Vaccination with Autologous Dendritic Cells Loaded with Autologous Tumour Homogenate After Curative Resection for Stage IV Colorectal Cancer.

Launched by ISTITUTO ROMAGNOLO PER LO STUDIO DEI TUMORI DINO AMADORI IRST S.R.L. IRCCS · Sep 28, 2016

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment approach for patients with stage IV colorectal cancer who have had surgery to remove their tumors. The treatment involves using a type of immune cell called dendritic cells, which are taken from the patient’s own body and loaded with pieces of their tumor. The goal of this trial is to see if this personalized vaccine is safe and if it can help the immune system recognize and fight any remaining cancer cells after surgery.

To be eligible for this study, participants must be at least 18 years old and have been treated for stage IV colorectal cancer with the intention of completely removing the cancer. They should be free of disease, as confirmed by recent medical scans, and have recovered well from their surgery. Patients will need to provide written consent and may need to follow specific health guidelines to ensure their safety during the trial. Participants can expect to be closely monitored throughout the study to check their health and response to the vaccine.

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Eligibility criteria

• Inclusion Criteria:
• • 1. Patients must have histologically confirmed stage IV colorectal cancer surgically treated with radical intent.
• • 2. The autologous surgical specimen must have been collected and sent to the Somatic Cell Therapy Lab of Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST IRCCS) and must fulfil all the acceptance criteria prescribed by the Good Manufacturing practise (GMP) procedures.
• • 3. The patient must be disease-free, as assessed by CT scan or MRI of the chest, abdomen, pelvis performed within 60 days before enrolment. If the resected lesions had occurred in other sites, these must be also included in the baseline CT scan and in all the subsequent evaluations.
• • 4. The patient must have recovered (grade 1 or less by CTCAE 4.0) from all the adverse events related to previous surgery.
• • 5. Age \>18 years.
• • 6. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1.
• 7. Patient must have acceptable organ function, defined as:
• • 1. Haemoglobin \>10 g/dl
• • 2. White blood cells ≥4000/μl.
• • 3. Absolute neutrophil count \>1500/μl.
• • 4. Platelets ≥100000/μl.
• • 5. aspartate aminotransferase (AST) and Alanine Aminotransferase (ALT) \<3 times the upper institutional reference level.
• • 6. Total bilirubin \<1.5 times the upper institutional reference level.
• • 7. Serum creatinine \<1.5 times the upper institutional reference level.
• • 8. Patients aged 70 years or older must have left ventricular ejection fraction not lower than 55% as assessed by echocardiography.
• • 9. Female patients of childbearing potential and all male patients must accept and be compliant with an highly effective contraceptive method (i.e. with a failure rate of \<1% per year: double barrier method, one barrier method plus spermicidal, intrauterine device, or oral contraception) from informed consent signature and up to three months after end of study. For this purpose are considered of childbearing potential all female subjects after puberty unless they are post-menopausal for at least two years or are surgically sterile. Complete abstinence from sexual intercourses is acceptable if patients' lifestyle guarantees his/her strict compliance with this prescription in the judgement of the Investigator.
• • 10. The patient is willing and able to give written informed consent for the study.
• Exclusion Criteria:
• • 1. Patients with residual disease after surgery. Marginal resection of any lesion in the absence of clinically evident residual disease is acceptable.
• • 2. Patients who relapsed within 6 months since primary treatment of stage I-III colorectal cancer. If adjuvant chemotherapy had been administered, the term must be computed since last chemotherapy dose.
• • 3. Patient who completed surgery more than 60 days before study enrolment.
• • 4. History of other neoplastic diseases in the previous 5 years, except basal cell carcinoma of the skin and in situ carcinoma of the cervix uteri treated with curative surgery.
• • 5. History of congenital or acquired immunodeficiency, including history of organ transplantation.
• • 6. Any positivity for the serologic markers of hepatitis B virus (HBV) (including at least anti-HBs antibodies and anti-hepatitis B core (HBc) antibodies), hepatitis C virus (HCV), HIV or Treponema pallidum. The serologic tests must have been performed within 30 days before any GMP-regulated activity (i.e. surgical resection and leukapheresis). The sole positivity for antibodies against the HBV S antigen (i.e. with all other HBV markers negative) is indicative of previous HBV vaccination and therefore is acceptable.
• • 7. Female patients who are pregnant or nursing.
• • 8. Patients undergone surgery after preoperatory chemotherapy with a fluoropyrimidine plus oxaliplatin, unless they are not candidate for postoperatory chemotherapy with the same schedule in the opinion of the Investigator (e.g. for unacceptable toxicity) or refuse completion of the perioperatory treatment.
• • 9. Participation in another clinical trial with any investigational agent within 30 days prior to study screening.
• • 10. Any active inflammatory or autoimmune disease requiring systemic steroids or other immunomodulatory agents as detailed in section 6.4, or potentially requiring such treatments during the study treatment in the judgement of the Investigator.
• • 11. Any clinical condition that, in the opinion of the Investigator or the Transfusion Medicine specialist, is a contraindication to leukapheresis. In addition, all patients aged 70 or older must be evaluated by a cardiology specialist before the procedure to exclude any clinically relevant cardiac condition and any grade 3-4 cardiac arrhythmia, even if asymptomatic.
• • 12. Any clinical condition that, in the opinion of the Investigator, contraindicates the subcutaneous administration of low-dose IL-2 as per protocol (see section 6.2 for details).
• • 13. Any uncontrolled serious intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations potentially impacting patient safety and compliance in the opinion of the Investigator.
• • 14. Refusal of giving written informed consent.