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OncoMatch/Clinical Trials/NCT02919644

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

Is NCT02919644 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including autologous dendritic cells loaded with autologous tumour homogenate and IL2 for stage iv colorectal cancer.

Phase 2RecruitingIstituto Romagnolo per lo Studio dei Tumori Dino Amadori IRST S.r.l. IRCCSNCT02919644Data as of Jun 2026Location: Italy

Treatment: autologous dendritic cells loaded with autologous tumour homogenate · IL2Single-arm, monocentric trial to assess safety and immunological efficacy of adjuvant vaccination with autologous dendritic cells loaded with autologous tumour homogenate after curative resection for stage IV colorectal cancer

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Extracted eligibility criteria

Treatments studied

Other

autologous dendritic cells loaded with autologous tumour homogenateIL2

Cancer type

Colorectal Cancer

Disease stage

Required: Stage IV

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≥ 19

Prior therapy

Must have received: surgery — curative resection for stage IV colorectal cancer

surgically treated with radical intent

Cannot have received: preoperatory chemotherapy with a fluoropyrimidine plus oxaliplatin

Exception: unless not candidate for postoperatory chemotherapy with the same schedule (e.g. for unacceptable toxicity) or refuse completion of the perioperatory treatment

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

Lab requirements

Blood counts

haemoglobin >10 g/dl; white blood cells ≥4000/μl; absolute neutrophil count >1500/μl; platelets ≥100000/μl

Kidney function

serum creatinine <1.5 times the upper institutional reference level

Liver function

ast and alt <3 times the upper institutional reference level; total bilirubin <1.5 times the upper institutional reference level

Cardiac function

patients aged 70 years or older must have left ventricular ejection fraction not lower than 55% as assessed by echocardiography

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT02919644 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior preoperatory chemotherapy with a fluoropyrimidine plus oxaliplatin disqualifies patients from enrollment.

What disease stage is eligible?

Stage IV is required.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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