Patient-derived mouse xenografts from pediatric liver cancer predict tumor recurrence and advise clinical management

Hepatology ◽  
2016 ◽  
Vol 64 (4) ◽  
pp. 1121-1135 ◽  
Author(s):  
Delphine Nicolle ◽  
Monique Fabre ◽  
Marina Simon-Coma ◽  
Aurore Gorse ◽  
Roland Kappler ◽  
...  
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Fabien K Baksh ◽  
Sanja Dacic ◽  
Sydney D Finkelstein ◽  
Patricia A Swalsky ◽  
Siva Raja ◽  
...  

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Sarah Jane Commander ◽  
Tu-Anh Ha ◽  
Huirong Zhu ◽  
Jorge Portuondo ◽  
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2021 ◽  
pp. candisc.1809.2020
Author(s):  
Theo Z Hirsch ◽  
Jill Pilet ◽  
Guillaume Morcrette ◽  
Amelie Roehrig ◽  
Benedict JE Monteiro ◽  
...  

2003 ◽  
Vol 43 (2) ◽  
pp. 146-151 ◽  
Author(s):  
Martin G Friedrich ◽  
Angelika Hellstern ◽  
Marieta I Toma ◽  
Peter Hammerer ◽  
Hartwig Huland

Cancers ◽  
2020 ◽  
Vol 12 (3) ◽  
pp. 720 ◽  
Author(s):  
Rakesh Sindhi ◽  
Vinayak Rohan ◽  
Andrew Bukowinski ◽  
Sameh Tadros ◽  
Jean de Ville de Goyet ◽  
...  

Unresectable hepatocellular carcinoma (HCC) was first removed successfully with total hepatectomy and liver transplantation (LT) in a child over five decades ago. Since then, children with unresectable liver cancer have benefitted greatly from LT and a confluence of several equally important endeavors. Regional and trans-continental collaborations have accelerated the development and standardization of chemotherapy regimens, which provide disease control to enable LT, and also serve as a test of unresectability. In the process, tumor histology, imaging protocols, and tumor staging have also matured to better assess response and LT candidacy. Significant trends include a steady increase in the incidence of and use of LT for hepatoblastoma, and a significant improvement in survival after LT for HCC with each decade. Although LT is curative for most unresectable primary liver sarcomas, such as embryonal sarcoma, the malignant rhabdoid tumor appears relapse-prone despite chemotherapy and LT. Pediatric liver tumors remain rare, and diagnostic uncertainty in some settings can potentially delay treatment or lead to the selection of less effective chemotherapy. We review the current knowledge relevant to diagnosis, LT candidacy, and post-transplant outcomes for these tumors, emphasizing recent observations made from large registries or larger series.


2014 ◽  
Vol 50 ◽  
pp. 25
Author(s):  
M. Fabre ◽  
D. Nicolle ◽  
A. Gorse ◽  
O. Déas ◽  
C. Mussini ◽  
...  

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