Benefit of Adding Trastuzumab to Second Line Chemotherapy in Breast Cancer Patients Previously Treated With Trastuzumab

Breast Cancer Clinical Trial

Official title:

Randomized Trial to Assess the Benefit of Adding Trastuzumab to Capecitabine and Vinorelbine as Second Line for HER2positive Breast Cancer Patients With Locally Advanced or Metastatic Disease, Previously Treated With Trastuzumab and Taxanes

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00130507
• Other study ID #: GEICAM 2004-06
• Status: Terminated
• Phase: Phase 2
• Start date: November 4, 2005
• Est. completion date: July 25, 2009

Study information

• Verified date: February 2019
• Source: Spanish Breast Cancer Research Group
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Eligible patients must receive vinorelbine plus capecitabine, with or without trastuzumab, until disease progression or unbearable toxicity. Cycles will be administered every 3 weeks.Human epidermal growth factor receptor 2 (HER2) status must be locally assessed by immunohistochemistry (IHC). All 3+ patients are eligible. In 2+ patients, HER2 status must be confirmed by fluorescence in situ hybridization (FISH).

Description:

Principal outcome is clinical benefit (complete + partial responses + stable disease). Sample size in each arm has been estimated with the Fleming method. Previous data show a clinical benefit rate of vinorelbine plus capecitabine around 50%. The researchers assume trastuzumab can increase it by 20%. With an alpha error of 0.05 and 80% power, 37 patients per arm are needed.

This is a randomised phase II trial. With a minimum expected benefit rate of 50%, at least 36 patients are needed to choose, with a 90% of probability to be right, the best treatment arm, providing it increases benefit rate at least by 15%.

Assuming a drop-out rate of 10%, the total number of patients needed is 82, 41 per treatment arm.

Patients will be stratified as per investigational site, and presence of visceral metastatic lesion (liver, lung, pleura, heart, peritoneum, suprarenal glands). All patients must receive 2 cycles. If no disease progression is detected, treatment must continue until progression or unbearable toxicity.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 14
• Est. completion date: July 25, 2009
• Est. primary completion date: June 2009
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Written informed consent.

• Women older than 18 years old.

• HER2 positive breast cancer with histological diagnoses.

• Non-operable locally advanced or metastatic disease, previously treated with trastuzumab and taxanes.

• Measurable or non-measurable disease as per Response Evaluation Criteria in Solid Tumors (RECIST).

• Disease progression during or after treatment with trastuzumab and taxanes.

• Maximum of 1 previous chemotherapy line for advanced or metastatic disease.

• Previous radiotherapy is allowed if radiated area is not the only documented lesion.

• At least 4 weeks since the last administration of antineoplastic treatment and all toxicities resolved.

• Performance status Eastern Cooperative Oncology Group (ECOG) >=2.

• Life expectancy of at least 12 weeks.

• Left Ventricular Ejection Fraction (LVEF) evaluation (>=50%) in previous 4 weeks.

• Hematology:

• neutrophils >=1.5 x 10e9/l;

• platelets >= 100 x 10e9/l;

• hemoglobin >= 10 mg/dl

• Hepatic function:

• total bilirubin <= 1.5 x under normal limit (UNL);

• Aspartate aminotransferase (SGOT) and Alanine aminotransferase (SGPT) and alkaline phosphatase <= 2.5 x UNL, or <=5 x UNL if hepatic lesions present

• Renal function:

• creatinine <= 175 µmol/l (2 mg/dl);

• creatinine clearance >= 60 ml/min.

• Patients able to comply with treatment and follow-up.

• Negative pregnancy test in the previous 14 days. Adequate contraceptive method during treatment and up to 3 months after finalised.

• Brain metastatic lesions are allowed provided all other criteria are met.

• Male who met inclusion criteria are eligible.

Exclusion Criteria:

• History of hypersensitivity to vinorelbine, trastuzumab, rat proteins or trastuzumab components.

• History of dyspnea at rest, or chronic oxygen therapy required.

• Active infection.

• Second malignancy, except for cervical in situ carcinoma, basal skin carcinoma, adequately treated. Previous malignancies with a 5 year disease free survival are allowed.

• Pregnant or lactating women.

• Any other serious medical pathology, such as congestive heart failure, unstable angina, history of myocardial infarction during the previous year, uncontrolled hypertension or high risk arrhythmias.

• History of neurological or psychiatric disorders, which could preclude the patients to free informed consent.

• Active uncontrolled infection.

• Active peptic ulcer, unstable diabetes mellitus.

• Concomitant treatment with other investigational products. Participation in other clinical trials with a non-marketed drug in the 30 previous days before randomization.

• Concomitant treatment with other therapy for cancer.

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Drug:
• Vinorelbine

• Capecitabine

• Trastuzumab

Locations

Country	Name	City	State
Spain	Spanish Breast Cancer Research Group (GEICAM)	San Sebastián de los Reyes	Madrid

Sponsors (2)

Lead Sponsor	Collaborator
Spanish Breast Cancer Research Group	Hoffmann-La Roche

Country where clinical trial is conducted

Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical benefit rate	Clinical benefit rate is defined as the rate of objective responses (complete responses and partial responses to treatment) and stabilizations, with a minimum duration of 24 weeks.	Through study completion, an average of 1 year
Secondary	Time to progression (TTP)	Tumor assessments will be performed until disease progression in order to evaluate the TTP. TTP is defined as the time from the date of the first dose to the first date of objectively determined progressive disease. For patients not known to have objectively-determined progressive disease, TTP will be censored at the date of the last objective progression-free assessment. For patients who receive subsequent systemic anticancer therapy (after discontinuation from the study treatment) prior to objective disease progression, TTP will be censored at the date of last objective progression-free assessment prior to the initiation of postdiscontinuation systemic anticancer therapy.	Through study completion, an average of 1 year
Secondary	Objective Response Rate (ORR)	Tumor response will be assessed using RECIST criteria. The best response across all treatment will be recorded. ORR is defined as the percentage of patients with a complete or partial response out of the patients who had measurable disease at baseline.	Through study completion, an average of 1 year
Secondary	Response Duration (RD)	RD is defined as the time from the date when the measurement criteria are met for complete response (CR) or partial response (PR) (whichever status is recorded first) until the date of first observation of disease progression or death occurred. For responding patients not known to have died as of the data cut-off date and who do not have progression, duration of response will be censored at the date of last visit with adequate assessment. For responding patients who receive subsequent anticancer therapy (after discontinuation from the study treatment) prior to progression, duration of response will be censored at the date of last visit with adequate assessment prior to the initiation of post-discontinuation anticancer therapy.	Through study completion, an average of 1 year
Secondary	The Number of Participants Who Experienced Adverse Events (AE)	All AE suffered by patients will be recorded and graduated by the NCI CTCAE v1.0.	Through study completion, an average of 1 year
Secondary	Overall Survival (OS)	OS was defined as the time elapsed from first treatment until death from any cause.	Through study completion, an average of 1 year

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