Current partner codePEPTIDESDE
NCT00935558·Phase 2·INTERVENTIONAL

Dendritic Cell Based Therapy for Breast Cancer Patients

Status

Withdrawn

Phase

Phase 2

Enrollment

0

Locations

1

Results

Not posted

Publications

2

Study summary

What the protocol is testing.

The primary aim of this study is to investigate time to progression in breast cancer patients vaccinated with autologous dendritic cells pulsed with peptides in combination with adjuvant aromatase inhibitor (AI), Thymosin 1 alpha and interleukin-2. The secondary aim is to investigate whether a measurable immune response can be induced, and to evaluate the clinical effect (objective response rate) of the vaccination regime.

Full detailed description

Only patients who have tumors \> 5 % positive for p53 by IHC can be referred to this treatment. All patients will receive standard dosage of AI +/- p53-DC vaccination. Patients who express HLA-A2 will also receive DC vaccination. Patients that do not express HLA-A2 will receive only AI and be regarded as controls. The vaccination regime consists of primary 10 intradermal injections of 1-2 weeks interval (q1w x 4 → q2w x 6) with p53 peptide-pulsed dendritic cells, followed by monthly injections until progression; proleukin and Zadaxin are used as vaccine adjuvants. Defined procedures are employed for generation of autologous dendritic cells for clinical application in a classified laboratory. Unmobilized leukapheresis will be used for isolation of large-scale mononuclear cells, and dendritic cells will be generated from monocytes by cytokine stimulation and loaded with p53 peptides. Frozen preparations of dendritic cells will be prepared using automated cryopreservation.Each patient will receive a minimum of 5x10\^6 dendritic cells per treatment supplemented with interleukin-2 6 MIU/m² sc per vaccine and 1.6 mg Thymosin 1 alpha sc x 2/week. Toxicity including autoimmunity will be evaluated using the common Toxicity Criteria (CTC).

Interventions

Treatment arms and agents.

BIOLOGICAL

DC vaccine

DC vaccination regime consist of primary 10 intradermal injections of 1-2 weeks interval. At the time of each vaccine 6 MIU/m² IL-2 will be administered sc. Zadaxin 1.6 mg is injected sc twice a week. and tablet Aromatase inhibitor is administered ; Exemestane 25 mg (tablet) is administered PO daily or Femar 2,5 mg (tablet) is administered PO daily or Arimidex 1 mg (tablet) is administered PO daily

DRUG

aromatase inhibitor

Exemestane 25 mg (tablet) is administered PO daily or Femar 2,5 mg (tablet) is administered PO daily or Arimidex 1 mg (tablet) is administered PO daily

Timeline

From registration to results.

  1. First posted

    Jul 9, 2009

  2. Study start

    Jul 2009

  3. Primary completion

    May 2012

  4. Study completion

    Not reported

  5. Results posted

    Not reported

  6. Registry updated

    May 31, 2012

Outcomes

What the study measures.

Primary outcomes

To determine time to progression

Time frame · after 8 and 16 weeks

Secondary outcomes

To evaluate safety of DC vaccination in combination with AI, to evaluate clinical tumor response, to evaluate treatment induced immune response to p53 end to evaluate duration of tumor and immune responses

Time frame · Weekly the first 4 weeks, thereafter biweekly for five months, thereafter monthly

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
Not reported
Sex
FEMALE
Healthy volunteers
No

Inclusion Criteria: * Patients with histological proven metastatic or locally advanced ER+/PGR+ breast cancer in progression after receiving 1. line endocrine therapy. * Further inclusion criteria: p53+ tumour, PS≤1, postmenopausal. Age \>18, PS ≤ 1 and acceptable CBC and blood chemistry results Exclusion Criteria: * Patients with a history of any other neoplastic disease less than 5 years ago (excepting treated carcinoma in situ of the cervix and basal/squamous carcinoma of the skin) * Patients with metastatic disease in the central nervous system * Patients with other significant illness including severe allergy, asthma, DM, angina pectoris or congestive heart failure * Patients with acute or chronic infection including HIV, hepatitis og TB * Patients who received antineoplastic therapy including chemotherapy, radiation, immunotherapy or other agents, less than 4 weeks before the beginning of the trial * Patients who received corticosteroids or other immunosuppressive agents * Patients with active autoimmune diseases such as lupus erythematosus, rheumatoid arthritis or thyroiditis * Severe hypercalcemia

Study locations

1 registered sites.

Denmark. Showing up to 24 locations stored in the fast local snapshot.

Department of Oncology, Copenhagen University Hospital, Herlev

Herlev, Denmark

Related trials

More studies on Thymosin Alpha-1.

Related PeptideStat pages

Put the record in context.

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