Post Mortem Tissue Donation of Pediatric Tumor Tissues and Cells

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorAnn & Robert H Lurie Children's Hospital of Chicago

About this trial

The objective of this study is to utilize all donated pediatric tumor tissues and cells obtained from autopsy to prospectively develop novel patient derived orthotopic xenograft (PDOX) mouse models as well as in vitro cell culture model systems for pediatric cancers, and also provide tissue samples to other researchers and organizations (eg, CBTN, DIPG Registry, COG).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Pediatric patients with cancer and non-cancer tumor types (solid, liquid, neuro-oncology)

Signed consent for post mortem tissue donation and autopsy

Disqualifiers

Signed consent for post mortem tissue donation and autopsy not obtained

Trial population

Pediatric patients with cancer and non-cancer tumor types (solid, liquid, neuro-oncology)

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Collection of post mortem tissue donation

    Other intervention

    Collection of post mortem tissue from pediatric participants with cancer and non-cancer tumor types from whom post mortem tissue donation and autopsy consent is obtained.

Treatment groups

150 Participants
are divided into 1 treatment group
Group A: Pediatric patients with cancer and non-cancer tumor types1 intervention

Trial outcomes

Primary outcomes

1

Procurement of pediatric cancer and non-cancer tumor tissue during autopsy with signed consent

Procurement of pediatric cancer and non-cancer tumor tissue during autopsy with signed consent. Tissue will be collected through a research tissue collection autopsy of the original tumor and other sites that are appropriate. Samples of both tumor and normal cells will be collected in addition to body fluids such as cerebrospinal fluid (CSF), blood, bone marrow, and skin biopsies for genomic testing.

Time frame
Up to 5 years from procurement

Secondary outcomes

Other outcomes

Sponsors and contacts

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