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Analysis of the serial circulating tumor cell count during neoadjuvant chemotherapy in breast cancer patients

  • Sung chan Gwark
  • , Jisun Kim
  • , Cham Han Lee
  • , Young Hun Kim
  • , Myoung Shin Kim
  • , Sung Woo Hong
  • , Mi Young Choi
  • , Byung Hee Jeon
  • , Nak Jung Kwon
  • , Kyoung Yeon Kim
  • , Yongnam Kim
  • , Suhwan Chang
  • , Jong Han Yu
  • , Ji Yeon Park
  • , Jin Hee Ahn
  • , Kyung Hae Jung
  • , Sung Bae Kim
  • , Hee Jin Lee
  • , Gyung Yub Gong
  • , Sae Byul Lee
  • Il Yong Chung, Beom Seok Ko, Hee Jeong Kim, Jong Won Lee, Byung Ho Son, Sei Hyun Ahn
  • University of Ulsan
  • Cytogen Inc
  • Macrogen Inc
  • Sungkyunkwan University

Research output: Contribution to journalArticlepeer-review

Abstract

We evaluated the prognostic implications of the circulating tumor cell (CTC) count in non-metastatic, HER2-negative breast cancer patients who failed to achieve pathologic complete response (pCR) after neoadjuvant chemotherapy (NCT). A total of 173, non-metastatic breast cancer patients treated with NCT were prospectively enrolled. CTCs were obtained from blood drawn pre-NCT and post-NCT using a SMART BIOPSY SYSTEM isolation kit (Cytogen Inc., Seoul, Korea) with immunofluorescence staining. Excluding 26 HER2-positive patients, Relapse-free survival (RFS) and overall survival (OS) related to the CTC count and the association of the CTC count with the treatment response to given therapy were analyzed in 147 HER2-negative patients. Among 147 HER2-negative patients, 28 relapses (19.0%) and 13 deaths (8.8%, all breast cancer-specific) were observed during a median follow-up of 37.3 months. One hundred and seven patients (72.8%) were hormone receptor-positive, and 40 patients (27.2%) had triple-negative breast cancer (TNBC). One or more CTCs were identified in 88 of the 147 patients (59.9%) before NCT and 77 of the 134 patients (52.4%) after NCT. In the entire HER2-negative patient cohort, the initial nodal status was the most significant factor influencing RFS and OS. In TNBC, 11 patients (27.5%) achieved pCR and patients that failed to achieve pCR with ≥ 5 CTCs after NCT, showed worse RFS (HR, 10.66; 95% CI, 1.80–63.07; p = 0.009) and OS (HR, 14.00; 95% CI, 1.26–155.53; p = 0.032). The patients with residual tumor and a high number of the CTCs after NCT displayed the worse outcome. These findings could provide justification to launch a future, well designed trial with longer follow-up data to obtain regulatory approval for clinical use of the assay, especially for the ER-positive, HER2-negative breast cancer subset.

Original languageEnglish
Article number17466
JournalScientific Reports
Volume10
Issue number1
DOIs
StatePublished - 1 Dec 2020
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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