Childhood Cancer Data Initiative Annual Symposium (Abstract Registration): Submission #76
Submission information
Submission Number: 76
Submission ID: 192391
Submission UUID: 315c3ecd-4d04-43e3-8d65-90f2993da697
Submission URI: /nci/ccdisymposium/abstract?utm_source=aug18_2025abstract&utm_medium=email&utm_campaign=2026ccdisymposium
Submission Update: /nci/ccdisymposium/abstract?utm_source=aug18_2025abstract&utm_medium=email&utm_campaign=2026ccdisymposium&token=SUrtn0RNFO3uHEnNSFUp1SCG5Avc8youX8QGg4Bj7Wo
Created: Wed, 08/26/2026 - 15:12
Completed: Wed, 08/26/2026 - 15:17
Changed: Wed, 08/26/2026 - 15:17
Remote IP address: 10.208.24.244
Submitted by: Anonymous
Language: English
Is draft: No
serial: '76'
sid: '192391'
uuid: 315c3ecd-4d04-43e3-8d65-90f2993da697
uri: '/nci/ccdisymposium/abstract?utm_source=aug18_2025abstract&utm_medium=email&utm_campaign=2026ccdisymposium'
created: '1787771549'
completed: '1787771862'
changed: '1787771862'
in_draft: '0'
current_page: ''
remote_addr: 10.208.24.244
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langcode: en
webform_id: ccdi_symposium_abstract
entity_type: node
entity_id: '2139'
locked: '0'
sticky: '0'
notes: ''
metatag: meta
data:
authors_:
- add_author_degree: PharmD
add_author_first_name: Min
add_author_last_name: Kang
add_author_middle: H
add_author_organization: 'Texas Tech University Health Sciences Center'
- add_author_degree: PhD
add_author_first_name: In-Hyoung
add_author_last_name: Yang
add_author_middle: ''
add_author_organization: 'Texas Tech University Health Sciences Center'
- add_author_degree: PhD
add_author_first_name: Nighat
add_author_last_name: Noureen
add_author_middle: ''
add_author_organization: 'Texas Tech University Health Sciences Center'
- add_author_degree: MS
add_author_first_name: Kristyn
add_author_last_name: McCoy
add_author_middle: ''
add_author_organization: 'Texas Tech University Health Sciences Center'
- add_author_degree: BS
add_author_first_name: Jonas
add_author_last_name: Nance
add_author_middle: ''
add_author_organization: 'Texas Tech University Health Sciences Center'
- add_author_degree: BS
add_author_first_name: Diana
add_author_last_name: Ixlamati-Nava
add_author_middle: ''
add_author_organization: 'Texas Tech University Health Sciences Center'
- add_author_degree: PhD
add_author_first_name: Ashly
add_author_last_name: Hindle
add_author_middle: ''
add_author_organization: 'Texas Tech University Health Sciences Center'
- add_author_degree: MD
add_author_first_name: Meredith
add_author_last_name: Erwin
add_author_middle: S
add_author_organization: 'Hospital for Sick Children, University of Toronto'
- add_author_degree: MD
add_author_first_name: Michael
add_author_last_name: Hogarty
add_author_middle: D
add_author_organization: "Children's Hospital of Philadelphia and University of Pennsylvania"
- add_author_degree: 'MD, PhD'
add_author_first_name: Charles
add_author_last_name: Reynolds
add_author_middle: P
add_author_organization: 'Texas Tech University Health Sciences Center'
abstract: 'Tumor biopsies are often not obtained at the time of progressive disease (PD) in neuroblastoma (NB). Patient-derived xenografts (PDXs) established from bone marrow or blood of NB patients enable studies to define molecular mechanisms and approaches to overcome therapy resistance. Tumor, marrow, or peripheral blood samples from 40 high-risk patients, 19 at diagnosis (Dx) and 21 at PD (12 of 21 at post-mortem), were received via Children’s Oncology Group (COG) protocol ANBL00B1 and established as PDXs. PDXs were classified by the response to chemotherapy (Cyclo/Topo, cyclophosphamide + topotecan, 3 x 21-day cycles, or TMZ/IRI, relapse chemo, temozolomide + irinotecan, 2 x 21-day cycles) as non-responders (NR), stable disease (SD), partial responders (PR), and complete responders (CR). Engraftment rates were 17% for Dx and 24% for PD samples. Based on an algorithm we developed for PDX response evaluation, Cyclo/Topo responses were NR (n=11), SD (n=2), PR (n=9), and CR (n=18), and 9 of 11 showed CR to TMZ/IRN. Nine of 13 (69%) of the NR+SD PDXs were established from post-mortem PD (PD-PM) samples, while 12 of 18 (67%) of the CR group were from Dx samples. The response of PDXs to Cyclo/Topo was greater for pretherapy (Dx) PDXs than for PD-PM or PD PDXs; six of the 11 PD models showed significantly better EFS for TMZ/IRN relative to Cyclo/Topo (P<0.05, n=6 PDXs). This panel of 40 NB PDXs, characterized for their response to chemotherapy, will enable studies to define the molecular mechanisms of NB therapy resistance and is available at www.CCcells.org. '
abstract_title_: 'Characterizing the Children’s Oncology Group panel of neuroblastoma patient-derived xenografts for response to induction and salvage chemotherapy'
email_address_: min.kang@ttuhsc.edu
institution_: 'Texas Tech University Health Sciences Center'
presenting_author_: 'Min H. Kang'