[A Case Report of Triple-Negative Breast Cancer with High Ki-67 Expression That Responded to Neoadjuvant Pembrolizumab Therapy].
증례보고
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
추출되지 않음
I · Intervention 중재 / 시술
partial mastectomy
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Seven months later, she has shown no signs of recurrence. We report a case of TNBC with high Ki-67 expression that responded well to neoadjuvant pembrolizumab therapy.
Drug therapy including pembrolizumab is expected to improve treatment outcomes for triple-negative breast cancer (TNBC).
APA
Yao S, Goi T, et al. (2025). [A Case Report of Triple-Negative Breast Cancer with High Ki-67 Expression That Responded to Neoadjuvant Pembrolizumab Therapy].. Gan to kagaku ryoho. Cancer & chemotherapy, 52(13), 1123-1125.
MLA
Yao S, et al.. "[A Case Report of Triple-Negative Breast Cancer with High Ki-67 Expression That Responded to Neoadjuvant Pembrolizumab Therapy].." Gan to kagaku ryoho. Cancer & chemotherapy, vol. 52, no. 13, 2025, pp. 1123-1125.
PMID
41546269
Abstract
Drug therapy including pembrolizumab is expected to improve treatment outcomes for triple-negative breast cancer (TNBC). We experienced a case of early-stage TNBC with high Ki-67 expression and a high risk of recurrence, in which neoadjuvant pembrolizumab therapy was effective. A 72-year-old woman with TNBC who developed secondary adrenal insufficiency due to hypopituitarism during pembrolizumab treatment. Symptoms rapidly improved with steroid replacement therapy, pembrolizumab was discontinued. Later, the patient had experienced severe infections during subsequent chemotherapy but recovered, and underwent partial mastectomy. Pathological findings showed treatment effect Grade 1a with negative margins. Seven months later, she has shown no signs of recurrence. We report a case of TNBC with high Ki-67 expression that responded well to neoadjuvant pembrolizumab therapy.
MeSH Terms
Humans; Female; Neoadjuvant Therapy; Aged; Triple Negative Breast Neoplasms; Antibodies, Monoclonal, Humanized; Ki-67 Antigen; Antineoplastic Agents, Immunological
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