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标题: 哎呀:数据支持替诺福韦超过恩替卡韦用于乙型肝炎撤回 仍 [打印本页]

作者: StephenW    时间: 2019-4-26 11:47     标题: 哎呀:数据支持替诺福韦超过恩替卡韦用于乙型肝炎撤回 仍


Oops: Data Supporting Tenofovir Over Entecavir for Hepatitis B Retracted
Still superior for preventing liver cancer, but mortality/transplant advantage disappears
  
    by Molly Walker, Staff Writer, MedPage Today
    April 25, 2019

Maybe tenofovir diproxil fumarate (TDF, Viread) isn't better than entecavir (Baraclude) for keeping hepatitis B alive and transplant-free after all.

Data from a Korean study published online last September, indicating reduced risk for mortality or transplant with TDF versus entecavir, have been retracted and replaced, according to a letter in the April 25 issue of JAMA Oncology from two of the original paper's authors.

Citing "inadvertent errors" in determining follow-up duration for participants, the researchers recalculated the hazard ratio for mortality or transplant and found that it no longer significantly favored TDF (HR 0.89, 95% CI 0.73-1.07), according to Young-Suk Lim, MD, PhD, and Min Jung Ko, PhD, both of the University of Ulsan College of Medicine in Seoul.

"We sincerely apologize for these unintentional errors, and considering the extent of the corrections, we have requested that the original article be retracted and replaced," Lim and Ko wrote.

Their study gained prominence after being cited earlier this month at the European Association for the Study of the Liver (EASL) annual meeting. A study in a cohort out of Hong Kong -- with similar large numbers of patients on entecavir therapy and smaller numbers of patients on tenofovir -- was presented as a late-breaker abstract that indicated TDF was superior for preventing development of hepatocellular carcinoma.

At an EASL press conference, moderator Francesco Negro, MD, of the University Hospital of Geneva in Switzerland, urged caution with those results, with additional researchers saying there may be other factors that were not included in the Hong Kong study's propensity score analysis.

A January editorial in JAMA Oncology accompanying the Korean study's print publication, by Jennifer A. Flemming, MD, of Queen's University in Kingston, Ontario, and Norah A. Terrault, MD, of the University of California San Francisco, also backed a wait-and-see approach.

"We would advocate for additional observational cohorts with data on liver disease severity, virologic response, and adherence to surveillance to evaluate this important question," the editorialists wrote. "This study should not lead to a widespread paradigm shift in selecting TDF over [entecavir]."

The April 25 JAMA Oncology also carried three letters of comment on the Korean study, although Lim and Ko only referred to one from Yuanyuan Kong, PhD, of Beijing Friendship Hospital in China, which cited "inconsistent data presentations."

Lim and Ko said that following this letter, they conduced an "extensive and thorough review" of the data. In addition to the corrected hazard ratio for mortality and transplant in the TDF group, they included the following corrections:

    Number of reported mortality or transplant cases changed from 281 to 269 in the entecavir group, and from 228 to 190 in the tenofovir treatment group
    Hazard ratios for hepatocellular carcinoma in the full TDF cohort changed from 0.61 (95% CI 0.54-0.70) to 0.68 (95% CI 0.59-0.77) relative to entecavir, which remained statistically significant

Douglas Dieterich, MD, of the Icahn School of Medicine at Mount Sinai in New York City, who was not involved in the research, said that "the data is going in both directions" when looking at TDF versus entecavir in this population.

He also noted "all sorts of confounders" in this type of analysis, including time on the drug and potential entecavir resistance.

"There's a signal, it's just not clear which way the signal is pointing. We need somebody to combine all these studies together and do a super meta-analysis looking at all the factors," Dieterich told MedPage Today.

He included the caveat that his team at Mount Sinai is also looking at a similar type of analysis of tenofovir in a multi-ethnic cohort of patients with chronic hepatitis B infection. Their early data suggests tenofovir may be better at treating HBV, he said.

"We're not saying [our study] can settle it, but there's clearly something going on. We'll need to wait until we have enough data to make a decision about how to evaluate [TDF vs entecavir] in different sample sizes," Dieterich said.

Lim disclosed support from Gilead Sciences and Bayer Healthcare.

Ko disclosed no conflicts of interest.

    Primary Source
    JAMA Oncology
    Source Reference: Lim Y-S, Ko MJ "Notice of Retraction and Replacement. Choi et al. Risk of hepatocellular carcinoma in patients treated with entecavir vs tenofovir for chronic hepatitis B: a Korean nationwide cohort study. JAMA Oncol. 2019;5(1):30-36" JAMA Oncol 2019; DOI: 10.1001/jamaoncol.2019.0576.


作者: StephenW    时间: 2019-4-26 11:48

哎呀:数据支持替诺福韦超过恩替卡韦用于乙型肝炎撤回
仍然优于预防肝癌,但死亡率/移植优势消失

作者:Molly Walker,编剧,MedPage Today
2019年4月25日

也许替诺福韦的富马酸diproxil(TDF,Viread)并不比恩替卡韦(Baraclude)更好,因为它可以使乙型肝炎保持活力和无移植。

根据两篇原始论文作者在4月25日出版的JAMA Oncology上的一封信中所述,去年9月在线发表的一项韩国研究数据显示,TDF与恩替卡韦的死亡或移植风险降低,已经被撤回和替换。

根据Young-Suk的研究,在确定参与者的随访时间时,研究人员引用了“无意中的错误”,重新计算了死亡率或移植率的风险比,并发现它不再显着有利于TDF(HR 0.89,95%CI 0.73-1.07)。 Lim,MD,PhD和Min Jung Ko,博士,均为首尔蔚山医学院。

“我们真诚地为这些无意的错误道歉,并考虑到更正的程度,我们要求撤回和替换原始文章,”Lim和Ko写道。

他们的研究在本月早些时候在欧洲肝脏研究协会(EASL)年会上被引用后获得了突出地位。一项针对香港一个队列的研究 - 恩替卡韦治疗患者数量相似且替诺福韦患者的数量 - 被提出作为一种晚期的摘要,表明TDF对预防肝细胞癌的发展具有优势。

在EASL新闻发布会上,瑞士日内瓦大学医院的主持人Francesco Negro博士敦促谨慎对待这些结果,其他研究人员表示,香港研究的倾向评分分析中可能还有其他因素未包括在内。

安大略省金斯敦女王大学的医学博士Jennifer A. Flemming和加利福尼亚大学旧金山分校医学博士Norah A. Terrault在韩国研究的印刷出版物上发表了一篇关于JAMA Oncology的一篇社论,并支持等待 - 而且看到方法。

“我们会提倡额外的观察队列,其中包括有关肝病严重程度,病毒学反应和遵守监测的数据,以评估这一重要问题,”社论作者写道。 “这项研究不应导致选择TDF超过[恩替卡韦]的广泛范式转变。”

4月25日,JAMA Oncology还就韩国研究发表了三封评论信,尽管Lim和Ko仅提到了中国北京友谊医院的Yuanyuan Kong博士,其中引用了“不一致的数据表达”。

Lim和Ko说,在这封信之后,他们对数据进行了“广泛而彻底的审查”。除了TDF组中死亡率和移植的校正风险比之外,它们还包括以下更正:

报告的死亡率或移植病例数在恩替卡韦组中从281变为269,在替诺福韦治疗组中从228变为190
相对于恩替卡韦,完整TDF队列中肝细胞癌的危险比从0.61(95%CI 0.54-0.70)变为0.68(95%CI 0.59-0.77),这仍然具有统计学意义

纽约市西奈山伊坎医学院的医学博士道格拉斯·迪特里希(Douglas Dieterich)没有参与这项研究,他说,在这一人群中观察TDF与恩替卡韦时,“数据是双向的”。

他还指出了此类分析中的“各种混杂因素”,包括药物的时间和潜在的恩替卡韦耐药性。

“有一个信号,不知道信号指向哪个方向。我们需要有人将所有这些研究结合在一起,并进行超级荟萃分析,查看所有因素,”Dieterich告诉MedPage Today。

他指出,他在西奈山的团队也正在研究一项类似的对替诺福韦的慢性乙型肝炎感染患者群体中的替诺福韦分析。他们说,他们的早期数据表明替诺福韦可能更好地治疗HBV。

“我们并没有说[我们的研究]可以解决它,但显然还有一些事情发生。我们需要等到有足够的数据来决定如何评估不同样本量的[TDF vs恩替卡韦], “迪特里希说。

Lim公布了Gilead Sciences和Bayer Healthcare的支持。

Ko透露没有利益冲突。

主要资源
JAMA肿瘤学
来源参考文献:Lim YS,Ko MJ“撤回和替代的通知.Choi等。恩替卡韦治疗慢性乙型肝炎患者肝细胞癌风险与替诺福韦治疗:韩国全国队列研究.JAMA Oncol。2019; 5(1) :30-36“JAMA Oncol 2019; DOI:10.1001 / jamaoncol.2019.0576。
作者: jinpaimanman    时间: 2019-4-27 15:59

本帖最后由 jinpaimanman 于 2019-4-27 15:59 编辑

回复 StephenW 的帖子

这个撤回跟之前香港的试验报告减下68%的文章是同一篇吗?
作者: StephenW    时间: 2019-4-27 16:06

回复 jinpaimanman 的帖子

不是. 只有韩国的研究撤回.




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