Trial Using CTCs to Make Therapy Decisions

Publication
Article
Oncology NEWS InternationalOncology NEWS International Vol 15 No 12
Volume 15
Issue 12

Immunicon Corporation has announced that a major clinical trial using the CellSearch Assay has opened to enrollment. The randomized phase III trial (S0500), conducted by the Southwest Oncology Group (SWOG), is testing the strategy of changing therapy vs maintaining therapy for metastatic breast cancer patients who have elevated circulating tumors cells (CTCs) at first follow-up assessment. Immunicon will perform CTC testing for participating sites.

HUNTINGDON VALLEY, Pennsylvania—Immunicon Corporation has announced that a major clinical trial using the CellSearch Assay has opened to enrollment. The randomized phase III trial (S0500), conducted by the Southwest Oncology Group (SWOG), is testing the strategy of changing therapy vs maintaining therapy for metastatic breast cancer patients who have elevated circulating tumors cells (CTCs) at first follow-up assessment. Immunicon will perform CTC testing for participating sites.

Eligible patients are those with confirmed breast cancer and clinical evidence of metastatic disease who are entering their first line of chemotherapy for their metastatic disease. Prior use of hormonal therapy, bisphosphonate, trastuzumab (Herceptin), and/or bevacizumab (Avastin) in the metastatic setting is allowed.

Jeffrey B. Smerage, MD, PhD, of the University of Michigan Comprehensive Cancer Center, and PI for the study, commented, "The SWOG study is a natural extension of the pivotal trial that Immunicon conducted for FDA clearance [of the CellSearch Assay]. The original study demonstrated that CTCs can be used to predict survival at multiple time points during therapy. The data suggest that effective therapy that eliminates CTCs does indeed positively impact survival."

Recent Videos
Leading experts in the breast cancer field highlight the use of CDK4/6 inhibitors, antibody-drug conjugates, and other treatment modalities.
Patients with node-negative disease who are older and have comorbidities may not be suitable to receive CDK4/6 inhibitors.
An observed carryover effect with CDK4/6 inhibitors may reduce the risk of recurrence years after a patient stops treatment.
Breast oncologist Jade E. Jones, MD, says she tries to send patients with BRCA-mutant HR-positive TNBC to clinical trials that use PARP inhibitors.
Related Content