← back to search

Alicia Okines

Royal Marsden NHS Foundation Trust · GB
Area of research
Pulmonary and Respiratory Medicine · Oncology
Research interest
Research interests include HER2/EGFR in Cancer Research, Cancer Genomics and Diagnostics, Advanced Breast Cancer Therapies, and Gastric Cancer Management and Outcomes.
h-index
41
citations
12,857
works
269
NIH funding
primary concept
Medicine
email

Recent publications

Efficacy and Safety of Oral Progestogens (Megestrol Acetate and Medroxyprogesterone Acetate) in Heavily Pretreated Oestrogen Receptor-Positive Metastatic Breast Cancer: A 10-Year Multi-Site Study.
2026cited by 0position: contributordoi
LOX Inhibition Disrupts a Collagen-Integrin-MYC Axis to Suppress Progression of Invasive Lobular Carcinoma.
2026cited by 0position: contributordoi
UK real-world evidence on pembrolizumab and neoadjuvant chemotherapy for early-stage triple-negative breast cancer
ESMO Real World Data and Digital Oncology 2026cited by 0position: contributordoi
HER2CLIMB-05: A Phase III Study of Tucatinib Versus Placebo in Combination With Trastuzumab and Pertuzumab as First-Line Maintenance Therapy for HER2+ Metastatic Breast Cancer.
2025cited by 2position: contributordoi
Abstract GS01-10: HER2CLIMB-02: Randomized, Double-Blind Phase 3 Trial of Tucatinib and Trastuzumab Emtansine for Previously Treated HER2-Positive Metastatic Breast Cancer
Cancer Research 2024cited by 34position: middledoi
Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer.
2024cited by 33position: contributordoi
Resistance to Targeted Inhibitors of the PI3K/AKT/mTOR Pathway in Advanced Oestrogen-Receptor-Positive Breast Cancer.
2024cited by 23position: contributordoi
Real world study of sacituzumab govitecan in metastatic triple-negative breast cancer in the United Kingdom.
2024cited by 23position: contributordoi
The Clinical Features and Outcomes of Pseudocirrhosis in Breast Cancer.
2024cited by 2position: contributordoi
Supplementary Table S4 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Figure S1 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Table S6 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Table S1 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Table S2 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Table S4 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Figure S2 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Data from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Table S5 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Data from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Table S5 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Table S3 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Table S1 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Figure S2 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Figure S1 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Table S2 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Table S3 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Supplementary Table S6 from Comparison of Circulating Tumor DNA Assays for Molecular Residual Disease Detection in Early-Stage Triple-Negative Breast Cancer
2024cited by 0position: contributordoi
Tucatinib and Trastuzumab for Previously Treated Human Epidermal Growth Factor Receptor 2–Positive Metastatic Biliary Tract Cancer (SGNTUC-019): A Phase II Basket Study
Journal of Clinical Oncology 2023cited by 98position: middledoi
Tucatinib and Trastuzumab for Previously Treated Human Epidermal Growth Factor Receptor 2-Positive Metastatic Biliary Tract Cancer (SGNTUC-019): A Phase II Basket Study.
2023cited by 76position: contributordoi
Systemic Therapy for Metastatic Triple Negative Breast Cancer: Current Treatments and Future Directions.
2023cited by 18position: contributordoi

Grants

No grants ingested yet.

Frequent collaborators

· 45 papers (2021–2026) · 33 papers (2020–2023)Michael Hubank · Genomics (United Kingdom)18 papers (2020–2023)Alex Pearson · University of California, Santa Cruz18 papers (2020–2023) · 18 papers (2020–2023) · 18 papers (2021–2024)Iain R. Macpherson · University of Dundee18 papers (2021–2024)Anne Armstrong · University of Manchester18 papers (2020–2023)Emma Hall · University of Glasgow17 papers (2021–2023) · 17 papers (2021–2023) · 17 papers (2021–2023)Timothy A. Yap · The University of Texas MD Anderson Cancer Center17 papers (2021–2023)Karen E. Swales · Institute of Cancer Research17 papers (2021–2023)Maria Teresa Herrera-Abreu · 17 papers (2021–2023)Ruth Ruddle · Institute of Cancer Research17 papers (2021–2023)Clare M. Isacke · Institute of Cancer Research16 papers (2021–2023)Adam Mills · Institute of Cancer Research15 papers (2022–2023)Andrew Tutt · Breast Cancer Now15 papers (2022–2023)Marjan Iravani · King's College London15 papers (2022–2023) · 15 papers (2022–2023)