Evidence map›Paper›PMID 29171941›Full record

Trial reportLiver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society2018

Extracorporeal cellular therapy (ELAD) in severe alcoholic hepatitis: A multinational, prospective, controlled, randomized trial.

Julie Thompson, Natasha Jones, Ali Al-Khafaji, Shahid Malik, David Reich, Santiago Munoz, Ross MacNicholas, Tarek Hassanein, Lewis Teperman, Lance Stein and 34 more

Open access · hybridAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 2 pooled it
10.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

57 citing papers in PubMed, 2 syntheses or guidelines pooled it, 140 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Bacterial Infections in Patients With Severe Alcohol-Associated Hepatitis: Drivers of Organ Failure and Mortality.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Trial
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. A Systematic Review on Artificial Liver for Implantation.Journal of functional biomaterials · 2026
    Review
  10. Article
  11. [Research progress on bioartificial liver].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2025
    Review
  12. Article
  13. Review
  14. Potential therapies for acute-on-chronic liver failure.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Review
  15. Liver support systems and liver transplantation in acute liver failure.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Review
  16. Extracorporeal liver support and liver transplantation for acute-on-chronic liver failure.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Review
  17. Article
  18. Article
  19. Observational
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

44 authors at 20 institutions in 4 countries.

Julie ThompsonUniversity of Minnesota Medical Center, Minneapolis, MN.
Natasha JonesEmory University School of Medicine, Atlanta, GA.
Ali Al-KhafajiUniversity of Pittsburgh Medical Center, Pittsburgh, PA.
Shahid MalikUniversity of Pittsburgh Medical Center, Pittsburgh, PA.
David ReichDrexel University, Philadelphia, PA.
Santiago MunozDrexel University, Philadelphia, PA.
Ross MacNicholasSir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
Tarek HassaneinSouthern California Gastrointestinal and Liver Centers, Coronado, CA.
Lewis TepermanNew York University Medical, New York City, NY.
Lance SteinPiedmont Atlanta Hospital, Atlanta, GA.
Andrés Duarte-RojoUniversity of Arkansas for Medical Sciences, Little Rock, AK.ORCID 0000-0002-5377-9295
Raza MalikBeth Israel Deaconess Medical Center, Boston, MA.
Talal AdhamiCleveland Clinic Foundation in Cleveland, OH.
Sumeet AsraniBaylor University Medical Center, Dallas, TX.
Nikunj ShahRush University Medical Center, Chicago, IL.
Paul GaglioMontefiore Medical Center, Bronx, NY.
Anupama DuddempudiNorth Shore University Hospital, Manhasset, NY.
Brian BorgUniversity of Mississippi Medical Center, Jackson, MS.
Rajiv JalanRoyal Free Hospital, London, United Kingdom.
Robert BrownColumbia University Medical Center, New York City, NY.
Heather PattonUniversity of California, San Diego Medical Center, San Diego, CA.
Rohit SatoskarGeorgetown University, Washington, DC.
Simona RossiAlbert Einstein Medical Center, Philadelphia, PA.
Amay ParikhRutgers University Medical Center, New Brunswick, NJ.
Ahmed ElSharkawyQueen Elizabeth Hospital/University of Birmingham, Birmingham, United Kingdom.
Parvez MantryMethodist Dallas Medical Center, Dallas, TX.
Linda SherUniversity of Southern California, Los Angeles, CA.
David WolfWestchester Medical Center, Valhalla, NY.
Marquis HartSwedish Medical Center, Seattle, WA.
Charles LandisUniversity of Washington, Harborview, Seattle, WA.
Alan WiggFlinders Medical Centre, Adelaide, Bedford Park, South Australia, Australia.
Shahid HabibUniversity of Arizona Medical Center, Tucson, AZ.
Geoffrey McCaughanRoyal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Steven ColquhounCedars-Sinai Medical Center, Los Angeles, CA.
Alyssa HenryVital Therapies Inc., San Diego, CA.
Patricia BedardVital Therapies Inc., San Diego, CA.
Lee LandeenVital Therapies Inc., San Diego, CA.
Michael MillisUniversity of Chicago, Chicago, IL.
Robert AshleyVital Therapies Inc., San Diego, CA.
William FrankVital Therapies Inc., San Diego, CA.
Andrew HenryVital Therapies Inc., San Diego, CA.
Jan StangeVital Therapies Inc., San Diego, CA.
Ram SubramanianEmory University School of Medicine, Atlanta, GA.
VTI-208 Study Group
Vital Therapies (United States) · USDrexel University · USEmory University · USUniversity of Pittsburgh Medical Center · USBanner - University Medical Center Tucson · USBaylor University Medical Center · USBeth Israel Deaconess Medical Center · USCedars-Sinai Medical Center · USCleveland Clinic · USColumbia University Irving Medical Center · USEinstein Medical Center Philadelphia · USFlinders Medical Centre · AUGeorgetown University · USJackson Memorial Hospital · USMethodist Dallas Medical Center · USMontefiore Medical Center · USNew York University · USNorth Shore University Hospital · USPiedmont Atlanta Hospital · USQueen Elizabeth Hospital Birmingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe alcoholic hepatitis (sAH) is associated with a poor prognosis. There is no proven effective treatment for sAH, which is why early transplantation has been increasingly discussed. Hepatoblastoma-derived C3A cells express anti-inflammatory proteins and growth factors and were tested in an extracorporeal cellular therapy (ELAD) study to establish their effect on survival for subjects with sAH. Adults with sAH, bilirubin ≥8 mg/dL, Maddrey's discriminant function ≥ 32, and Model for End-Stage Liver Disease (MELD) score ≤ 35 were randomized to receive standard of care (SOC) only or 3-5 days of continuous ELAD treatment plus SOC. After a minimum follow-up of 91 days, overall survival (OS) was assessed by using a Kaplan-Meier survival analysis. A total of 203 subjects were enrolled (96 ELAD and 107 SOC) at 40 sites worldwide. Comparison of baseline characteristics showed no significant differences between groups and within subgroups. There was no significant difference in serious adverse events between the 2 groups. In an analysis of the intent-to-treat population, there was no difference in OS (51.0% versus 49.5%). The study failed its primary and secondary end point in a population with sAH and with a MELD ranging from 18 to 35 and no upper age limit. In the prespecified analysis of subjects with MELD < 28 (n = 120), ELAD was associated with a trend toward higher OS at 91 days (68.6% versus 53.6%; P = .08). Regression analysis identified high creatinine and international normalized ratio, but not bilirubin, as the MELD components predicting negative outcomes with ELAD. A new trial investigating a potential benefit of ELAD in younger subjects with sufficient renal function and less severe coagulopathy has been initiated. Liver Transplantation 24 380-393 2018 AASLD.

Indexed as

AdultAustraliaCell Line, TumorExtracorporeal CirculationFemaleHepatitis, AlcoholicHepatoblastomaHumansIntention to Treat AnalysisKaplan-Meier EstimateLiver NeoplasmsMaleMiddle AgedProspective StudiesRisk FactorsSeverity of Illness Index

Identifiers

PMID29171941
PMCPMC5873437
OpenAlexW2768152453

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.