China CellSearch Study

A Multi-Center, Prospective Study to Evaluate the Ability of CTC Enumeration Using the CellSearch® Circulating Tumor Cell Kit to Predict Prognosis and to Assess the Agreement Between CTC and Imaging Determined Response in MBC Patients 一项评价CellSearch® 循环肿瘤细胞检测试剂盒对复发转移性乳腺癌患者进行循环肿瘤细胞检测 以预测病人预后的能力及循环肿瘤细胞检测和影像学疗效判断之间一致性的多中心、前瞻性的研究

The study is designed to confirm the current indication (below) of the CellSearch® Circulating Tumor Cell Kit in metastatic breast cancer (MBC) patients for use of the kit in China.

The CellSearch® Circulating Tumor Cell Kit is intended for the enumeration of circulating tumor cells (CTC) of epithelial origin (CD45-, EpCAM+, and cytokeratins 8, 18+, and/or 19+) in whole blood.

The presence of CTC in the peripheral blood, as detected by the CellSearch® Circulating Tumor Cell Kit, is associated with decreased progression free survival and decreased overall survival in patients treated for metastatic breast cancer. This test is to be used as an aid in the monitoring of patients with metastatic breast cancer. Serial testing for CTC should be used in conjunction with other clinical methods for monitoring metastatic breast cancer. Evaluation of CTC at any time during the course of disease allows assessment of patient prognosis and is predictive of progression free survival and overall survival.

Study Overview

• Status: Completed
• Conditions: Metastatic Breast Cancer; Benign Breast Disease

Detailed Description

A longitudinal, multi-center, prospective study will be conducted in MBC patients to evaluate the ability of CTC to predict the patients' prognosis. A separate population of healthy and benign disease subjects will serve as controls to compare the CTC incidence in this control group versus the MBC group at baseline. Correlation between CTC and radiographic response to the systemic therapies in the MBC study group will also be assessed.

300 MBC patients, each of whom will provide a series of at least 3 blood draws (baseline, 3-4 weeks and 6-8 weeks after the initiation of the systemic therapy) for CTC analysis, will be enrolled. All MBC patients will be followed for a maximum of 36 months for disease progression and survival.

200 healthy and benign disease volunteers, each of whom will donate blood 1 time for CTC analysis, will be enrolled as controls.

• Study Type: Observational
• Enrollment (Anticipated): 500

Contacts and Locations

Study Locations

• China
  • Beijing, China
    • 307 Hosptial of PLA

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 70 years (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: Female

• Sampling Method: Non-Probability Sample

Study Population

The hazard ratio of disease progression in patients with unfavorable versus favorable CTC counts at baseline, 3-4 weeks and 6-8 weeks after the initiation of therapy will be estimated using Cox regression.

Kaplan-Meier plots for PFS will be constructed using the favorable and unfavorable CTC patient groups. The log-rank test will be used to determine if the curves for the two CTC groups are statistically significantly different.

The hazard ratio of death in patients with unfavorable versus favorable CTC counts at each blood draw time point will be estimated using Cox regression. Kaplan-Meier plots for OS will be constructed using the favorable and unfavorable CTC patient groups.

Description

Inclusion Criteria

• Female
• over 18 and less than 70 years of age
• Subject having agreed to participate in the study and follow the study procedures by providing written informed consent prior entering the study.
• For MBC Subject Set only Confirmed metastatic breast cancer patient with at least one measurable solid tumor according to the RECIST guideline Starting a new line of systemic therapy which is recommended in the Chinese edition of NCCN Clinical Practice Guidelines in Oncology Breast Cancer Guideline 2009 line of chemotherapy should be over 3 ECOG performance grade of 0 to 2 Life expectancy over 3 months
• For Healthy Subject Set only Medical examinations detect no breast benign and malignant tumors
• For Benign Breast Disease Subject Set only Pathology diagnosed breast benign tumor disease

Exclusion Criteria

• Self reported pregnancy
• For MBC Subject Set only Prior history of other malignancy Patients who have surgery to remove any metastatic lesions or receive radiation therapy during her participation in the study
• For Healthy Subject Set only Prior history of breast benign tumor disease or any malignancy Any conditions inappropriate for blood drawing
• For Benign Breast Disease Subject Set only Prior history of any malignancy Any conditions inappropriate for blood drawing

Study Plan

How is the study designed?

Number of groups / cohorts

3

Cohorts and Interventions

Group / Cohort
MBC patients; 300 MBC patients, each of whom will provide a series of at least 3 blood draws (baseline, 3-4 weeks and 6-8 weeks after the initiation of the systemic therapy) for CTC analysis, will be enrolled. All MBC patients will be followed for a maximum of 36 months for disease progression and survival.
Benign disease volunteers; 100 Benign disease volunteers whom will donate blood 1 time for CTC analysis, will be enrolled as controls.
Healthy volunteers; 100 Healthy volunteers whom will donate blood 1 time for CTC analysis, will be enrolled as controls.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Ability of CTC levels to predict progression-free survival (PFS) in MBC patients.	12 months

Secondary Outcome Measures

Outcome Measure	Time Frame
Ability of CTC levels to predict overall survival (OS) in MBC patients.	3 years
Agreement between CTC counts (3-4 weeks and 6-8 weeks) after the initiation of a new line of systemic therapy and the patient's response as determined by imaging evaluation (6-8 weeks after the initiation of therapy) in MBC patients.	12 months

Collaborators and Investigators

• Sponsor: Johnson & Johnson Medical, China
• Investigators: Study Chair: Zefei Jiang, Doctor, 307 Hosptial of PLA; Principal Investigator: Zhimin Shao, Doctor, Shanghai Cancer Hosptial; Principal Investigator: Tao Ouyang, Doctor, Beijing Cancer Hosptial; Principal Investigator: Erwei Song, Doctor, Zhongshan 2nd Hospital; Principal Investigator: Ning Liao, Doctor, Guangdong People's Hospital; Principal Investigator: Xiaojia Wang, Doctor, Zhejiang Cancer Hosptial; Principal Investigator: Zhongsheng Tong, Doctor, Tianjin cancer hospital

Study record dates

Study Major Dates

• Study Start (Actual): March 25, 2010
• Primary Completion (Actual): June 22, 2011
• Study Completion (Actual): January 6, 2014

Study Registration Dates

• First Submitted: May 4, 2010
• First Submitted That Met QC Criteria: May 4, 2010
• First Posted (Estimate): May 5, 2010

Study Record Updates

• Last Update Posted (Actual): November 15, 2019
• Last Update Submitted That Met QC Criteria: November 13, 2019
• Last Verified: November 1, 2019

More Information

Terms related to this study

• Keywords: Healthy; MBC; Benign disease; Confirmed metastatic breast cancer patient with at least one measurable solid tumor according to the RECIST guideline; Medical examinations detect no breast benign and malignant tumors; Benign Breast Disease; Pathology diagnosed breast benign tumor disease
• Additional Relevant MeSH Terms: Skin Diseases; Breast Diseases; Fibrocystic Breast Disease
• Other Study ID Numbers: 200901