Phase II Study With Trastuzumab + Paclitaxel in Locally Advanced HER2+ Tumors or Epirubicin + Taxotere in HER2- Tumors

Breast Neoplasms Clinical Trial

Official title:

Antitumor Immune Responses in Breast Cancer Patients Treated With Neoadjuvant Chemotherapy: a Phase II Study With Trastuzumab and Concomitant Weekly Paclitaxel in Patients With HER2+ Tumors or Epirubicin + Taxotere in HER2- Tumors.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02307227
• Other study ID #: CRO-18-2006
• Status: Completed
• Phase: Phase 2
• First received: November 26, 2014
• Last updated: December 1, 2014
• Start date: April 2006
• Est. completion date: April 2014

Study information

• Verified date: December 2014
• Source: Centro di Riferimento Oncologico - Aviano
• Contact: n/a
• Is FDA regulated: No
• Health authority: Italy: The Italian Medicines Agency
• Study type: Interventional

Clinical Trial Summary

Prospective, monoinstitutional, phase II study. Patients with HER 2 positive locally advanced breast cancer will be treated with 3 initial cycles (12 weeks) of trastuzumab plus paclitaxel and then if responding further 12 weeks and then with surgical resection, patients with HER2 negative breast carcinoma will be treated with 4 cycles (12 weeks) of epirubicin and taxotere. If responding 4 more cycles (12 weeks). Patients progressing will be treated depending on physician's and patient's preference

Description:

Primary Objective: to determine the pathological complete response (pCR) and correlation with immune response.

Secondary Objectives:

• to determine the progression free survival (PFS) and overall survival (OS);

• to evaluate the safety of the treatment with particular attention to cardiac safety.

Inclusion Criteria:

• Histologically proven breast carcinoma evaluated for HER 2 status and immune status

• Locally advanced carcinoma (UICC stage II-III)

• Age < 70 years

• measurable lesions

• ECOG Performance Status 0-2

• Life expectancy > 3 months

• Adequate bone marrow and hepatic functions

• Creatinine Clearance > 40 ml/min

• Written informed consent

• Patients must be accessible for treatment and follow up

Exclusion criteria:

• Prior chemotherapy or hormonal treatments

• Brain metastases.

• Past or current history of neoplasm other than curatively treated.

• Concurrent treatment with other experimental drugs.

• Left Ventricular Ejection Fraction (LVEF) <50 %

• History of significant neurological or psychiatric disorders.

Treatment HER2 positive (defined as 3+ at Herceptest or FISH/CISH positive) Herceptin 4mg/kg first time, then 2 mg/kg weekly with concomitant paclitaxel 80 mg/mq weekly (one cycle corresponding to 4 weeks) for 12 weeks (3 cycles). Clinical and instrumental evaluation, in responding patients continue for additional 12 weeks (total 6 cycles), then surgical excision

HER2 negative:

Epirubicin 90 mg/mq and docetaxel 75 mg/mq every 3 weeks for 4 cycles. Clinical and instrumental evaluation, in responding patients continue for additional 12 weeks (total 8 cycles), then surgical excision.

Main Parameters of Activity:

• Complete Remission (CR): complete disappearance of all previously detectable disease for a period of at least 28 days, and no new lesions.

• Partial Remission (PR): more than 30% reduction in the longest diameter of target lesions, and no new lesions.

• Stable Disease (SD): less than 30% reduction and less than 20% increase in the longest diameter of target lesions and no new lesions.

• Progressive Disease (PD): an increase in size of more than 20% of at least one lesion of previously documented disease. Or the appearance of disease at any site.

• Progression Free Survival (PFS) will be measured from the first day of the treatment until the first observation of disease progression or death due to any cause or the last date the patient was known to be progression free and alive.

• Overall Survival (OS) will be computed as the time between the first day of treatment and the date of death or the last date the patient was known to be alive.

Main Parameters of Safety:

• Adverse events, laboratory parameters.

• All toxicity will be graded using the NCI common toxicity criteria (Appendix II). Cardiac events (CHF) will be graded according to NYHA

Study procedure:

• At Baseline:

• Complete medical history, ECOG PS, physical examination (including a neurological examination, height, weight,),

• ECG

• Left ventricular ejection fraction evaluation (LVEF, evaluated by echocardiography).

• Blood chemistry (fasting blood sugar, transaminases, serum alkaline phosphatase, total bilirubin, total protein, albumin, creatinine, PT, fìbrinogen)

• Complete blood count and differential

• Calculated Creatinine Clearance/24 h

• Chest X- ray

• Abdomen computer tomography (CT) or ultrasound

• Bone scan and X-ray (if appropriate)

• Written informed consent.

• During Treatment - Every Cycle:

• Blood chemistry

• Complete blood count and differential

• Toxicity evaluation

• Physical examination

• During Treatment - Every 12 weeks (3-4 cycles):

• Breast ultrasound

• Surgical and medical evaluation

• Left ventricular ejection fraction evaluation (LVEF) evaluated by echocardiography

• ECOG PS

• Before surgery:

• Mammography, Ultrasound and Magnetic resonance

• Long term Follow up - Every 3 months for the first 2 years, every 6 months years 3-5 then yearly

• Survival

Statistical Considerations:

The aim of this phase II clinical trial is to detect 20% improvement in the pCR (i.e., from 25% to 54%). Simon's methods will be used to calculate sample size. Accrual of 46 patients has been planned considering a 80% of power to detect a 20% difference (two-sided type I error =0.05). The Chi-square test and Fisher's exact test will be used for qualitative parameters.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 46
• Est. completion date: April 2014
• Est. primary completion date: April 2009
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Histologically proven breast carcinoma evaluated for HER 2 status and immune status

• Locally advanced carcinoma (UICC stage II-III)

• Age < 70 years

• measurable lesions

• ECOG Performance Status 0-2

• Life expectancy > 3 months

• Adequate bone marrow and hepatic functions

• Creatinine Clearance > 40 ml/min

• Written informed consent

• Patients must be accessible for treatment and follow up.

Exclusion Criteria:

• Prior chemotherapy or hormonal treatments

• Brain metastases.

• Past or current history of neoplasm other than curatively treated.

• Concurrent treatment with other experimental drugs.

• Left Ventricular Ejection Fraction (LVEF) <50 %

• History of significant neurological or psychiatric disorders.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Breast Neoplasms

Intervention

Drug:
• Trastuzumab

• Paclitaxel

• Epirubicin

• Docetaxel

Locations

Country	Name	City	State
Italy	Centro di Riferimento Oncologico	Aviano	Pordenone

Sponsors (1)

Lead Sponsor	Collaborator
Centro di Riferimento Oncologico - Aviano

Country where clinical trial is conducted

Italy, 

References & Publications (1)

Muraro E, Martorelli D, Turchet E, Miolo G, Scalone S, Comaro E, Talamini R, Mastorci K, Lombardi D, Perin T, Carbone A, Veronesi A, Crivellari D, Dolcetti R. A different immunologic profile characterizes patients with HER-2-overexpressing and HER-2-negative locally advanced breast cancer: implications for immune-based therapies. Breast Cancer Res. 2011;13(6):R117. doi: 10.1186/bcr3060. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pathological complete response (pCR)	pCR was defined as no evidence of microscopic residual invasive cancer, both in breast and ipsilateral axillary lymph nodes, or residual carcinoma in situ in the absence of invasive breast cancer	60 months	Yes
Secondary	Progression free survival	From the first day of treatment to progression or death due to any cause or last contact patient was to be known progression free or alive	60 months	Yes
Secondary	Overall survival	Time between the date of first day of treatment and the date of death from any cause or the last date the patient was known to be alive.	60 months	Yes
Secondary	Cardiac safety	Number of patients with adverse cardiac events. The intensity of clinical adverse events will be graded according to the NCI Common Toxicity Criteria grading system in the toxicity categories that have recommended gradings	60 months	Yes
Secondary	Host immune response	Multiple parameters were investigated: T-cell responses against 13 immunogenic HLA-A*0201-restricted nonamer (9-mer) peptides; Immune cells subsets (CD3+ T cells, CD19+ B cells, CD3-CD16+CD56+ NK cells, CD3+CD4+ T cells, CD3+CD8+ T cells, CD3+CD4+CD25+CD127-/lowFoxP3+ Treg cells, CD3+CD4+IL17+ Th17 cells. Among CD3+CD4+ and CD3+CD8+ T cells, CCR7+CD45RA+ naïve T cells , CCR7+CD45RA- Central Memory T cells, CCR7-CD45RA- Effector Memory T cells , CCR7-CD45RA+ Terminally Differentiated T cells, trastuzumab-dependent ADCC in the HER-2+ arm. Measure of immunologic parameters: changes from baseline recorded at 12 and 24 weeks of treatment	60 months	No