1. Novel prognostic and predictive markers for systemic therapies in childhood and adult malignancies
2. Next-generation sequencing in diagnosis and monitoring of residual disease in myeloproliferative malignancies
3. The alterations of lipid metabolism in various mailignancies
4. Genetic and epigenetic features of selected human malignancies as a tool for early cancer detection and prediction of response to chemotherapy and immunotherapy
5. Liquid biopsy in solid tumours (circulating tumour cells, circulating tumour DNA, tumour educated platelets, exosomes) for early prognosis, prediction, and monitoring of treatment response
Coordinator #1 | Coordinator #2 | Coordinator #3 | |
---|---|---|---|
Name and surname | Anna Żaczek | Michał Bieńkowski | Marcin Skrzypski |
Academic degree | Prof. Dr. Habil. | Ph.D. | Dr. Habil. |
Employment unit | Laboratory of Translational Oncology | Department of Pathomorphology | Department of Oncology & Radiotherapy |
Polish Platform of Medical Research | Prof. Dr. Habil. Anna Żaczek | Michał Bieńkowski, Ph.D. | Dr. Habil. Marcin Skrzypski |
anna.zaczek@gumed.edu.pl | michal.bienkowski@gumed.edu.pl | marcin.skrzypski@gumed.edu.pl | |
Phone number | +48 58 523 63 20 | +48 58 349 37 40 | +48 58 584 45 10 |
photos Paweł Sudara/MUG
1. Liquid biopsy and cell free DNA for the assessment of response to treatment in patients with Hodgkin’s lymphoma
2. Clinical relevance of plasma metabolomics, educated blood platelets sequencing, tumour mutational burden and gene expression in NSCLC patients administered curative radiotherapy
3. Novel biochemical markers in predicting response to treatment in childhood acute lymphoblastic leukaemia
4. Epigenetic biomarkers for prediction of response to immunotherapy
5. Genetic features of Reed-Sternberg cells and their interplay with tumour-infiltrating macrophages in classical Hodgkin lymphoma: identification of drug resistance and disease relapse mechanisms
Funding agency/grant number | Title of the project | Years | |
---|---|---|---|
1. | Medical Research Agency/ RAFTING-2019/ 2019/ABM/01/00060 | Radiation-free therapy for the initial treatment of good prognosis early non-bulky HL, defined by a low metabolic tumour volume and a negative interim PET after 2 chemotherapy cycles | 2021-2026 |
2. | The Health Research Council of New Zealand/ 18/144 | Epigenomic profiling to predict patient response to melanoma immunotherapy | 2018-2021 |
3. | NCBiR (1st Polish-Chinese/Chinese-Polish Joint Research) WPC1/HESCAP/2019 | Highly efficient enrichment, single-cell analysis, and drug screening of circulating tumour cells for personalized medicine | 2019-2022 |
Foreign partner (unit name) | Principal investigator(s) | Area of cooperation | |
---|---|---|---|
1. | Mayo Clinic; Rochester, Minnesota; USA | Fergus J. Couch | Triple-negative breast cancer (a role of BARD1 gene in the pathogenesis of TNBC) |
2. | Laboratory of Pathology, National Cancer Institute, Bethesda, USA | Markku Miettinen; Jerzy Lasota | Molecular characterization of sarcomas |
3. | Brigham and Women’s Hospital, Harvard Medical School, USA | Mariana Castells | Mastocytosis, drug allergy |
4. | The Francis Crick Institute, UK | Charles Swanton | Prognostic gene expression signatures for early stage NSCLC patients |
5. | University College London, Cancer Institute, UK | Sergio Quezada; Charles Swanton | Immunological basis of cachexia and sarcopenia in long cancer |
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