TY - JOUR
T1 - A 10-miRNA risk score-based prediction model for pathological complete response to neoadjuvant chemotherapy in hormone receptor-positive breast cancer
AU - Gong, Chang
AU - Cheng, Ziliang
AU - Yang, Yaping
AU - Shen, Jun
AU - Zhu, Yingying
AU - Ling, Li
AU - Lin, Wanyi
AU - Yu, Zhigang
AU - Li, Zhihua
AU - Tan, Weige
AU - Zheng, Chushan
AU - Zheng, Wenbo
AU - Zhong, Jiajie
AU - Zhang, Xiang
AU - Zeng, Yunjie
AU - Liu, Qiang
AU - Huang, R. Stephanie
AU - Komorowski, Andrzej L.
AU - Yang, Eddy S.
AU - Bertucci, François
AU - Ricci, Francesco
AU - Orlandi, Armando
AU - Franceschini, Gianluca
AU - Takabe, Kazuaki
AU - Klimberg, Suzanne
AU - Ishii, Naohiro
AU - Toss, Angela
AU - Tan, Mona P.
AU - Cherian, Mathew A.
AU - Song, Erwei
N1 - Publisher Copyright:
© 2022, Science China Press and Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2022/11
Y1 - 2022/11
N2 - Patients with hormone receptor (HR)-positive tumors breast cancer usually experience a relatively low pathological complete response (pCR) to neoadjuvant chemotherapy (NAC). Here, we derived a 10-microRNA risk score (10-miRNA RS)-based model with better performance in the prediction of pCR and validated its relation with the disease-free survival (DFS) in 755 HR-positive breast cancer patients (273, 265, and 217 in the training, internal, and external validation sets, respectively). This model, presented as a nomogram, included four parameters: the 10-miRNA RS found in our previous study, progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2) status, and volume transfer constant (Ktrans). Favorable calibration and discrimination of 10-miRNA RS-based model with areas under the curve (AUC) of 0.865, 0.811, and 0.804 were shown in the training, internal, and external validation sets, respectively. Patients who have higher nomogram score (>92.2) with NAC treatment would have longer DFS (hazard ratio=0.57; 95%CI: 0.39–0.83; P=0.004). In summary, our data showed the 10-miRNA RS-based model could precisely identify more patients who can attain pCR to NAC, which may help clinicians formulate the personalized initial treatment strategy and consequently achieves better clinical prognosis for patients with HR-positive breast cancer.
AB - Patients with hormone receptor (HR)-positive tumors breast cancer usually experience a relatively low pathological complete response (pCR) to neoadjuvant chemotherapy (NAC). Here, we derived a 10-microRNA risk score (10-miRNA RS)-based model with better performance in the prediction of pCR and validated its relation with the disease-free survival (DFS) in 755 HR-positive breast cancer patients (273, 265, and 217 in the training, internal, and external validation sets, respectively). This model, presented as a nomogram, included four parameters: the 10-miRNA RS found in our previous study, progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2) status, and volume transfer constant (Ktrans). Favorable calibration and discrimination of 10-miRNA RS-based model with areas under the curve (AUC) of 0.865, 0.811, and 0.804 were shown in the training, internal, and external validation sets, respectively. Patients who have higher nomogram score (>92.2) with NAC treatment would have longer DFS (hazard ratio=0.57; 95%CI: 0.39–0.83; P=0.004). In summary, our data showed the 10-miRNA RS-based model could precisely identify more patients who can attain pCR to NAC, which may help clinicians formulate the personalized initial treatment strategy and consequently achieves better clinical prognosis for patients with HR-positive breast cancer.
KW - dynamic contrast-enhanced magnetic resonance imaging
KW - hormone receptor-positive breast cancer
KW - microRNA signature
KW - neoadjuvant chemotherapy
KW - nomogram
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U2 - 10.1007/s11427-022-2104-3
DO - 10.1007/s11427-022-2104-3
M3 - Article
C2 - 35579777
AN - SCOPUS:85130305337
SN - 1674-7305
VL - 65
SP - 2205
EP - 2217
JO - Science China Life Sciences
JF - Science China Life Sciences
IS - 11
ER -