首页> 外文期刊>Modern Pathology >Phosphohistone H3 expression has much stronger prognostic value than classical prognosticators in invasive lymph node-negative breast cancer patients less than 55 years of age
【24h】

Phosphohistone H3 expression has much stronger prognostic value than classical prognosticators in invasive lymph node-negative breast cancer patients less than 55 years of age

机译:在年龄小于55岁的浸润性淋巴结阴性乳腺癌患者中,磷酸化H3表达的预后价值比经典预后要强得多

获取原文
       

摘要

The proliferation factor mitotic activity index is the strongest prognostic factor in early breast cancer, but it may lack reproducibility. We analyzed the prognostic value of phosphohistone H3, a marker of cells in late G2 and M phase, measuring highly standardized immunohistochemical nuclear phosphohistone H3 expression by subjective counts and digital image analysis. Expression was compared with classical clinico-pathologic prognostic variables and the mitotic activity index in 119 node-negative invasive breast cancers in patients less than 55 years old treated with adjuvant systemic chemotherapy with long-term follow-up (median 168 months). Nineteen patients (16%) developed distant metastases and 16 (13%) died. Strong phosphohistone H3 expression occurred preferentially in the peripheral growing front; counts were highly reproducible between observers (R=0.92) and highly consistent with digital image analysis (R=0.96). Phosphohistone H3 correlated (Pn=53; 45% of all cases) vs phosphohistone H313 (n=66; 55% of all cases) was the strongest prognostic threshold, with 20-year recurrence-free survival of distant metastases of 96 and 58%, respectively (P=0.0002, HR=9.6). Mitotic activity index was the second strongest prognostic variable (P=0.003, HR=3.9). In multivariate analysis, phosphohistone H3 vs13 exceeded the prognostic value of the mitotic activity index. None of the other classical prognostic factors examined offered prognostic value additional to phosphohistone H3. Phosphohistone H3 is by far the strongest prognostic variable in early invasive node-negative breast cancer patients less than 55 years old with long-term follow-up.
机译:增殖因子有丝分裂活性指数是早期乳腺癌中最强的预后因子,但可能缺乏可重复性。我们通过主观计数和数字图像分析来分析高度标准化的免疫组织化学核磷酸化组蛋白H3表达,从而分析了G2和M期晚期细胞标志物–磷酸组蛋白H3的预后价值。将表达与经典临床病理学预后变量和有丝分裂活性指数进行了比较,该研究在接受长期全身性辅助化疗(年龄168个月)的55岁以下的119名淋巴结阴性浸润性乳腺癌中。 19例患者(16%)发生远处转移,死亡16例(13%)。强烈的磷酸化组蛋白H3表达优先出现在外围生长前沿。观察者之间的计数可高度重现(R = 0.92),并且与数字图像分析高度一致(R = 0.96)。磷酸化组蛋白H3相关性(Pn = 53;占所有病例的45%)vs磷酸化组蛋白H313(n = 66;占所有病例的55%)是最强的预后阈值,远处转移的20年无复发生存率分别为96和53%。分别为58%(P = 0.0002,HR = 9.6)。有丝分裂活动指数是第二强的预后变量(P = 0.003,HR = 3.9)。在多变量分析中,组蛋白H3 vs13超过了有丝分裂活动指数的预后值。所检查的其他经典预后因素均未提供除组蛋白H3以外的其他预后价值。迄今为止,对于年龄小于55岁且早期随访的侵袭性淋巴结阴性的早期乳腺癌患者,磷酸化H3是最强的预后变量。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号