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首页> 外文期刊>BMC Cancer >CTCs as a prognostic and predictive biomarker for stage II/III Colon Cancer: a companion study to the PePiTA trial
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CTCs as a prognostic and predictive biomarker for stage II/III Colon Cancer: a companion study to the PePiTA trial

机译:CTC作为阶段II / III结肠癌的预后和预测生物标志物:对Pepita试验的伴侣研究

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摘要

Adjuvant therapy improves the prognosis of stage II & III colon cancer patients. Unfortunately, most patients do not benefit from this treatment. PePITA (NCT00994864) is a prospective, multicenter, non-randomized study whose primary objective is to predict the outcome of adjuvant therapy in colon cancer. The primary objective was to determine the prognostic and predictive value of circulating tumor cell (CTC) detection before therapy and after one course of preoperative FOLFOX. Out of the 58 first patients accrued in PePiTA trial, 36 patients participated in the CTC companion study, of whom 32 had at least one evaluable sample. Only 5 patients (14, 95% CI?=?5-30%) had ≥1 CTC/22.5?ml blood in at least one of the two timepoints with 2 patients having ≥1 CTC/22.5?ml at baseline (6, 95% CI: 1-19%). The detection rate of patients with CTCs at baseline being lower than expected, the inclusion of patients in the PePiTA CTC substudy was stopped. The limited sample size did not allow us to investigate the prognostic and predictive value of CTCs in locally advanced colon cancer. Our data illustrate the need for further standardized studies in order to find the most reliable prognostic/predictive biomarker in early-stage colon cancer. This trial was prospectively registered at Jules Bordet institute ( NCT00994864 ) on the October 14, 2009.
机译:佐剂治疗改善了II和III阶段癌症患者的预后。不幸的是,大多数患者不会受益于这种治疗。 PEPITA(NCT00994864)是一项前瞻性,多中心,非随机化研究,其主要目标是预测结肠癌佐剂治疗的结果。主要目的是确定治疗前循环肿瘤细胞(CTC)检测的预测和预测值,并在术前对FOLFOX之后进行术语。在Pepita试验中的58名患者中,36名患者参加了CTC伴侣学习,其中32名至少有一个可评估样品。只有5名患者(14,95%CI?= 5-30%)≥12例时的两个时间点中的至少一种血液中的血液中的至少一种,其中2名患者在基线(6,6,)在基线时≥1ctc/ 22.5?ml(6, 95%CI:1-19%)。基线CTCs患者的检出率低于预期,将患者纳入肽CTC血栓制中止损。有限的样品大小不允许我们探讨CTC在局部晚期结肠癌中的预后和预测值。我们的数据说明了需要进一步标准化的研究,以便在早期结肠癌中找到最可靠的预后/预测生物标志物。本次审判于2009年10月14日在Jules Bordet Institute(NCT00994864)上注册。

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