A Multicenter Phase II Study of Pazopanib in Patients with Unresectable Dermatofibrosarcoma Protuberans.
Adult
Aged
Biomarkers, Tumor
/ antagonists & inhibitors
Dermatofibrosarcoma
/ drug therapy
Drug Resistance, Neoplasm
/ genetics
Epidermal Growth Factor
/ genetics
ErbB Receptors
/ antagonists & inhibitors
Female
Gene Expression Profiling
Gene Expression Regulation, Neoplastic
Humans
Indazoles
/ administration & dosage
Male
Middle Aged
Protein Kinase Inhibitors
/ administration & dosage
Pyrimidines
/ administration & dosage
Response Evaluation Criteria in Solid Tumors
Skin
/ drug effects
Skin Neoplasms
/ drug therapy
Sulfonamides
/ administration & dosage
Tumor Burden
/ drug effects
Journal
The Journal of investigative dermatology
ISSN: 1523-1747
Titre abrégé: J Invest Dermatol
Pays: United States
ID NLM: 0426720
Informations de publication
Date de publication:
04 2021
04 2021
Historique:
received:
26
02
2020
revised:
23
06
2020
accepted:
29
06
2020
pubmed:
22
9
2020
medline:
8
10
2021
entrez:
21
9
2020
Statut:
ppublish
Résumé
Dermatofibrosarcoma protuberans (DFSP) is a soft-tissue sarcoma characterized by a high risk of local infiltration. The identification of the COL1A1-PDGFB t(17;22) translocation activating the PDGF pathway led to the use of imatinib in unresectable DFSP, with a response rate of 36-80%. Pazopanib is a multitarget tyrosine kinase inhibitor approved for soft-tissue sarcomas. We conducted a phase II study of patients with unresectable DFSP to evaluate the efficacy and safety of pazopanib. Patients received 800 mg of pazopanib daily. The primary endpoint was the objective response rate defined as the reduction of the largest diameter of the tumor by ≥30% at 6 months or at surgery. A total of 23 patients, including one pretreated with imatinib, were enrolled. With a median follow-up of 6.2 months (interquartile range = 5.6-7.8 months), five patients (22%, 95% confidence interval = 7-22%) had a partial response to pazopanib. The best objective response rate was 30% (95% confidence interval = 13-53%) using Response Evaluation Criteria in Solid Tumors. One patient with metastatic DFSP previously treated with imatinib died after 2.4 months. Nine patients (39%) discontinued the treatment owing to adverse events. Pharmacodynamics analyses of tumor samples were conducted: the enrichment of EGF and the EGFR-associated gene panel was associated with resistance, suggesting that EGFR-targeted therapies could be a therapeutic option to explore in DFSP. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT01059656.
Identifiants
pubmed: 32956651
pii: S0022-202X(20)32067-4
doi: 10.1016/j.jid.2020.06.039
pii:
doi:
Substances chimiques
Biomarkers, Tumor
0
Indazoles
0
Protein Kinase Inhibitors
0
Pyrimidines
0
Sulfonamides
0
Epidermal Growth Factor
62229-50-9
pazopanib
7RN5DR86CK
EGFR protein, human
EC 2.7.10.1
ErbB Receptors
EC 2.7.10.1
Banques de données
ClinicalTrials.gov
['NCT01059656']
Types de publication
Clinical Trial, Phase II
Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
761-769.e2Informations de copyright
Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.