volume 25 issue 9 pages 2699-2707

A Phase I, Open-Label, Multicenter, Dose-escalation Study of the Oral Selective FGFR Inhibitor Debio 1347 in Patients with Advanced Solid Tumors Harboring FGFR Gene Alterations

Martin Voss 1
Cinta Hierro 2
Rebecca S. Heist 3
James M Cleary 4
Funda Meric-Bernstam 5
Filip Janku 5
Leena Gandhi 6
A. John Iafrate 3
Darrell R. Borger 3
Nobuya Ishii 7
Youyou Hu 8
Yulia Kirpicheva 8
Valérie Nicolas-Métral 8
Anna Pokorska-Bocci 8
Anne Vaslin Chessex 8
Claudio Zanna 8
Keith T. Flaherty 3
José Baselga 1, 2
Publication typeJournal Article
Publication date2019-05-01
scimago Q1
wos Q1
SJR4.800
CiteScore19.0
Impact factor10.2
ISSN10780432, 15573265
Cancer Research
Oncology
Abstract
Purpose:

To investigate tolerability, efficacy, and pharmacokinetics/pharmacodynamics of Debio 1347, a selective FGFR inhibitor.

Patients and Methods:

This was a first-in-human, multicenter, open-label study in patients with advanced solid tumors harboring FGFR1–3 gene alterations. Eligible patients received oral Debio 1347 at escalating doses once daily until disease progression or intolerable toxicity. Dose-limiting toxicities (DLT) were evaluated during the first 4 weeks on treatment, pharmacokinetics/pharmacodynamics postfirst dose and after 4 weeks.

Results:

A total of 71 patients were screened and 58 treated with Debio 1347 at doses from 10 to 150 mg/day. Predominant tumor types were breast and biliary duct cancer, most common gene alterations were FGFR1 amplifications (40%) and mutations in FGFR2 (12%) and FGFR3 (17%); 12 patients (21%) showed FGFR fusions. Five patients at three dose levels had six DLTs (dry mouth/eyes, hyperamylasemia, hypercalcemia, hyperbilirubinemia, hyperphosphatemia, and stomatitis). The maximum tolerated dose was not reached, but dermatologic toxicity became sometimes dose limiting beyond the DLT period at ≥80 mg/day. Adverse events required dose modifications in 52% of patients, mostly due to dose-dependent, asymptomatic hyperphosphatemia (22%). RECIST responses were seen across tumor types and mechanisms of FGFR activation. Six patients, 3 with FGFR fusions, demonstrated partial responses, 10 additional patients' tumor size regressions of ≤30%. Plasma half-life was 11.5 hours. Serum phosphate increased with Debio 1347 plasma levels and confirmed target engagement at doses ≥60 mg/day.

Conclusions:

Preliminary efficacy was encouraging and tolerability acceptable up to 80 mg/day, which is now used in an extension part of the study.

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GOST |
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GOST Copy
Voss M. et al. A Phase I, Open-Label, Multicenter, Dose-escalation Study of the Oral Selective FGFR Inhibitor Debio 1347 in Patients with Advanced Solid Tumors Harboring FGFR Gene Alterations // Clinical Cancer Research. 2019. Vol. 25. No. 9. pp. 2699-2707.
GOST all authors (up to 50) Copy
Voss M., Hierro C., Heist R. S., Cleary J. M., Meric-Bernstam F., Tabernero J., Janku F., Gandhi L., Iafrate A. J., Borger D. R., Ishii N., Hu Y., Kirpicheva Y., Nicolas-Métral V., Pokorska-Bocci A., Vaslin Chessex A., Zanna C., Flaherty K. T., Baselga J. A Phase I, Open-Label, Multicenter, Dose-escalation Study of the Oral Selective FGFR Inhibitor Debio 1347 in Patients with Advanced Solid Tumors Harboring FGFR Gene Alterations // Clinical Cancer Research. 2019. Vol. 25. No. 9. pp. 2699-2707.
RIS |
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RIS Copy
TY - JOUR
DO - 10.1158/1078-0432.ccr-18-1959
UR - https://doi.org/10.1158/1078-0432.ccr-18-1959
TI - A Phase I, Open-Label, Multicenter, Dose-escalation Study of the Oral Selective FGFR Inhibitor Debio 1347 in Patients with Advanced Solid Tumors Harboring FGFR Gene Alterations
T2 - Clinical Cancer Research
AU - Voss, Martin
AU - Hierro, Cinta
AU - Heist, Rebecca S.
AU - Cleary, James M
AU - Meric-Bernstam, Funda
AU - Tabernero, Josep
AU - Janku, Filip
AU - Gandhi, Leena
AU - Iafrate, A. John
AU - Borger, Darrell R.
AU - Ishii, Nobuya
AU - Hu, Youyou
AU - Kirpicheva, Yulia
AU - Nicolas-Métral, Valérie
AU - Pokorska-Bocci, Anna
AU - Vaslin Chessex, Anne
AU - Zanna, Claudio
AU - Flaherty, Keith T.
AU - Baselga, José
PY - 2019
DA - 2019/05/01
PB - American Association for Cancer Research (AACR)
SP - 2699-2707
IS - 9
VL - 25
PMID - 30745300
SN - 1078-0432
SN - 1557-3265
ER -
BibTex |
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BibTex (up to 50 authors) Copy
@article{2019_Voss,
author = {Martin Voss and Cinta Hierro and Rebecca S. Heist and James M Cleary and Funda Meric-Bernstam and Josep Tabernero and Filip Janku and Leena Gandhi and A. John Iafrate and Darrell R. Borger and Nobuya Ishii and Youyou Hu and Yulia Kirpicheva and Valérie Nicolas-Métral and Anna Pokorska-Bocci and Anne Vaslin Chessex and Claudio Zanna and Keith T. Flaherty and José Baselga},
title = {A Phase I, Open-Label, Multicenter, Dose-escalation Study of the Oral Selective FGFR Inhibitor Debio 1347 in Patients with Advanced Solid Tumors Harboring FGFR Gene Alterations},
journal = {Clinical Cancer Research},
year = {2019},
volume = {25},
publisher = {American Association for Cancer Research (AACR)},
month = {may},
url = {https://doi.org/10.1158/1078-0432.ccr-18-1959},
number = {9},
pages = {2699--2707},
doi = {10.1158/1078-0432.ccr-18-1959}
}
MLA
Cite this
MLA Copy
Voss, Martin, et al. “A Phase I, Open-Label, Multicenter, Dose-escalation Study of the Oral Selective FGFR Inhibitor Debio 1347 in Patients with Advanced Solid Tumors Harboring FGFR Gene Alterations.” Clinical Cancer Research, vol. 25, no. 9, May. 2019, pp. 2699-2707. https://doi.org/10.1158/1078-0432.ccr-18-1959.