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首页> 外文期刊>European Journal of Surgical Oncology: The Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology >Validation of the Joensuu risk criteria for primary resectable gastrointestinal stromal tumour - the impact of tumour rupture on patient outcomes.
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Validation of the Joensuu risk criteria for primary resectable gastrointestinal stromal tumour - the impact of tumour rupture on patient outcomes.

机译:Joensuu原发性可切除胃肠道间质瘤风险标准的验证-肿瘤破裂对患者预后的影响。

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BACKGROUND: Approval of imatinib for adjuvant treatment of gastrointestinal stromal tumours (GIST) raised discussion about accuracy of prognostic factors in GIST and the clinical significance of the available risk stratification criteria. METHODS: We studied the influence of a new modification of the NIH Consensus Criteria (the Joensuu risk criteria), NCCN-AFIP criteria, and several clinicopathological factors, including tumour rupture, on relapse-free survival (RFS) in a prospectively collected tumour registry series consisting of 640 consecutive patients with primary, resectable, CD117-immunopositive GIST. The median follow-up time after tumour resection was 39 months. None of the patients received adjuvant imatinib. RESULTS: The median RFS time after surgery was 50 months. In univariable analyses, high Joensuu risk group, tumour mitotic count >5/50 HPF, size >5 cm, non-gastric location, tumour rupture (7% of cases; P = 0.0014) and male gender had adverse influence on RFS. In a multivariable analysis mitotic count >5/50HPF, tumour size >5 cm and non-gastric location were independent adverse prognostic factors. Forty, 151, 86 and 348 patients were assigned according to the Joensuu criteria to very low, low, intermediate and high risk groups and had 5-year RFS of 94%, 94%, 86% and 29%, respectively. CONCLUSION: The Joensuu criteria, which include 4 prognostic factors (tumour size, site, mitotic count and rupture) and 3 categories for the mitotic count, were found to be a reliable tool for assessing prognosis of operable GIST. The Joensuu criteria identified particularly well high risk patients, who are likely the proper candidates for adjuvant therapy.
机译:背景:伊马替尼用于胃肠道间质瘤(GIST)的辅助治疗的批准引发了关于GIST预后因素的准确性以及可用风险分层标准的临床意义的讨论。方法:我们在前瞻性收集的肿瘤登记资料中研究了美国国立卫生研究院共识标准(Joensuu风险标准),NCCN-AFIP标准以及一些临床病理因素(包括肿瘤破裂)的新修改对无复发生存(RFS)的影响。系列由640例连续的原发性,可切除的CD117免疫阳性GIST患者组成。肿瘤切除后的中位随访时间为39个月。所有患者均未接受伊马替尼辅助治疗。结果:手术后中位RFS时间为50个月。在单变量分析中,高Joensuu高危组,肿瘤有丝分裂计数> 5/50 HPF,大小> 5 cm,非胃位置,肿瘤破裂(7%病例; P = 0.0014)和男性对RFS有不利影响。在多变量分析中,有丝分裂计数> 5 / 50HPF,肿瘤大小> 5 cm和非胃位置是独立的不良预后因素。根据Joensuu标准,分别将40、151、86和348位患者分为极低,低,中和高风险组,其5年RFS分别为94%,94%,86%和29%。结论:Joensuu标准包括4个预后因素(肿瘤大小,部位,有丝分裂计数和破裂)和3个有丝分裂计数类别,是评估可手术GIST预后的可靠工具。约恩苏(Joensuu)标准确定了风险特别高的患者,他们很可能是辅助治疗的合适人选。

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