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发表于 2018-2-22 15:13 |只看该作者 |倒序浏览 |打印
New AASLD Guidelines for Hepatocellular Carcinoma: The Big Questions Tackled

David A. Johnson, MD
Disclosures

February 21, 2018

11:22
Screening for Hepatocellular Carcinoma

Hello. I'm Dr David Johnson, professor of medicine and chief of gastroenterology at Eastern Virginia Medical School in Norfolk, Virginia.

When we see patients with cirrhosis in the clinic, we are concerned about screening for hepatocellular carcinoma (HCC). I'm not a transplant hepatologist, but I deal with these patients all the time, as you do.

HCC is an incredibly common disease. It's the fifth most common tumor in the world and the second leading cause of cancer-related death.[1] In the United States, there are an estimated 39,000 new cases per year and over 27,000 related deaths[2,3]; the incidence is likely to rise at least until 2030.[4] This problem is not going away.

Why is that? It's about cirrhosis. The majority of HCCs, 85%-95%, occur in patients with cirrhosis[5,6]—the exception to the rule being hepatitis B, where patients do not need to be cirrhotic. The incidence of HCC in patients with cirrhosis that I quote to my patients is 2%-4% per year.[7] Thus, it is recommended that we screen these patients because early screening may lead to earlier diagnosis and appropriate interventions.

It's very pragmatic, at this point, to review new guidelines issued by the American Association for the Study of Liver Diseases (AASLD)[2] in the January 2018 issue of Hepatology. They used a graded system for their recommendations and provide strength of evidence and support of the recommendation. Let's focus on the 10 questions and answers from this evidence-based analysis and recommendation.
AASLD Guidelines: Questions and Answers
Should Patients With Cirrhosis Undergo Surveillance for HCC?

Should adults with cirrhosis undergo surveillance for HCC? The answer is yes. But which surveillance test is best? Ultrasound is still the best. It's relatively cheap and [may be used] with or without alpha-fetoprotein (AFP). According to the recommendation, [surveillance should occur] every 4-8 months; we use 6 months [in my clinic]. You can choose to couple that with AFP, but that is not a strong recommendation.
Multiphasic CT or Multiphasic MRI for Diagnostic Evaluation?

Should adults with suspected HCC and cirrhosis undergo multiphasic CT or multiphasic MRI for diagnostic evaluation? The data are fairly mixed. There may be a little marginal data bias toward MRI on smaller lesions, but the available evidence suggests that both are equivocal. There are some variable differences. CT is more available and may result in repetitive radiation exposure, and MRI is a lot more expensive. There may be issues of claustrophobia, and patients with large-volume ascites may have movement issues during their positioning in the MRI. These are potential reasons to choose one versus the other. The evidence suggests that we could use either at this point.

Which Diagnostic Evaluation Should Patients With Cirrhosis and an Indeterminate Nodule Undergo?

Should adults with cirrhosis and an indeterminate nodule undergo biopsy, repeat imaging, or alternative imaging? According to the current guideline, all three are acceptable. This is a difference from the previous AASLD guideline. Now they say to consider these things but not biopsy every individual indeterminate nodule because the majority of them are likely benign and potentially subject to sampling bias. Repeat imaging by another alternative may be the best course of action. Consider all three as viable options under these new evidence-based recommendations.

How Should Patients With Child-Pugh Class A Cirrhosis and Early-Stage HCC Be Managed?

Is resection or locoregional therapy recommended for a patient with Child-Pugh class A cirrhosis and early-stage HCC (T1 or T2)? If you want to do an intervention that is not a transplant, resection in the viable candidate is recommended. A good surgeon is really the course of action.

The diagnosis now for these lesions begins at ≥ 10 mm by radiologic CT or MRI diagnostic criteria. T1-stage HCC is potentially referred to the transplant center and T2-stage HCC is now the threshold for transplant evaluation. T2-stage HCC, by radiologic imaging, is a single lesion ≥ 2 cm, or two to three lesions that are 1-3 cm.
Is Adjuvant Therapy Recommended for Resected or Ablated HCC?

Should patients with cirrhosis and successfully resected or ablated HCC undergo adjuvant therapy? Probably not. The weak recommendation is conditional and based on histology and radiologic imaging. The broad recommendation is that these patients need not receive adjuvant therapy.
Should Patients With T1 HCC and Cirrhosis Be Treated or Undergo Observation?

Should adults with T1 HCC and cirrhosis be treated or undergo observation? If you treat these patients, you may take them out of the transplant window, so observation is really the best course of action. Stay in close concert with a transplant center and be ready to transplant these patients when they hit that threshold. Waiting and watching may be somewhat disconcerting to a lot of people, but that is how they get into the transplant window.
Transplantation Alone or Transplantation With Bridging?

Should patients with cirrhosis awaiting liver transplant undergo transplant alone or transplant with bridging therapy? Bridging therapy is adjuvant locoregional therapy. Provided that the patient is a good candidate and you have expertise, bridging therapy is recommended because you do not want them to progress and migrate out of the transplant window. The transplant window may be an extended period of time, depending on where the transplant center is. Bridging therapy should be considered.
Is Transplant After Downstaging Recommended?

Should patients with cirrhosis and HCC beyond Milan criteria (T3) be transplanted following downstaging? The answer is yes. They should be considered for transplant once they have been downstaged. It's a weak recommendation and conditional. This is something that needs to be driven by the transplant center, but it's important that you understand this when conversing with your patients.
Is Embolization/External Radiation Recommended for Advanced HCC?

Should patients with cirrhosis and HCC (T2 or T3, but no vascular involvement) who are not candidates for a resection or transplantation undergo treatment with transarterial chemoembolization, transarterial radioembolization, or external radiation? The answer is yes. If those options are available, they are reasonable things to offer. The recommendation did not pick one over the other; that is something that is substantive to your local expertise.
Therapy or No Therapy for Patients With Advanced HCC?

Should a patient with Child-Pugh class A/B cirrhosis and advanced HCC with evidence of macrovascular involvement and/or metastatic disease be treated with systemic, locoregional, or no therapy? The answer is: Treat them if they are good candidates. This needs to be considered on an individual, case-by-case basis.
Takeaway Message

These are AASLD's 10 evidence-based-focused questions. Most of these recommendations are based on weak evidence and are conditional; nonetheless, this is where we are. We need to understand this as we communicate with our patients and transplant centers, but even more so as we screen patients and manage them once a diagnosis of HCC is made.

This evidence-based guideline has been extremely helpful for me. As a gastroenterologist and not a transplant hepatologist, I've tried to give my perspective on what I do in my clinical practice. Hopefully this will be helpful for your practice.

I'm Dr David Johnson. Thanks again for listening. I'll see you next time.

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发表于 2018-2-22 15:14 |只看该作者
新的AASLD肝细胞癌指南:解决的重大问题

医学博士David A. Johnson
披露

2018年2月21日

11:22
筛选肝细胞癌

你好。我是弗吉尼亚州诺福克东弗吉尼亚州医学院的医学教授兼肠胃病学教授大卫约翰逊博士。

当我们在临床中看到肝硬化患者时,我们担心筛查肝细胞癌(HCC)。我不是移植肝病专家,但我一直都在和这些病人打交道,就像你一样。

HCC是一种非常常见的疾病。这是世界上第五大常见肿瘤,也是癌症相关死亡的第二大原因[1]。在美国,每年估计有39,000新病例和27,000以上相关死亡[2,3];发病率至少可能上升到2030年。[4]这个问题不会消失。

这是为什么?这是关于肝硬化。大多数HCC的发生率为85%-95%,发生于肝硬化患者[5,6],这一规则是乙肝的例外,患者不需要肝硬化。我引用我的患者的肝硬化患者的HCC发病率为每年2%-4%[7]。因此,建议我们筛查这些患者,因为早期筛查可能会导致更早的诊断和适当的干预措施。

在这一点上,非常务实的是,在2018年1月的肝病学期刊中回顾由美国肝病研究协会(AASLD)发布的新指南[2]。他们使用分级系统提供建议,并提供证据的力量和对建议的支持。我们来关注这个基于证据的分析和推荐的10个问题和答案。
AASLD指南:问题和答案
肝硬化患者是否应该对HCC进行监测?

肝硬化患者是否应接受HCC监测?答案是肯定的。但哪种监测测试最好?超声仍然是最好的。它相对便宜,[可以使用]有或没有甲胎蛋白(AFP)。根据建议,每4-8个月应[监测];我们使用6个月[在我的诊所]。你可以选择将它与法新社结合起来,但这不是一个强有力的建议。
多相CT或多相MRI用于诊断评估?

怀疑HCC和肝硬化的成年人是否应接受多相CT或多相MRI进行诊断评估?数据相当混杂。在较小的病灶中,MRI可能存在少量边缘数据偏倚,但现有证据表明两者都不明确。有一些可变的差异。 CT更容易获得,并可能导致重复性的辐射照射,并且MRI更昂贵。可能存在幽闭恐怖症,大量腹水患者在MRI定位时可能会出现运动问题。这些是选择一个与另一个的潜在原因。证据表明我们可以在这一点上使用。
肝硬化和不确定结节患者的诊断评估

肝硬化和不确定结节的成人是否应接受活检,重复成像或其他影像检查?根据目前的准则,所有三个都可以接受。这与以前的AASLD指南有所不同。现在他们说要考虑这些事情,但不要对每个不确定的结节进行活检,因为它们中的大多数可能是良性的并且可能受到取样偏差的影响。用另一种替代方法重复成像可能是最佳的行动方案。在这些新的基于证据的建议下,将所有三个视为可行的选择。

Child-Pugh A级肝硬化患者和早期HCC患者应如何管理?

对Child-Pugh A级肝硬化和早期HCC(T1或T2)患者推荐切除或局部治疗?如果您想进行非移植手术,建议切除可行的候选人。一个好的外科医生确实是一个行动的过程。

现在对这些病变的诊断是在放射学CT或MRI诊断标准下开始≥10mm。 T1期HCC可能是指移植中心,而T2期HCC现在是移植评估的门槛。通过影像学检查,T2期HCC是≥2cm的单一病变,或2-3 cm的2〜3个病灶。
辅助治疗推荐用于切除或消除的HCC?

肝硬化并成功切除或消融HCC的患者是否应接受辅助治疗?可能不会。弱推荐是有条件的,并且基于组织学和放射学成像。广泛的建议是这些患者不需要接受辅助治疗。
是否应对T1肝癌和肝硬化患者进行治疗或观察?

患有T1 HCC和肝硬化的成人是否应该接受治疗或接受观察?如果你治疗这些患者,你可以将它们从移植窗口中取出,所以观察确实是最佳的方法。与移植中心保持密切的合作关系,并准备在这些患者达到阈值时移植这些患者。等待和观望对许多人来说可能有点令人不安,但这就是他们进入移植窗口的方式。
单独移植还是移植与桥接?

是否应该等待肝移植的肝硬化患者单独进行移植或移植桥接治疗?桥接治疗是辅助局部治疗。假如病人是一个很好的候选人并且你有专业知识,建议使用桥接治疗,因为你不希望他们进展并移出移植窗口。移植窗口可能会延长一段时间,这取决于移植中心的位置。应考虑桥接治疗。
降级后移植是否推荐?

肝硬化和HCC超出米兰标准(T3)的患者是否应该在移植后进行移植?答案是肯定的。一旦他们下台,他们应该考虑移植。这是一个薄弱的建议和有条件的。这是移植中心需要推动的事情,但重要的是,当你与患者交谈时,你能理解这一点。
是推荐用于高级HCC的栓塞/外部放射?

肝硬化和HCC患者(T2或T3,但无血管受累者)是否应接受经动脉化疗栓塞,经动脉栓塞或外部放射治疗?答案是肯定的。如果这些选项可用,它们是合理的东西。该建议没有选择一个;这对您当地的专业知识而言是实质性的。
治疗或不治疗晚期HCC患者?

Child-Pugh分期A / B期肝硬化和晚期HCC伴有大血管受累和/或转移性疾病的患者是否应该接受系统性,局部治疗或无治疗?答案是:如果他们是好人选,就对待他们。这需要根据具体情况逐个考虑。
外卖消息

这些是AASLD的10个基于证据的问题。这些建议大部分都是基于薄弱的证据,并且是有条件的;尽管如此,这就是我们所处的位置。当我们与患者和移植中心进行交流时,我们需要了解这一点,但是更加如此,因为我们筛选患者并在确诊HCC后进行管理。

这种循证指南对我来说非常有帮助。作为胃肠病专家而不是移植肝病专家,我试图对我在临床实践中做什么给予自己的观点。希望这会对你的练习有所帮助。

我是戴维约翰逊博士。再次感谢您的聆听。我下次见。

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