Pancreatic Cancer ResectableNCT06495749
Early Diagnosis of Pancreatic Cancer Via Deciphering Multi-modal Immunological Signatures
An observational study of Pancreatic Cancer Resectable, run by Zhejiang University at 2 sites in China.
Trial summary
Prospective inclusion of 1000 patients with pancreatic cancer (early-stage pancreatic cancer accounts for approximately 75% of cases), 1000 patients with benign pancreatic diseases, and 1000 healthy individuals as controls. Read more about this study
- Who is it for?
- Any ageHealthy volunteers can take part
- Conditions the study is for
- Pancreatic Cancer Resectable
- How many people
- 3,000 participants
- Where
- 2 sitesChina
- Study dates
- 1 Aug 2024to 31 Dec 2027
- 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 Any age
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: Prospective inclusion of 1000 patients with pancreatic cancer (early-stage pancreatic cancer accounts for approximately 75% of cases), 1000 patients with benign pancreatic diseases, and 1000 healthy individuals as controls. Peripheral blood samples were collected from newly diagnosed pancreatic cancer patients and healthy individuals. Using techniques such as plasma TCR-seq, CyTOF, and plasma proteomics, multi-modal individual immune characteristics were obtained and analyzed along with clinical information. An artificial intelligence predictive model was built based on these multi-modal individual immune characteristics to establish an early screening technique for pancreatic cancer.
Who may be able to join
- Sign the informed consent form;
- Initial diagnosis as patients with pancreatic cancer, patients with benign pancreatic lesions, or healthy controls.
Who cannot join
- History of other malignancies;
- Presence of organ dysfunction;
- Concurrent immunodeficiency syndrome, active tuberculosis, HIV infection, etc.;
- Allogeneic transplantation requiring immunosuppressive therapy;
- Poor follow-up compliance.
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
China2 sites
First Affiliated Hospital, Medical College of Zhejiang University
Hangzhou, Zhejiang, 310003
the First Affiliated Hospital, School of Medicine, Zhejiang University
Hangzhou, Zhejiang, 310009
About this study
Prospective inclusion of 1000 patients with pancreatic cancer (early-stage pancreatic cancer accounts for approximately 75% of cases), 1000 patients with benign pancreatic diseases, and 1000 healthy individuals as controls. Peripheral blood samples were collected from newly diagnosed pancreatic cancer patients and healthy individuals. Using techniques such as plasma TCR/BCR-seq, CyTOF, and plasma proteomics, multi-modal individual immune characteristics were obtained and analyzed along with clinical information. An artificial intelligence predictive model was built based on these multi-modal individual immune characteristics to establish an early screening technique for pancreatic cancer. The sensitivity and specificity of this artificial intelligence model for early pancreatic cancer diagnosis were evaluated using an external multicenter sample test set.
Read the detailed description
Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive cancers and currently ranks as the seventh leading cause of cancer-related deaths in China. The nonspecific symptoms of early PDAC are one of the most significant reasons for its low 5-year survival rate. Additionally, PDAC lacks highly sensitive and specific biomarkers for early detection and preventive screening. For the majority of advanced PDAC cases, pathological confirmation often requires tissue biopsies obtained through invasive procedures, and due to the scarcity of tumor cells in these biopsies, pathology may be unclear in up to 20% of cases. On the other hand, there are currently no effective and targeted treatments for PDAC, with surgical resection being the only available option. However, this is only applicable to a small fraction of early-stage PDAC patients, as more than 80% of PDAC patients are diagnosed with distant metastasis at initial diagnosis, where only adjuvant therapy is feasible.
Early diagnosis and detection of PDAC can significantly improve patient prognosis. To date, the only diagnostic biomarker for PDAC is serum Carbohydrate antigen199(CA199) levels, which are neither diagnostic nor specific. High CA199 levels are uncommon in early PDAC but most common in late-stage PDAC. Furthermore, elevated CA199 levels are frequently detected in various benign and malignant diseases, including pancreatitis, cholestasis, and cancer. Additionally, due to screening limitations, imaging modalities such as computed tomography (CT), magnetic resonance imaging (MRI), and endoscopic ultrasound (EUS) are insufficient for early detection of PDAC.
Ideally, the investigators aim to obtain non-invasive, reliable, and repeatable biological markers with clinical potential for early cancer diagnosis. Early studies have identified circulating tumor DNA (ctDNA), circulating tumor cells (CTC), extracellular vesicles (EV), plasma proteomics, and circulating tumor cells (CTCs) as promising real-time and remote tools for this purpose. Compared to other solid tumors, especially lung and breast cancer, some of these circulating biomarkers have entered clinical practice, while blood-derived biomarkers for PDAC diagnosis or monitoring are very limited (excluding CA199), and CA199 is largely underdeveloped compared to other tumors. One example is the use of EpCAM(Epithelial cell adhesion molecule) and cytokeratin for CellSearch system diagnostics, an FDA(Food and Drug Administration)-approved method for diagnosing metastatic breast, colon, and prostate cancers, which was evaluated for PDAC diagnosis, achieving an accuracy rate of 11-78.5%, indicating a wide variation in PDAC detection rates. Other molecular features for diagnosing PDAC, including KRAS mutations in CTCs, miRNA in EVs, and heparan sulfate proteoglycan glypican 1 (GPC1) in extracellular vesicles, unfortunately, exhibit significant differences in sensitivity and predictive performance across different studies, particularly between tumor and CTC status. One study found that in 97% of patients with tumors carrying mutated KRAS, only 18% of CTCs carried the wild-type KRAS allele, even from metastatic tumors. Therefore, due to genetic limitations associated with CTC enrichment and identification, ctDNA isolation, etc., using a single biomarker may only capture partial tumor biological characteristics, leading to low consistency and false negatives. Given the challenges of early diagnosis of PDAC, it is imperative to develop one or more new biological markers for early PDAC diagnosis to capture more possible biological characteristics of primary and metastatic tumors.
The immune system is an extremely important defense system in the human body. Through specific and non-specific biological processes, the immune system can detect various pathogens and harmful substances ranging from viruses to parasites, and differentiate them from healthy cells and tissues in the body under normal circumstances. Therefore, there is a close connection between the immune system and the overall health of an individual. Tumor development remains under constant surveillance by the immune system, and in the early stages of disease, the immune system responds and immune features undergo changes. However, when clinical symptoms appear, it indicates that the immune system is struggling to overcome the presence of harmful substances, and at this point, the disease has already progressed to the middle or late stage. By establishing a large-scale early pancreatic cancer clinical cohort, collecting high-quality multi-modal immune data from individuals, and integrating cutting-edge artificial intelligence models, it is possible to decode individual immune features and develop early diagnostic techniques for pancreatic cancer based on capturing immune status and response signals. This approach can help identify early risk factors for pancreatic cancer by analyzing abnormal immune responses before disease progression, enabling early diagnosis of pancreatic cancer.
- Conditions
- Pancreatic Cancer Resectable
- Keywords
- Early diagnosis, Pancreatic cancer, Artificial intelligence, Immunity decoding
- Medical subject headings
- Disease, Pancreatic Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Pancreatic Cancer | The patient is diagnosed with pancreatic cancer for the first time and has not received any tumor treatment. | |
| Benign Pancreatic Diseases | The patient is diagnosed with a benign pancreatic disease ,such as SCN、MCN、IPMN.and has not undergone any treatment. | |
| Healthy controls | A healthy population without any pancreatic-related diseases or other cancers. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Peripheral blood mononuclear cell
Using RNA seq technology to analyze differentially expressed genes in peripheral immune cells
Measured: During the 1-7 day period before surgery
Peripheral blood mononuclear cell
TCR/BCR-seq:Using multiple amplification to obtain the CDR3(complementarities determining region3) region of TCR and BCR and analyzing the VDJ rearrangement pattern
Measured: During the 1-7 day period before surgery
Peripheral blood mononuclear cell
Analyzing RNA expression in individual cells using scRNA-seq
Measured: During the 1-7 day period before surgery
Peripheral blood mononuclear cell
scTCR/BCR-seq:Using multiple amplification to obtain the CDR3(complementarities determining region3) region of TCR and BCR and analyzing the VDJ rearrangement pattern in individual cells
Measured: During the 1-7 day period before surgery
Peripheral blood mononuclear cell
Identification of open chromatin regions in individual cells using scATAC-seq technology
Measured: During the 1-7 day period before surgery
Peripheral blood mononuclear cell
Detecting the abundance and type of some markers for peripheral blood mononuclear cell using CYTOF technology
Measured: During the 1-7 day period before surgery
CT
Imaging data from the patient's initial visit
Measured: Within 1 month before surgery
MRI
Imaging data from the patient's initial visit
Measured: Within 1 month before surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Jul 2024
- Study start1 Aug 2024 (estimated)
- Primary completion1 Jan 2027 (estimated)
- Study completion31 Dec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pancreatic Cancer ResectableStudies of the same condition, open and under way.
- More trials run by Zhejiang UniversityThe 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
- Cohort
- Time perspective
- Prospective
- Enrolment
- 3,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Zhejiang University
- Sponsor type
- University, hospital or other
- Collaborators
- The Affiliated Hospital of the Chinese Academy of Military Medical Sciences, Nanjing Medical University
- Responsible party
- Principal investigator, TingBo Liang, Zhejiang University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06495749
- Sponsor's protocol ID
- MULTIMODAL-1
- Status last verified
- Jul 2024
- First submitted
- 23 Jun 2024
- Last updated
- 16 Jul 2024
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 16 Jul 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Early Diagnosis of Pancreatic Cancer Via Deciphering Multi-modal Immunological Signatures
- ClinicalTrials.gov ID
- NCT06495749
- Acronym / sponsor ID
- MULTIMODAL-1
- Conditions
- Pancreatic Cancer Resectable
- Keywords
- Early diagnosis, Pancreatic cancer, Artificial intelligence, Immunity decoding
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 3,000 participants (estimated)
- Lead sponsor
- Zhejiang UniversityUniversity, hospital or other
- Collaborators
- The Affiliated Hospital of the Chinese Academy of Military Medical Sciences, Nanjing Medical University
- Study start
- 1 Aug 2024 (estimated)
- Primary completion
- 1 Jan 2027 (estimated)
- Study completion
- 31 Dec 2027 (estimated)
- First posted
- 11 Jul 2024 (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.
Prospective inclusion of 1000 patients with pancreatic cancer (early-stage pancreatic cancer accounts for approximately 75% of cases), 1000 patients with benign pancreatic diseases, and 1000 healthy individuals as controls. Peripheral blood samples were collected from newly diagnosed pancreatic cancer patients and healthy individuals. Using techniques such as plasma TCR/BCR-seq, CyTOF, and plasma proteomics, multi-modal individual immune characteristics were obtained and analyzed along with clinical information. An artificial intelligence predictive model was built based on these multi-modal individual immune characteristics to establish an early screening technique for pancreatic cancer. The sensitivity and specificity of this artificial intelligence model for early pancreatic cancer diagnosis were evaluated using an external multicenter sample test set.
Detailed description
Pancreatic ductal adenocarcinoma (PDAC) is one of the most aggressive cancers and currently ranks as the seventh leading cause of cancer-related deaths in China. The nonspecific symptoms of early PDAC are one of the most significant reasons for its low 5-year survival rate. Additionally, PDAC lacks highly sensitive and specific biomarkers for early detection and preventive screening. For the majority of advanced PDAC cases, pathological confirmation often requires tissue biopsies obtained through invasive procedures, and due to the scarcity of tumor cells in these biopsies, pathology may be unclear in up to 20% of cases. On the other hand, there are currently no effective and targeted treatments for PDAC, with surgical resection being the only available option. However, this is only applicable to a small fraction of early-stage PDAC patients, as more than 80% of PDAC patients are diagnosed with distant metastasis at initial diagnosis, where only adjuvant therapy is feasible.
Early diagnosis and detection of PDAC can significantly improve patient prognosis. To date, the only diagnostic biomarker for PDAC is serum Carbohydrate antigen199(CA199) levels, which are neither diagnostic nor specific. High CA199 levels are uncommon in early PDAC but most common in late-stage PDAC. Furthermore, elevated CA199 levels are frequently detected in various benign and malignant diseases, including pancreatitis, cholestasis, and cancer. Additionally, due to screening limitations, imaging modalities such as computed tomography (CT), magnetic resonance imaging (MRI), and endoscopic ultrasound (EUS) are insufficient for early detection of PDAC.
Ideally, the investigators aim to obtain non-invasive, reliable, and repeatable biological markers with clinical potential for early cancer diagnosis. Early studies have identified circulating tumor DNA (ctDNA), circulating tumor cells (CTC), extracellular vesicles (EV), plasma proteomics, and circulating tumor cells (CTCs) as promising real-time and remote tools for this purpose. Compared to other solid tumors, especially lung and breast cancer, some of these circulating biomarkers have entered clinical practice, while blood-derived biomarkers for PDAC diagnosis or monitoring are very limited (excluding CA199), and CA199 is largely underdeveloped compared to other tumors. One example is the use of EpCAM(Epithelial cell adhesion molecule) and cytokeratin for CellSearch system diagnostics, an FDA(Food and Drug Administration)-approved method for diagnosing metastatic breast, colon, and prostate cancers, which was evaluated for PDAC diagnosis, achieving an accuracy rate of 11-78.5%, indicating a wide variation in PDAC detection rates. Other molecular features for diagnosing PDAC, including KRAS mutations in CTCs, miRNA in EVs, and heparan sulfate proteoglycan glypican 1 (GPC1) in extracellular vesicles, unfortunately, exhibit significant differences in sensitivity and predictive performance across different studies, particularly between tumor and CTC status. One study found that in 97% of patients with tumors carrying mutated KRAS, only 18% of CTCs carried the wild-type KRAS allele, even from metastatic tumors. Therefore, due to genetic limitations associated with CTC enrichment and identification, ctDNA isolation, etc., using a single biomarker may only capture partial tumor biological characteristics, leading to low consistency and false negatives. Given the challenges of early diagnosis of PDAC, it is imperative to develop one or more new biological markers for early PDAC diagnosis to capture more possible biological characteristics of primary and metastatic tumors.
The immune system is an extremely important defense system in the human body. Through specific and non-specific biological processes, the immune system can detect various pathogens and harmful substances ranging from viruses to parasites, and differentiate them from healthy cells and tissues in the body under normal circumstances. Therefore, there is a close connection between the immune system and the overall health of an individual. Tumor development remains under constant surveillance by the immune system, and in the early stages of disease, the immune system responds and immune features undergo changes. However, when clinical symptoms appear, it indicates that the immune system is struggling to overcome the presence of harmful substances, and at this point, the disease has already progressed to the middle or late stage. By establishing a large-scale early pancreatic cancer clinical cohort, collecting high-quality multi-modal immune data from individuals, and integrating cutting-edge artificial intelligence models, it is possible to decode individual immune features and develop early diagnostic techniques for pancreatic cancer based on capturing immune status and response signals. This approach can help identify early risk factors for pancreatic cancer by analyzing abnormal immune responses before disease progression, enabling early diagnosis of pancreatic cancer.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Pancreatic Cancer | – | –The patient is diagnosed with pancreatic cancer for the first time and has not received any tumor treatment. |
| Benign Pancreatic Diseases | – | –The patient is diagnosed with a benign pancreatic disease ,such as SCN、MCN、IPMN.and has not undergone any treatment. |
| Healthy controls | – | –A healthy population without any pancreatic-related diseases or other cancers. |
Who may qualify
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Prospective inclusion of 1000 patients with pancreatic cancer (early-stage pancreatic cancer accounts for approximately 75% of cases), 1000 patients with benign pancreatic diseases, and 1000 healthy individuals as controls. Peripheral blood samples were collected from newly diagnosed pancreatic cancer patients and healthy individuals. Using techniques such as plasma TCR-seq, CyTOF, and plasma proteomics, multi-modal individual immune characteristics were obtained and analyzed along with clinical information. An artificial intelligence predictive model was built based on these multi-modal individual immune characteristics to establish an early screening technique for pancreatic cancer.
Key inclusion criteria (2 listed)
- Sign the informed consent form;
- Initial diagnosis as patients with pancreatic cancer, patients with benign pancreatic lesions, or healthy controls.
Key exclusion criteria (5 listed)
- History of other malignancies;
- Presence of organ dysfunction;
- Concurrent immunodeficiency syndrome, active tuberculosis, HIV infection, etc.;
- Allogeneic transplantation requiring immunosuppressive therapy;
- Poor follow-up compliance.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Peripheral blood mononuclear cell
Time frame: During the 1-7 day period before surgery
Using RNA seq technology to analyze differentially expressed genes in peripheral immune cells
Peripheral blood mononuclear cell
Time frame: During the 1-7 day period before surgery
TCR/BCR-seq:Using multiple amplification to obtain the CDR3(complementarities determining region3) region of TCR and BCR and analyzing the VDJ rearrangement pattern
Peripheral blood mononuclear cell
Time frame: During the 1-7 day period before surgery
Analyzing RNA expression in individual cells using scRNA-seq
Peripheral blood mononuclear cell
Time frame: During the 1-7 day period before surgery
scTCR/BCR-seq:Using multiple amplification to obtain the CDR3(complementarities determining region3) region of TCR and BCR and analyzing the VDJ rearrangement pattern in individual cells
Peripheral blood mononuclear cell
Time frame: During the 1-7 day period before surgery
Identification of open chromatin regions in individual cells using scATAC-seq technology
Peripheral blood mononuclear cell
Time frame: During the 1-7 day period before surgery
Detecting the abundance and type of some markers for peripheral blood mononuclear cell using CYTOF technology
CT
Time frame: Within 1 month before surgery
Imaging data from the patient's initial visit
MRI
Time frame: Within 1 month before surgery
Imaging data from the patient's initial visit
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 16 Jul 2024.
- Individual participant dataSharing planned: No
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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.
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Pancreatic Cancer Resectable, run by Zhejiang University at 2 sites in China.
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 5 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 16 Jul 2024. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in China. 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 Qi Zhang, Associate professor (13819137113, qi.zhang@zju.edu.cn), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Peripheral blood mononuclear cell (time frame: During the 1-7 day period before surgery). The study lists 8 primary outcomes in all. 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 16 Jul 2024.