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ctDNA Detected after Neoadjuvant Therapy for HER2-Positive Breast Cancer Is Associated with Inferior Outcomes and May Inform Adjuvant Therapy.

1/5 보강
Cancer research communications 2026 Vol.6(1) p. 105-114
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 3/4)

유사 논문
P · Population 대상 환자/모집단
117 patients enrolled, 25 patients achieved pCR after NAT and 92 patients did not.
I · Intervention 중재 / 시술
adjuvant T-DM1, whereas 99 patients did not
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
In conclusion, the presence of ctDNA after NAT in patients with HER2+ EBC is associated with a poor prognosis and may indicate adjuvant T-DM1.

Lin PH, Tsai LW, Lo C, Kuo SH, Ni CC, Yu CH, Huang CS

📝 환자 설명용 한 줄

[UNLABELLED] ctDNA has been reported as a predictor of the progression of metastatic breast cancer and recurrence in early breast cancer (EBC).

🔬 핵심 임상 통계 (초록에서 자동 추출 — 원문 검증 권장)
  • p-value P = 0.001
  • p-value P = 0.008

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APA Lin PH, Tsai LW, et al. (2026). ctDNA Detected after Neoadjuvant Therapy for HER2-Positive Breast Cancer Is Associated with Inferior Outcomes and May Inform Adjuvant Therapy.. Cancer research communications, 6(1), 105-114. https://doi.org/10.1158/2767-9764.CRC-24-0234
MLA Lin PH, et al.. "ctDNA Detected after Neoadjuvant Therapy for HER2-Positive Breast Cancer Is Associated with Inferior Outcomes and May Inform Adjuvant Therapy.." Cancer research communications, vol. 6, no. 1, 2026, pp. 105-114.
PMID 41543393

Abstract

[UNLABELLED] ctDNA has been reported as a predictor of the progression of metastatic breast cancer and recurrence in early breast cancer (EBC). This study explored whether ctDNA persistence in patients with HER2-positive (HER2+) EBC who achieved pathologic complete response (pCR) after neoadjuvant therapy (NAT) indicates a poor prognosis and the need for adjuvant T-DM1. Of the 117 patients enrolled, 25 patients achieved pCR after NAT and 92 patients did not. Six of the 25 pCR patients showed positive ctDNA after NAT, whereas 26 of the 92 non-pCR patients were ctDNA-positive. Eighteen patients received adjuvant T-DM1, whereas 99 patients did not. Among the non-T-DM1 group, ctDNA positivity after NAT independently predicted recurrence (HR, 5.505; 95% confidence interval, 1.950-15.540; P = 0.001). pCR patients with ctDNA positivity experienced a shorter recurrence-free survival (RFS) compared with pCR and ctDNA-negative patients after NAT(P = 0.008), whereas non-pCR patients with ctDNA-negative tumors had a better RFS compared with non-pCR patients with ctDNA-positive status (P = 0.001). In the 79 patients who were ctDNA-positive before NAT, clearance of ctDNA by NAT was associated with significantly better RFS than nonclearance (P < 0.001). Adjuvant T-DM1 also significantly improved the ctDNA clearance rate (P = 0.035) compared with non-T-DM1 therapy in patients with ctDNA positivity after NAT during serial tests. We classified the 117 patients as T-DM1/non-T-DM1 and ctDNA-positive/negative, and a significantly shorter RFS was observed in patients with ctDNA-positive/non-T-DM1 (P = 0.029) than in the other three patient groups. In conclusion, the presence of ctDNA after NAT in patients with HER2+ EBC is associated with a poor prognosis and may indicate adjuvant T-DM1.

[SIGNIFICANCE] Adjuvant T-DM1 can improve the survival of HER2+ EBC patients who don't achieve pCR. Our study showed that ctDNA positivity after NAT was associated with decreased RFS. ctDNA-positive status after NAT can be switched to ctDNA-negative status in patients treated with T-DM1. Patients who were ctDNA-positive and treated with T-DM1 had a similar RFS to those who were ctDNA-negative, indicating that "ctDNA positivity" could be a marker determining adjuvant T-DM1 therapy.

MeSH Terms

Humans; Female; Breast Neoplasms; Neoadjuvant Therapy; Erb-b2 Receptor Tyrosine Kinases; Middle Aged; Circulating Tumor DNA; Adult; Chemotherapy, Adjuvant; Prognosis; Aged; Biomarkers, Tumor; Neoplasm Recurrence, Local; Trastuzumab; Treatment Outcome; Retrospective Studies

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