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Targeted Therapies in Pheochromocytoma and Paraganglioma

Wang, Katharina (författare)
Ludwig Maximilian Univ Munich, Univ Hosp, Dept Internal Med 4, LMU Klinikum, D-80336 Munich, Germany.
Crona, Joakim (författare)
Uppsala universitet,Endokrin tumörbiologi
Beuschlein, Felix (författare)
Ludwig Maximilian Univ Munich, Univ Hosp, Dept Internal Med 4, LMU Klinikum, D-80336 Munich, Germany.;Univ Hosp Zurich USZ, Dept Endocrinol Diabetol & Clin Nutr, Ramistr 100, CH-8091 Zurich, Switzerland.;Univ Zurich UZH, Ramistr 100, CH-8091 Zurich, Switzerland.
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Grossman, Ashley B. (författare)
Univ Oxford, Green Templeton Coll, Oxford OX2 6HG, England.;Royal Free Hosp, ENETS Ctr Excellence, NET Unit, London NW3 2QG, England.
Pacak, Karel (författare)
Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, NIH, Bethesda, MD 20892 USA.
Nölting, Svenja (författare)
Ludwig Maximilian Univ Munich, Univ Hosp, Dept Internal Med 4, LMU Klinikum, D-80336 Munich, Germany.;Univ Hosp Zurich USZ, Dept Endocrinol Diabetol & Clin Nutr, Ramistr 100, CH-8091 Zurich, Switzerland.;Univ Zurich UZH, Ramistr 100, CH-8091 Zurich, Switzerland.
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Ludwig Maximilian Univ Munich, Univ Hosp, Dept Internal Med 4, LMU Klinikum, D-80336 Munich, Germany Endokrin tumörbiologi (creator_code:org_t)
2022-08-17
2022
Engelska.
Ingår i: Journal of Clinical Endocrinology and Metabolism. - : Oxford University Press. - 0021-972X .- 1945-7197. ; 107:11, s. 2963-2972
  • Forskningsöversikt (refereegranskat)
Abstract Ämnesord
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  • Molecular targeted therapy plays an increasingly important role in the treatment of metastatic pheochromocytomas and paragangliomas (PPGLs), which are rare tumors but remain difficult to treat. This mini-review provides an overview of established molecular targeted therapies in present use, and perspectives on those currently under development and evaluation in clinical trials. Recently published research articles, guidelines, and expert views on molecular targeted therapies in PPGLs are systematically reviewed and summarized. Some tyrosine kinase inhibitors (sunitinib, cabozantinib) are already in clinical use with some promising results, but without formal approval for the treatment of PPGLs. Sunitinib is the only therapeutic option which has been investigated in a randomized placebo-controlled clinical trial. It is clinically used as a first-, second-, or third-line therapeutic option for the treatment of progressive metastatic PPGLs. Some other promising molecular targeted therapies (hypoxia-inducible factor 2 alpha [HIF2 alpha] inhibitors, tumor vaccination together with checkpoint inhibitors, antiangiogenic therapies, kinase signaling inhibitors) are under evaluation in clinical trials. The HIF2 alpha inhibitor belzutifan may prove to be particularly interesting for cluster 1B-/VHL/EPAS1-related PPGLs, whereas antiangiogenic therapies seem to be primarily effective in cluster 1A-/SDHx-related PPGLs. Some combination therapies currently being evaluated in clinical trials, such as temozolomide/olaparib, temozolomide/talazoparib, or cabozantinib/atezolizumab, will provide data for novel therapy for metastatic PPGLs. It is likely that advances in such molecular targeted therapies will play an essential role in the future treatment of these tumors, with more personalized therapy options paving the way towards improved therapeutic outcomes.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

Nyckelord

molecular targeted therapy
metastatic
pheochromocytoma
paraganglioma

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