Chemotherapy Effect, Colorectal Neoplasms, Molecular Sequence Variation
Conditions
Brief summary
Patients meeting the inclusion criteria will be randomized 1:1 into Cohort A (n ≈ 177) or Cohort BC (n ≈ 177). Cohort A is the control: patients receive combination chemotherapy with FOLFOX plus anti-EGFR therapy (panitumumab or cetuximab) based on RAS/BRAF wild-type data, according to clinical guidelines. The BC cohort begins FOLFOX chemotherapy and simultaneously undergoes extensive molecular genetic profiling. Further, the BC cohort, depending on the profile, is divided into cohort B - patients without changes in alternative oncogenes, and cohort C - with changes in alternative oncogenes. The expected cohort ratio is 3:1 (\ 120 and \ 40 patients). Cohort B begins to receive anti-EGFR therapy in addition to chemotherapy, and the potentially resistant cohort C continues to receive chemotherapy alone or begins to receive bevacizumab if there are no contraindications.
Detailed description
In total, the study plans to include 355 patients diagnosed with unresectable metastatic colorectal cancer with a left-sided localization of the primary tumor, who have not previously received systemic therapy for metastatic disease, have wild-type KRAS/NRAS/BRAF, or have wild-type KRAS/NRAS with unknown BRAF status in no contraindications to targeted therapy (cetuximab/panitumumab/bevacizumab). Patients meeting the inclusion criteria will be randomized 1:1 into Cohort A (n ≈ 177) or Cohort BC (n ≈ 177). Cohort A is the control: patients receive combination chemotherapy with FOLFOX plus anti-EGFR therapy (panitumumab or cetuximab) based on RAS/BRAF wild-type data, according to clinical guidelines. Next, this cohort, after completion of the protocol, undergoes extended profiling, according to the results of which it is divided into cohorts A1 and A2. Cohort A1 includes patients without changes in alternative oncogenes (N ≈ 120), cohort A2 includes patients with changes (N ≈ 40). The BC cohort begins FOLFOX chemotherapy and simultaneously undergoes extensive molecular genetic profiling. Further, the BC cohort, depending on the profile, is divided into cohort B - patients without changes in alternative oncogenes, and cohort C - with changes in alternative oncogenes. The expected cohort ratio is 3:1 (\ 120 and \ 40 patients). Cohort B begins to receive anti-EGFR therapy in addition to chemotherapy, and the potentially resistant cohort C continues to receive chemotherapy alone or begins to receive bevacizumab if there are no contraindications.
Interventions
DRUGCetuximab
FOLFOX+cetuximab/panitumumab q2w until desease progression, deescalation to de Gramont+cetuximab/panitumumab is allowed after 8 cycles
Sponsors
Atlas Biomed
N.N. Blokhin National Medical Research Center of Oncology
Moscow MultidisciplinaryClinical Center Kommunarka
City Clinical Oncology Hospital No 1
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
randomize and compare contol and experimental groups
Eligibility
Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No
Inclusion criteria
1. Informed consent signed before commencing any procedures related to the clinical trial. 2. Age ≥18 years. 3. ECOG status 0-2. 4. Life expectancy greater than 12 weeks as assessed by the investigator. 5. Verified diagnosis of colorectal adenocarcinoma (C18.5, C19, C20). 6. Metastatic unresectable form of the disease that has not previously received any systemic therapy for the metastatic process (previous neo-/adjuvant therapy completed at least 6 months before the detection of metastases is allowed). 7. Left-sided localization of the primary tumor (from the splenic flexure of the colon inclusive). 8. Verified wild type KRAS, NRAS determined from tumor tissue. 9. Satisfactory function of hematopoiesis and internal organs: * absolute number of neutrophils ≥ 1.5×10 9 /l; * platelets ≥ 100×10 9 /l; * hemoglobin ≥ 90 g/l. * creatinine clearance above 50 ml/min; * total bilirubin \<1.5 X the upper limit of normal; * ALT or AST \>5 X the upper limit of normal in the presence of liver metastases or \>2.5 X the upper limit of normal in the absence of liver metastases. 10. Availability of a sufficient amount of tumor material for molecular genetic research. Tumor material must be collected no more than 24 months before inclusion in the study.
Exclusion criteria
1. Previous systemic therapy for metastatic disease. 2. Presence of KRAS/NRAS/V600E mutations (except for unknown BRAF status). 3. Uncertain KRAS/NRAS status 4. The presence of any other malignant tumor, with the exception of radically treated basal cell carcinoma, cervical cancer in situ, currently or within 5 years before inclusion in the study. Pregnant and lactating women, as well as planning pregnancy during the period of therapy in a clinical trial and 6 months after the end of therapy. 5. HIV infection, active hepatitis B, active hepatitis C. 6. Complicated primary tumor, requiring urgent surgical intervention. After it is eliminated, the patient can participate in the study. 7. The presence of a disease or condition that, in the opinion of the investigator, prevents the patient from participating in the study. 8. Impossibility of organizing central venous access.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| progression-free survival | through study completion, an average of 3 years | Intention to treat, Calculated from start of therapy to date of disease progression or death |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| edverse events | through study completion, an average of 3 years | all AE based on CTC criteria v. 5 |
| overall survival | through study completion, an average of 3 years | Calculated from start of therapy to date of last contact or death |
| progression-free survival based (per protocol) | through study completion, an average of 3 years | — |
Countries
Russia
Contacts
Primary ContactIlya Pokataev, phD
Backup ContactMaria Byakhova, phD
Outcome results
None listed