Page last updated: 2024-11-04

vorinostat and Dysplastic Nevus Syndrome, Hereditary

vorinostat has been researched along with Dysplastic Nevus Syndrome, Hereditary in 2 studies

Vorinostat: A hydroxamic acid and anilide derivative that acts as a HISTONE DEACETYLASE inhibitor. It is used in the treatment of CUTANEOUS T-CELL LYMPHOMA and SEZARY SYNDROME.
vorinostat : A dicarboxylic acid diamide comprising suberic (octanedioic) acid coupled to aniline and hydroxylamine. A histone deacetylase inhibitor, it is marketed under the name Zolinza for the treatment of cutaneous T cell lymphoma (CTCL).

Research Excerpts

ExcerptRelevanceReference
"Vorinostat is a small molecule inhibitor of class I and II histone deacetylases with preclinical activity in melanoma."9.19Phase II trial of vorinostat in advanced melanoma. ( Adams, PD; Alpaugh, RK; Haas, NB; Hotte, S; Litwin, S; Martin, LP; McBryan, T; McWhirter, E; Oza, A; Polintan, R; Quirt, I; vonMehren, M; Wang, L; Zweibel, J, 2014)
"Vorinostat is a small molecule inhibitor of class I and II histone deacetylases with preclinical activity in melanoma."5.19Phase II trial of vorinostat in advanced melanoma. ( Adams, PD; Alpaugh, RK; Haas, NB; Hotte, S; Litwin, S; Martin, LP; McBryan, T; McWhirter, E; Oza, A; Polintan, R; Quirt, I; vonMehren, M; Wang, L; Zweibel, J, 2014)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's1 (50.00)2.80

Authors

AuthorsStudies
Gassenmaier, M1
Rentschler, M1
Fehrenbacher, B1
Eigentler, TK1
Ikenberg, K1
Kosnopfel, C1
Sinnberg, T1
Niessner, H1
Bösmüller, H1
Wagner, NB1
Schaller, M1
Garbe, C1
Röcken, M1
Haas, NB1
Quirt, I1
Hotte, S1
McWhirter, E1
Polintan, R1
Litwin, S1
Adams, PD1
McBryan, T1
Wang, L1
Martin, LP1
vonMehren, M1
Alpaugh, RK1
Zweibel, J1
Oza, A1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Phase II Study of Vorinostat in Patients With Advanced Melanoma[NCT00121225]Phase 232 participants (Actual)Interventional2005-09-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Comparison of VEGF Serum Levels to Response to Vorinostat

Blood specimens were collected from participants on Day 1 Cycle 1 prior to treatment (baseline), Day 1 3-4 hours following Vorinostat ingestion, Day 8 and Day 15. VEGF serum concentrations were detected using the Luminex multiplexed assay, where the median fluorescence intensity results were analyzed by a weighted five-parameter logistic method. The values were averaged across all time points per participant. (NCT00121225)
Timeframe: Baseline, Day 1, Day 8 and Day 15

Interventionpg (Mean)
Arm 1 Vorinostat203

Objective Response Rate Assessed by Response Evaluation Criteria for Solid Tumors (RECIST)

Per Response Evaluation Criteria in Solid Tumours Criteria (RECIST v1.0) for target lesions and are assessed by MRI: Complete Response (CR), disappearance of all target lesions; Partial Response (PR), at least 30% decrease in sum of longest diameter of target lesions; Objective Response (OR) = CR+ PR. (NCT00121225)
Timeframe: Up to 5 years

Interventionparticipants (Number)
Arm I2

Time to Progression Assessed by RECIST

(NCT00121225)
Timeframe: Up to 5 years

Interventionmonths (Median)
Arm 1 Vorinostat4

Difference in HP1 and MacroH2A Nuclear Foci Expression Between Progressive Minus Stable Disease Outcomes

Macro H2A and HP1 expression levels were compared through analysis of log fold changes in antibody expression in a multivariate general linear model between progressive disease and stable disease outcomes. (NCT00121225)
Timeframe: Baseline and day 15

Interventionlog fold change (Mean)
MacroH2A1.1MacroH2A1.2HP1
Arm 1 Vorinostat0.149-0.748-0.077

Number of Patients With p53 Allelic Variations (72R or 72P)

Participants were assessed for p53 allelic variation at baseline (NCT00121225)
Timeframe: Baseline

Interventionparticipants (Number)
Wild TypeMutant
Arm 1 Vorinostat2011

Trials

1 trial available for vorinostat and Dysplastic Nevus Syndrome, Hereditary

ArticleYear
Phase II trial of vorinostat in advanced melanoma.
    Investigational new drugs, 2014, Volume: 32, Issue:3

    Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Biomarkers; Disease-Free Survival; Female; Fi

2014

Other Studies

1 other study available for vorinostat and Dysplastic Nevus Syndrome, Hereditary

ArticleYear
Expression of DNA Methyltransferase 1 Is a Hallmark of Melanoma, Correlating with Proliferation and Response to B-Raf and Mitogen-Activated Protein Kinase Inhibition in Melanocytic Tumors.
    The American journal of pathology, 2020, Volume: 190, Issue:10

    Topics: Cell Line, Tumor; Cell Proliferation; DNA; Histone Deacetylase Inhibitors; Humans; Melanocytes; Mela

2020