volume 31 issue 9 pages OF1-OF9

Phase 1 trial of selinexor in pediatric recurrent/refractory solid and CNS tumors (ADVL1414): A Children's Oncology Group Phase 1 Consortium Trial

Adam S. Green 1, 2, 3
Charles G Minard 4, 5
Xiaowei Liu 6, 7
Stephanie L. Safgren 8, 9
Kerice Pinkney 10, 11
Lauren Harris 2, 12
Gabrielle Link 1, 2
John DeSisto 1, 2
Stephan Voss 13, 14
Marvin D. Nelson 15, 16
Joel Reid 8, 9
Elizabeth Fox 17, 18
Brenda J Weigel 19, 20
Julia Glade-Bender 21, 22
6
 
Children's Oncology Group, Monrovia, CA, United States
7
 
4Children’s Oncology Group, Monrovia, California.
10
 
Joe DiMaggio Children's Hospital, United States
11
 
6Joe DiMaggio Children’s Hospital, Hollywood, Florida.
Publication typeJournal Article
Publication date2025-02-25
scimago Q1
wos Q1
SJR4.800
CiteScore19.0
Impact factor10.2
ISSN10780432, 15573265
Abstract
Purpose:

Selinexor is a first-in-class, central nervous system (CNS)–penetrant, oral inhibitor of exportin 1 (XPO1), the main nuclear exporter of many key tumor suppressors. We report a phase I trial of selinexor in children and adolescents with recurrent CNS and solid tumors (NCT02323880).

Patients and Methods:

A rolling six design was used to evaluate the maximum tolerated dose (MTD) and first dose pharmacokinetics of selinexor administered once (35–45 mg/m2) or twice (20–35 mg/m2) weekly during a 28-day cycle (part A). Ten additional patients with high-grade glioma (HGG) were treated at the MTD administered once weekly (part B).

Results:

In part A, 49 patients were enrolled. Continuous twice weekly dosing was limited by extended hematologic toxicity. The MTD on a twice weekly schedule for 3 weeks on/1 week off (twice weekly 3/1) was 20 mg/m2/dose. Dose-limiting toxicities (DLTs) on this schedule included fatigue, acute reversible neurologic changes, neutropenia, thrombocytopenia, and aspartate aminotransferase/alanine aminotransferase increase. On a continuous once weekly schedule, the MTD was 35 mg/m2/dose; DLTs included seizure and thrombocytopenia. In part B (HGG expansion), there were no additional DLTs observed. Non-DLTs included lymphopenia, leukopenia, neutropenia, thrombocytopenia, anorexia, fatigue, hypophosphatemia, nausea, and vomiting. There were no objective responses. The median number of cycles received was 1 (range, 1–9); eight of 59 patients (13.5%) received 5 to 9 cycles, five of whom had HGG.

Conclusions:

Selinexor-related toxicities were primarily hematologic and neurologic, requiring dose or dose-frequency reduction. The MTD and recommended initial phase II dose of selinexor in children and adolescents with recurrent solid and CNS tumors is 35 mg/m2/dose once weekly.

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Green A. S. et al. Phase 1 trial of selinexor in pediatric recurrent/refractory solid and CNS tumors (ADVL1414): A Children's Oncology Group Phase 1 Consortium Trial // Clinical Cancer Research. 2025. Vol. 31. No. 9. p. OF1-OF9.
GOST all authors (up to 50) Copy
Green A. S., Minard C. G., Liu X., Safgren S. L., Pinkney K., Harris L., Link G., DeSisto J., Voss S., Nelson M. D., Reid J., Fox E., Weigel B. J., Glade-Bender J. Phase 1 trial of selinexor in pediatric recurrent/refractory solid and CNS tumors (ADVL1414): A Children's Oncology Group Phase 1 Consortium Trial // Clinical Cancer Research. 2025. Vol. 31. No. 9. p. OF1-OF9.
RIS |
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RIS Copy
TY - JOUR
DO - 10.1158/1078-0432.ccr-24-2754
UR - https://aacrjournals.org/clincancerres/article/doi/10.1158/1078-0432.CCR-24-2754/752095/Phase-1-trial-of-selinexor-in-pediatric-recurrent
TI - Phase 1 trial of selinexor in pediatric recurrent/refractory solid and CNS tumors (ADVL1414): A Children's Oncology Group Phase 1 Consortium Trial
T2 - Clinical Cancer Research
AU - Green, Adam S.
AU - Minard, Charles G
AU - Liu, Xiaowei
AU - Safgren, Stephanie L.
AU - Pinkney, Kerice
AU - Harris, Lauren
AU - Link, Gabrielle
AU - DeSisto, John
AU - Voss, Stephan
AU - Nelson, Marvin D.
AU - Reid, Joel
AU - Fox, Elizabeth
AU - Weigel, Brenda J
AU - Glade-Bender, Julia
PY - 2025
DA - 2025/02/25
PB - American Association for Cancer Research (AACR)
SP - OF1-OF9
IS - 9
VL - 31
SN - 1078-0432
SN - 1557-3265
ER -
BibTex |
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BibTex (up to 50 authors) Copy
@article{2025_Green,
author = {Adam S. Green and Charles G Minard and Xiaowei Liu and Stephanie L. Safgren and Kerice Pinkney and Lauren Harris and Gabrielle Link and John DeSisto and Stephan Voss and Marvin D. Nelson and Joel Reid and Elizabeth Fox and Brenda J Weigel and Julia Glade-Bender},
title = {Phase 1 trial of selinexor in pediatric recurrent/refractory solid and CNS tumors (ADVL1414): A Children's Oncology Group Phase 1 Consortium Trial},
journal = {Clinical Cancer Research},
year = {2025},
volume = {31},
publisher = {American Association for Cancer Research (AACR)},
month = {feb},
url = {https://aacrjournals.org/clincancerres/article/doi/10.1158/1078-0432.CCR-24-2754/752095/Phase-1-trial-of-selinexor-in-pediatric-recurrent},
number = {9},
pages = {OF1--OF9},
doi = {10.1158/1078-0432.ccr-24-2754}
}
MLA
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MLA Copy
Green, Adam S., et al. “Phase 1 trial of selinexor in pediatric recurrent/refractory solid and CNS tumors (ADVL1414): A Children's Oncology Group Phase 1 Consortium Trial.” Clinical Cancer Research, vol. 31, no. 9, Feb. 2025, pp. OF1-OF9. https://aacrjournals.org/clincancerres/article/doi/10.1158/1078-0432.CCR-24-2754/752095/Phase-1-trial-of-selinexor-in-pediatric-recurrent.
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