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Trial With Autologous Dendritic Cell Vaccination in Patients With Stage II-III HER2 Negative Breast Cancer

Phase II Trial With Autologous Dendritic Cell Vaccination in Patients With Stage II-III HER2 Negative Breast Cancer

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01431196
Enrollment
29
Registered
2011-09-09
Start date
2011-02-28
Completion date
2013-12-31
Last updated
2016-05-19

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

Conditions

Stage II Breast Cancer, Stage III Breast Cancer

Keywords

breast cancer, neoadjuvant chemotherapy, autologous dendritic cell vaccination

Brief summary

Molecular expression in breast cancer (BC) defines special fenotypes with different prognostic and predictive features.Since the addition of trastuzumab and lapatinib to chemotherapy, HER2 overexpressing tumors have become the best responders to systemic therapies, reaching pathologic complete response rates (pCR) around 50%. But HER2 negative tumors (luminal A and triple negative) are characterized by low chemosensitivity (luminal A) or early distant relapse after diagnosis (triple negative BC) . In this open, prospective, non-randomized and multicentric phase II study the investigators include stage II and III HER2 negative BC patients that are going to receive neoadjuvant sequential chemotherapy Epirubicin+Ciclofosfamide x 4 and then Docetaxel x 4)with an individualized vaccination with autologous dendritic cells pulsed with their own tumor. The hypothesis is that the reinforcement of the immune system with the autologous dendritic cell vaccination against HER2 negative BC could increase pathologic complete responses (pCR) and disease free survival(DFS), when added to chemo, surgery and radiation therapy and in a maintenance schedule.

Detailed description

Chemotherapy schedule: * dose dense epirubucin 100 mgr/m2 plus ciclofosfamide 600 mgr/m2 every two weeks for four cycles with with GM-CSF support on day +1 (pegylated filgastrim) or on days +5 to +9 (filgastrim) subcutaneously * docetaxel 80-100 mgr/m2 every three weeks for four cycles. Addition of GM-CSF if docetaxel doses are \> 85 mgr/m2

Interventions

Autologous dendritic cell vaccination. Dendritic cells are pulsed with their own tumor antigens

Sponsors

Spanish Clinical Research Network - SCReN
CollaboratorNETWORK
National Institutes of Health (NIH)
CollaboratorNIH
Clinica Universidad de Navarra, Universidad de Navarra
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* HER2 negative and stage II and III Breast cancer patients who benefit with neoadjuvant chemotherapy * age 18-75 * to get enough tumoral sample to elaborate the vaccine

Exclusion criteria

* pregnancy * severe diseases * hepatitis or HIV * need to be on immunosuppressant drugs

Design outcomes

Primary

MeasureTime frame
pathologic complete response (pCR) in the breast and the axilla6 months after starting chemotherapy

Secondary

MeasureTime frameDescription
Number of participants with adverse eventsDuring the 6-24 months of administration of the vaccine
Impact of the vaccine on patients DFS and OSthree to five years after the diagnosis of breast cancerWe will compare our cohort of patients vaccinated and treated with chemotherapy, surgery and radiation therapy with an historic cohort in our center treated with the same schedule of chemotherapy , surgery and radiation therapy without the vaccine
EORTC quality of lifeFrom 9 months and up to two years
Correlation among the specific immune response induced in patients and the pathologic response of the tumor6-24 monthsSpecific immune response will be evaluated as delayed hipesrsensitivity (DTH), humoral response by cuantification antibodies against tumoral cells (ELISA)and cellullar response (proliferation assay and citokines production)

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026