Cadonilimab Combined With Fruquintinib and SBRT as Athird-line and Posterior Line Treatment in Patients With MSS CRC

Trial Title: Cadonilimab Combined With Fruquintinib and SBRT as Athird-line and Posterior Line Treatment in Patients With MSS CRC

NCT ID: NCT06551207

Condition: Metastatic Colorectal Cancer

Conditions: Official terms:
Colorectal Neoplasms

Study type: Interventional

Study phase: N/A

Overall status: Recruiting

Study design:

Allocation: Randomized

Intervention model: Parallel Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: Fruquintinib
Description: Fruquintinib:5mg ,qd,po, d1-d14, q3w
Arm group label: Fuquintinib combined with cardonilizumab and SBRT
Arm group label: fuquintinib

Intervention type: Drug
Intervention name: Cadonilimab
Description: Cadonilimab:10mg/kg, ivgtt, d1, q3w
Arm group label: Fuquintinib combined with cardonilizumab and SBRT

Intervention type: Radiation
Intervention name: SBRT
Description: SBRT:8-10Gy×5F, god, in 10 days
Arm group label: Fuquintinib combined with cardonilizumab and SBRT

Summary: An assessment of 6-month progression-free survival in patients with mCRC with third-line and postline metastatic colorectal cancer in combination with cardonilizumab and fuquinitinib and SBRT compared with fuquinitinib monotherapy

Criteria for eligibility:
Criteria:
Inclusion Criteria:• Provision of written Informed Consent Form (IC) prior to any study specific procedures - Age = 18 years, $75 years - Histologically or cytologically confirmed advanced Stage IV primary colorectal cancer - MSI status: MSS - At least two or more standard systemic therapies prior treatment (based on Fu, oxaliplatin, irinotecan, bevacizumab and cetuximab) of cytotoxic chemotherapy, treatment failure or intolerable toxicities - ECOG 0-1 - Patients must have measurable lesions - Expected overall survival ≥ 12 weeks - AST, ALT and alkaline phosphatase s 2.5 times the upper limit of normal (ULN), Serum bilirubin s 1.5 x ULN, creatinine 2 (except those who only show a small amount of ascites on imaging without clinical symptoms); Uncontrolled or moderate or higher pleural effusion or pericardial effusion - History of gastrointestinal bleeding or a definite tendency to gastrointestinal bleeding within 6 months before the start of treatment - Abdominal fistula, gastrointestinal perforation, or abdominal abscess developed within 6 months before the start of study treatment - Known hereditary or acquired bleeding (e.g. coagulation dysfunction) or thrombotic tendencies, e.g. in hemophiliacs; Currently or recently (within 10 days prior to the start of study therapy) used full dose oral or injectable anticoagulants or thrombolytic agents for therapeutic purposes (allowing prophylactic use of low-dose aspirin, low molecular weight heparin) - Aspirin (> 325 mg / day (maximum antiplatelet dose) or dipyridamole, ticlopidine, clopidogrel (≥ 75 mg) and clostazol are currently used or have been used recently (within 10 days before the start of study treatment) - Thrombosis or embolism events such as cerebrovascular accident (including transient ischemic attack, cerebral hemorrhage, cerebral infarction) and pulmonary embolism occurred within 6 months before the start of the study - Patient with an active infection, heart failure, heart attack, unstable angina pectoris, or unstable arrhythmia within the last 6 months - Physical examination or clinical trial findings that the investigator believes may interfere with the results or put the patient at increased risk for treatment complications, or other uncontrollable diseases - The researchers believe that the patient has a lesion and needs emergency palliative radiotherapy / emergency surgery (spinal cord compression, brain hernia, pathological fracture) - Lactating or pregnant women - History of immunodeficiency, including HIV positive, other acquired or congenital immunodeficiency diseases, or organ transplantation - Patients with mental illness, substance abuse, or social problems that affect compliance will not be enrolled after researcher's review - Known active infection and active tuberculosis infection were not included in the group; However, patients with hepatitis B virus (HBV) and hepatitis C virus (HCV) infection can be included in the group if their condition is stable after antiviral treatment - Patients who received live vaccine within 30 days prior to enrollment - Have clinical symptoms or diseases of the heart that are not well controlled - Systolic blood pressure > 140mmg or diastolic blood pressure > 90mmg regardless of any antihypertensive drugs; or a history of hypertensive crisis or hypertensive encephalopathy - Major vascular disease (such as aortic aneurysms requiring surgical repair or recent peripheral arterial thrombosis developed within 6 months - Severe, unhealed or open wounds and active ulcers or untreated fractures - Received major surgery within 4 weeks prior to the start of study treatment (except for diagnosis or expected to require major surgery during the study period - Inability to swallow tablets, malabsorption syndrome or any condition affecting gastrointestinal absorption - Had a history of intestinal obstruction and/or had clinical signs or symptoms of gastrointestinal obstruction within 6 months prior to initiation of study therapy, including incomplete obstruction related to pre-existing disease or requiring routine parenteral hydration, parenteral nutrition, or tube feeding - Patients with signs/symptoms of incomplete obstruction/obstructive syndrome/ileus at initial diagnosis may be admitted to the study if they have received definitive (surgical) treatment to resolve symptoms - There is evidence of abdominal gas accumulation that cannot be explained by puncture or recent surgical procedures - Metastatic disease involvina a maior airway or blood vessel or a large mediastinal tumor mass located in the center (<30 mm from the crest) - Patients with a history of hepatic encephalopathy For those who currentlv have interstitial oneumonia or interstitial luna disease, or who have a history of interstitial pneumonia or interstitial luna disease requiring hormone therapv. Or other - Patients with a history of hepatic encephalopathy - For those who currently have interstitial pneumonia or interstitial lung disease, or who have a history of interstitial pneumonia or interstitial lung disease requiring hormone therapy, Or other subjects with pulmonary fibrosis, institutionalized pneumonia, pneumoconiosis, drug-related pneumonia, idiopathic pneumonia that may interfere with the judgment and management of immune-related pulmonary toxicity, or with evidence of active pneumonia or severe impairment of lung function visible on chest CT during the screening period, radiation pneumonia is allowed in the radiation field: Active tuberculosis - Presence of active autoimmune disease or history of autoimmune disease with possible recurrence; Participants with non-systemic skin diseases such as vitiligo, psoriasis, and alopecia, controlled type 1 diabetes treated with insulin, or asthma in complete remission in childhood, were enrolled without any intervention as adults; Patients with asthma who require medical intervention with bronchodilators are not included - Use of immunosuppressants or systemic hormone therapy for immunosuppression within 14 days prior to initiation of study therapy - Known history of severe allergy to any monoclonal antibody, anti-angiogenesis targeting drug Severe infection, including but not limited to hospitalization for complications of infection, bacteremia, or severe pneumonia, in the 4 weeks prior to initiation of study treatment; Therapeutic antibiotics were given orally or intravenously within 2 weeks prior to the start of study therapy - According to the investigator's judgment, the patient has other factors that may affect the study results or lead to the forced termination of the study. There are serious abnormalities in laboratory examination, accompanied by family or social factors, which will affect the safety of the patient

Gender: All

Minimum age: 18 Years

Maximum age: 75 Years

Healthy volunteers: No

Locations:

Facility:
Name: Huazhong University of Science and Technology

Address:
City: Wuhan
Zip: 430000
Country: China

Status: Recruiting

Contact:
Last name: Xianglin Yuan, PhD,MD

Phone: 8627-83663406
Email: xlyuan1020@163.com

Start date: August 20, 2024

Completion date: December 30, 2027

Lead sponsor:
Agency: Liu Huang
Agency class: Other

Source: Tongji Hospital

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06551207