Patients' preference in androgen deprivation therapy

Abstract

Huggins et al. introduced surgical castration for prostate cancer treatment in 1941. Currently, androgen deprivation therapy (ADT) is key in treating advanced prostate cancer, especially in elderly patients. With the development of gonadotropin-releasing hormone (GnRH) medications, ADT transitioned from surgical to medical castration. From 1985 onwards, various GnRH agonists like Leuprorelin and Goserelin acetate have been used as ADT for prostate cancer. By 2012, a GnRH antagonist, degarelix, was introduced in Japan. A study at Yokohama City University Medical Center analyzed 851 hormonal injections between August 2018 and February 2019. It assessed the duration from prescription to injection completion and the perceived physical and mental load on patients. Results showed degarelix injections took significantly longer than other treatments. Leuprorelin 22.5mg reduced hospital stays the most, largely due to its 6-month duration and kit formulation. The lengthy process for degarelix, which requires drug dilution and cooling at the injection site due to potential skin reactions, increases its administration time. Concerning patient burden, leuprorelin 22.5mg ranked the lowest, with little variance from the oral form. A limitation of this study is the administration method of leuprorelin in Japan, which differs from other countries. In summary, the 6-month leuprorelin 22.5mg regimen minimizes hospital time, while degarelix tends to cause the most discomfort for patients.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This study did not receive any funding

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

IRB of Yokohama City University Medical Center gave ethical approval for this work

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the authors

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