NOLUS 评分在预测接受新辅助化疗的 HR 阳性 HER2 阴性早期乳腺癌患者的 pCR 和 iDFS 中的作用

Cancer diagnosis & prognosis Pub Date : 2024-11-03 eCollection Date: 2024-11-01 DOI:10.21873/cdp.10395
Anna-Lea Amylidi, Loukas Kontovinis, George Douganiotis, Ioannis Natsiopoulos, Konstantinos Papazisis
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引用次数: 0

摘要

背景/目的:乳腺癌仍然是一项重大的健康挑战,新辅助化疗(NACT)改善了某些亚型的临床疗效。然而,NACT在激素受体阳性、HER2-阴性(HR+/HER2-)乳腺癌中的作用尚不明确,因为结果各异,病理完全反应(pCR)率普遍较低。本研究将非管腔疾病评分(NOLUS)作为一种潜在的预测工具,用于评估这些病例对 NACT 的反应:我们回顾性评估了2009年至2023年在本院接受NACT治疗的局部晚期HR+/HER2-乳腺癌患者。研究探讨了NOLUS与pCR率之间的关系。NOLUS根据肿瘤细胞中雌激素受体、孕激素受体和Ki-67的百分比计算为阳性或阴性。我们还研究了pCR和无浸润生存期(iDFS)之间的相关性,并考察了不同年龄组的NOLUS阳性率:共有 149 例患者符合纳入标准。NOLUS阳性患者的pCR率为33.33%,明显高于NOLUS阴性患者的10.4%(P=0.0031)。中位随访时间为2.47年,NOLUS阳性患者获得pCR的iDFS率为100%,反映了三阴性患者的pCR与残留疾病模式。在22-50岁的患者中,NOLUS阳性率为20.43%,而在50岁以上的患者中,NOLUS阳性率为8.93%,但这一差异无统计学意义:NOLUS在预测HR+/HER2-乳腺癌的pCR方面具有潜力,可作为基因组检测的一种经济有效的替代方法。
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The Role of the NOLUS Score in Predicting pCR and iDFS in HR-positive HER2-negative Early Breast Cancer Patients who Received Neoadjuvant Chemotherapy.

Background/aim: Breast cancer remains a significant health challenge, with neoadjuvant chemotherapy (NACT) improving clinical outcomes in certain subtypes. However, the role of NACT in hormone receptor-positive, HER2-negative (HR+/HER2-) breast cancer is unclear due to various outcomes and generally low rates of pathologic complete response (pCR). This study introduces the Non-Luminal Disease Score (NOLUS) as a potential predictive tool for assessing the response to NACT in these cases.

Patients and methods: We retrospectively assessed patients diagnosed with locally advanced HR+/HER2- breast cancer who received NACT at our institution from 2009 to 2023. The study explored the association between NOLUS and pCR rates. NOLUS was calculated as positive or negative based on the percentage of estrogen receptor, progesterone receptor, and Ki-67 in tumor cells. We also investigated the correlation between pCR and invasive disease-free survival (iDFS), and examined NOLUS positivity across different age groups.

Results: A total of 149 patients met the inclusion criteria. NOLUS-positive patients exhibited a significantly higher pCR rate of 33.33% compared to 10.4% in NOLUS-negative patients (p=0.0031). With a median follow-up of 2.47 years, NOLUS-positive patients who achieved pCR had a 100% iDFS rate, mirroring the pCR versus residual disease patterns seen in triple-negative patients. NOLUS positivity was observed in 20.43% of patients aged 22-50, compared to 8.93% in those over 50, though this difference was not statistically significant.

Conclusion: NOLUS exhibits potential in predicting pCR in HR+/HER2- breast cancer, serving as a cost-effective substitute for genomic tests.

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