Channing Division of Network Medicine, Department of Medicine, Brigham & Women's Hospital, and Harvard Medical School, Boston, Massachusetts.
Department of Epidemiology, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Cancer Epidemiol Biomarkers Prev. 2022 Oct 4;31(10):1926-1934. doi: 10.1158/1055-9965.EPI-22-0672.
The relationships between PTEN loss and/or PIK3CA mutation and breast cancer prognosis remain controversial. We aim to examine the associations in large epidemiologic cohorts.
We followed women with invasive breast cancer from the Nurses' Health Studies with available data on tumor PTEN expression (n = 4,111) and PIK3CA mutation (n = 2,930). PTEN expression was evaluated by IHC and digitally scored (0%-100%). Pyrosequencing of six hotspot mutations of PIK3CA was performed.
We found loss of PTEN expression (≤10%) occurred in 17% of cases, and PIK3CA mutations were detected in 11% of cases. After adjusting for clinical and lifestyle factors, PTEN loss was not associated with worse breast cancer-specific mortality among all samples [HR, 0.85; 95% confidence intervals (CI), 0.71-1.03] or among estrogen receptor (ER)-positive tumors (HR, 0.99; 95% CI, 0.79-1.24). However, among ER-negative tumors, PTEN loss was associated with lower breast cancer-specific mortality (HR, 0.68; 95% CI, 0.48-0.95). PIK3CA mutation was not strongly associated with breast cancer-specific mortality (HR, 0.89; 95% CI, 0.67-1.17). Compared with tumors without PTEN loss and without PIK3CA mutation, those with alterations (n = 540) were not at higher risk (HR, 1.07; 95% CI, 0.86-1.34). However, women with both PTEN loss and PIK3CA mutation (n = 38) were at an increased risk of breast cancer-specific mortality (HR, 1.65; 95% CI, 0.83-3.26).
In this large epidemiologic study, the PTEN-mortality association was more pronounced for ER-negative tumors, and the joint PTEN loss and PIK3CA mutation may be associated with worse prognosis.
Further studies with a larger sample of ER-negative tumors are needed to replicate our findings and elucidate underlying mechanisms.
PTEN 缺失和/或 PIK3CA 突变与乳腺癌预后之间的关系仍存在争议。我们旨在通过大型流行病学队列研究来检验这些关联。
我们随访了有肿瘤 PTEN 表达(n=4111)和 PIK3CA 突变(n=2930)数据的“护士健康研究”中的浸润性乳腺癌女性患者。通过免疫组化(IHC)和数字评分(0%-100%)评估 PTEN 表达。对 PIK3CA 的六个热点突变进行焦磷酸测序。
我们发现 17%的病例存在 PTEN 表达缺失(≤10%),11%的病例存在 PIK3CA 突变。在调整了临床和生活方式因素后,PTEN 缺失与所有样本的乳腺癌特异性死亡率无显著相关性[风险比(HR),0.85;95%置信区间(CI),0.71-1.03],或与雌激素受体(ER)阳性肿瘤无显著相关性(HR,0.99;95%CI,0.79-1.24)。然而,在 ER 阴性肿瘤中,PTEN 缺失与较低的乳腺癌特异性死亡率相关(HR,0.68;95%CI,0.48-0.95)。PIK3CA 突变与乳腺癌特异性死亡率无显著相关性(HR,0.89;95%CI,0.67-1.17)。与没有 PTEN 缺失和没有 PIK3CA 突变的肿瘤相比,同时存在这两种改变(n=540)的肿瘤并未表现出更高的风险(HR,1.07;95%CI,0.86-1.34)。然而,同时存在 PTEN 缺失和 PIK3CA 突变的女性(n=38)的乳腺癌特异性死亡率升高(HR,1.65;95%CI,0.83-3.26)。
在这项大型流行病学研究中,PTEN 与死亡率的关联在 ER 阴性肿瘤中更为显著,并且 PTEN 缺失和 PIK3CA 突变的联合可能与更差的预后相关。
需要进一步开展针对更大样本量 ER 阴性肿瘤的研究来复制我们的发现并阐明潜在机制。