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Amid a boom in organ donation, a heightened focus on cancer risk in transplant recipients 随着器官捐赠的蓬勃发展,对移植受者癌症风险的高度关注:免疫抑制、传染性感染和肿瘤,以及器官受者长期生存率的提高,要求对皮肤癌和其他恶性肿瘤提高警惕。
IF 3.2 3区 医学 Q3 ONCOLOGY Pub Date : 2025-01-20 DOI: 10.1002/cncy.22932
Bryn Nelson PhD, William Faquin MD, PhD

In 2023, the United States set a record for organ transplants, with more than 46,00 transplants performed with organs procured from more than 16,000 deceased donors and nearly 7000 living ones.1 With this encouraging trend reported by the Organ Procurement and Transplantation Network (OPTN), though, experts have stressed that the lifesaving operations can carry a tradeoff. Although it has happened only rarely, some donors’ metabolic disorders or nascent tumors have evaded detection before the transplant, the latter resulting in the documented transmission of glioblastoma multiforme and lung, breast, colorectal, kidney, and other cancers.

More commonly, donors can transmit parasitic, fungal, bacterial, or viral infections, including some cancer-linked pathogens such as Helicobacter pylori, hepatitis B, and hepatitis C, as well as more ubiquitous viruses such as Epstein–Barr virus and human papillomavirus (HPV). H. pylori has been linked to gastric cancer, chronic hepatitis, and liver cancer; Epstein–Barr to non-Hodgkin lymphoma; and HPV to cervical, anal, penile, and oropharyngeal cancers.

A 2021 study by OPTN’s Disease Transmission Advisory Committee (DTAC) suggested that donor-derived disease transmission occurs in less than 1% of all transplant recipients. Of the proven or probable donor transmission events, 67% involved infections, 29% included malignancies, and 6% involved other disease processes (a small percentage involved more than one kind of event).2

Gerald Berry, MD, a professor of surgical pathology at Stanford University in Palo Alto, California, and a cancer expert on the DTAC, says that the committee first tries to determine whether a transmissible event is donor-derived or originates in the recipient. “Then the subcategory is, even if it’s donor derived, was it there at the time of transplant and too small to actually detect?”

The DTAC’s work toward determining whether a malignancy can be traced back to the donor, even years after the fact, can help to establish the risk for the remaining cohort of transplant recipients. “Many times, the donor is providing organs for more than one recipient, so the biggest concern is when a recipient develops a malignancy, are the other recipients at risk?” Dr Berry says. The risk can be further characterized according to tumor type: A donor’s brain tumor that has metastasized, for example, would pose a considerably bigger danger than a far more treatable thyroid tumor.

The most significant cancer-related risk for organ transplant recipients, however, is associated with the very immunosuppressive medications that are required to prevent rejection of the organs but also can render the immune system less able to identify and kill tumor cells or battle cancer-linked infections. “The patients are so heavily immunosuppressed as part of the transplant protocol that the host versus the virus mechani

2023年,美国创下了器官移植的纪录,从1.6万多名已故捐赠者和近7000名活着的捐赠者那里获得的器官进行了4.6万多例移植尽管器官获取和移植网络(OPTN)报告了这一令人鼓舞的趋势,但专家们强调,挽救生命的手术可能会带来权衡。虽然这种情况很少发生,但一些供体的代谢紊乱或新生肿瘤在移植前没有被发现,后者导致多形性胶质母细胞瘤和肺癌、乳腺癌、结肠直肠癌、肾癌和其他癌症的传播。更常见的是,捐赠者可以传播寄生虫、真菌、细菌或病毒感染,包括一些与癌症相关的病原体,如幽门螺杆菌、乙型肝炎和丙型肝炎,以及更普遍的病毒,如爱泼斯坦-巴尔病毒和人类乳头瘤病毒(HPV)。幽门螺旋杆菌与胃癌、慢性肝炎和肝癌有关;Epstein-Barr到非霍奇金淋巴瘤;HPV对宫颈癌、肛门癌、阴茎癌和口咽癌的影响。OPTN疾病传播咨询委员会(DTAC) 2021年的一项研究表明,供体来源的疾病传播发生在所有移植受者的不到1%。在已证实或可能的供体传播事件中,67%涉及感染,29%包括恶性肿瘤,6%涉及其他疾病过程(一小部分涉及一种以上事件)Gerald Berry医学博士是加州帕洛阿尔托斯坦福大学的外科病理学教授,也是DTAC的癌症专家,他说该委员会首先试图确定传播事件是源自供体还是源自受体。“那么子类别是,即使它来自供体,在移植时是否存在并且太小而无法实际检测?”DTAC的工作是确定恶性肿瘤是否可以追溯到捐赠者,甚至在事实发生多年之后,这有助于确定移植接受者的剩余队列的风险。“很多时候,捐赠者为不止一个接受者提供器官,所以最大的担忧是,当一个接受者患上恶性肿瘤时,其他接受者是否有风险?”贝里博士说。风险可以根据肿瘤类型进一步确定:例如,供体的脑肿瘤已经转移,比可治疗得多的甲状腺肿瘤造成的危险要大得多。然而,对于器官移植受者来说,最重要的癌症相关风险与免疫抑制药物有关,这些药物是防止器官排异反应所必需的,但也会降低免疫系统识别和杀死肿瘤细胞或对抗癌症相关感染的能力。贝瑞博士说:“作为移植方案的一部分,患者的免疫受到严重抑制,宿主对抗病毒的机制被扭曲,因此类似的事情就会扩散。”与一般人群相比,移植受者患多种癌症的风险高出2至4倍。例如,芬兰一项为期30年的队列研究对大约6500名移植接受者进行了调查,发现近四分之一的人最终患上了癌症;这意味着风险增加了3.6倍对于非黑色素瘤皮肤癌,如基底细胞癌和鳞状细胞癌,发病率甚至更高:研究表明,其风险增加了25至250倍波士顿马萨诸塞州眼耳科头颈癌外科主任Kevin Emerick医学博士说,虽然这些癌症大多是相对良性的,但移植受者也会发展成更多的局部晚期或晚期皮肤恶性肿瘤。“随着我们做越来越多的移植手术,我们将会有越来越多的这样的病人,”埃默里克博士说,他也是诊所非黑色素瘤皮肤癌多学科临床和项目的联合主任。“因此,也许一个好的趋势是对这些患者需要的特殊护理的认可和承认。”随着更多的患者在移植后存活时间延长,更多的患者需要长期随访。他指出,在许多学术医疗中心,皮肤科正在开设高风险诊所,专门为越来越多的实体器官移植患者提供服务,其中一些患者需要每6或12周看一次。根据意大利一项对1300多名心脏或肾脏移植患者的研究,“患皮肤癌的总体风险从移植后5年的累计发病率5.8%增加到移植后10年的发病率10.8%。”其他国家的研究记录了更高的比例。埃默里克博士说,一个重要的信息是,需要专门的提供者进行常规监测,并需要足够的基础设施和团队来照顾那些患皮肤癌的患者。 与其他癌症的风险相比,皮肤癌的风险主要是基于受体的免疫抑制和癌症病变逃避免疫监视的能力。“我们的免疫系统在帮助抑制和清除DNA损伤方面起着至关重要的作用,我们的皮肤上都有大量的DNA损伤,”埃默里克博士说。“所以,如果你把我们免疫系统的监视作用拿走,这就是为什么患者患皮肤癌的几率要高得多。”因此,与普通大众相比,与新肝脏相关的癌症风险可能更高,但与新心脏相关的风险甚至更高。同样,小肠和肺移植患者往往有更高的移植后淋巴增殖性疾病发病率,这是一种危及生命的淋巴瘤,也见于造血干细胞移植后,白细胞不受控制地增殖。移植肾患者生活数年或数十年可能会减少他们的免疫抑制方案,老年患者通常免疫系统活性较低;相反,随着时间的推移,移植器官的寿命延长会增加风险。对于一些患者,转换免疫抑制剂(例如,从他克莫司到西罗莫司)可能会降低患皮肤癌的风险。“这就是为什么与人们的移植团队合作是如此重要,”埃默里克博士说。“他们是找到合适的免疫抑制水平的真正专家,(移植受者)需要维持他们的器官,这对这些人来说非常重要,尤其是我们的心脏和肺移植患者。”降低风险的策略,例如为患者接种乙型肝炎和人乳头瘤病毒疫苗,并优先宣传预防信息(例如,强调避免更多阳光照射的紫外线辐射的重要性),即使患者在器官移植等待名单上,也可能使他们受益。皮肤色素较多的患者患非黑色素瘤和黑色素瘤皮肤癌的风险较低,包括在器官移植后,因为黑色素对紫外线辐射的累积暴露具有保护作用。即便如此,埃默里克博士说,他们患其他癌症的风险仍然很高,需要时刻保持警惕。器官移植后发生的晚期皮肤癌的一个残酷的讽刺是,免疫疗法是一种关键的抗癌治疗方法。“皮肤癌是免疫疗法最容易治疗的癌症,”埃默里克博士说。“不幸的是,免疫疗法伴随着失去移植器官的巨大风险。”抗癌免疫疗法可以用于一些肾移植患者,他说,“很大程度上是因为如果他们的器官衰竭,你可以考虑透析。”同样的选择不适用于肺、心脏和大多数肝脏移植患者,因为失去器官会杀死他们。埃默里克博士和其他专家说,免疫抑制有助于防止对捐赠器官的排斥,但会增加许多其他疾病的风险,这一事实加强了对移植患者进行长期癌症监测和早期检测的重要性。因此,一种传播性恶性肿瘤可能直到移植后数年才在临床上表现出来,贝里博士补充道。他说:“我们不仅要研究那些不幸患上肿瘤的贫穷受者的生存风险或发病率-死亡率风险,而且还要研究其余受者的风险分层。”幸运的是,大多数这样的患者在移植后定期就诊,这些就诊为筛查和风险评估提供了充足和关键的机会。
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引用次数: 0
Cytologic diagnosis of fumarate hydratase-deficient renal cell carcinoma: A single-institutional experience 富马酸水合酶缺乏肾细胞癌的细胞学诊断:单一机构的经验。
IF 3.2 3区 医学 Q3 ONCOLOGY Pub Date : 2025-01-13 DOI: 10.1002/cncy.22931
Patrick C. Mullane MD, Xiaohua Qian MD, PhD, Hubert D. Lau MD, Alarice Cheng-Yi Lowe MD

Background

Fumarate hydratase-deficient renal cell carcinoma (FHRCC) is an aggressive carcinoma that typically presents as advanced-stage disease. Prompt recognition of FHRCC is critical for appropriate clinical care and genetic counseling for patients and family members. However, diagnosing FHRCC from cytology specimens is challenging, with limited characterization and no reports describing prospectively identified cases.

Methods

Cytology fine-needle aspiration (FNA) cases diagnosed as FHRCC were reviewed, including two prospectively identified cases.

Results

Five cases of FHRCC diagnosed by FNA cytology were identified in five unique patients. The cytologic samples included four FNAs with core biopsy and one FNA with cell block. Biopsy sites included kidney (n = 1), chest wall (n = 1), omentum (n = 1), lung (n = 1), and cervical lymph node (n = 1). All cases demonstrated cytologically malignant epithelial cells characterized by enlarged, round nuclei with variable pleomorphism, irregular nuclear membranes, prominent nucleoli, and moderate-to-abundant amounts of cytoplasm. Perinucleolar halos characterized by chromatin margination and pallor around macronucleoli were seen in all cases. Cytologic features not previously described included cytoplasmic macrovacuoles and eosinophilic globules, cytophagocytosis, and floral groups. Papillary architecture was rarely present on aspirate smears. Cell block sections showed variable architectural patterns. By immunohistochemistry, FH was definitively lost in three of five cases (60%), and 2-succinocysteine was positive in all 5 cases (100%).

Conclusions

Cytologic specimens of FHRCC demonstrate salient cytomorphologic features that can support their initial diagnosis. Confirmatory immunohistochemical testing using a dual panel of fumarate hydratase and 2-succinocysteine is recommended for the diagnosis in limited biopsy samples.

背景:富马酸水合酶缺陷肾细胞癌(FHRCC)是一种侵袭性癌症,通常表现为晚期疾病。及时识别FHRCC对于患者和家属进行适当的临床护理和遗传咨询至关重要。然而,从细胞学标本中诊断FHRCC具有挑战性,具有有限的特征,并且没有报告描述前瞻性确定的病例。方法:回顾性分析经细胞学细针穿刺(FNA)诊断为FHRCC的病例,包括2例前瞻性诊断病例。结果:5例独特的FNA细胞学诊断为FHRCC。细胞学样本包括4例核心活检的FNA和1例细胞阻滞的FNA。活检部位包括肾脏(n = 1)、胸壁(n = 1)、大网膜(n = 1)、肺(n = 1)和颈部淋巴结(n = 1)。所有病例均表现为细胞学上的恶性上皮细胞,其特征是核肿大、圆形,具有可变多形性,核膜不规则,核仁突出,细胞质含量中等至丰富。所有病例均可见核周晕,其特征为染色质边缘和大核仁周围的苍白。先前未描述的细胞学特征包括细胞质大空泡和嗜酸性球,细胞吞噬和花群。吸痰涂片上乳头状结构很少出现。细胞块切片显示了不同的建筑模式。免疫组化结果显示,5例患者中3例(60%)FH完全消失,5例患者中2-琥珀酸半胱氨酸均呈阳性(100%)。结论:FHRCC的细胞学标本显示出明显的细胞形态学特征,可以支持其初步诊断。在有限的活检样本中,推荐使用富马酸水合酶和2-琥珀酸半胱氨酸双组进行确证性免疫组织化学检测。
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引用次数: 0
Counseling gap may worsen endometrial cancer disparities in Black women 咨询差距可能会加剧黑人女性子宫内膜癌的差异:一项研究发现,黑人或非洲血统的女性比白人女性有更少的癌症相关基因突变,但获得遗传咨询的机会更少。
IF 3.2 3区 医学 Q3 ONCOLOGY Pub Date : 2025-01-02 DOI: 10.1002/cncy.22928
Bryn Nelson PhD, William Faquin MD, PhD
<p>Cancer of the endometrium, or the lining of the uterus, is the most common gynecologic cancer. Its incidence is accelerating, especially in younger women and among racial and ethnic minorities; it is one of the few cancers with worsening mortality rates.<span><sup>1</sup></span> The trend is most pronounced in Black women, who are two-fold more likely to die of endometrial cancer than their White counterparts.</p><p>Research has shown that mutations in dozens of cancer predisposition genes, or germline pathogenic variants, can increase the risk. A recent study that grouped 1625 women with endometrial cancer by self-reported race, ethnicity, and Ashkenazi Jewish ancestry, however, has pointed to a more troubling contributor to disparities in patient outcomes. Although the genetic mutation rates were lowest in women who identified as being Black or of African ancestry, so too were their rates of genetic counseling, which could help them to assess treatment options.<span><sup>2</sup></span> </p><p>The study, led by oncologist Ying Liu, MD, MPH, at Memorial Sloan Kettering Cancer Center in New York, suggests that the counseling disparities also could dampen subsequent counseling rates for at-risk relatives. Social determinants then could be making endometrial cancer morbidity and mortality disparities worse in Black women despite a genetic contribution to risk that is equivalent to or lower than that in White women.</p><p>Given the growing use of such germline assessments, Dr Liu and her colleagues emphasize the need to understand variations related to patients’ ancestry, correlations between genetic findings and tumor traits, and “downstream implications on treatment and cancer prevention and the potential contribution to racial disparities in outcomes.”</p><p>Oladapo Yeku, MD, PhD, assistant professor of medicine at Harvard University, says that he is not surprised by Dr Liu’s findings “but very concerned because it gave numbers to some of the things that a lot of doctors in the community and academic centers have known for some time.” Many physicians had sensed that women in underserved communities were not getting appropriate referrals for genetic counseling. “But it was hard to get a number on it; it hadn’t been rigorously studied,” Dr Yeku says. “What this single institution report did was actually put some numbers to what some people had feared the whole time.”</p><p>The referral gap is even more concerning because tumor mutation testing and guideline-based recommendations for managing newly diagnosed, advanced, and recurrent endometrial cancer generally have increased in availability. As Dr Yeku wrote in an editorial accompanying the study, “disparities in testing, referral to clinical genetics, and participation in clinical trials are persistent contributors to poor outcomes in this patient population.”<span><sup>3</sup></span> </p><p>Lack of access, in fact, has been a consistent theme in multiple aspects of care
子宫内膜癌,或子宫内膜癌,是最常见的妇科癌症。其发病率正在加速上升,特别是在年轻妇女和少数种族和族裔群体中;它是少数几种死亡率越来越高的癌症之一这一趋势在黑人女性中最为明显,她们死于子宫内膜癌的可能性是白人女性的两倍。研究表明,数十种癌症易感性基因的突变或种系致病变异会增加患癌风险。然而,最近的一项研究将1625名患有子宫内膜癌的女性按自我报告的种族、民族和德系犹太人血统分组,指出了导致患者结果差异的一个更令人不安的因素。尽管被认定为黑人或非洲血统的妇女的基因突变率最低,但她们接受遗传咨询的比率也最低,这可以帮助她们评估治疗方案这项研究由纽约纪念斯隆-凯特琳癌症中心的肿瘤学家刘颖(医学博士、公共卫生硕士)领导,研究表明,咨询的差异也会降低风险亲属的后续咨询率。社会决定因素可能会使黑人女性的子宫内膜癌发病率和死亡率差距更大,尽管遗传因素对风险的影响与白人女性相当或更低。鉴于越来越多地使用这种生殖系评估,刘博士和她的同事强调有必要了解与患者祖先相关的变异,遗传发现与肿瘤特征之间的相关性,以及“对治疗和癌症预防的下游影响以及对结果的种族差异的潜在贡献”。哈佛大学医学助理教授Oladapo Yeku博士说,他对刘博士的发现并不感到惊讶,“但非常担心,因为它提供了一些数字,许多社区和学术中心的医生已经知道了一段时间。”许多医生已经意识到,在服务不足的社区,妇女没有得到适当的遗传咨询转诊。“但很难得到一个具体数字;它没有经过严格的研究,”耶库博士说。“这份单一机构的报告实际上是为一些人一直以来所担心的事情提供了一些数字。”转诊差距更令人担忧,因为肿瘤突变检测和基于指南的治疗新诊断、晚期和复发子宫内膜癌的建议普遍增加了。正如Yeku博士在该研究的一篇社论中所写的那样,“在检测、转诊到临床遗传学和参与临床试验方面的差异是导致这一患者群体预后不佳的持续因素。事实上,缺乏机会一直是少数民族子宫内膜癌妇女护理的多个方面的一致主题。Yeku博士说,对于DNA错配修复机制存在缺陷的一部分患者,两种强效药物(称为免疫检查点抑制剂)的出现在延长生命方面已经“改变了游戏规则”。他说,美国食品和药物管理局(FDA)批准派姆单抗和多斯达单抗用于治疗晚期或复发性子宫内膜癌的妇女是“毫不含糊的全打”。即便如此,导致FDA批准的开创性临床试验同样受到Yeku博士所说的少数族裔女性“糟糕”代表的困扰。他说,从理论上讲,任何拥有正确基因突变的人都可以获得挽救生命的精准药物。然而,实际情况却截然不同。他说:“有一部分人有机会获得这种药物,而且情况很好,而另一部分人有同样的突变,但从未及早获得这些药物。”换句话说,一些女性在诊断和治疗两方面都被排除在尖端癌症护理之外。在其他癌症中也有同样的普遍现象。例如,刘博士和她的同事在他们最近的研究中指出,他们之前的研究报告了所有肿瘤类型在护理方面的类似差异。“即使在排除了许多障碍之后,非白人,尤其是黑人患者也不太可能得到推荐的基因治疗,这可能会影响他们的癌症治疗和家庭。研究人员正试图分析造成这些令人不安的差异的潜在社会经济因素,一些人认为,是否能获得检测和咨询——从而获得知情的护理——可能在一定程度上取决于人们住在哪里。例如,2008年一项被广泛引用的针对老年女性乳腺癌患者的研究得出的结论是:“生活在隔离地区的人接受乳腺癌适当治疗的可能性较小。”这份研究报告是最早明确地将种族隔离与较差的护理联系起来的报告之一。 根据最新的研究,一些研究人员提出,适合的少数族裔患者是否接受基因检测和咨询的关键点可能是癌症差异的主要原因,也是实际解决方案的关键目标。Yeku博士说,展望未来,最重要的优先事项之一应该是对患者和从业人员,特别是患者的初级保健医生进行教育。应该让患者了解他们的基因图谱的结果和影响,包括他们可以传递给后代的种系变异,以及帮助他们确定治疗方案的肿瘤相关图谱。因此,一个关键的问题是,该结果是否应促使转介给临床遗传学家,以讨论对患者及其家属的风险。另一个问题是,研究结果是否指向一项患者可以参加的临床试验。然而,Yeku博士说,患者教育本身是不够的。原发肿瘤学家、转诊肿瘤学家、初级保健提供者、妇科医生或其他提供者应该意识到询问基因检测结果的必要性,询问他们是如何讨论的,与患者协商最相关的问题,然后将他们转介给临床遗传学家寻求答案。他说:“在我看来,这将是在基层加强教育的最佳途径之一。”患者导航员(通常是护士)或值得信赖的初级保健提供者可能比三级保健中心不熟悉的医生更适合弥合诊断和治疗差距。Yeku博士说:“如果你在社区中考虑一下,对很多病人来说,是家庭成员为他们扮演了这个角色。”“我怀疑这些患者往往更容易获得转诊,他们可能更精明。”在实践中,教育还意味着提醒患者和医生注意与遗传条件相关的子宫内膜癌风险增加,如林奇综合征,以及早期预警信号,如绝经后出血——这是一个女性通常没有报告的危险信号。Yeku博士说:“他们可能看到的从业人员没有充分了解绝经后妇女可能存在的风险因素。”缺乏关注可能会导致一系列下游影响,降低患者的生存几率,例如在疾病的后期诊断,缺乏基因检测,咨询或临床试验的登记。Yeku博士说:“早期诊断、早期检测必须是解决之道。”他说,当来自服务不足人群的患者确实得到转诊去看临床遗传学家时,绝大多数人都会坚持到底。弄清楚如何让他们更好地获得这一关键资源,可能会在这种趋势日益令人担忧的疾病中产生可喜的转机。
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引用次数: 0
Same-day molecular testing for targetable mutations in solid tumor cytopathology—The next frontier of the rapid on-site evaluation 实体瘤细胞病理学中可靶向突变的当日分子检测——快速现场评估的下一个前沿领域。
IF 3.2 3区 医学 Q3 ONCOLOGY Pub Date : 2025-01-02 DOI: 10.1002/cncy.22930
J. Bryan Iorgulescu MD, MPH, Richard Kenneth Yang MD, PhD, Sinchita Roy-Chowdhuri MD, PhD, Gloria Hopkins Sura MD

Introduction

This study aimed to assess the feasibility of implementing the Idylla system, an ultra-rapid, cartridge-based assay, as an extension of rapid on-site evaluation (ROSE) in cytology. The authors conducted a pilot validation study on specimens from non–small cell lung carcinoma, thyroid carcinoma, and melanoma, evaluating four assays designed to detect alterations in KRAS, EGFR, BRAF, gene fusions, and expression imbalances in ALK, ROS1, RET, NTRK1/2/3, and MET exon 14 skipping transcripts. They investigated the feasibility of providing accurate biomarker molecular testing results in a cytopathology laboratory within hours of specimen collection.

Methods

The authors evaluated the performance characteristics and turn-around-time of the Idylla system by testing a total of 144 cartridge assays across various specimen types, including fine-needle aspirate smears, formalin-fixed paraffin-embedded (FFPE) cell blocks, small tissue biopsy FFPE blocks, and control cell line FFPE scrolls.

Results

The average time from specimen input to results output was 2–3 hours. Accuracy across the four cartridge types was: KRAS assay: 100%, EGFR assay: 94%, BRAF assay: 100%, and GeneFusion assay: 94%. Analytical sensitivity ranged from 1% to 5% variant allele frequency for all assays. Inter-assay precision and analytical specificity were both 100%.

Conclusion

Using the Idylla system, actionable genetic alterations can be reliably detected within 2–3 hours from cytology and small biopsy samples with minimal input requirements. The findings of this study demonstrate the feasibility of incorporating same-day molecular testing as part of ROSE procedures in the cytopathology laboratory, ultimately shortening the time from procedure to personalized treatment for cancer patients.

简介本研究旨在评估 Idylla 系统的可行性,该系统是一种基于试剂盒的超快速检测方法,是快速现场评估 (ROSE) 在细胞学中的延伸。作者对来自非小细胞肺癌、甲状腺癌和黑色素瘤的标本进行了试点验证研究,评估了四种检测方法,旨在检测 KRAS、EGFR、BRAF、基因融合的改变,以及 ALK、ROS1、RET、NTRK1/2/3 和 MET 第 14 号外显子跳越转录本的表达失衡。他们研究了细胞病理学实验室在标本采集后数小时内提供准确的生物标志物分子检测结果的可行性:作者评估了 Idylla 系统的性能特点和周转时间,在各种标本类型(包括细针抽吸涂片、福尔马林固定石蜡包埋(FFPE)细胞块、小组织活检 FFPE 块和对照细胞系 FFPE 卷)中测试了总共 144 项盒式检测:结果:从样本输入到结果输出的平均时间为 2-3 小时。四种试剂盒的准确性如下KRAS检测100%,表皮生长因子受体检测94%,BRAF 检测100%,基因融合检测94%.所有检测方法的分析灵敏度在 1%至 5%的变异等位基因频率之间。测定间精密度和分析特异性均为 100%:结论:使用 Idylla 系统,可在 2-3 小时内从细胞学和小型活检样本中可靠地检测出可操作的基因改变,且对输入的要求极低。这项研究结果表明,将当天分子检测作为细胞病理学实验室 ROSE 程序的一部分,最终缩短癌症患者从手术到个性化治疗的时间是可行的。
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引用次数: 0
State pathology societies—valuable resources for trainees 国家病理学会——学员的宝贵资源。
IF 3.2 3区 医学 Q3 ONCOLOGY Pub Date : 2025-01-02 DOI: 10.1002/cncy.22926
Myles R. McCrary MD, PHD, Carmen Gomez-Fernandez MD

The importance of large, national/international organizations like the College of American Pathologists (CAP) and the US and Canadian Academy of Pathology for resident and fellow training cannot be overstated. However, many opportunities also exist at the locoregional level, such as pathology state societies, which vary widely in size, structure, and level of engagement but can provide valuable resources and networking opportunities for trainees. What are some specific resources, initiatives, and mechanisms that might be beneficial for local, state, and regional pathology society groups to enhance trainee experiences? The Florida Society of Pathologists (FSP) enjoys a long history of representing the interests of Florida pathologists and is an impressive example of a large state society. Key areas addressed for residents and fellows who participate in the FSP include engagement, networking, education, and advocacy. Here, we summarize several programs and initiatives that the FSP has pursued to cater to the needs of Florida's resident/fellow trainees, and we hope that this information will benefit other locoregional and state societies.

美国病理学家学会(CAP)、美国和加拿大病理学学会等大型国家/国际组织对住院医师和同事培训的重要性怎么强调也不为过。然而,在地方区域层面也存在许多机会,例如病理国家协会,它们在规模、结构和参与程度上差异很大,但可以为学员提供宝贵的资源和交流机会。有哪些具体的资源、倡议和机制可能对地方、州和地区病理学会团体有益,以增强实习生的经验?佛罗里达病理学家协会(FSP)有着悠久的历史,代表着佛罗里达病理学家的利益,是一个令人印象深刻的大国家社会的例子。为参加FSP的住院医师和研究员解决的关键领域包括参与、网络、教育和宣传。在这里,我们总结了FSP为满足佛罗里达州居民/学员的需求而进行的几个项目和倡议,我们希望这些信息能使其他地方和州的社会受益。
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引用次数: 0
Rapid on-site evaluation using telecytology: Quality assurance study at a high-volume cancer center 使用远程技术的快速现场评估:高容量癌症中心的质量保证研究。
IF 3.2 3区 医学 Q3 ONCOLOGY Pub Date : 2025-01-02 DOI: 10.1002/cncy.22929
Mohamed Alhamar MD, Dorota Rudomina MBA, CT (ASCP), Lu Wang BS, CT (ASCP), Rusmir Feratovic MHA, CT (ASCP), Handy Oen MBA, CT, MB (ASCP), Oscar Lin MD, PhD, Xiao-Jun Wei MD

Background

Telecytology-assisted rapid on-site evaluation (ROSE) offers a cost-effective method to enhance minimally invasive biopsies like fine needle aspiration and core biopsies with touch preparation. By reducing nondiagnostic sampling and the need for repeat procedures, ROSE via telecytology facilitates prompt triage for ancillary tests, improving patient management. This study examines cases initially deemed adequate for diagnosis during telecytology-assisted ROSE but later categorized as nondiagnostic at final evaluation (NDIS).

Design

We performed a retrospective analysis of telecytology-assisted ROSE cases over 7 years at a major cancer center, focusing on fine needle aspiration and touch preparation of core biopsies. Each case was thoroughly reviewed, correlating with clinical data and concurrent core biopsies or subsequent excisions. The study identified leading factors contributing to NDIS.

Results

The average NDIS rate was 0.06% (42/70,612). Misinterpretation of benign or reactive cells as neoplastic was the leading cause (76.2%) of discrepancies between original ROSE and final diagnosis. Kidney biopsies had the highest NDIS rate (0.90%), primarily because of misinterpreting nonneoplastic cells. Thyroid biopsies were linked to quantitative threshold issues (0.10%). NDIS events were most associated with misinterpretation in kidney, pancreas, gastrointestinal tract, and lung biopsies.

Conclusion

In conclusion, the NDIS rate in telecytology-assisted ROSE is low, but quality assurance identified areas for improvement. Recognizing site-specific pitfalls during telecytology-assisted ROSE can enhance diagnostic accuracy and optimize patient care.

背景:远程细胞学辅助快速现场评估(ROSE)提供了一种经济有效的方法来加强微创活检,如细针穿刺和触摸准备的核心活检。通过减少非诊断性抽样和重复程序的需要,ROSE通过远程细胞学促进了辅助测试的及时分诊,改善了患者管理。本研究检查了在远程细胞学辅助的ROSE中最初被认为足以诊断的病例,但后来在最终评估(NDIS)中被归类为不可诊断的病例。设计:我们对一家大型癌症中心7年来远程细胞学辅助的ROSE病例进行了回顾性分析,重点是细针穿刺和触摸准备核心活检。每个病例都经过彻底的审查,并与临床数据和同时进行的核心活检或随后的切除相关联。该研究确定了导致NDIS的主要因素。结果:NDIS平均发生率为0.06%(42/70,612)。将良性或反应性细胞误解为肿瘤是导致最初ROSE和最终诊断不一致的主要原因(76.2%)。肾活检的NDIS率最高(0.90%),主要是因为误诊了非肿瘤细胞。甲状腺活检与定量阈值问题有关(0.10%)。NDIS事件与肾、胰腺、胃肠道和肺活检的误读最相关。结论:远程细胞学辅助ROSE的NDIS率较低,但质量保证有待改进。在远程细胞学辅助的ROSE中识别特定部位的缺陷可以提高诊断准确性并优化患者护理。
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引用次数: 0
A rapid turnaround time workflow for a cytological liquid biopsy assay using FNA supernatant specimens 利用 FNA 上清液标本进行细胞学液体活检化验的快速周转时间工作流程。
IF 3.2 3区 医学 Q3 ONCOLOGY Pub Date : 2024-12-20 DOI: 10.1002/cncy.22925
Mohamed H. Maher PharmD, PhD, Dzifa Y. Duose PhD, Ignacio I. Wistuba MD, Rajyalakshmi Luthra MD, Srividya Arjuna PhD, Sinchita Roy-Chowdhuri MD, PhD

Background

Genomic profiling is essential in the management of non–small cell lung cancer. However, this may often be challenging because of limited cytological tissue and extended turnaround time (TAT) for next-generation sequencing (NGS). This study aims to describe a rapid TAT workflow for molecular profiling using fine-needle aspiration (FNA) supernatants.

Methods

A fully automated total nucleic acid extraction using the Genexus Integrated System was compared to a manual extraction using FNA supernatants from 50 patients with non–small cell lung cancer. Molecular profiling using the 50 gene Oncomine Precision Assay GX panel was performed and NGS results were compared with those of paired tissue samples.

Results

The FNA samples processed using the automated Genexus purification system (n = 42) and the manual extraction method (n = 8) showed comparable quality control metrics with a median total nucleic acid yield of 1230 ng (18–17720 ng) and 1068 ng (777–1740 ng), respectively. The Genexus purification system reduced the hands-on time from 120 to 30 minutes, enhancing workflow efficiency and decreasing the overall TAT. Of the 50 samples extracted, NGS was performed on 26 samples: seven via manual extraction and 19 using automated extraction. NGS quality control metrics were also comparable between both extraction methods. The overall TAT of the automated NGS workflow from specimen received to test result was 24 hours, providing rapid and reliable molecular results for timely clinical decision-making and improved patient outcomes.

背景:基因组分析在非小细胞肺癌的治疗中是必不可少的。然而,由于下一代测序(NGS)有限的细胞学组织和延长的周转时间(TAT),这通常是具有挑战性的。本研究旨在描述使用细针抽吸(FNA)上清液进行分子分析的快速TAT工作流程。方法:采用Genexus集成系统对50例非小细胞肺癌患者进行全自动总核酸提取,并与人工提取FNA上清液进行比较。使用50基因Oncomine Precision Assay GX面板进行分子分析,并将NGS结果与配对组织样本的结果进行比较。结果:采用Genexus自动纯化系统(n = 42)和人工提取方法(n = 8)处理的FNA样品的质量控制指标相当,中位总核酸产率分别为1230 ng (18-17720 ng)和1068 ng (777-1740 ng)。Genexus净化系统将操作时间从120分钟减少到30分钟,提高了工作效率,降低了总体TAT。在提取的50个样本中,对26个样本进行了NGS: 7个通过人工提取,19个使用自动提取。两种提取方法之间的NGS质量控制指标也具有可比性。从收到标本到检测结果的自动化NGS工作流程的总体TAT为24小时,为及时的临床决策和改善患者预后提供了快速可靠的分子结果。
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引用次数: 0
A pilot study of the value of micronucleus count in urinary cytology samples in the follow-up of patients with urothelial carcinoma: Implications for diagnosis and prognosis 尿路上皮癌患者随访中尿细胞学样本微核计数价值的初步研究:对诊断和预后的影响。
IF 3.2 3区 医学 Q3 ONCOLOGY Pub Date : 2024-12-10 DOI: 10.1002/cncy.22923
Tuba Dilay Kökenek Ünal MD, Ayşegül Aksoy Altınboğa MD

Background

Nuclear protrusions such as micronuclei (MNs) and nuclear budding (NB) are morphological findings of chromosomal instability and indicators of genotoxic damage. They are increased in malignancies, and their high frequency may be used in the diagnosis of cancers and the follow-up of patients. Urothelial carcinomas are common tumors that cause morbidity and mortality, and cytology is a commonly used method for the monitoring and screening of urothelial carcinoma. Although the cytological evaluation of urinary samples is mainly based on nuclear features, there is limited research focusing on MN frequency in urinary cytology. This study aimed to investigate MN and NB counts in various diagnostic categories of urinary samples.

Methods

This study included 117 urinary cytology samples categorized according to The Paris System for Reporting of Urinary Cytology. Two observers, blinded to the diagnosis, counted the frequency of MNs and NB per 1000 cells on May-Grünwald-Giemsa– and Papanicolaou-stained slides.

Results

MN and NB counts significantly differed among the groups (p < .001 for each) with a large effect (Ɛ2 = 0.509). MN and NB counts were significantly higher in cases with high-grade urothelial carcinoma (HGUC) than in control cases and in cases that were negative for HGUC or with atypical urothelial cells (p < .001 for each). Any MN count greater than 2.5 per 1000 cells indicated HGUC with a 55% sensitivity and 92.4% specificity.

Conclusions

Because increased MN and NB frequencies are closely associated with an increased risk of malignancy, these could be integrated into The Paris System for Reporting of Urinary Cytology.

背景:核突出如微核(MNs)和核出芽(NB)是染色体不稳定的形态学表现和基因毒性损伤的指标。它们在恶性肿瘤中增加,其高频率可用于癌症的诊断和患者的随访。尿路上皮癌是引起发病率和死亡率的常见肿瘤,细胞学是监测和筛查尿路上皮癌的常用方法。虽然尿液样本的细胞学评价主要基于核特征,但对尿液细胞学中MN频率的研究有限。本研究旨在探讨不同诊断类别尿液样本中MN和NB计数。方法:本研究纳入117例泌尿细胞学样本,按巴黎泌尿细胞学报告系统分类。两名不知道诊断结果的观察者在may - gr nwald- giemsa和papanicolao染色玻片上计算每1000个细胞中MNs和NB的频率。结果:组间MN、NB计数差异有统计学意义(p 2 = 0.509)。高级别尿路上皮癌(HGUC)患者的MN和NB计数明显高于对照组和HGUC阴性或非典型尿路上皮细胞的患者(p结论:由于MN和NB频率的增加与恶性肿瘤风险的增加密切相关,这些可以整合到巴黎尿细胞学报告系统中。
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引用次数: 0
The deadliness of loneliness 孤独的致命
IF 3.2 3区 医学 Q3 ONCOLOGY Pub Date : 2024-12-02 DOI: 10.1002/cncy.22924
Bryn Nelson PhD, William Faquin MD, PhD
<p>In May 2023, US Surgeon General Vivek Murthy, MD, MBA, issued a stark health advisory. “Our epidemic of loneliness and isolation has been an underappreciated public health crisis that has harmed individual and societal health,” he asserted. Dr Murthy cited research suggesting that poor social connections increase the risk of depression, anxiety, heart disease, stroke, dementia in older adults, and premature death. The World Health Organization likewise declared loneliness a global health threat in 2023, and other countries have raised the alarm on a problem likely exacerbated by social distancing during the coronavirus disease 2019 pandemic.</p><p>Studies of people who are lonely, socially isolated, or living alone have expanded the potential consequences to include a higher risk of developing and dying of cancer, increasing the urgency of understanding the problem, its contributing factors, and the potential solutions.</p><p>Despite the flurry of attention, Frank Infurna, PhD, a professor of psychology at Arizona State University in Tempe, says that the loneliness “epidemic” has been more of an endemic but growing problem in the United States, particularly within the Baby Boomer and Gen X generations. “We’re seeing over multiple generations, over multiple cohorts, that loneliness levels within the US are elevated. So, it’s been a problem not just recently; it’s been a problem for a while,” he says.</p><p>Kerri Winters-Stone, PhD, an exercise scientist and professor in the Division of Oncological Sciences at the Oregon Health & Science University in Portland, began shifting her work to focus on loneliness among cancer survivors a few years ago. “I think it’s a bigger problem than we’re acknowledging,” she says. If loneliness and isolation should be treated as cancer-abetting threats akin to smoking and the human papillomavirus, however, studies have not yet settled on how to similarly tamp down the danger.</p><p>The problem is complicated by related but different kinds of “aloneness.” <i>Social isolation</i>, for example, refers to a small or nonexistent social network or a lack of meaningful engagement with others, whereas <i>loneliness</i> refers to a mismatch between desired and actual social connections—the unwanted feeling of being alone or not close to others. “A person can be socially isolated but may not feel lonely, and vice versa,” says Hyunjung Lee, PhD, MS, MPP, MBA, a principal scientist on the American Cancer Society’s Cancer Disparities Research Team (the American Cancer Society publishes <i>Cancer Cytopathology</i>).</p><p>Living alone, by contrast, is a more objective measure “that can be easily assessed with a single question on the number of people in the household,” Dr Lee says. “People who live alone are more likely to be socially isolated or feel lonely, although this is not always the case.” Research also suggests that older people are more likely to live alone in the United States than elsewhere around the world—in
2023年5月,美国卫生局局长、医学博士、工商管理硕士维韦克·默蒂(Vivek Murthy)发布了一份严厉的健康建议。他说:“我们的孤独和孤立流行病一直是一场未得到充分重视的公共卫生危机,损害了个人和社会的健康。”默蒂博士引用了一项研究,该研究表明,不良的社会关系会增加抑郁、焦虑、心脏病、中风、老年人痴呆和过早死亡的风险。世界卫生组织同样在2023年宣布孤独是全球健康威胁,其他国家也对2019年冠状病毒大流行期间社交距离可能加剧的问题发出了警告。对孤独、社会孤立或独居人群的研究扩大了潜在后果,包括患癌症和死于癌症的风险更高,增加了了解问题、其影响因素和潜在解决方案的紧迫性。尽管引起了一阵关注,但坦佩亚利桑那州立大学的心理学教授弗兰克·因弗纳博士表示,孤独“流行病”在美国更像是一种地方性问题,但日益严重,尤其是在婴儿潮一代和X世代中。“我们看到,在多代人、多群人中,美国人的孤独感正在上升。所以,这不是最近才出现的问题;这个问题已经存在一段时间了。”Kerri Winters-Stone博士是一名运动科学家,同时也是俄勒冈健康与健康中心肿瘤科学部的教授。几年前,她开始将工作重点转向癌症幸存者的孤独感。“我认为这是一个比我们承认的更大的问题,”她说。然而,如果孤独和孤立应该像吸烟和人类乳头瘤病毒一样被视为诱发癌症的威胁,研究还没有确定如何以同样的方式降低这种危险。相关但不同种类的“孤独”使问题变得复杂。例如,社会隔离指的是一个小的或不存在的社会网络,或者缺乏与他人有意义的接触,而孤独指的是期望的和实际的社会联系之间的不匹配——一种不想要的孤独或不接近他人的感觉。“一个人可以在社会上被孤立,但可能不会感到孤独,反之亦然,”Hyunjung Lee博士,MS, MPP, MBA,美国癌症协会癌症差异研究小组(美国癌症协会出版癌症细胞病理学)的首席科学家说。李博士说,相比之下,独居是一种更客观的衡量标准,“可以很容易地用一个关于家庭人数的问题来评估”。“独居的人更有可能被社会孤立或感到孤独,尽管情况并非总是如此。”研究还表明,与世界其他地方相比,美国的老年人更有可能独自生活——这与研究表明他们也更有可能被孤立和孤独的研究结果一致。李博士于2023年领导的一项研究发现,独居的美国工作年龄成年人,因此更有可能被孤立,与与他人同住的成年人相比,患癌症相关死亡的风险更高她说:“被社会孤立的人更有可能吸烟,但不太可能保持健康的饮食、睡眠和身体活动,也不太可能在需要时寻求并坚持医疗护理。”“社交孤立还与压力、抑郁和孤独有关,这涉及到下丘脑-垂体-肾上腺轴和自主神经系统,导致血管生成,促进肿瘤生长,从而加速癌症的进展和死亡。”独居与癌症死亡率增加之间的关联在非西班牙裔白人成年人中最为显著,在非西班牙裔黑人成年人中不那么显著,而在西班牙裔、美洲印第安人或阿拉斯加原住民和亚洲成年人中则不存在。李博士认为,其中一些差异可能部分是由于个人更广泛的社区的社会支持水平。强有力的支持可以减轻独居带来的一些负面影响,尽管她强调需要对这些影响因素进行更多的研究。2023年,一项对来自高收入国家的90项研究进行的单独荟萃分析发现,“社会孤立和孤独都与全因死亡率和癌症死亡率的风险增加显著相关。”越来越多的证据表明,这个问题在美国更为严重:研究发现,与外国同行相比,美国人的社会孤立与全因死亡率之间的关联要大得多。更糟糕的是,其他证据表明,美国的孤独感和孤立感都在增加。 在一项对来自美国和13个欧洲国家的45至65岁人群的研究中,因弗纳博士和他的同事发现,婴儿潮一代的整体孤独感最高,而美国婴儿潮一代的孤独感远远超过了他们的国际同龄人“这当然是一个惊喜,”他说。“这真的让我们停下来,暂停了一下。”事实上,研究发现,美国人的整体孤独感水平一直高于所有其他被调查的国家。怎样才能扭转这个日益严重的问题呢?李博士说,对于独居的患者,患者导航项目可能有助于增加对癌症筛查的接受和坚持。她说,这种援助反过来可以帮助“及时诊断、治疗和参加医疗预约,特别是在历史上被边缘化的人群中”。更一般地说,因弗纳博士建议,找到更多参与社区活动的方法,比如做志愿者或加入教堂、俱乐部或健身房,可能有助于培养更有意义的互动、友谊和相互支持。事实上,温特斯-斯通博士已经收集了一些初步数据,指出群体锻炼的潜在好处。她和她的同事招募了几百名患有前列腺癌的男性参加一项试验,最初的目的是评估教练指导的团体锻炼项目对减少激素治疗相关跌倒的影响。然而,通过倾听参与者的谈话,她意识到小组练习也可能减少孤独感,于是她开始对145名男性进行跟踪调查。这一组中大约87%的男性已婚。即便如此,大约70%的人报告说,由于她所说的与癌症相关的孤独,他们经历了某种程度的孤立和脱节:“你没有人可以和你谈论和倾诉你的癌症诊断。”这个项目现在几乎在Zoom上进行,其中包括让男人们通过分组讨论室进行社交互动的机会。去年11月,温特斯-斯通博士在西雅图举行的美国老年学学会年会上公布了初步研究结果。研究结果表明,参与者与癌症相关的孤独感在6个月的时间里下降了,而那些最初报告孤独感最高的人下降幅度最大。她指出,对于男性来说,男性气概的观念和与癌症相关的耻辱可能会阻止那些需要帮助的人寻求帮助。一些癌症应对机制会表现为愤怒,一些药物会导致易怒;两者都可能进一步孤立某人。温特斯-斯通博士说:“对我来说,关于我们为什么需要其他类型的社会支持的想法一直在响。”虽然传统的支持团体对一些患者来说可能不那么可取,但锻炼或其他亲和团体仍然可以提供有益的联系机会。她和其他专家说,至少,让关于孤独和孤立的对话正常化,是迈向更持久、更能挽救生命的解决方案的重要一步。
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引用次数: 0
Thin-layer cervical sample evaluation: Conventional light microscopy versus digital whole-slide imaging 薄层宫颈样本评估:传统光学显微镜与数字全切片成像的对比。
IF 3.2 3区 医学 Q3 ONCOLOGY Pub Date : 2024-11-21 DOI: 10.1002/cncy.22921
Jessica Viti MSc, Chiara Di Stefano MSc, Serena Giunti MSc, Giampaolo Pompeo MSc, Paola Pezzati MD, Alessandro Terreni MSc, Cristina Sani MSc, The Cytology Working Group

Background

Whole-slide imaging (WSI) has been adopted in many fields of pathology for education, quality assurance, and remote diagnostics. In 2021, the College of American Pathologists (CAP) updated guidelines to support pathology laboratories regarding the WSI systems validation process. However, the majority of published literature refers to histopathology rather than cytology. The aim of this study was to compare conventional light microscopy (CLM) and WSI in thin-layer cervical samples evaluation according to CAP guideline.

Methods

A sample set of 64 thin-layer cervical specimens from women 25–64 years old who participated in cervical cancer screening programs in Tuscany was distributed among five cytologists at Institute for Cancer Research, Prevention and Clinical Network (Florence, Italy) for CLM analysis. After 2 weeks, the corresponding 64 digitally scanned slides were available at several magnifications for WSI evaluation.

Results

Substantial/near perfect agreement between CLM and WSI evaluation (0.77 ≥ κ ≥1) was observed for the negative for intraepithelial lesion or malignancy (NILM) class with concordance rates from 83.3% to 100%.Variability in concordance was observed among all the cytologists: 50%–85.7% for low-grade squamous intraepithelial lesion (LSIL), 47.1%–100% for high-grade squamous intraepithelial lesion (HSIL), 50%–100% for atypical glandular cells (AGCs) favors adenocarcinoma (ADK) with moderate/near perfect agreement (0.47 ≥ κ ≥1). Concordance and agreement rates were also variable within the “borderline” cytological categories of atypical squamous cells of undetermined significance (ASC-US), atypical squamous cells cannot exclude an HSIL (ASC-H), and AGCs with lower or not computable kappa for some readers. The overall intralaboratory concordance between CLM and WSI was 92.9% with a near perfect agreement (κ = 0.84) for NILM. Substantial agreement (κ ≥0.65) was assessed for LSIL, HSIL/squamous cell carcinoma, AGCs, and ADK categories whereas the agreement was lower (κ ≤0.39) for ASC-US and ASC-H.

Conclusions

This study showed an overall substantial/near perfect agreement between CLM and WSI for all the cytological categories except the “borderline” ASC-US and ASC-H. Further progress in cytology WSI systems are needed before introducing it in routine diagnostics.

背景:全滑动成像(WSI)已被许多病理学领域采用,用于教育、质量保证和远程诊断。2021 年,美国病理学家学会(CAP)更新了指南,为病理实验室的 WSI 系统验证过程提供支持。然而,已发表的文献大多涉及组织病理学而非细胞学。本研究的目的是比较传统光学显微镜(CLM)和 WSI 在根据 CAP 指南评估薄层宫颈样本中的应用:方法:托斯卡纳区癌症研究、预防和临床网络研究所(意大利佛罗伦萨)的五位细胞学专家对参加宫颈癌筛查项目的 25-64 岁女性的 64 份薄层宫颈样本进行了 CLM 分析。2 周后,相应的 64 张数字扫描切片以不同的放大倍数提供给 WSI 评估:在上皮内病变或恶性肿瘤阴性(NILM)类别中,CLM 和 WSI 评估之间的一致性非常高(0.77 ≥ κ ≥1),一致性从 83.3% 到 100% 不等:低度鳞状上皮内病变(LSIL)的吻合率为 50%-85.7%,高度鳞状上皮内病变(HSIL)的吻合率为 47.1%-100%,非典型腺细胞(AGCs)的吻合率为 50%-100%,腺癌(ADK)的吻合率为中等/接近完全吻合(0.47 ≥ κ ≥1)。在意义未定的非典型鳞状细胞(ASC-US)、不能排除 HSIL 的非典型鳞状细胞(ASC-H)和一些读者卡帕值较低或无法计算的 AGC 等 "边缘 "细胞学类别中,一致性和一致率也存在差异。CLM和WSI的实验室内总体一致性为92.9%,NILM的一致性接近完美(κ = 0.84)。LSIL、HSIL/鳞状细胞癌、AGC和ADK类别的评估结果基本一致(κ≥0.65),而ASC-US和ASC-H的一致性较低(κ≤0.39):本研究表明,除 "边缘 "ASC-US 和 ASC-H 外,CLM 和 WSI 在所有细胞学类别中的总体一致性都很高/接近完美。在将 WSI 系统引入常规诊断之前,细胞学 WSI 系统还需要进一步改进。
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引用次数: 0
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Cancer Cytopathology
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