Colorectal CancerNCT06504901
Evaluation of Efficacy and Safety of PD-1 Monoclonal Antibody in Combination With rhG-CSF, IL-2, and CapeOX in Initially Resectable Synchronous Colorectal Liver Metastases
An observational study of Colorectal Cancer, run by The First Affiliated Hospital with Nanjing Medical University.
Trial summary
This study attempts to employ a combination therapy using rhG-CSF, IL-2, and PD-1 inhibitors, aiming to overcome the limitations of monotherapy in immunotherapy through multi-faceted immune regulation. Read more about this study
- Who is it for?
- Ages 18 to 75 years
- Conditions the study is for
- Colorectal Cancer
- What is being tested?
- Tislelizumab, Interleukin-2 and Capecitabine
- How many people
- 30 participants
- Where
- No sites listed yet
- Study dates
- 10 Jul 2024to 10 Jul 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 18 to 75 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: 1. Age ≥18 years and ≤75 years 2. Histologically confirmed colorectal adenocarcinoma 3. pMMR (proficient mismatch repair) or MSI-L (microsatellite instability-low) or MSS (microsatellite stable) 4. Synchronous liver metastases 5. Achievable NED (No Evidence of Disease) status 6. CRS (Clinical Risk Score) of 3-4 points 7. ECOG (Eastern Cooperative Oncology Group) Performance Status score ≤ 1
Who may be able to join
- Age ≥18 years and ≤75 years
- Histologically confirmed colorectal adenocarcinoma
- pMMR (proficient mismatch repair) or MSI-L (microsatellite instability-low) or MSS (microsatellite stable)
- Synchronous liver metastases
- Achievable NED (No Evidence of Disease) status
- CRS (Clinical Risk Score) of 3-4 points
- ECOG (Eastern Cooperative Oncology Group) Performance Status score ≤ 1
Who cannot join
- Recurrent colorectal cancer with active bleeding, perforation, or complex conditions requiring urgent surgery; or concurrent non-colorectal cancer malignancies.
- Patients who have previously received systemic anticancer therapy for colorectal cancer; or have been treated with PD-1, PD-L1, or CTLA-4 antibodies.
- Patients with any active autoimmune disease; known or tested positive for Human Immunodeficiency Virus (HIV) or Acquired Immunodeficiency Syndrome (AIDS); or a history requiring steroid or immunosuppressive drug treatment.
- Patients with interstitial lung disease, non-infectious pneumonitis, or uncontrolled systemic diseases (such as diabetes, hypertension, pulmonary fibrosis, and acute pneumonia).
- Patients who experienced any Grade 2 or higher toxicities due to prior treatments (as classified by the Common Terminology Criteria for Adverse Events [CTCAE] version 5), which have not resolved (excluding anemia, alopecia, and skin pigmentation changes); known or suspected history of hypersensitivity to any of the drugs used in the trial.
- Pregnant or breastfeeding women.
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Evaluation of Efficacy and Safety of PD-1 Monoclonal Antibody in Combination With rhG-CSF, IL-2, and CapeOX in Initially Resectable Synchronous Colorectal Liver Metastases: A Single-Center, Single-Arm, Open-Label Clinical Study (PRICE)
This study attempts to employ a combination therapy using rhG-CSF, IL-2, and PD-1 inhibitors, aiming to overcome the limitations of monotherapy in immunotherapy through multi-faceted immune regulation. By modulating the immune microenvironment to enhance immune cell infiltration, and breaking through the physical and immunosuppressive barriers of tumors, it seeks to augment the efficacy of immunotherapy. This approach explores the effectiveness of a neoadjuvant treatment model in cases of liver metastasis.
Read the detailed description
Colorectal cancer stands as a prominent global health issue, ranking among the most prevalent malignancies worldwide. Its incidence exhibits distinct geographical variations, with higher rates observed in developed countries. Age is a significant risk factor, primarily affecting individuals aged 50 and above, although a concerning trend of increasing incidence in younger adults has emerged in recent years. There exists a gender disparity, with a slightly higher prevalence in males. Notably, lifestyle factors, including dietary choices, sedentary habits, smoking, and obesity, play pivotal roles in its pathogenesis. These epidemiological patterns underscore the urgency of implementing effective prevention strategies and advancing early detection methods to mitigate the impact of the disease.
The poor prognosis in colorectal cancer patients primarily stems from the tumor's aggressive biological properties and its propensity for distant metastasis. The unique anatomy of the liver, endowed with both the portal venous and hepatic arterial systems, and abundant blood supply, renders it the most common site for distant metastasis from colorectal cancer. Currently, radical surgical resection remains the primary treatment for colorectal liver metastases; however, due to tumor burden and clinical complications, only 17% to 20% of patients with colorectal liver metastases are amenable to surgery. With advancements in therapeutic modalities and the precision of medical approaches, a comprehensive treatment paradigm combining surgery, radiofrequency ablation, postoperative targeted drugs, and interventional therapies has gradually taken shape. Although this has enriched treatment options for colorectal liver metastases and improved outcomes, many patients present with multifocal intrahepatic metastases and severe complications at diagnosis, precluding further surgical intervention and resulting in limited survival and poor prognosis. In recent years, immunotherapy for tumors has garnered unprecedented attention and extensive clinical application, fundamentally relying on enhancing the patient's own immune capabilities to bolster antitumor activity. The ongoing in-depth investigation into the programmed cell death receptor 1 (PD1)/programmed cell death ligand 1 (PDL1) signaling pathway has also presented new opportunities for patients with colorectal liver metastases.
In colorectal cancer, the PD-1 inhibitory pathway plays a central role in regulating immune cell exhaustion. However, a majority of colorectal cancer patients exhibit limited response to monotherapy targeting PD-1, suggesting that combinations of PD1 inhibitors with other immunostimulatory agents may address this challenge. Some of these combination therapies have made progress in animal models and are being tested in clinical studies. Among them, interleukin-2 (IL-2) emerges as a promising candidate to synergize with PD-1 blockade in exerting antitumor effects. Meanwhile, recombinant human granulocyte colony-stimulating factor (rhG-CSF) has been primarily utilized in oncology for two purposes: first, to prevent and treat neutropenia induced by chemotherapy or radiotherapy; second, as a priming strategy to augment the efficacy of chemotherapy. Our study aims to explore a combination therapy employing rhG-CSF, IL-2, and PD-1 inhibitors, with the objective of overcoming the limitations of single-agent immunotherapy through multifaceted immune modulation. By modulating the immune microenvironment to enhance immune cell infiltration and breach the physical and immunosuppressive barriers of tumors, we seek to potentiate the effects of immunotherapy and investigate the efficacy of a neoadjuvant treatment model in liver metastases.
- Conditions
- Colorectal Cancer
- Being tested
- Tislelizumab, Interleukin-2, Capecitabine, Oxaliplatin, Neupogen
- Keywords
- Tislelizumab, Interleukin-2, MSS/pMMR colorectal cancer, rhG-CSF
- Medical subject headings
- Colorectal Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
TislelizumabDrug
Tislelizumab 200mg ivd D1
Interleukin-2Drug
Interleukin 2 100IU HD,QOD d1-d14
CapecitabineDrug
Capecitabine: 1000mg/m2 bid po, d1-d14
OxaliplatinDrug
Oxaliplatin 130mg/m2 ivd, d1
NeupogenDrug
rhG-CSF 5mcg/kg HD, QD d1-d14
| Study group | Role | What they receive |
|---|---|---|
| CapeOX+PD-1+IL-2+rhG-CSF | Tislelizumab 200mg ivd D1 + Interleukin 2 100IU HD,QOD d1-d14+rhG-CSF 5mcg/kg HD, QD d1-d14 +CapeOX (Capecitabine: 1000mg/m2 bid po, d1-d14;Oxaliplatin 130mg/m2 ivd, d1) 6 cycles Receives: Drug: Tislelizumab; Drug: Interleukin-2; Drug: Capecitabine; Drug: Oxaliplatin; Drug: Neupogen |
What is being measured
The primary outcome is the main question the study is designed to answer.
CR rate (cCR + local excision pCR)
Complete Response rate," which includes both "complete clinical response" (cCR)
Measured: 3 years
Secondary outcomes (2)
Event-Free Survival rates
Event-Free Survival (EFS) is the length of time after treatment during which the patient survives without any events of interest occurring, such as disease progression, recurrence, or death. Therefore, the 1/2/3-year EFS rates refer to the percentages of patients surviving without these events at 1, 2, and 3 years.
Measured: 5 years
Overall Survival rates
Overall Survival (OS) is the most common endpoint in cancer clinical trials, measuring the proportion of patients still alive at specific time points after the start of treatment. Thus, the 1/2/3-year OS rates represent the percentages of patients still alive at 1, 2, and 3 years post-treatment.
Measured: 5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Jul 2024
- Study start10 Jul 2024 (estimated)
- Primary completion10 Jul 2025 (estimated)
- Study completion10 Jul 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Colorectal CancerStudies of the same condition, open and under way.
- More trials run by The First Affiliated Hospital with Nanjing Medical 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
- Case crossover
- Time perspective
- Cross-sectional
- Enrolment
- 30 participants (estimated)
Sponsor and investigators
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06504901
- Sponsor's protocol ID
- PRICE202407
- Status last verified
- Jul 2024
- First submitted
- 11 Jul 2024
- Last updated
- 17 Jul 2024
- Results posted
- No
- Data monitoring committee
- Yes
- 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 17 Jul 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of Efficacy and Safety of PD-1 Monoclonal Antibody in Combination With rhG-CSF, IL-2, and CapeOX in Initially Resectable Synchronous Colorectal Liver Metastases: A Single-Center, Single-Arm, Open-Label Clinical Study (PRICE)
- ClinicalTrials.gov ID
- NCT06504901
- Acronym / sponsor ID
- PRICE202407
- Conditions
- Colorectal Cancer
- Keywords
- Tislelizumab, Interleukin-2, MSS/pMMR colorectal cancer, rhG-CSF
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 30 participants (estimated)
- Lead sponsor
- The First Affiliated Hospital with Nanjing Medical UniversityUniversity, hospital or other
- Study start
- 10 Jul 2024 (estimated)
- Primary completion
- 10 Jul 2025 (estimated)
- Study completion
- 10 Jul 2027 (estimated)
- First posted
- 17 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.
This study attempts to employ a combination therapy using rhG-CSF, IL-2, and PD-1 inhibitors, aiming to overcome the limitations of monotherapy in immunotherapy through multi-faceted immune regulation. By modulating the immune microenvironment to enhance immune cell infiltration, and breaking through the physical and immunosuppressive barriers of tumors, it seeks to augment the efficacy of immunotherapy. This approach explores the effectiveness of a neoadjuvant treatment model in cases of liver metastasis.
Detailed description
Colorectal cancer stands as a prominent global health issue, ranking among the most prevalent malignancies worldwide. Its incidence exhibits distinct geographical variations, with higher rates observed in developed countries. Age is a significant risk factor, primarily affecting individuals aged 50 and above, although a concerning trend of increasing incidence in younger adults has emerged in recent years. There exists a gender disparity, with a slightly higher prevalence in males. Notably, lifestyle factors, including dietary choices, sedentary habits, smoking, and obesity, play pivotal roles in its pathogenesis. These epidemiological patterns underscore the urgency of implementing effective prevention strategies and advancing early detection methods to mitigate the impact of the disease.
The poor prognosis in colorectal cancer patients primarily stems from the tumor's aggressive biological properties and its propensity for distant metastasis. The unique anatomy of the liver, endowed with both the portal venous and hepatic arterial systems, and abundant blood supply, renders it the most common site for distant metastasis from colorectal cancer. Currently, radical surgical resection remains the primary treatment for colorectal liver metastases; however, due to tumor burden and clinical complications, only 17% to 20% of patients with colorectal liver metastases are amenable to surgery. With advancements in therapeutic modalities and the precision of medical approaches, a comprehensive treatment paradigm combining surgery, radiofrequency ablation, postoperative targeted drugs, and interventional therapies has gradually taken shape. Although this has enriched treatment options for colorectal liver metastases and improved outcomes, many patients present with multifocal intrahepatic metastases and severe complications at diagnosis, precluding further surgical intervention and resulting in limited survival and poor prognosis. In recent years, immunotherapy for tumors has garnered unprecedented attention and extensive clinical application, fundamentally relying on enhancing the patient's own immune capabilities to bolster antitumor activity. The ongoing in-depth investigation into the programmed cell death receptor 1 (PD1)/programmed cell death ligand 1 (PDL1) signaling pathway has also presented new opportunities for patients with colorectal liver metastases.
In colorectal cancer, the PD-1 inhibitory pathway plays a central role in regulating immune cell exhaustion. However, a majority of colorectal cancer patients exhibit limited response to monotherapy targeting PD-1, suggesting that combinations of PD1 inhibitors with other immunostimulatory agents may address this challenge. Some of these combination therapies have made progress in animal models and are being tested in clinical studies. Among them, interleukin-2 (IL-2) emerges as a promising candidate to synergize with PD-1 blockade in exerting antitumor effects. Meanwhile, recombinant human granulocyte colony-stimulating factor (rhG-CSF) has been primarily utilized in oncology for two purposes: first, to prevent and treat neutropenia induced by chemotherapy or radiotherapy; second, as a priming strategy to augment the efficacy of chemotherapy. Our study aims to explore a combination therapy employing rhG-CSF, IL-2, and PD-1 inhibitors, with the objective of overcoming the limitations of single-agent immunotherapy through multifaceted immune modulation. By modulating the immune microenvironment to enhance immune cell infiltration and breach the physical and immunosuppressive barriers of tumors, we seek to potentiate the effects of immunotherapy and investigate the efficacy of a neoadjuvant treatment model in liver metastases.
Study design
- Observational model
- Case crossover
- Time perspective
- Cross-sectional
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| CapeOX+PD-1+IL-2+rhG-CSF | – | Drug: Tislelizumab, Drug: Interleukin-2, Drug: Capecitabine, Drug: Oxaliplatin, Drug: NeupogenTislelizumab 200mg ivd D1 + Interleukin 2 100IU HD,QOD d1-d14+rhG-CSF 5mcg/kg HD, QD d1-d14 +CapeOX (Capecitabine: 1000mg/m2 bid po, d1-d14;Oxaliplatin 130mg/m2 ivd, d1) 6 cycles |
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- 1. Age ≥18 years and ≤75 years 2. Histologically confirmed colorectal adenocarcinoma 3. pMMR (proficient mismatch repair) or MSI-L (microsatellite instability-low) or MSS (microsatellite stable) 4. Synchronous liver metastases 5. Achievable NED (No Evidence of Disease) status 6. CRS (Clinical Risk Score) of 3-4 points 7. ECOG (Eastern Cooperative Oncology Group) Performance Status score ≤ 1
Key inclusion criteria (7 listed)
- Age ≥18 years and ≤75 years
- Histologically confirmed colorectal adenocarcinoma
- pMMR (proficient mismatch repair) or MSI-L (microsatellite instability-low) or MSS (microsatellite stable)
- Synchronous liver metastases
- Achievable NED (No Evidence of Disease) status
Key exclusion criteria (6 listed)
- Recurrent colorectal cancer with active bleeding, perforation, or complex conditions requiring urgent surgery; or concurrent non-colorectal cancer malignancies.
- Patients who have previously received systemic anticancer therapy for colorectal cancer; or have been treated with PD-1, PD-L1, or CTLA-4 antibodies.
- Patients with any active autoimmune disease; known or tested positive for Human Immunodeficiency Virus (HIV) or Acquired Immunodeficiency Syndrome (AIDS); or a history requiring steroid or immunosuppressive drug treatment.
- Patients with interstitial lung disease, non-infectious pneumonitis, or uncontrolled systemic diseases (such as diabetes, hypertension, pulmonary fibrosis, and acute pneumonia).
- Patients who experienced any Grade 2 or higher toxicities due to prior treatments (as classified by the Common Terminology Criteria for Adverse Events [CTCAE] version 5), which have not resolved (excluding anemia, alopecia, and skin pigmentation changes); known or suspected history of hypersensitivity to any of the drugs used in the trial.
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 |
|---|---|---|
| TislelizumabTislelizumab 200mg ivd D1 | Drug | CapeOX+PD-1+IL-2+rhG-CSF |
| Interleukin-2Interleukin 2 100IU HD,QOD d1-d14 | Drug | CapeOX+PD-1+IL-2+rhG-CSF |
| CapecitabineCapecitabine: 1000mg/m2 bid po, d1-d14 | Drug | CapeOX+PD-1+IL-2+rhG-CSF |
| OxaliplatinOxaliplatin 130mg/m2 ivd, d1 | Drug | CapeOX+PD-1+IL-2+rhG-CSF |
| NeupogenrhG-CSF 5mcg/kg HD, QD d1-d14 | Drug | CapeOX+PD-1+IL-2+rhG-CSF |
Primary outcome
CR rate (cCR + local excision pCR)
Time frame: 3 years
Complete Response rate," which includes both "complete clinical response" (cCR)
2 secondary outcomes
Event-Free Survival rates
Time frame: 5 years
Overall Survival rates
Time frame: 5 years
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 17 Jul 2024.
- Individual participant dataSharing planned: Undecided
Related trials for Colorectal Cancer
Not yet recruitingPhase 1
Hepatic Artery Infusion of Carfilzomib in Participants With Liver Metastatic Disease Previously Treated With Hepatic Artery Infusion Pump Therapy
Colorectal Neoplasms, Neoplasms
Active, not recruiting
Streamlined Geriatric and Oncological Evaluation Based On IC Technology
Breast Cancer, Comorbidities and Coexisting Conditions
RecruitingObservational study
Pre- and On-treatment Multi-omics Profiling of Locally Advanced Rectal Cancer
Rectal Neoplasms
Enrolling by invitationObservational study
Natural History Study of Early Life Exposures in Agriculture (ELEA)
Prostate Cancer, Leukemia
RecruitingPhase 2
Tislelizumab in People With Colorectal Cancer
Colorectal Cancer
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.
Questions about this trial
What is this clinical trial studying?
An observational study of Colorectal Cancer, run by The First Affiliated Hospital with Nanjing Medical University.
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 7 inclusion and 6 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 17 Jul 2024. Status can change between updates, so confirm with the study contact before making plans.
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 Yueming Sun, MD (862568306026, sunyueming@njmu.edu.cn), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
CR rate (cCR + local excision pCR) (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 17 Jul 2024.