Literature DB >> 35391541

Study protocol of Phase 2 open-label multicenter randomized controlled trial for granulocyte-colony stimulating factor (GCSF) in post-Kasai Type 3 biliary atresia.

Hoa Pham Anh Nguyen1, Jinma Ren2, Marilyn Butler3, Henri Li3, Saqib Qazi4, Kamran Sadiq4, Hieu Trung Dao5, AiXuan Holterman6.   

Abstract

Animal studies support RCT findings of improved liver function and short-term benefits using repurposed Granulocyte Colonic Stimulating Factor GCSF in adults with decompensated cirrhosis. We describe the protocol for phase 2 RCT of sequential Kasai-GCSF under an FDA-approved IND to test that GCSF improves early bile flow and post-Kasai biliary atresia BA clinical outcome. Immediate post-Kasai neonates, age 15-180 days, with biopsy-confirmed type 3 BA, without access to early liver transplantation, will be randomized 1:1 to standard of care SOC + GCSF at 10 ug/kg in 3 daily doses within 4 days of Kasai vs SOC + NO-GCSF (ClinicalTrials.gov NCT0437391). They will be recruited from children's hospitals in Vietnam, Pakistan and one US center. The primary objective is to demonstrate that GCSF decreases the proportion of subjects with a 3-month post-Kasai serum Total Bilirubin ≥ 34 umol/L by 20%, (for a = 0.05, b = 0.80, i.e., calculated sample size of 218 subjects). The secondary objectives are to demonstrate that the frequency of post-Kasai cholangitis at 6-month and 24-month transplant-free survival are improved. The benefits are that GCSF is an affordable BA adjunct therapy, especially in developing countries, to improve biliary complications, enhance quality of liver and survival while diminishing costly liver transplantation.Clinical trial registration: A phase 1 for GCSF dose and safety determination under ClinicalTrials.gov identifier NCT03395028 was completed in 2019. The current Phase 2 trial was registered under NCT04373941.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Biliary atresia; GCSF; Kasai, Randomized controlled trial; Low middle income country

Mesh:

Substances:

Year:  2022        PMID: 35391541     DOI: 10.1007/s00383-022-05115-0

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  55 in total

1.  Derivation of hepatocytes from bone marrow cells in mice after radiation-induced myeloablation.

Authors:  N D Theise; S Badve; R Saxena; O Henegariu; S Sell; J M Crawford; D S Krause
Journal:  Hepatology       Date:  2000-01       Impact factor: 17.425

2.  G-CSF-primed hematopoietic stem cells or G-CSF per se accelerate recovery and improve survival after liver injury, predominantly by promoting endogenous repair programs.

Authors:  Evangelia Yannaki; Evangelia Athanasiou; Angeliki Xagorari; Varnavas Constantinou; Ioannis Batsis; Panagiotis Kaloyannidis; Evangelia Proya; Achilles Anagnostopoulos; Athanasios Fassas
Journal:  Exp Hematol       Date:  2005-01       Impact factor: 3.084

3.  Immunomodulatory action of G-CSF in a rat model of endotoxin-induced liver injury: an intravital microscopic analysis of Kupffer cell and leukocyte response.

Authors:  B Vollmar; S Messner; G A Wanner; T Hartung; M D Menger
Journal:  J Leukoc Biol       Date:  1997-12       Impact factor: 4.962

4.  Liver from bone marrow in humans.

Authors:  N D Theise; M Nimmakayalu; R Gardner; P B Illei; G Morgan; L Teperman; O Henegariu; D S Krause
Journal:  Hepatology       Date:  2000-07       Impact factor: 17.425

5.  Intermittent dosing of G-CSF to ameliorate carbon tetrachloride-induced liver fibrosis in mice.

Authors:  Baijun Fang; Suxia Luo; Yongping Song; Ning Li; Huixiang Li; Robert Chunhua Zhao
Journal:  Toxicology       Date:  2009-12-11       Impact factor: 4.221

6.  Granulocyte colony-stimulating factor (G-CSF) reduces not only gram-negative but also gram-positive infection-associated proinflammatory cytokine release by interaction between Kupffer cells and leukocytes.

Authors:  C J Busch; G A Wanner; M D Menger; B Vollmar
Journal:  Inflamm Res       Date:  2004-04-21       Impact factor: 4.575

Review 7.  Biliary Atresia: Clinical and Research Challenges for the Twenty-First Century.

Authors:  Jorge A Bezerra; Rebecca G Wells; Cara L Mack; Saul J Karpen; Jay H Hoofnagle; Edward Doo; Ronald J Sokol
Journal:  Hepatology       Date:  2018-09       Impact factor: 17.425

Review 8.  Cellular Mechanisms of Liver Regeneration and Cell-Based Therapies of Liver Diseases.

Authors:  Irina V Kholodenko; Konstantin N Yarygin
Journal:  Biomed Res Int       Date:  2017-01-22       Impact factor: 3.411

Review 9.  Cytokine-induced hematopoietic stem and progenitor cell mobilization: unraveling interactions between stem cells and their niche.

Authors:  Evert-Jan F M de Kruijf; Willem E Fibbe; Melissa van Pel
Journal:  Ann N Y Acad Sci       Date:  2019-04-21       Impact factor: 5.691

Review 10.  Cell therapy for advanced liver diseases: Repair or rebuild.

Authors:  Benjamin J Dwyer; Mark T Macmillan; Paul N Brennan; Stuart J Forbes
Journal:  J Hepatol       Date:  2020-09-22       Impact factor: 25.083

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