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The role of theragnostics in oncology: an interview with Stefano Buono 诊断学在肿瘤学中的作用:Stefano Buono访谈
IF 1.2 Pub Date : 2017-06-09 DOI: 10.2217/ije-2017-0014
S. Buono
Stefano Buono* speaks to Commissioning Editor, Sebastian Dennis-Beron: Stefano Buono is the Chief Executive Officer, a member of the board of directors, and a founder of Advanced Accelerator Applications (AAA). He has been responsible for overseeing AAA operations, including the development and commercialization of the current portfolio of diagnostic and therapeutic molecular nuclear medicine products, and listing AAA on Nasdaq (stock symbol: AAAP). Prior to founding the company in 2002, he worked as a physicist at the Centre for Advanced Studies, Research and Development, or CRS4, in Italy. During his 6-year tenure with CRS4, he headed a team of engineers working on different international research projects in the field of energy production and nuclear waste transmutation. Before working at CRS4, and alongside his appointment at CRS4, he worked with Physics Nobel Laureate Carlo Rubbia at The European Organization for Nuclear Research (CERN), the world’s largest research laboratory for particle physics, i...
Stefano Buono*与调试编辑Sebastian Dennis Beron交谈:Stefano Bouono是首席执行官、董事会成员,也是高级加速器应用程序(AAA)的创始人。他一直负责监督AAA的运营,包括当前诊断和治疗分子核医学产品组合的开发和商业化,并在纳斯达克上市(股票代码:AAAP)。在2002年创立该公司之前,他曾在意大利高级研究、研究与发展中心(CRS4)担任物理学家。在CRS4的6年任期内,他领导了一个工程师团队,从事能源生产和核废料嬗变领域的不同国际研究项目。在CRS4工作之前,以及在CRS4任职期间,他曾与诺贝尔物理学奖获得者Carlo Rubbia在世界上最大的粒子物理研究实验室欧洲核研究组织(CERN)共事。。。
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引用次数: 1
The evolving landscape of systemic therapy for well-differentiated neuroendocrine tumors of the lung 分化良好的肺神经内分泌肿瘤系统治疗的发展前景
IF 1.2 Pub Date : 2017-05-15 DOI: 10.2217/IJE-2017-0003
James C. Yao
James Yao*, MD, is professor and chairman of gastrointestinal medical oncology at the MD Anderson Cancer Center (TX, USA). He is the chair emeritus of the North American Neuroendocrine Tumor Society (NANETS). He has numerous awards including the American Society of Clinical Oncology Career Development Award 2003, and the Carcinoid Cancer Foundation Research Award 2006, MD Anderson Distinguished Alumni Award 2009, Irwin H. Krakoff Excellence in Clinical Research Award 2011, and The Murray Brennan Distinguished Lecturer, Memorial Sloan-Kettering Cancer Center, 2012. In 1995, Dr. Yao received his doctorate of medicine at Baylor College of Medicine (TX, USA). His credentials include board of certification in internal medicine (ABIM) in 1999 and board of certification in medical oncology (ABIM) in 2003. Dr. Yao has special interests in neuroendocrine tumors and gastric cancer and has authored over 100 manuscripts including practice-changing articles in New England Journal of Medicine and The Lancet. He has als...
James Yao*,医学博士,美国德克萨斯州安德森医学博士癌症中心胃肠道医学肿瘤学教授兼主席。他是北美神经内分泌肿瘤学会(NANETS)的名誉主席。他获得了许多奖项,包括2003年美国临床肿瘤学会职业发展奖、2006年癌症基金会癌症研究奖、2009年MD Anderson杰出校友奖、2011年Irwin H.Krakoff临床研究卓越奖和2012年纪念斯隆-凯特林癌症中心Murray Brennan杰出讲师。1995年,姚博士在美国得克萨斯州贝勒医学院获得医学博士学位。他的资历包括1999年的内科认证委员会(ABIM)和2003年的医学肿瘤学认证委员会(ABIM)。姚博士对神经内分泌肿瘤和癌症有着特殊的兴趣,他在《新英格兰医学杂志》和《柳叶刀》上发表了100多篇论文,其中包括实用论文。他有。。。
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引用次数: 0
Epigenetics of human parathyroid tumors 人类甲状旁腺肿瘤的表观遗传学
IF 1.2 Pub Date : 2017-05-08 DOI: 10.2217/IJE-2017-0002
V. Chiara, Corbetta Sabrina
Parathyroid tumors are common endocrine neoplasia associated with primary hyperparathyroidism, a metabolic disorder sustained by parathormone hypersecretion. The epigenetic scenario in parathyroid tumors is beginning to be decoded. Here, main findings are reviewed: hypermethylation of specific DNA CpG islands has been described, despite global DNA promoter hypomethylation was not detectable; embryonic-related miRNAs, belonging to the C19MC and miR‐371-373 clusters, and miR‐296, are deregulated; expression of histone H1.2 and H2B is increased; expression of histone methyltransferase EZH2, BMI1 and RIZ1 is impaired; the tumor suppressor HIC1, MEN1 and CDC73 gene products, key molecules in parathyroid tumorigenesis, may be involved in epigenetic aberrant changes. Epigenetic changes are more frequent and more consistent in parathyroid malignancies, and positively correlated with severity of primary hyperparathyroidism.
甲状旁腺瘤是一种常见的内分泌肿瘤,与原发性甲状旁腺功能亢进有关,甲状旁腺功能亢进是一种由甲状旁腺激素分泌过多引起的代谢紊乱。甲状旁腺肿瘤的表观遗传机制开始被破译。在这里,主要研究结果进行了回顾:尽管没有检测到全局DNA启动子低甲基化,但已经描述了特定DNA CpG岛的超甲基化;属于C19MC和miR‐371-373簇以及miR‐296的胚胎相关mirna被解除调控;组蛋白H1.2、H2B表达升高;组蛋白甲基转移酶EZH2、BMI1、RIZ1表达受损;肿瘤抑制因子HIC1、MEN1和CDC73基因产物是甲状旁腺肿瘤发生的关键分子,可能参与了表观遗传异常改变。表观遗传改变在甲状旁腺恶性肿瘤中更为频繁和一致,并与原发性甲状旁腺功能亢进的严重程度呈正相关。
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引用次数: 3
Using genetics to develop new treatment possibilities for ovarian cancer 利用遗传学为卵巢癌开发新的治疗方法
IF 1.2 Pub Date : 2017-05-08 DOI: 10.2217/IJE-2017-0006
J. Delaney, D. Stupack
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引用次数: 0
Bilateral extramedullary adrenal plasmacytoma: case report and review of the literature. 双侧髓外肾上腺浆细胞瘤:病例报告和文献综述。
IF 1.2 Pub Date : 2017-05-01 Epub Date: 2017-05-03 DOI: 10.2217/ije-2016-0023
Philip J Townend, Gabriel Kraus, Luke Coyle, David Nevell, Anton Engelsman, Stan B Sidhu

Extramedullary plasmacytoma (EMP) accounts for only 3% of plasma cell malignancies; others include multiple myeloma, plasma cell leukemia and solitary plasmacytoma of bone. The majority of EMPs are found in the upper respiratory tract. Other sites include the GI tract, bladder, CNS, thyroid, breast, testes, parotid gland, lymph nodes and skin. There are eight cases in the literature of adrenal plasmacytoma, however, only two were bilateral. We describe our recent experience of bilateral adrenal plasmacytoma and review of the literature. While EMP may present as aggressive locally destructive lesions, excellent local control can be achieved in a majority of cases. Follow-up should be lifelong due to risk of progression to multiple myeloma.

髓外浆细胞瘤(EMP)仅占浆细胞恶性肿瘤的 3%,其他包括多发性骨髓瘤、浆细胞白血病和骨单发浆细胞瘤。大多数 EMP 发现于上呼吸道。其他部位包括消化道、膀胱、中枢神经系统、甲状腺、乳腺、睾丸、腮腺、淋巴结和皮肤。文献中有八例肾上腺浆细胞瘤,但只有两例是双侧的。我们介绍了最近的双侧肾上腺浆细胞瘤病例,并回顾了相关文献。虽然EMP可能表现为侵袭性局部破坏性病变,但大多数病例都能获得很好的局部控制。由于存在进展为多发性骨髓瘤的风险,因此应终身随访。
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引用次数: 0
11-Deoxycortisol may be superior to cortisol in confirming a successful adrenal vein catheterization without cosyntropin: a pilot study. 一项初步研究表明,去氧皮质醇可能优于皮质醇,可证实无共syntropin的肾上腺静脉导管置入术成功。
IF 1.2 Pub Date : 2017-05-01 Epub Date: 2017-04-27 DOI: 10.2217/ije-2016-0020
Naris Nilubol, Steven J Soldin, Dhaval Patel, Muthoni Rwenji, Jianghong Gu, Likhona S Masika, Richard Chang, Constantine A Stratakis, Electron Kebebew

Aim: We aimed to compare the performance of nine adrenal steroids in confirming the correct catheter position during adrenal venous sampling (AVS) without cosyntropin in patients with primary hyperaldosteronism.

Materials & methods: A successful adrenal vein catheterization without cosyntropin was defined as the ratio of steroids from adrenal to peripheral veins being >3:1. AVS samples from four patients with primary hyperaldosteronism were analyzed.

Results: Compared with the mean ratio of cortisol without cosyntropin, the ratios of 11-deoxycortisol (p = 0.008), dehydroepiandrosterone (p = 0.01) and androstenedione (p = 0.008) were significantly higher. None of the ratios (n = 8) of cortisol from adrenal to peripheral veins exceeded 3:1, while all ratios of 11-deoxycortisol (p < 0.001) were >3.

Conclusion: Cosyntropin infusion during AVS may not be necessary if 11-deoxycortisol is used to confirm catheter position.

目的:比较原发性高醛固酮增多症患者在无共syntropin的情况下进行肾上腺静脉取样(AVS)时,九种肾上腺激素在确定正确导管位置方面的表现。材料与方法:肾上腺静脉置管成功的标准是肾上腺静脉与外周静脉的类固醇比例大于3:1。分析了4例原发性高醛固酮增多症患者的AVS样本。结果:与不含共syntropin的皮质醇的平均比值相比,11-脱氧皮质醇(p = 0.008)、脱氢表雄酮(p = 0.01)和雄烯二酮(p = 0.008)的比值显著升高。肾上腺皮质皮质醇与外周静脉的比值均未超过3:1 (n = 8),而11-脱氧皮质醇的比值均>3 (p < 0.001)。结论:如果使用11-脱氧皮质醇来确定导管位置,AVS期间可能不需要注射共syntropin。
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引用次数: 14
Recent advances in the management of endocrine malignancies associated with hereditary hyperparathyroidism syndromes 遗传性甲状旁腺功能亢进综合征相关内分泌恶性肿瘤的治疗进展
IF 1.2 Pub Date : 2017-04-27 DOI: 10.2217/IJE-2016-0018
Yulong Li, W. Simonds
Hereditary hyperparathyroidism syndromes, such as multiple endocrine neoplasm type 1, type 2A and the hyperparathyroidism-jaw tumor syndrome, are associated with an increased incidence of malignancies involving the neuroendocrine tissue of the pancreas and thymus, parathyroid and thyroid glands. The natural history of these endocrine tumors can differ from nonhereditary malignancies. The surgical approach, the only potentially curative treatment option for these endocrine malignancies, has evolved considerably in recent years. Newer targeted therapies, such as small molecule kinase inhibitors, somatostatin analogs and peptide receptor radionuclide therapy, are being developed. We provide here a comprehensive review of the current standards of treatment and emerging novel therapies for the endocrine malignancies commonly associated with hereditary hyperparathyroidism syndromes.
遗传性甲状旁腺功能亢进综合征,如1型、2A型多发性内分泌肿瘤和甲状旁腺功能亢进颌骨肿瘤综合征,与涉及胰腺和胸腺神经内分泌组织、甲状旁腺和甲状腺的恶性肿瘤发病率增加有关。这些内分泌肿瘤的自然病史可能与非遗传性恶性肿瘤不同。外科手术是治疗这些内分泌恶性肿瘤的唯一潜在治疗选择,近年来已经有了很大的发展。正在开发新的靶向疗法,如小分子激酶抑制剂、生长抑素类似物和肽受体放射性核素疗法。我们在这里对目前的治疗标准和新出现的内分泌恶性肿瘤的新疗法进行了全面的综述,这些肿瘤通常与遗传性甲状旁腺功能亢进综合征有关。
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引用次数: 0
Von Hippel-Lindau disease: a multidisciplinary neoplasia syndrome Von Hippel-Lindau病:一种多学科肿瘤综合征
IF 1.2 Pub Date : 2017-04-03 DOI: 10.2217/IJE-2016-0021
K. Dreijerink, A. N. Horst-Schrivers, T. Links, R. Giles
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引用次数: 0
Novel targets in the treatment of neuroendocrine tumors: RBP2 治疗神经内分泌肿瘤的新靶点:RBP2
IF 1.2 Pub Date : 2017-03-23 DOI: 10.2217/IJE-2016-0022
E. Maggi, J. Crabtree
Retinoblastoma binding protein 2, also known as RBP2, JARID1A or KDM5A, is an H3K4 demethylase implicated in a variety of non-neuroendocrine, and more recently, neuroendocrine tumors (NETs). NETs are tumors that form from neuroendocrine cells in tissues of the GI tract, endocrine pancreas, lung, skin and other tissues. RBP2 is expressed at abnormally high levels in NETs and recent work demonstrates that modulation of RBP2 in vitro and in vivo impacts end points of tumorigenesis. Interestingly, the demethylase activity of RBP2 is not exclusively responsible for these changes, as RBP2's binding partners may mediate its activity in a tissue- or context-dependent manner. Here, we discuss the features of RBP2 and its role in cell cycle regulation, angiogenesis and drug resistance in cancer.
视网膜母细胞瘤结合蛋白2,也被称为RBP2、JARID1A或KDM5A,是一种H3K4去甲基化酶,与多种非神经内分泌和最近的神经内分泌肿瘤(NETs)有关。NETs是由胃肠道、内分泌胰腺、肺、皮肤等组织中的神经内分泌细胞形成的肿瘤。在NETs中,RBP2的表达水平异常高,最近的研究表明,体外和体内对RBP2的调节会影响肿瘤发生的终点。有趣的是,RBP2的去甲基酶活性并不是这些变化的唯一原因,因为RBP2的结合伙伴可能以组织或环境依赖的方式调节其活性。在此,我们讨论了RBP2的特点及其在肿瘤细胞周期调节、血管生成和耐药中的作用。
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引用次数: 1
Factors influencing Ki67 calculation in neuroendocrine neoplasia 影响神经内分泌肿瘤Ki67计算的因素
IF 1.2 Pub Date : 2017-03-23 DOI: 10.2217/IJE-2016-0011
C. Castañeda, Miluska Castillo, Juvenal Sanchez, S. Casavilca, C. Gonzalez, C. Flores, Luis Cano, Carolina Belmar-López, Rosario Villa-Robles, Gabriela Rios-Martini, Yun Wu
Aim: We compared different methodologies to evaluate Ki67 in neuroendocrine neoplasia (NEN). Patients & methods: ki67 was evaluated using three methods in 70 NEN cases: manual-count, eyeballed estimate made by three pathologists and ImmunoRatio-software. Manual-count was the standard method and agreement with it was evaluated through intraclass correlation (ICC). Results: Agreement between manual-count and eyeballed estimate had ICC: 0.887–0.929. Eyeballed estimate by three pathologists produced upgradation in 5.7–32.9% and downgradation in 5.7% of NEN cases. Agreement for ImmunoRatio-count had ICC: 0.989. Immunoratio produced upgradation in 17.1% and downgradation in 8.5% cases. Agreement between all methods was higher at low-Ki67. Cellularity, immune-cell infiltration, staining and sample quality did not affect agreement. Conclusion: Eyeballed estimate and ImmunoRatio showed good accuracy, especially at low-Ki67.
目的:比较不同方法对神经内分泌瘤(NEN) Ki67的评价。患者与方法:对70例NEN病例采用三种方法对ki67进行评估:手工计数、三名病理学家的目测和ImmunoRatio-software。手工计数为标准方法,并通过类内相关性(ICC)评价其一致性。结果:手工计数与目测的一致性ICC: 0.887-0.929。三名病理学家的肉眼估计导致5.7-32.9%的NEN病例升级,5.7%的NEN病例降级。免疫协议计数ICC: 0.989。免疫接种导致17.1%的患者升级,8.5%的患者降级。在低ki67时,所有方法之间的一致性更高。细胞结构、免疫细胞浸润、染色和样品质量不影响一致性。结论:肉眼估计和免疫比具有良好的准确性,特别是在低ki67时。
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引用次数: 0
期刊
International Journal of Endocrine Oncology
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