TY - JOUR
T1 - Estetrol Prevents Hot Flushes and Improves Quality of Life in Patients with Advanced Prostate Cancer Treated with Androgen Deprivation Therapy
T2 - The PCombi Study
AU - Zimmerman, Yvette
AU - Frydenberg, Mark
AU - van Poppel, Hendrik
AU - van Moorselaar, R. Jeroen A.
AU - Roos, Erik P. M.
AU - Somford, Diederik M.
AU - Roeleveld, Ton A.
AU - de Haan, Tjard D.
AU - van Melick, Harm H. E.
AU - Reisman, Yacov
AU - Krijgh, Jan
AU - Debruyne, Frans M. J.
AU - Coelingh Bennink, Herjan J. T.
N1 - Funding Information: Financial disclosures: Herjan J.T. Coelingh Bennink certifies that all conflicts of interest, including specific financial interests and relationships and affiliations relevant to the subject matter or materials discussed in the manuscript (eg, employment/affiliation, grants or funding, consultancies, honoraria, stock ownership or options, expert testimony, royalties, or patents filed, received, or pending), are the following: Jeroen A. van Moorselaar has received grants and fees from Astellas, Ipsen, AstraZeneca, Bayer, and Janssen. Diederik M. Somford is an advisor/consultant for Astellas, Janssen, Bayer, and MSD; has received institutional research funding from Astellas, Besins, and the Dutch Cancer Society; and has performed contracted institutional research for Janssen, Eli Lilly, Astellas, Blue Earth Diagnostics, Bayer, SPL Medical, and QED Therapeutics. Frans M.J. Debruyne is a consultant for Pantarhei Oncology BV. Yvette Zimmerman is chief executive officer and a shareholder of Pantarhei Oncology. Jan Krijgh is chief medical officer of Pantarhei Oncology. Herjan J.T. Coelingh Bennink is president and a shareholder of Pantarhei Oncology, an affiliate of Pantarhei Bioscience BV. The remaining authors have nothing to disclose. Funding Information: Funding/Support and role of the sponsor: Funding for the study was provided by Pantarhei Oncology. The sponsor played a role in the design and conduct of the study, and in the collection, management, and analysis of the data. Employees of the sponsor participated in interpretation of the data; in preparation, review, and approval of the manuscript; and in the decision to submit the manuscript for publication. Publisher Copyright: © 2022 The Author(s)
PY - 2022/11/1
Y1 - 2022/11/1
N2 - Background: Androgen deprivation therapy (ADT) for prostate cancer (PCa) is accompanied by side effects affecting health-related quality of life (HRQL). Objective: To assess the effects of the fetal estrogen estetrol (E4) on symptoms related to estrogen and androgen deficiency, and on HRQL measured using the validated Functional Assessment of Cancer Therapy-Prostate (FACT-P) questionnaire. Design, setting, and participants: This was a phase 2, double-blind, randomized, placebo-controlled study in patients with advanced PCa. Intervention: Patients receiving ADT were randomly assigned at a 2:1 ratio to daily treatment with a high dose of E4 (HDE4; n = 41) or placebo (n = 21) for 24 wk. Outcome measurements and statistical analysis: The primary outcome was the effect of HDE4 cotreatment on hot flushes (HFs). Secondary outcomes were the Q-Man questionnaire for evaluation of the effect on estrogen and androgen deficiency symptoms, and the FACT-P questionnaire for evaluating HRQL. Results and limitations: At 24 wk, the number of patients experiencing HFs was significantly lower in the HDE4 group than in the placebo group (14.3% vs 60.0%; p < 0.001). HDE4 treatment was associated with lower incidence of night sweats, arthralgia, and fatigue, but more nipple tenderness and gynecomastia. At 24 wk, the mean HRQL score favored HDE4 over placebo for the FACT-P total score (122.2 ± 12.3 vs 118.7 ± 19.7) and for several other FACT subscales. Conclusions: Daily HDE4 coadministration almost completely prevented HFs in patients with advanced PCa treated with ADT. HDE4 also had positive effects on HRQL and counteracted other estrogen deficiency symptoms caused by ADT. These data support the dual efficacy concept of ADT and HDE4 to improve HRQL and increase the antitumor effect of ADT. Patient summary: For patients on androgen deprivation therapy for advanced prostate cancer, cotreatment with a high dose of estetrol almost completely prevents the occurrence of hot flushes and improves quality of life and well-being, but nipple sensitivity and an increase in breast size may occur.
AB - Background: Androgen deprivation therapy (ADT) for prostate cancer (PCa) is accompanied by side effects affecting health-related quality of life (HRQL). Objective: To assess the effects of the fetal estrogen estetrol (E4) on symptoms related to estrogen and androgen deficiency, and on HRQL measured using the validated Functional Assessment of Cancer Therapy-Prostate (FACT-P) questionnaire. Design, setting, and participants: This was a phase 2, double-blind, randomized, placebo-controlled study in patients with advanced PCa. Intervention: Patients receiving ADT were randomly assigned at a 2:1 ratio to daily treatment with a high dose of E4 (HDE4; n = 41) or placebo (n = 21) for 24 wk. Outcome measurements and statistical analysis: The primary outcome was the effect of HDE4 cotreatment on hot flushes (HFs). Secondary outcomes were the Q-Man questionnaire for evaluation of the effect on estrogen and androgen deficiency symptoms, and the FACT-P questionnaire for evaluating HRQL. Results and limitations: At 24 wk, the number of patients experiencing HFs was significantly lower in the HDE4 group than in the placebo group (14.3% vs 60.0%; p < 0.001). HDE4 treatment was associated with lower incidence of night sweats, arthralgia, and fatigue, but more nipple tenderness and gynecomastia. At 24 wk, the mean HRQL score favored HDE4 over placebo for the FACT-P total score (122.2 ± 12.3 vs 118.7 ± 19.7) and for several other FACT subscales. Conclusions: Daily HDE4 coadministration almost completely prevented HFs in patients with advanced PCa treated with ADT. HDE4 also had positive effects on HRQL and counteracted other estrogen deficiency symptoms caused by ADT. These data support the dual efficacy concept of ADT and HDE4 to improve HRQL and increase the antitumor effect of ADT. Patient summary: For patients on androgen deprivation therapy for advanced prostate cancer, cotreatment with a high dose of estetrol almost completely prevents the occurrence of hot flushes and improves quality of life and well-being, but nipple sensitivity and an increase in breast size may occur.
KW - Advanced prostate cancer
KW - Androgen deprivation therapy
KW - Estetrol
KW - Estrogen deficiency
KW - Health-related quality of life
KW - Hot flushes
KW - PCombi trial
UR - http://www.scopus.com/inward/record.url?scp=85139324568&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.euros.2022.09.006
DO - https://doi.org/10.1016/j.euros.2022.09.006
M3 - Article
C2 - 36353657
SN - 2666-1691
VL - 45
SP - 59
EP - 67
JO - European urology open science
JF - European urology open science
ER -