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Clinical study of autologous tumor lysate-pulsed dendritic cell therapy for advanced colorectal cancer (Stage3, 4)

Clinical study of autologous tumor lysate-pulsed dendritic cell therapy for advanced colorectal cancer (Stage3, 4) - Clinical study of autologous tumor lysate-pulsed dendritic cell therapy for advanced colorectal cancer (Stage3, 4)

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005929
Enrollment
15
Registered
2011-07-05
Start date
2011-07-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

colorectal cancer (Stage3, 4)

Interventions

Patients of stage 3a recieved UFT+l-LV( day1-28) and autologous tumor lysate-pulsed dendritic cells (day8,22) every 2 weeks.This treatment repeats 6 courses, or recieved capecitabine (day1-14) and au

Sponsors

Tomishiro Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Colorectal cancer patients who are histopathologically diagnosed as Stage3b or 4 and adenocarcinoma; (1)Tumor tissue is preserved after resection and tumor lysate is aseptically prepared; (2)No serious abnormality in heart, lung, bone marrow, liver, and renal functions; (3)Performance Status is 0-1; (4)Apheresis is feasibile.

Exclusion criteria

Exclusion criteria: Patients who have: (1)Pulmonary fibrosis or interstitial pneumonia, or history or predisposition of them (2)Serious drug allergy (3)Serious cardiac disease (4)Active autoimmune disease (5)Other cancers (6)Drainage is necessary (pleural/ascites effusion ) (7)Brain metastasis with symptoms (8)Edema which needs treatment (9)Positive for HIV or HTLV-1 (10)Continuous systematic administration of steroids within 4 weeks (20mg or more on a predonine conversion basis) (11)Uncontrollable infection (12)Pregnant or lactating (13)Gelling of plasma, cryoglobulinemia (14)Any reason why, in the opinion of the investigator, the patient should not participate.

Design outcomes

Primary

MeasureTime frame
Safety

Secondary

MeasureTime frame
Immunological responses Antitumor effect progression-free survival event-free survival overall survival

Countries

Japan

Contacts

Public ContactAtsushi Ochiai

Tomishiro Central Hospital Office of Clinical Trial

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026