Marrow-ablative consolidation chemotherapy and molecular targeted therapy delivered in a risk-adapted manner for newly diagnosed children with choroid plexus carcinoma: A work in progress

Author:

Yankelevich Maxim1,Zaky Wafik2,Lafay-Cousin Lucie3,Osorio Diana2,Adamski Jenny4,Kordes Uwe5,Finlay Jonathan L6ORCID,Prados Michael7,Mueller Sabine7

Affiliation:

1. Division of Oncology, St. Cristopher’s Hospital for Children , Philadelphia , Pennsylvania , USA

2. Department of Pediatrics, MD Anderson Cancer Center , Houston, Texas , USA

3. Department of Pediatrics and Oncology, Alberta Children’s Hospital , Calgary, Alberta , Canada

4. Birmingham Women’s and Children’s Hospital NHS Foundation Trust , Birmingham , UK

5. Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf , Hamburg , Germany

6. Ohio State University College of Medicine, The Ohio State University , Columbus , Ohio , USA

7. Departments of Pediatrics and Neurosurgery, University of California-San Francisco , San Francisco, California , USA

Abstract

Abstract Choroid plexus carcinomas (CPC) are early childhood cancers characterized by loss of TP53 function and poor survival. We are analyzing data on TP53 status, survival, and second cancers from the largest cohort of CPC receiving chemotherapy followed by consolidation with marrow-ablative chemotherapy (HDCx). Additionally, we discuss the rationale for targeted therapies for CPC patients. Currently, 8 of the 13 with Li-Fraumeni Syndrome-associated CPC were treated and continued CPC-free, indicating that HDCx improves CPC-free survival in young children with TP53-mutated CPC. These data justify the inclusion of HDCx in the planned prospective international trial for children with TP53-mutated CPC.

Publisher

Oxford University Press (OUP)

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