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Development and validation of a prognostic nomogram for recurrence-free survival after complete surgical resection of localised primary gastrointestinal stromal tumour: a retrospective analysis.

机译:局限性原发性胃肠道间质瘤完全手术切除后无复发生存的预后诺模图的开发和验证:回顾性分析。

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BACKGROUND: Adjuvant imatinib mesylate prolongs recurrence-free survival (RFS) after resection of localised primary gastrointestinal stromal tumours (GIST). We aimed to develop a nomogram to predict RFS after surgery in the absence of adjuvant therapy to help guide patient selection for adjuvant imatinib therapy. METHODS: A nomogram to predict RFS based on tumour size (cm), location (stomach, small intestine, colon/rectum, or other), and mitotic index (<5 or > or =5 mitoses per 50 high-power fields) was developed from 127 patients treated at Memorial Sloan-Kettering Cancer Center (MSKCC), New York, NY, USA. The nomogram was tested in patients from the Spanish Group for Research on Sarcomas (GEIS; n=212) and the Mayo Clinic, Rochester, MN, USA (Mayo; n=148). The nomogram was assessed by calculating concordance probabilities and testing calibration of predicted RFS with observed RFS. Concordance probabilities were also compared with those of three commonly used staging systems. FINDINGS: The nomogram had a concordance probability of 0.78 (SE 0.02) in the MSKCC dataset, and 0.76 (0.03) and 0.80 (0.02) in the validation cohorts. Nomogram predictions were well calibrated. Inclusion of tyrosine kinase mutation status in the nomogram did not improve its discriminatory ability. Concordance probabilities of the nomogram were better than those of the two NIH staging systems (0.76 [0.03] vs 0.70 [0.04, p=0.04] and 0.66 [0.04, p=0.01] in the GEIS validation cohort; 0.80 [0.02] vs 0.74 [0.02, p=0.04] and 0.78 [0.02, p=0.05] in the Mayo cohort) and similar to those of the AFIP-Miettinen staging system (0.76 [0.03] vs 0.73 [0.004, p=0.28] in the GEIS cohort; 0.80 [0.02] vs 0.76 [0.003, p=0.09] in the Mayo cohort). Nomogram predictions of RFS seemed better calibrated than predictions made with the AFIP-Miettinen system. INTERPRETATION: The nomogram accurately predicts RFS after resection of localised primary GIST and could be used to select patients for adjuvant imatinib therapy.
机译:背景:甲磺酸伊马替尼辅助治疗可切除局部原发性胃肠道间质瘤(GIST)后延长无复发生存期(RFS)。我们旨在开发诺模图来预测在没有辅助治疗的情况下手术后的RFS,以帮助指导患者选择辅助伊马替尼治疗。方法:根据肿瘤大小(cm),位置(胃,小肠,结肠/直肠或其他)和有丝分裂指数(每50个高倍视野<5或>或= 5个有丝分裂)来预测RFS的诺模图为从在美国纽约州纪念斯隆-凯特琳癌症中心(MSKCC)治疗的127名患者中获得了成功。在西班牙肉瘤研究小组(GEIS; n = 212)和美国明尼苏达州罗彻斯特的梅奥诊所(Mayo; n = 148)的患者中测试了诺模图。通过计算一致性概率并用观察到的RFS测试预测的RFS来评估列线图。还将一致性概率与三个常用分期系统的一致性概率进行了比较。结果:在MSKCC数据集中,诺模图的一致性概率为0.78(SE 0.02),在验证队列中,一致性概率为0.76(0.03)和0.80(0.02)。诺法图预测已得到很好的校准。在诺模图中包括酪氨酸激酶突变状态并没有改善其鉴别能力。诺模图的一致性概率优于两个NIH分级系统(GEIS验证队列中的0.76 [0.03] vs 0.70 [0.04,p = 0.04]和0.66 [0.04,p = 0.01]); 0.80 [0.02] vs 0.74在Mayo队列中[0.02,p = 0.04]和0.78 [0.02,p = 0.05]),与AFIP-Miettinen分期系统的相似(在GEIS队列中为0.76 [0.03]对0.73 [0.004,p = 0.28]) ;在Mayo队列中为0.80 [0.02]与0.76 [0.003,p = 0.09]。与AFIP-Miettinen系统所做的预测相比,RFS的线照相术预测似乎更好地进行了校准。解释:诺模图可准确预测局部原发GIST切除后的RFS,可用于选择伊马替尼辅助治疗的患者。

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