TY - JOUR
T1 - A Single-Arm Phase 2 Trial of Trametinib in Patients with Locally Advanced or Metastatic Epithelioid Hemangioendothelioma
AU - Schuetze, Scott M.
AU - Ballman, Karla V.
AU - Heise, Rachel
AU - Ganjoo, Kristen N.
AU - Davis, Elizabeth J.
AU - George, Suzanne
AU - Burgess, Melissa A.
AU - Choy, Edwin
AU - Shepard, Dale R.
AU - Tinoco, Gabriel
AU - Kelly, Ciara M.
AU - Hirbe, Angela
AU - Attia, Steven
AU - Deshpande, Hari A.
AU - Schwartz, Gary K.
AU - Siontis, Brittany L.
AU - Riedel, Richard F.
AU - von Mehren, Margaret
AU - Kozlowski, Erin
AU - Chen, Helen X.
AU - Astbury, Caroline
AU - Rubin, Brian P.
N1 - ©2024 American Association for Cancer Research.
PY - 2024/10/15
Y1 - 2024/10/15
N2 - PURPOSE: Epithelioid hemangioendothelioma (EHE) is a rare vascular cancer with pathogenic TAZ-CAMTA1 (calmodulinbinding transcription activator 1) operating as an oncogenic driver through activation of the MAPK pathway. Trametinib is an inhibitor of MEK, a critical kinase in the MAPK pathway. We sought to evaluate the effect of trametinib in patients with EHE.PATIENTS AND METHODS: A phase 2 trial of trametinib was conducted in patients with locally advanced or metastatic EHE. Eligibility requirements included evidence of tumor progression or presence of EHE-related pain requiring opiates for management before enrollment. The primary endpoint was objective response rate (ORR) as per RECIST1.1 in cases with TAZ- CAMTA1 confirmed by fusion-FISH. Secondary objectives were to estimate ORR for all patients, median progression-free survival (PFS), 2-year overall survival (OS) rate, patient safety, and change in patient-reported global health and pain scores per PROMIS questionnaires.RESULTS: 44 patients enrolled and 42 started trametinib. TAZ- CAMTA1 was detected in 27 tumor samples. TheORRwas 3.7%[95% confidence interval (CI), 0.094-19.0], median PFS was 10.4 months (95%CI, 7.1-NA), and 2-year OS rate was 33.3%(95%CI, 19.1-58.2) in the target population. Median pain intensity and interference scores improved significantly after 4 weeks of trametinib in patients using opiates. Common adverse events related to trametinib were rash, fatigue, nausea/vomiting, diarrhea/constipation, alopecia, and edema; one grade 5 ARDS/pneumonitis was related to trametinib.CONCLUSIONS: Trametinib was associated with reduction in EHE-related pain and median PFS of more than 6 months, providing palliative benefit in patients with advanced EHE, but the trial did not meet the ORR goal. See related commentary by Van Tine and Haarberg, p. 4552.
AB - PURPOSE: Epithelioid hemangioendothelioma (EHE) is a rare vascular cancer with pathogenic TAZ-CAMTA1 (calmodulinbinding transcription activator 1) operating as an oncogenic driver through activation of the MAPK pathway. Trametinib is an inhibitor of MEK, a critical kinase in the MAPK pathway. We sought to evaluate the effect of trametinib in patients with EHE.PATIENTS AND METHODS: A phase 2 trial of trametinib was conducted in patients with locally advanced or metastatic EHE. Eligibility requirements included evidence of tumor progression or presence of EHE-related pain requiring opiates for management before enrollment. The primary endpoint was objective response rate (ORR) as per RECIST1.1 in cases with TAZ- CAMTA1 confirmed by fusion-FISH. Secondary objectives were to estimate ORR for all patients, median progression-free survival (PFS), 2-year overall survival (OS) rate, patient safety, and change in patient-reported global health and pain scores per PROMIS questionnaires.RESULTS: 44 patients enrolled and 42 started trametinib. TAZ- CAMTA1 was detected in 27 tumor samples. TheORRwas 3.7%[95% confidence interval (CI), 0.094-19.0], median PFS was 10.4 months (95%CI, 7.1-NA), and 2-year OS rate was 33.3%(95%CI, 19.1-58.2) in the target population. Median pain intensity and interference scores improved significantly after 4 weeks of trametinib in patients using opiates. Common adverse events related to trametinib were rash, fatigue, nausea/vomiting, diarrhea/constipation, alopecia, and edema; one grade 5 ARDS/pneumonitis was related to trametinib.CONCLUSIONS: Trametinib was associated with reduction in EHE-related pain and median PFS of more than 6 months, providing palliative benefit in patients with advanced EHE, but the trial did not meet the ORR goal. See related commentary by Van Tine and Haarberg, p. 4552.
KW - Adult
KW - Aged
KW - Aged, 80 and over
KW - Calcium-Binding Proteins
KW - Female
KW - Hemangioendothelioma, Epithelioid/drug therapy
KW - Humans
KW - Male
KW - Middle Aged
KW - Protein Kinase Inhibitors/therapeutic use
KW - Pyridones/therapeutic use
KW - Pyrimidinones/therapeutic use
KW - Trans-Activators
KW - Transcriptional Coactivator with PDZ-Binding Motif Proteins
KW - Young Adult
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:001338631000016&DestLinkType=FullRecord&DestApp=WOS_CPL
UR - http://www.scopus.com/inward/record.url?scp=85197992565&partnerID=8YFLogxK
U2 - 10.1158/1078-0432.CCR-23-3817
DO - 10.1158/1078-0432.CCR-23-3817
M3 - Article
C2 - 38446990
SN - 1078-0432
VL - 30
SP - 4584
EP - 4592
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 20
ER -