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KHA-CARI guideline: KHA-CARI adaptation of the KDIGO Clinical Practice Guideline for Acute Kidney Injury

机译:B-Curry指南:针对急性肾脏损伤的T Kadig临床实践指南的B-Curry改编

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INTRODUCTION:: The International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society classification of lung adenocarcinoma recommends identification of pathologic patterns in metastatic samples where possible. We investigated the clinical relevance of these patterns. METHODS:: Patients with a surgical biopsy of lung adenocarcinoma from a metastatic site were included. Slides were reviewed by an anatomical pathologist identifying the histologic patterns of solid with mucin, acinar, micropapillary, papillary, and assigning a major adenocarcinoma subtype according to the International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society classification. EGFR and KRAS mutation testing were performed on formalin-fixed, paraffin-embedded blocks. Mutations were detected by high resolution melting assay with high resolution melting-positive samples confirmed by Sanger sequencing. RESULTS:: One-hundred patients were included. The major histologic subtype prevalence was as follows: solid (50), acinar (29), micropapillary (20), and papillary (1). Of 100 patients, 45 received no systemic therapy with no overall survival differences seen by histologic subtype and 55 received systemic therapy (chemoradiotherapy with curative intent or palliative chemotherapy). Worse survival was seen in the major solid histologic subtype compared with major acinar (hazard ratio 0.32 [95% confidence interval 0.15-0.68], p = 0.003) and micropapillary subtypes (hazard ratio 0.34 [95% confidence interval, 0.17-0.69], p = 0.003). The major solid histologic subtype was less likely to harbor EGFR mutations (p = 0.006) and was less frequent in never smokers (p = 0.010) compared with other histologic subtypes. CONCLUSION:: The major solid histologic subtype of lung adenocarcinoma at metastatic sites is associated with shorter overall survival on systemic anticancer therapy. Furthermore, the major solid histologic subtype is less likely to harbor EGFR mutations. These results require validation in larger cohorts.
机译:简介:国际肺癌研究协会/美国胸科学会/欧洲呼吸学会对肺腺癌的分类建议在可能的情况下鉴定转移性样本的病理模式。我们调查了这些模式的临床相关性。方法:包括来自转移部位的肺腺癌手术活检的患者。根据国际肺癌研究协会/美国胸腔学会/欧洲呼吸学会的分类,解剖病理学家对载玻片进行了审查,确定了粘蛋白,腺泡,微乳头,乳头状固体的组织学模式,并指定了主要的腺癌亚型。 EGFR和KRAS突变测试是在福尔马林固定的石蜡包埋块上进行的。通过高分辨率熔解测定法检测突变,并通过Sanger测序确认高分辨率熔解阳性样品。结果:包括一百例患者。主要的组织学亚型患病率如下:实体(50),腺泡(29),微乳头(20)和乳头(1)。在100例患者中,有45例未接受全身治疗,没有通过组织学亚型观察到总体生存率差异,还有55例接受了全身治疗(放化疗与治愈性或姑息性化疗)。与主要腺泡(危险比0.32 [95%置信区间0.15-0.68],p = 0.003)和微乳头亚型(危险比0.34 [95%置信区间0.17-0.69])相比,主要实体组织学亚型的生存率较差, p = 0.003)。与其他组织学亚型相比,主要的实体组织学亚型不太可能携带EGFR突变(p = 0.006),并且从不吸烟的人较少(p = 0.010)。结论:转移性部位肺腺癌的主要实体组织学亚型与全身抗癌治疗的总体生存期缩短有关。此外,主要的实体组织学亚型不太可能携带EGFR突变。这些结果需要在更大的队列中进行验证。

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