Department of Oncology, University of Pécs, Edesanyak street 17, 7624 Pecs, Hungary.
J Cancer Res Clin Oncol. 2012 Mar;138(3):387-95. doi: 10.1007/s00432-011-1110-1. Epub 2011 Dec 8.
The response to neoadjuvant chemoradiotherapy (CRT) varies greatly in patients suffering from locally advanced rectal cancer. Our aim was to correlate the response to CRT with the pre-treatment expression of heat shock protein 90 (Hsp90), small heat shock protein 16.2 (sHsp 16.2), phospho-Akt (p-Akt), growth hormone-releasing hormone receptor (GHRH-R) and heme-binding protein 2 (SOUL) in order to try to identify one or more as a predictive marker.
Sixty-nine patients receiving combined CRT for locally advanced rectal cancer were examined retrospectively. Surgical resection was carried out 6-9 weeks following CRT. The histopathological response to neoadjuvant treatment was determined according to the modified Mandard score. Using immunohistochemistry, we investigated the relationship between the expression of the five cited proteins in the pre-operative samples as well as various clinical parameters and the histopathological regression of the tumors.
Thirty-one patients (48%) were good responders, and 33 patients (52%) were found to respond poorly to neoadjuvant therapy. Among patients undergoing surgery 7 weeks following CRT, there were significantly more good responders than among patients who underwent surgery sooner (63% vs. 37%). High levels of expression of GHRH-R and Hsp90 were shown to be significantly correlated with minor or absent histological regression.
GHRH-R and Hsp90 were found to be independent predictive factors of histopathological response to neoadjuvant RCT. Since GHRH-R antagonists and Hsp90 inhibitors are currently being tested as potential anticancer agents, our study implies the possible elaboration of an effective and individualized treatment of poor responders.
接受新辅助放化疗(CRT)的局部晚期直肠癌患者的反应差异很大。我们的目的是将 CRT 的反应与 HSP90、小热休克蛋白 16.2(sHsp 16.2)、磷酸化 Akt(p-Akt)、生长激素释放激素受体(GHRH-R)和血红素结合蛋白 2(SOUL)在治疗前的表达相关联,试图确定一个或多个作为预测标志物。
回顾性检查了 69 例接受联合 CRT 治疗的局部晚期直肠癌患者。CRT 后 6-9 周进行手术切除。根据改良 Mandard 评分确定新辅助治疗的组织病理学反应。使用免疫组织化学,我们研究了术前样本中这五种蛋白质的表达与各种临床参数以及肿瘤组织学消退之间的关系。
31 例(48%)患者为良好反应者,33 例(52%)患者对新辅助治疗反应不佳。在 CRT 后 7 周接受手术的患者中,良好反应者明显多于更早接受手术的患者(63%比 37%)。GHRH-R 和 HSP90 的高表达与组织学上轻微或不存在的消退明显相关。
GHRH-R 和 HSP90 被发现是新辅助 RCT 组织病理学反应的独立预测因素。由于 GHRH-R 拮抗剂和 HSP90 抑制剂目前正在作为潜在的抗癌药物进行测试,我们的研究意味着可能制定出针对不良反应者的有效和个体化治疗方案。