SABCS 2017: Circulating Tumor Cells May Predict Late Recurrence in Patients With Hormone Receptor–Positive Breast Cancer

Key Points

  • Among 546 patients enrolled, 4.8% had a positive CTC assay result; among patients with hormone receptor–positive breast cancer, 5.1% had a positive CTC result; among those with hormone receptor–negative disease, 4.3% had a positive CTC result.
  • After a median follow-up of 1.6 years, a positive CTC assay result was associated with a nearly 20-fold increased risk of breast cancer recurrence in patients with hormone receptor–positive disease. 
  • The positive predictive value of a positive CTC assay for recurrence by 2 years in patients with hormone receptor–positive disease was 35%, and the negative predictive value for patients in this cohort was 98%.
  • A positive CTC assay was not associated with recurrence in the hormone receptor–negative group.

Among patients with hormone receptor–positive HER2-negative stage II–III breast cancer without clinical evidence of recurrence, those who had circulating tumor cells (CTCs) detected in blood 5 years after diagnosis had an increased risk for late recurrence of breast cancer, according to data presented by Sparano et al at the 2017 San Antonio Breast Cancer Symposium (Abstract GS6-03).

“We found that a single positive CTC assay result 5 years after diagnosis provides independent prognostic information for late recurrence,” said Joseph A. Sparano, MD, Associate Director for Clinical Research, Montefiore Einstein Center for Cancer Care, Albert Einstein Cancer Center, New York. “This provides proof of concept that liquid biopsy–based biomarkers may be used to stratify risk for late recurrence and possibly inform treatment or clinical trial options.”

Despite advances in breast cancer treatment in recent years, many women still have late-recurrent disease 5 years or more after the initial diagnosis. Hormone receptor–positive breast cancers, which make up more than half of all breast cancer cases, have an increased risk of late recurrence, noted Dr. Sparano. “Biomarkers for late recurrence that may help guide therapy are needed,” he stressed.

Study Details

Participants in the study, designed and conducted by Dr. Sparano and colleagues in the ECOG-ACRIN Cancer Research Group, were previously enrolled in ECOG-ACRIN clinical trial E5103, which assessed the addition of bevacizumab (Avastin), a vascular endothelial growth factor (VEGF) inhibitor, to chemotherapy as adjuvant treatment following surgery. They measured CTCs in blood samples from patients using the CELLSEARCH CTC assay between 4.5 and 7.5 years after an initial diagnosis of HER2-negative stage II–III breast cancer. No patients had clinical evidence of recurrence at the time of enrollment. Of patients with hormone receptor–positive breast cancer, 4.5% had recurrence of the disease; this result compares with a recurrence rate of 0.5% in the hormone receptor–negative group.

Of the 546 patients enrolled in the study, 4.8% had a positive CTC assay result. Among patients with hormone receptor–positive breast cancer, 5.1% had a positive CTC result; among those with hormone receptor–negative disease, 4.3% had a positive CTC result. After a median follow-up of 1.6 years, a positive CTC assay result was associated with a nearly 20-fold increased risk of breast cancer recurrence in patients with hormone receptor–positive disease.

The positive predictive value of a positive CTC assay for recurrence by 2 years in patients with hormone receptor–positive disease was 35%, and the negative predictive value for patients in this cohort was 98%. A positive CTC assay was not associated with recurrence in the hormone receptor–negative group.

Unexpected Findings

Dr. Sparano commented that these results were somewhat unexpected. “We were surprised to see that 5% of patients had CTCs about 5 or more years after their initial diagnosis,” he said. “Although we were expecting that CTC-positive patients would have a higher recurrence rate, we weren’t expecting the risk of recurrence to be this high after a relatively short period.”

“This study provides strong evidence of the clinical validity of the CTC assay as a prognostic biomarker for late recurrence in hormone receptor–positive breast cancer, which accounts for about one-half of all recurrences,” Dr. Sparano said. “Utilizing the CTC assay for prognostic analysis may aid in a more accurate identification of patients who would most benefit from extended adjuvant endocrine therapy or other treatment options,” he noted.

Next steps include studying how a single negative CTC test or serial negative tests could serve as a negative predictive marker that may allow sparing of extended adjuvant endocrine therapy beyond 5 or more years. 

Limitations of the study include short follow-up after the CTC assay, with an average time of 1.6 years. Dr. Sparano noted that additional follow-up is required and that further study will be necessary to determine the clinical utility of the CTC assay in this setting. 

Disclosure: ECOG-ACRIN received funding for this study from the Breast Cancer Research Foundation, Susan G. Komen, and the National Cancer Institute. Dr. Sparano reported no conflicts of interest.

The content in this post has not been reviewed by the American Society of Clinical Oncology, Inc. (ASCO®) and does not necessarily reflect the ideas and opinions of ASCO®.


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