Deliverables

ChiLTERN deliverables are tangible items such as a report or website that have to be documented by the lead and uploaded via the Participant Portal to the European Commission by the contracted deadline (). 

Deliverables

  • D1.1 Project Management Manual (6) UoB – submitted and approved
  • D1.2 Data Management Plan (6) UoB – submitted and approved
  • D2.1 Registration in ISRCTN (12) UoB – submitted and approved
  • D2.2 Protocol finalisation and submission to EC (12) UoB – submitted and approved
  • D2.3 Ethics & regulatory approval in UK and submission to EC (12) UoB – submitted and approved
  • D2.4 Ethics & regulatory approval in 50% of NCC countries (18) UoB – submitted 
  • D2.5 Trial Progress report (18) UoB – submitted and approved
  • D2.6 Mid-recruitment report (36) UoB – submitted
  • D2.7 Trial Progress report 3 (54) UoB
  • D2.8 Trial publication report (60) UoB
  • D2.9 Submission of approvals package to EC (60) UoB
  • D3.1 Report on biobanking activities (36) IGTP – submitted
  • D3.2 Website optimization to register sample collection (18) CINECA – submitted and approved
  • D3.3 Report on pathological review activities (36) UNIPD – submitted
  • D3.4 Report on the optimised panel of biomarkers (54) IGTP
  • D3.5 Report on validated biomarkers in diagnostic specimens (54) IGTP
  • D3.6 Report on new biomarkers identified in aggressive childhood cancers (54) LMU
  • D3.7 Report on similarities and differences between paediatric and adult HCC (54) UKB
  • D4.1 Report on the first step to a validation of the new clinical risk stratification CHIC HS (36) LMU
  • D4.2 Report of the validation of CHIC HS within the first part of the PHITT trial data (60) LMU
  • D4.3 Report of the inclusion of pathology and biology marker into a new clinical-pathological-biological version of the classification (60) LMU
  • D5.1Web-based surgical review platform (18) EKUT – submitted and approved
  • D5.2 Report on imaging data collection activities (36) EKUT
  • D5.3 Report on surgical review activities (36) EKUT
  • D5.4 Report on surgical review activitiesReport on the outcome of patients with PRETEXT III/IV HB undergoing surgery (54) EKUT
  • D5.5 Report on validated factors for surgical decision making (54) EKUT
  • D5.6 Report on factors identifying patients for computer assisted surgery planning (54) EKUT
  • D5.7 Report of clinical recommendations for children with PRETEXT III/IV Hepatoblastoma: extended resection or primary liver transplantation (60) EKUT
  • D6.1 Protocols for standardised collection of clinical samples and sample analysis (18) UNEW – submitted and approved
  • D6.2 Collection of samples and pharmacokinetic analysis (18) UNEW – submitted
  • D6.3 Collection of samples and biomarker analysis (18) UNEW
  • D6.4 Analysis of pharmacogenetic data (54) UNEW
  • D6.5 Final WP6 report (60) UNEW
  • D7.1 Dissemination and Communication Plan: and updated regularly (18) UoB – submitted and approved
  • D7.2 Publication Policy (18) UoB – submitted and approved
  • D7.3 Website activation (18) UoB – submitted and approved