitis B Virus (HBV) protein X (HBx), was the most enriched component of the virome in early-diagnosed UC patients, compared to both healthy subjects and Crohn's Disease patients. This factor was harbored by a specific cohort of UC patients (approximately 45% of the total analyzed), likely because of a zoonotic spillover event.
In vivo, HBx was shown as able to induce colitis per se independently of the other commensals, by interfering with the epithelial transcriptomic apparatus that causes the loss of appropriate barrier functions, in turn leading to the proinflammatory and immune sequelae of events within colonic mucosa, all these occurring independently of the microbiota. Indeed, HBx-treated mice displayed a reduction of neutrophils, dendritic and CD8+ T cells, indicating failure of the resolution phase (reduced neutrophils) and hampered defense against pathogens (dendritic and CD8+ T cells), all hallmarks consistent with the leading theory of UC pathogenesis. Moreover, it was shown that HBx shapes the transcriptomic state of the intestinal epithelium by binding regulatory DNA regions and activating the transcription of genes involved in the augmented epithelial cell proliferation and stemness. Notably, HBx overexpression in human colonic mucosa biopsies induced activation of biological processes related to the Wnt pathway, which is involved in colorectal carcinogenesis. This result is consistent with the HBx description in the context of HBV infection. Indeed, this viral protein is known to prevent the HBV-infected hepatocytes from efficiently repairing damaged DNA, thus leading to an accumulation of DNA mutations and, eventually, hepatocarcinogenesis.
Based on this evidence and preliminary results, it is believed that HBx-mediated epithelial alterations affect mucosal homeostasis, disrupting and driving intestinal chronic inflammation, which may progress to dysplastic lesions or adenocarcinoma.
For this reason, a multicenter retrospective study is being conducted to investigate the presence of HBx in patient-derived samples from individuals diagnosed with CAC. In detail, the study will employ reverse transcription polymerase chain reaction (RT-PCR) and Sanger sequencing techniques to analyze Formalin-Fixed Paraffin-Embedded (FFPE) tissue samples to detect HBx. A control group will be included, comprising CRC samples from patients without colitis and samples from patients with diverticulitis, indeterminate colitis (IC), and Crohn's disease (CD) without cancer.
The assessment of HBx in CAC samples could revolutionize clinical approaches by enabling earlier diagnosis and refining risk assessment for patients with UC. This finding may also lead to the development of personalized treatment strategies that specifically target HBx-related pathways, thereby advancing the understanding of the underlying disease mechanisms
- Being tested
- Transcriptomic Analysis
- Keywords
- Colorectal Cancer, Hepatitis Virus B, Hepatitis Virus B Protein X, IBD, Diverticulitis, Colitis, Crohn Disease, Colitis-associated Colorectal Cancer (CAC)
- Medical subject headings
- Colitis-Associated Neoplasms, Colorectal Neoplasms, Diverticulitis, Colitis, Crohn Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Transcriptomic AnalysisOther
FFPE tissue blocks from patients diagnosed with CAC, including low- and high-grade dysplasia and adenocarcinoma, obtained from pathological archives will be used. RNA will be extracted and analyzed using RT-PCR to detect and quantify HBx transcripts, with Sanger sequencing employed for further validation of the results.
Transcriptomic AnalysisOther
RNA will be extracted and analyzed using RT-PCR to detect and quantify HBx transcripts, with Sanger sequencing employed for further validation of the results. FFPE tissue blocks from CRC, diverticulitis, IC and CD without cancer patients will be utilized as controls.
| Study group | Role | What they receive |
|---|---|---|
| Control Group | 33 patients used as control including patients with CRC not associated with colitis, diverticulitis, IC and CD without cancer. Receives: Other: Transcriptomic Analysis | |
| Case Group | 33 patients diagnosed with CAC Receives: Other: Transcriptomic Analysis |
What is being measured
The primary outcome is the main question the study is designed to answer.
To define HBx as a predictive biomarker of CAC in UC patients
FFPE tissue blocks from patients diagnosed with CAC, including low- and high-grade dysplasia and adenocarcinoma, obtained from pathological archives will be used. RNA will be extracted and analyzed using RT-PCR to detect and quantify HBx transcripts, with Sanger sequencing employed for further validation of the results. Additionally, FFPE tissue blocks from CRC, diverticulitis, IC and CD without cancer patients will be utilized as controls. FFPE tissue blocks already present in the Pathology Unit will be used.
Measured: Being a retrospective study, we plan to collect FFPE stored from October 2021 to December 2024. Duration of total study period: 12 months.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Feb 2025
- Study start1 Apr 2025 (estimated)
- Primary completion1 Apr 2026 (estimated)
- Study completion1 Apr 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Colitis-associated Colorectal Cancer (CAC)Studies of the same condition, open and under way.
- More trials run by IRCCS San RaffaeleThe sponsor's other registered studies.
- 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
- Case-control
- Time perspective
- Retrospective
- Enrolment
- 66 participants (estimated)
Sponsor and investigators
- Lead sponsor
- IRCCS San Raffaele
- Sponsor type
- University, hospital or other
- Collaborators
- IRCCS Casa Sollievo della Sofferenza, Western University, Canada
- Responsible party
- Principal investigator, Silvio Danese, IRCCS San Raffaele
- Investigators
- Silvio Danese, PhD-MD, Study director, IRCCS San Raffaele
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06833021
- Sponsor's protocol ID
- HBx-CAC
- Status last verified
- Feb 2025
- First submitted
- 12 Feb 2025
- Last updated
- 20 Feb 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 20 Feb 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Multicenter Retrospective Study on Hepatitis B Virus Protein X (HBx) Screening in Patients With Colitis-associated Cancer (CAC)
- ClinicalTrials.gov ID
- NCT06833021
- Acronym / sponsor ID
- HBx-CAC
- Keywords
- Colorectal Cancer, Hepatitis Virus B, Hepatitis Virus B Protein X, IBD, Diverticulitis, Colitis, Crohn Disease, Colitis-associated Colorectal Cancer (CAC)
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 66 participants (estimated)
- Lead sponsor
- IRCCS San RaffaeleUniversity, hospital or other
- Collaborators
- IRCCS Casa Sollievo della Sofferenza, Western University, Canada
- Study start
- 1 Apr 2025 (estimated)
- Primary completion
- 1 Apr 2026 (estimated)
- Study completion
- 1 Apr 2026 (estimated)
- First posted
- 18 Feb 2025 (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.
It was recently discovered that a protein from the Hepatitis B Virus (HBV), called HBx, is highly present in patients who were recently diagnosed with Ulcerative Colitis (UC). This was more common in UC patients than in healthy individuals or those with Crohn's Disease. About 45% of the UC patients studied had this protein, possibly due to a virus jumping from animals to humans.
In experiments with mice, it was found that HBx alone can cause colitis (inflammation of the colon) by disrupting the normal function of the gut lining. This disruption leads to inflammation and immune system problems in the colon, even without other bacteria being involved. Mice treated with HBx showed fewer immune cells, which are crucial for resolving inflammation and fighting infections. This aligns with current theories about how UC develops.
Additionally, HBx affects the genes in the gut lining, promoting cell growth and changes that could lead to cancer. In human colon tissue samples, HBx activated processes linked to the Wnt pathway, which is known to be involved in colorectal cancer. This is similar to how HBx behaves in liver cells infected with HBV, where it prevents DNA repair and leads to cancer.
Based on these findings, it is believed that HBx disrupts the balance in the gut, causing chronic inflammation that could progress to cancer. To explore this further, a study is being conducted to detect HBx in tissue samples from patients with colitis-associated cancer (CAC). Advanced techniques will be used to analyze these samples and compare them with samples from patients with other conditions like diverticulitis, indeterminate colitis, and Crohn's disease without cancer
Detailed description
The human microbiota is a rich community of bacteria, viruses, fungi, protists, and archaea, and is an integral part of the body influencing its overall homeostasis. It colonizes all mucosal surfaces, with the gastrointestinal (GI) tract being the most densely populated. Although the most investigated gut colonizers are bacteria, emerging evidence highlights dysbiosis of the gut virome, made of both bacteriophages and eukaryotic targeting viruses, as responsible for influencing the overall intestinal microbiota composition and mucosal homeostasis by directly interacting with the other commensals, such as bacteria, or with the host, as for the eukaryotic-targeting viruses.
Eukaryotic viruses colonizing the mucosal surfaces may infect the host's cells without symptoms, and, even if asymptomatic, a virus-carrying host may hold a persistent immune response with a "continuum" of inflammatory mediators that might increase host susceptibility to disease. In parallel, eukaryotic viruses have been well-described as inducers of multiple mutational events, among which insertional mutagenesis, so viral infections are known to be responsible for about 20% of the global cancer burden. As an example, one of the most frequent infection-related cancers is hepatocarcinoma, mainly caused by the Hepatitis B virus (HBV).
Eukaryotic-targeting viruses have recently attracted considerable interest in gastrointestinal diseases such as ulcerative colitis (UC), a chronic inflammatory condition of the colonic tract, and colorectal cancer (CRC), the third most diagnosed malignancy and the fourth leading cause of cancer death in the world. UC and cancer share several factors influencing their etiogenesis, including intestinal dysbiosis. Of note, UC is a risk factor in developing colitis-associated colorectal cancer (CAC). Indeed, patients with UC have a risk of developing cancer approximately 2- to 3-fold more than the general population with poor prognosis. Dysplasia in CAC develops with different mechanisms in comparison to sporadic colorectal cancer. Patients affected by UC and CAC share a pro-inflammatory microenvironment within their mucosal tissues. Nevertheless, the mechanistic link between these two diseases is still missing.
It was recently reported that a factor derived from the Orthohepadnavirus genus, namely the Hepatitis B Virus (HBV) protein X (HBx), was the most enriched component of the virome in early-diagnosed UC patients, compared to both healthy subjects and Crohn's Disease patients. This factor was harbored by a specific cohort of UC patients (approximately 45% of the total analyzed), likely because of a zoonotic spillover event.
In vivo, HBx was shown as able to induce colitis per se independently of the other commensals, by interfering with the epithelial transcriptomic apparatus that causes the loss of appropriate barrier functions, in turn leading to the proinflammatory and immune sequelae of events within colonic mucosa, all these occurring independently of the microbiota. Indeed, HBx-treated mice displayed a reduction of neutrophils, dendritic and CD8+ T cells, indicating failure of the resolution phase (reduced neutrophils) and hampered defense against pathogens (dendritic and CD8+ T cells), all hallmarks consistent with the leading theory of UC pathogenesis. Moreover, it was shown that HBx shapes the transcriptomic state of the intestinal epithelium by binding regulatory DNA regions and activating the transcription of genes involved in the augmented epithelial cell proliferation and stemness. Notably, HBx overexpression in human colonic mucosa biopsies induced activation of biological processes related to the Wnt pathway, which is involved in colorectal carcinogenesis. This result is consistent with the HBx description in the context of HBV infection. Indeed, this viral protein is known to prevent the HBV-infected hepatocytes from efficiently repairing damaged DNA, thus leading to an accumulation of DNA mutations and, eventually, hepatocarcinogenesis.
Based on this evidence and preliminary results, it is believed that HBx-mediated epithelial alterations affect mucosal homeostasis, disrupting and driving intestinal chronic inflammation, which may progress to dysplastic lesions or adenocarcinoma.
For this reason, a multicenter retrospective study is being conducted to investigate the presence of HBx in patient-derived samples from individuals diagnosed with CAC. In detail, the study will employ reverse transcription polymerase chain reaction (RT-PCR) and Sanger sequencing techniques to analyze Formalin-Fixed Paraffin-Embedded (FFPE) tissue samples to detect HBx. A control group will be included, comprising CRC samples from patients without colitis and samples from patients with diverticulitis, indeterminate colitis (IC), and Crohn's disease (CD) without cancer.
The assessment of HBx in CAC samples could revolutionize clinical approaches by enabling earlier diagnosis and refining risk assessment for patients with UC. This finding may also lead to the development of personalized treatment strategies that specifically target HBx-related pathways, thereby advancing the understanding of the underlying disease mechanisms
Study design
- Observational model
- Case-control
- Time perspective
- Retrospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Control Group | – | Other: Transcriptomic Analysis33 patients used as control including patients with CRC not associated with colitis, diverticulitis, IC and CD without cancer. |
| Case Group | – | Other: Transcriptomic Analysis33 patients diagnosed with CAC |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- 66 total patients, of which 33 diagnosed with CAC and 33 representing the control group composed of CRC without colitis, diverticulitis, and CD without cancer. 20 patients will be enrolled at our center, and the remaining 40 will be equally distributed among the participating units: IRCCS Casa Sollievo della Sofferenza Hospital (San Giovanni Rotondo (FG), Italy) and Western University (London, Ontario, Canada).
Key inclusion criteria (3 listed)
- adult patients (age ≥18 years), both male and female, diagnosed with CAC, CRC, diverticulitis, IC or CD who had previously undergone endoscopic biopsy or surgical resection, according to standard clinical practice (from 2021 to 2024);
- patients with no documented history of HBV infection;
- patients who had already signed the informed consent authorizing the use of their clinical data for future scientific research.
Key exclusion criteria (3 listed)
- patients under 18 years of age;
- adult patients (age ≥18 years), both male and female diagnosed with CAC, CRC, diverticulitis, IC or CD with a documented history of HBV infection;
- patients who have not signed the informed consent authorizing the use of their clinical data for future scientific research.
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 |
|---|---|---|
| Transcriptomic AnalysisFFPE tissue blocks from patients diagnosed with CAC, including low- and high-grade dysplasia and adenocarcinoma, obtained from pathological archives will be used. RNA will be extracted and analyzed using RT-PCR to detect and quantify HBx transcripts, with Sanger sequencing employed for further validation of the results. | Other | Case Group |
| Transcriptomic AnalysisRNA will be extracted and analyzed using RT-PCR to detect and quantify HBx transcripts, with Sanger sequencing employed for further validation of the results. FFPE tissue blocks from CRC, diverticulitis, IC and CD without cancer patients will be utilized as controls. | Other | Control Group |
Primary outcome
To define HBx as a predictive biomarker of CAC in UC patients
Time frame: Being a retrospective study, we plan to collect FFPE stored from October 2021 to December 2024. Duration of total study period: 12 months.
FFPE tissue blocks from patients diagnosed with CAC, including low- and high-grade dysplasia and adenocarcinoma, obtained from pathological archives will be used. RNA will be extracted and analyzed using RT-PCR to detect and quantify HBx transcripts, with Sanger sequencing employed for further validation of the results. Additionally, FFPE tissue blocks from CRC, diverticulitis, IC and CD without cancer patients will be utilized as controls. FFPE tissue blocks already present in the Pathology Unit will be used.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Feb 2025.
- Individual participant dataSharing planned: Undecided
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.
Silvio Danese, PhD-MD study director
IRCCS San Raffaele
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 Colitis-associated Colorectal Cancer (CAC), run by IRCCS San Raffaele at 1 site in Italy.
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 3 inclusion and 3 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: opening soon, as of the sponsor's last update on 20 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 Italy. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Silvio Danese, PhD.-MD (+39 0226432807, danese.silvio@hsr.it), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
To define HBx as a predictive biomarker of CAC in UC patients (time frame: Being a retrospective study, we plan to collect FFPE stored from October 2021 to December 2024. Duration of total study period: 12 months.). 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 20 Feb 2025.