Improved Survival Benefit With the Use of Circulating Tumor Count Application in First-Line Metastatic Breast Cancer

Results from the phase 3 STIC CTC trial (NCT01710605) found an improved overall survival (OS) benefit when a circulating tumor cell (CTC) count approach was used to guide first-line treatment with chemotherapy or endocrine therapy vs physician’s choice CTC count for patients with hormone receptor–positive/HER2-negative breast cancer, which was presented at the 2022 San Antonio Breast Cancer Symposium (SABCS).¹

Data obtained after a median follow-up of 57 months from the study revealed better long-term outcomes with a treatment strategy based on CTC count in patients with discordant clinical/CTC profiles.

Specifically, among the 25% study participants who had a discordant profile as defined by a clinically low-risk profile but a high CTC count (≥5 CTCs/7.5 mL), patients treated with chemotherapy had an absolute gain in OS of 16 months compared with those treated with endocrine therapy, corresponding to a 47% reduction in the risk of death. These data suggest the utility of the CTC count as a biomarker for guiding treatment choice.

In this clinically low/CTC high group, the median OS was 51.8 months in the patients treated with chemotherapy compared with 35.4 months in those treated with endocrine therapy (HR, 0.53; 95% CI, 0.36-0.78; P = .001), Francois-Clement Bidard, MD, PhD, said during a press briefing.

In contrast, in those with the opposite discordant profile—a clinically high-risk profile and a low CTC count—there was no significant difference observed on progression-free survival (PFS) or OS whether patients received chemotherapy or endocrine therapy. In this group, the median PFS was 9.3 months in the CTC count–based arm, for whom endocrine therapy was chosen, vs 14.6 months in the standard arm, for whom chemotherapy was selected (P = .54), and median OS was 49.4 months vs 45.9 months (HR, 0.88; 95% CI, 0.51-1.51; P = .64), respectively.

Guidelines recommend prioritizing endocrine therapy before switching to chemotherapy to treat patients with metastatic breast cancer. This recommendation is based on the limited side effects of endocrine therapy compared with chemotherapy. Guidelines, however, provide an option to use chemotherapy in patients with aggressive disease and an unfavorable prognosis, which has led to highly heterogeneous treatment decisions, Bidard, professor of medical oncology at Institut Curie and Versailles Saint-Quentin University, Paris, France, noted during the presentation.

“STIC CTC is the first trial to demonstrate the clinical utility of CTC count in metastatic breast cancer,” he said. “The CTC count confirmed the allocated therapy in about 60% of patients and changed the allocated therapy in approximately 40% of HR-positive, HER2-negative patients.”

In STIC CTC, 755 women with metastatic, ER-negative breast cancer were randomly assigned 1:1 to the CTC-driven choice arm (n = 377; median age, 64 years), and the clinician-driven choice arm (n = 378; median age, 63 years). In the CTC-driven choice arm, patients with a low CTC count received endocrine therapy and those with a high CTC count received chemotherapy. In the clinician-driven choice arm, patients who were considered to have a clinically low profile received endocrine therapy while those with a clinically high profile received chemotherapy.

There were 61.4% of patients with concordant estimates: 48.2% with both a clinically low profile and a low CTC count and 13.2% with a clinically high profile and high CTC count. In the low/low cohort, for which endocrine therapy was used in both arms, the median OS was approximately 5 years. In the high/high cohort of patients treated with chemotherapy, the median OS was approximately 3 years.

In the overall population, including the 61.4% with concordant estimates and no change in treatment, noninferiority between treatments was previously established on the PFS endpoint. The median PFS in the CTC-driven choice arm was 15.5 months compared with 13.9 months in the clinician-driven choice arm, thereby meeting the primary endpoint of noninferiority.² “Longer follow-up substantiates that CTC-based choice is safe,” Bidard said.

The main limitation of the study was that it was designed before CDK4/6 inhibitors became the standard of care, he said. However, the dilemma between endocrine therapy and chemotherapy remains intact after patients progress on a CDK4/6 inhibitor given as first line or adjuvant therapy.

References

1. Bidard F-C, Klivue N, Alix-Panabières C, et al. Circulating tumor cells-driven choice of first line therapy for ER+ HER2- metastatic breast cancer: overall survival analysis of the randomized STIC CTC trial. Presented at: 2022 San Antonio Breast Cancer Symposium; December 6-10, 2022; San Antonio, TX. Abstract GS3-09.
2. Bidard F-C, Jacot W, Kiavue N, et al. Efficacy of circulating tumor cell count–driven vs clinician-driven first-line therapy choice in hormone receptor–positive, ERBB2-negative metastatic breast cancer: the STIC CTC randomized clinical trial. JAMA Oncol. 2021;7(1):34-41. doi:10.1001/jamaoncol.2020.5660.