John B. A. G. Haanen focuses on Internal medicine, Melanoma, Immunology, Oncology and Surgery. His Clinical trial, Dacarbazine, Adverse effect and Performance status study in the realm of Internal medicine connects with subjects such as Pharmacogenetics. His work in the fields of Melanoma, such as Vemurafenib, intersects with other areas such as Placebo.
His study in Immunology is interdisciplinary in nature, drawing from both Cytotoxic T cell and Cancer. His research on Oncology also deals with topics like
His scientific interests lie mostly in Internal medicine, Oncology, Melanoma, Immunology and Immunotherapy. His work in Internal medicine is not limited to one particular discipline; it also encompasses Surgery. His Oncology research is multidisciplinary, incorporating elements of Advanced melanoma, Clinical trial, Phases of clinical research, Targeted therapy and Metastasis.
In the field of Melanoma, his study on Vemurafenib and Dabrafenib overlaps with subjects such as Stage IIIC. His Immunology research focuses on Cytotoxic T cell and how it connects with Major histocompatibility complex. John B. A. G. Haanen works mostly in the field of Ipilimumab, limiting it down to concerns involving Nivolumab and, occasionally, Toxicity and Pembrolizumab.
John B. A. G. Haanen spends much of his time researching Internal medicine, Melanoma, Oncology, Cancer research and Cancer. As part of his studies on Internal medicine, he frequently links adjacent subjects like Gastroenterology. His Melanoma research integrates issues from Targeted therapy, Clinical trial, Cohort and Systemic therapy.
The Oncology study combines topics in areas such as Pembrolizumab, Immunotherapy, Toxicity and Confidence interval. His Cancer research research includes elements of Cytotoxic T cell, Cytokine, Immune system and T-cell receptor. Many of his studies on Ipilimumab involve topics that are commonly interrelated, such as Nivolumab.
His primary scientific interests are in Internal medicine, Oncology, Cancer, Melanoma and Ipilimumab. John B. A. G. Haanen regularly ties together related areas like Viral load in his Internal medicine studies. He has included themes like Prospective cohort study, Hepatitis B virus and Hazard ratio in his Oncology study.
John B. A. G. Haanen combines subjects such as Epidemiology, Cohort study, Vaccination, Lung cancer and Pandemic with his study of Cancer. He interconnects T cell, Long term follow up and Complete response in the investigation of issues within Melanoma. His research integrates issues of Gastroenterology, Blockade, Cutaneous melanoma, Nivolumab and Cohort in his study of Ipilimumab.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Improved Survival with Ipilimumab in Patients with Metastatic Melanoma.
F. Stephen Hodi;Steven J. O'Day;David F. McDermott;Robert W. Weber.
The New England Journal of Medicine (2010)
Improved Survival with Vemurafenib in Melanoma with BRAF V600E Mutation
Paul B. Chapman;Axel Hauschild;Caroline Robert;John B. Haanen.
The New England Journal of Medicine (2011)
Overall Survival with Combined Nivolumab and Ipilimumab in Advanced Melanoma
Jedd D. Wolchok;Vanna Chiarion-Sileni;Rene Gonzalez;Piotr Rutkowski.
The New England Journal of Medicine (2017)
Interleukin 10 (IL-10) and viral IL-10 strongly reduce antigen-specific human T cell proliferation by diminishing the antigen-presenting capacity of monocytes via downregulation of class II major histocompatibility complex expression.
R de Waal Malefyt;J Haanen;H Spits;M G Roncarolo.
Journal of Experimental Medicine (1991)
Combined BRAF and MEK Inhibition versus BRAF Inhibition Alone in Melanoma
G.V. Long;D. Stroyakovskiy;H. Gogas;E. Levchenko.
The New England Journal of Medicine (2014)
Management of toxicities from immunotherapy: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up
J. B. A. G. Haanen;F. Carbonnel;C. Robert;K. M. Kerr.
Annals of Oncology (2017)
Avelumab plus Axitinib versus Sunitinib for Advanced Renal-Cell Carcinoma
Robert J. Motzer;Konstantin Penkov;John Haanen;Brian Rini.
The New England Journal of Medicine (2019)
Dabrafenib and trametinib versus dabrafenib and placebo for Val600 BRAF-mutant melanoma: a multicentre, double-blind, phase 3 randomised controlled trial
Georgina V. Long;Georgina V. Long;Daniil Stroyakovskiy;Helen Gogas;Evgeny Levchenko.
The Lancet (2015)
Safety and efficacy of vemurafenib in BRAFV600E and BRAFV600K mutation-positive melanoma (BRIM-3): extended follow-up of a phase 3, randomised, open-label study
Grant A McArthur;Paul B Chapman;Caroline Robert;James Larkin.
Lancet Oncology (2014)
Tumor Exome Analysis Reveals Neoantigen-Specific T-Cell Reactivity in an Ipilimumab-Responsive Melanoma
Nienke van Rooij;Marit M. van Buuren;Daisy Philips;Arno Velds.
Journal of Clinical Oncology (2013)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
Antoni van Leeuwenhoek Hospital
Antoni van Leeuwenhoek Hospital
Antoni van Leeuwenhoek Hospital
Royal Marsden NHS Foundation Trust
University of Duisburg-Essen
Antoni van Leeuwenhoek Hospital
University of Paris-Saclay
University of Zurich
University of Manchester
Queen Mary University of London
Johns Hopkins University
University of Hong Kong
William & Mary
Spanish National Research Council
Nanyang Technological University
École Polytechnique
Sao Paulo State University
Kyoto University
Purdue University West Lafayette
University of Lausanne
Peking University
University of the Balearic Islands
University of Maryland, Baltimore
Columbia University
Columbia University
Pennsylvania State University