Engineered Anti‐GPC3 Immunotoxin, HN3‐ABD‐T20, Produces Regression in Mouse Liver Cancer Xenografts Through Prolonged Serum Retention-Reference-Cited by-同舟云学术

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Engineered Anti‐GPC3 Immunotoxin, HN3‐ABD‐T20, Produces Regression in Mouse Liver Cancer Xenografts Through Prolonged Serum Retention

Published:2020-01-27 Issue:5 Volume:71 Page:1696-1711
ISSN:0270-9139
Container-title:Hepatology
language:en
Short-container-title:Hepatology

Author:

Fleming Bryan D.¹^ORCID,Urban Daniel J.²,Hall Matthew D.²,Longerich Thomas³,Greten Tim F.⁴,Pastan Ira¹,Ho Mitchell¹^ORCID

Affiliation:

1. Laboratory of Molecular Biology National Cancer Institute Bethesda MD

2. NCATS Chemical Genomics Center National Center for Advancing Translational Sciences Rockville MD

3. Institute of Pathology University Hospital Heidelberg Germany

4. Thoracic and Gastrointestinal Oncology Branch National Cancer Institute Bethesda MD

Funder

National Cancer Institute

Publisher

Wiley

Subject

Hepatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/hep.30949

Reference42 articles.

1. Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012

2. Efficacy and safety of sorafenib in patients in the Asia-Pacific region with advanced hepatocellular carcinoma: a phase III randomised, double-blind, placebo-controlled trial

3. Regorafenib for patients with hepatocellular carcinoma who progressed on sorafenib treatment (RESORCE): a randomised, double-blind, placebo-controlled, phase 3 trial

4. Liver transplantation versus liver resection for hepatocellular carcinoma in intention to treat: An attempt to perform an ideal meta-analysis

5. Glypican-3-Specific Antibody Drug Conjugates Targeting Hepatocellular Carcinoma

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