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前瞻性验证一种新诊断卵巢癌反应预测的体外患者来源 3D 球体模型。

Prospective Validation of an Ex Vivo, Patient-Derived 3D Spheroid Model for Response Predictions in Newly Diagnosed Ovarian Cancer.

机构信息

KIYATEC, Inc., Greenville, South Carolina, USA.

USC School of Medicine, Greenville, South Carolina, USA.

出版信息

Sci Rep. 2019 Aug 1;9(1):11153. doi: 10.1038/s41598-019-47578-7.

Abstract

Although 70-80% of newly diagnosed ovarian cancer patients respond to first-line therapy, almost all relapse and five-year survival remains below 50%. One strategy to increase five-year survival is prolonging time to relapse by improving first-line therapy response. However, no biomarker today can accurately predict individual response to therapy. In this study, we present analytical and prospective clinical validation of a new test that utilizes primary patient tissue in 3D cell culture to make patient-specific response predictions prior to initiation of treatment in the clinic. Test results were generated within seven days of tissue receipt from newly diagnosed ovarian cancer patients obtained at standard surgical debulking or laparoscopic biopsy. Patients were followed for clinical response to chemotherapy. In a study population of 44, the 32 test-predicted Responders had a clinical response rate of 100% across both adjuvant and neoadjuvant treated populations with an overall prediction accuracy of 89% (39 of 44, p < 0.0001). The test also functioned as a prognostic readout with test-predicted Responders having a significantly increased progression-free survival compared to test-predicted Non-Responders, p = 0.01. This correlative accuracy establishes the test's potential to benefit ovarian cancer patients through accurate prediction of patient-specific response before treatment.

摘要

虽然 70-80%的新诊断卵巢癌患者对一线治疗有反应,但几乎所有患者都会复发,五年生存率仍低于 50%。增加五年生存率的一种策略是通过改善一线治疗反应来延长复发时间。然而,目前没有生物标志物可以准确预测个体对治疗的反应。在这项研究中,我们提出了一种新测试的分析和前瞻性临床验证,该测试利用原发性患者组织在 3D 细胞培养中进行,以便在临床治疗开始前对患者的特定反应进行预测。在从接受标准手术减瘤术或腹腔镜活检的新诊断卵巢癌患者中获得组织后的七天内生成测试结果。患者接受化疗的临床反应随访。在 44 名患者的研究人群中,32 名测试预测的反应者在辅助和新辅助治疗人群中的临床反应率均为 100%,总体预测准确性为 89%(44 例中的 39 例,p<0.0001)。该测试还可作为预后读出器,与预测非反应者相比,预测反应者的无进展生存期显著延长,p=0.01。这种相关性准确性确立了该测试通过在治疗前准确预测患者的特定反应来使卵巢癌患者受益的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0158/6671958/c0502f091436/41598_2019_47578_Fig1_HTML.jpg

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