Literature DB >> 18407326

Testosterone surge: rationale for gonadotropin-releasing hormone blockers?

Hendrik van Poppel1, Sten Nilsson.   

Abstract

Gonadotropin-releasing hormone (GnRH) agonists currently form the mainstay of management of advanced prostate cancer. They effectively suppress serum testosterone levels, which in turn inhibits tumor growth. However, the initial response to GnRH agonists is a transient increase in the serum testosterone levels. Known as a testosterone surge, this can lead to a worsening of symptoms and can adversely affect survival. Therefore, much interest exists in the development of a new class of drugs-GnRH antagonists-which produce immediate suppression of luteinizing hormone and testosterone without a testosterone surge. The most promising GnRH antagonist to date is degarelix.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18407326     DOI: 10.1016/j.urology.2007.12.070

Source DB:  PubMed          Journal:  Urology        ISSN: 0090-4295            Impact factor:   2.649


  37 in total

1.  The hypothalamic-pituitary-gonadal axis and prostate cancer: implications for androgen deprivation therapy.

Authors:  Luis A Kluth; Shahrokh F Shariat; Christian Kratzik; Scott Tagawa; Guru Sonpavde; Malte Rieken; Douglas S Scherr; Karl Pummer
Journal:  World J Urol       Date:  2013-09-03       Impact factor: 4.226

Review 2.  Pharmacotherapeutic Targeting of G Protein-Coupled Receptors in Oncology: Examples of Approved Therapies and Emerging Concepts.

Authors:  Rosamaria Lappano; Marcello Maggiolini
Journal:  Drugs       Date:  2017-06       Impact factor: 9.546

Review 3.  Sex steroid ablation: an immunoregenerative strategy for immunocompromised patients.

Authors:  E Velardi; J A Dudakov; M R M van den Brink
Journal:  Bone Marrow Transplant       Date:  2015-06       Impact factor: 5.483

4.  Gonadotropin-releasing hormone blockers and cardiovascular disease risk: analysis of prospective clinical trials of degarelix.

Authors:  Matthew R Smith; Laurence Klotz; Egbert van der Meulen; Enrico Colli; László B Tankó
Journal:  J Urol       Date:  2011-09-25       Impact factor: 7.450

Review 5.  Degarelix versus luteinizing hormone-releasing hormone agonists for the treatment of prostate cancer.

Authors:  Timothy N Clinton; Solomon L Woldu; Ganesh V Raj
Journal:  Expert Opin Pharmacother       Date:  2017-05-19       Impact factor: 3.889

Review 6.  Role of steroid receptor and coregulator mutations in hormone-dependent cancers.

Authors:  Anna C Groner; Myles Brown
Journal:  J Clin Invest       Date:  2017-04-03       Impact factor: 14.808

7.  ARv7 Represses Tumor-Suppressor Genes in Castration-Resistant Prostate Cancer.

Authors:  Laura Cato; Jonas de Tribolet-Hardy; Irene Lee; Jaice T Rottenberg; Ilsa Coleman; Diana Melchers; René Houtman; Tengfei Xiao; Wei Li; Takuma Uo; Shihua Sun; Nane C Kuznik; Bettina Göppert; Fatma Ozgun; Martin E van Royen; Adriaan B Houtsmuller; Raga Vadhi; Prakash K Rao; Lewyn Li; Steven P Balk; Robert B Den; Bruce J Trock; R Jeffrey Karnes; Robert B Jenkins; Eric A Klein; Elai Davicioni; Friederike J Gruhl; Henry W Long; X Shirley Liu; Andrew C B Cato; Nathan A Lack; Peter S Nelson; Stephen R Plymate; Anna C Groner; Myles Brown
Journal:  Cancer Cell       Date:  2019-02-14       Impact factor: 31.743

8.  Experience with degarelix in the treatment of prostate cancer.

Authors:  Neal D Shore
Journal:  Ther Adv Urol       Date:  2013-02

Review 9.  AR function in promoting metastatic prostate cancer.

Authors:  Michael A Augello; Robert B Den; Karen E Knudsen
Journal:  Cancer Metastasis Rev       Date:  2014-09       Impact factor: 9.264

Review 10.  Starving the addiction: new opportunities for durable suppression of AR signaling in prostate cancer.

Authors:  Karen E Knudsen; Howard I Scher
Journal:  Clin Cancer Res       Date:  2009-07-28       Impact factor: 12.531

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.