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Medicine and Health Sciences Commons

Open Access. Powered by Scholars. Published by Universities.®

Medical Specialties

2018

Edith Cowan University

Uveal melanoma

Articles 1 - 2 of 2

Full-Text Articles in Medicine and Health Sciences

Ipilimumab Activity In Advanced Uveal Melanoma: A Pooled Analysis, Muhammad A. Khattak, Elin Gray Jan 2018

Ipilimumab Activity In Advanced Uveal Melanoma: A Pooled Analysis, Muhammad A. Khattak, Elin Gray

Research outputs 2014 to 2021

Background

Uveal Melanoma is a rare tumour that displays different clinical behavior and molecular features compared with cutaneous melanoma. It is generally resistant to systemic therapy and there is no current standard effective therapy to treat patients with advanced disease.

Patients and methods

We searched Medline, PubMed, EMBASE and major oncology conference abstracts from the past 5 years to identify relevant studies evaluating ipilimumab monotherapy in uveal melanoma. Data were extracted on ipilimumab dose, sample size, Objective Response Rate (ORR), Progression Free Survival (PFS), median Overall Survival (mOS), Disease Control Rate (DCR), 1 year Overall Survival (1yrOS) and 2 year …


Clinical Application Of Circulating Tumor Cells And Circulating Tumor Dna In Uveal Melanoma, Aaron Beasley, Timothy Isaacs, Muhammad K. Khattak, James B. Freeman, Richard Allcock, Fred K. Chen, Michelle R. Pereira, Kyle Yau, Jaqueline Bentel, Tersia Vermeulen, Leslie Calapre, Michael Millward, Melanie R. Ziman, Elin S. Gray Jan 2018

Clinical Application Of Circulating Tumor Cells And Circulating Tumor Dna In Uveal Melanoma, Aaron Beasley, Timothy Isaacs, Muhammad K. Khattak, James B. Freeman, Richard Allcock, Fred K. Chen, Michelle R. Pereira, Kyle Yau, Jaqueline Bentel, Tersia Vermeulen, Leslie Calapre, Michael Millward, Melanie R. Ziman, Elin S. Gray

Research outputs 2014 to 2021

Purpose To evaluate the feasibility of using circulating tumor cells (CTCs) and circulating tumor DNA (ctDNA) for the management of uveal melanoma (UM).

Patients and Methods Low-coverage whole-genome sequencing was used to determine somatic chromosomal copy number alterations (SCNAs) in primary UM tumors, ctDNA, and whole-genome amplified CTCs. CTCs were immunocaptured using an antimelanoma-associated chondroitin sulfate antibody conjugated to magnetic beads and immunostained for melanoma antigen recognised by T cells 1 (MART1)/glycoprotein 100 (gp100)/S100 calcium-binding protein β (S100β). ctDNA was quantified using droplet digital polymerase chain reaction assay for mutations in the GNAQ, GNA11, PLCβ4, and CYSLTR2 …