|INVITED RESEARCH HIGHLIGHT
|Year : 2021 | Volume
| Issue : 3 | Page : 229-230
Relugolix as a promising novel oral GnRH antagonist for prostate cancer treatment
Jialu Lv1, Jianqing Lin2
1 Ningbo University Medical School, Ningbo 315211, China
2 The George Washington University School of Medicine and Health Sciences, Washington, DC 20037, USA
|Date of Submission||31-Aug-2020|
|Date of Acceptance||27-Sep-2020|
|Date of Web Publication||24-Nov-2020|
The George Washington University School of Medicine and Health Sciences, Washington, DC 20037
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Lv J, Lin J. Relugolix as a promising novel oral GnRH antagonist for prostate cancer treatment. Asian J Androl 2021;23:229-30
|How to cite this URL:|
Lv J, Lin J. Relugolix as a promising novel oral GnRH antagonist for prostate cancer treatment. Asian J Androl [serial online] 2021 [cited 2021 Sep 19];23:229-30. Available from: https://www.ajandrology.com/text.asp?2021/23/3/229/301469 - DOI: 10.4103/aja.aja_77_20
Continuous androgen deprivation therapy (ADT) is the mainstay of treatment for metastatic prostate cancer. Both injectable luteinizing hormone–releasing hormone (LHRH) agonists and antagonists (here LHRH interchangeable to gonadotropin-releasing hormone, GnRH) are the current standard of care for ADT in prostate cancer. The novel oral form of effective GnRH antagonist is a very promising alternative to the current landscape of ADT.
Most recently, a Phase III trial comparing oral GnRH antagonist relugolix (120 mg orally once daily) with leuprolide (injections every 3 months) in advanced prostate cancer was completed and published. The primary objective of the study was to compare the ability of these agents' sustained testosterone suppression to castrate levels (<50 ng dl−1) through a 48-week study period. Relugolix achieved rapid (compatible to another GnRH antagonist degarelix) castration level of testosterone that was superior to that with leuprolide, also very importantly, with a 54% lower risk of major adverse cardiovascular events (MACEs). Other side effects of relugolix were mild and expected. With final approval pending from regulatory agencies, this oral agent could be favored by both providers and patients and represent a very promising addition to the current prostate cancer treatment landscape.
Currently, degarelix is the only LHRH antagonist, while there are a few LHRH agonists in the USA market. These include leuprolide (in the formula of Eligard, Lupron Depot, etc.); goserelin (Zoladex); triptorelin (Trelstar); and histrelin (Vantas). Compared to LHRH agonists, degarelix has a pharmacological profile more closely matching orchiectomy, with an immediate onset of action and faster testosterone and prostate-specific antigen suppression, without a testosterone surge or microsurges. As a consequence, with this GnRH blocker, there is no risk of clinical flare and no need for concomitant antiandrogen flare protection. In addition to this pharmacodynamic advantage, degarelix likely has less cardiovascular side effects than LHRH agonist. A prospective Phase IIIb trial (PRONOUNCE, ClinicalTrials.gov NCT02663908) designed to compare the occurrence of MACE in patients with advanced prostate cancer and preexisting atherosclerotic cardiovascular disease receiving either a degarelix or a GnRH agonist (leuprolide) as ADT for 12 months was launched but on hold now after a feasibility analysis. However, pooled data from six Phase III prospective randomized trials that recruited 2328 men between 2005 and 2012 showed that among men with preexisting cardiovascular disease, the risk of cardiovascular events within 1 year of initiating therapy was significantly lower among men treated with a GnRH antagonist compared with those treated with a GnRH agonist (hazard ratio: 0.44; 95% confidence interval: 0.26–0.74; P = 0.002). Overall, these cardiovascular adverse event data of degarelix match well with that of relugolix based on a recent study [Table 1].
|Table 1: Cardiovascular complications post 1 year of ADT: MACE (%) in prospective trials|
Click here to view
Despite the advantages mentioned above, compared to LHRH agonist, degarelix is still less utilized probably due to the injection-site reaction, the requirement of monthly administration, and the less profit in practice. To seek an oral alternative seems very reasonable.
Oral medicine is one of the main methods for disease prevention and treatment because of its convenience and comfort, which leads to compliance. For patients who need treatment for many years, the oral format would be ideal. Even in the state of metastatic prostate cancer, the overall survival now could reach 9 years or 10 years thanks to a variety of therapeutic armamentaria including second-generation novel androgen receptor (AR) signaling inhibitors.,, Clinical trial data support the earlier use of these agents to improve prostate cancer-specific survival. These novel AR agents are able to achieve deep androgen suppression or near-completely blocking AR which is beneficial for cardiovascular function. In theory, the longer the duration of ADT, or the deeper the androgen suppression, the higher the chance of cardiovascular adverse events. In the setting of deep androgen suppression, there is no data about difference in MACE related to the use between LHRH agonists and degarelix. We would assume that using LHRH antagonist in combination with novel AR agents maybe safer.
In summary, both injectable GnRH antagonists and agonists are the current standard of care for ADT in prostate cancer. Compared to GnRH agonist, the antagonist degarelix has less cardiovascular side effects. An oral format of antagonist relugolix is recently studied in a prospective randomized Phase III trial showing similar pharmacodynamic effects to that of degarelix. More importantly, compared to leuprolide, relugolix causes less cardiovascular adverse events. Considering its convenience, efficacy, and potentially less long-term side effects, relugolix is a very promising addition and likely preferable in the current androgen deprivation therapy in prostate cancer.
| Author Contributions|| |
J Lv and J Lin contributed equally. Both authors reviewed the literature, drafted, read and approved the final manuscript.
| Competing Interests|| |
Both authors declare no competing interests.
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