Comparison of Oncological Outcomes of Conventional Androgen Deprivation Therapy (ADT) and ADT Plus Androgen Receptor Signaling Inhibitor in Older Patients With Metastatic Castration-Sensitive Prostate Cancer.
1/5 보강
[OBJECTIVES] Evidence on upfront androgen receptor signaling inhibitor (ARSI) plus androgen deprivation therapy (ADT) in the older population with metastatic castration-sensitive prostate cancer (mCSP
- p-value p < 0.05
APA
Yamamoto Y, Fujimoto S, et al. (2025). Comparison of Oncological Outcomes of Conventional Androgen Deprivation Therapy (ADT) and ADT Plus Androgen Receptor Signaling Inhibitor in Older Patients With Metastatic Castration-Sensitive Prostate Cancer.. International journal of urology : official journal of the Japanese Urological Association, 32(11), 1650-1659. https://doi.org/10.1111/iju.70202
MLA
Yamamoto Y, et al.. "Comparison of Oncological Outcomes of Conventional Androgen Deprivation Therapy (ADT) and ADT Plus Androgen Receptor Signaling Inhibitor in Older Patients With Metastatic Castration-Sensitive Prostate Cancer.." International journal of urology : official journal of the Japanese Urological Association, vol. 32, no. 11, 2025, pp. 1650-1659.
PMID
40813756 ↗
Abstract 한글 요약
[OBJECTIVES] Evidence on upfront androgen receptor signaling inhibitor (ARSI) plus androgen deprivation therapy (ADT) in the older population with metastatic castration-sensitive prostate cancer (mCSPC) is scarce. We aimed to compare the oncological outcomes of ARSI plus ADT (upfront doublet therapy) and conventional ADT in mCSPC patients aged ≥ 75 years in a real-world clinical practice.
[METHODS] Subjects were mCSPC patients aged ≥ 75 years who received upfront doublet therapy (upfront doublet group) or ADT, either alone or in combination with bicalutamide (conventional ADT group) as a first-line systemic therapy. Castration-resistant prostate cancer-free survival (CRPC-FS), overall survival (OS), and cancer-specific survival (CSS) were analyzed. Propensity score matching (PSM) was used to adjust the clinicopathological features.
[RESULTS] After PSM, a total of 200 mCSPC patients, 100 in the upfront doublet group and 100 in the conventional ADT group, were included. In the PSM population, median CRPC-FS was 30.8 months in the upfront doublet group and 12.1 months in the conventional ADT group (p < 0.05). Median OS was N.A. in the upfront doublet group and 45.2 months in the conventional ADT group (p < 0.05). Median CSS was also statistically different between the two groups (N.A. vs. 61.6 months; p < 0.05). In subgroup analyses, the upfront doublet group showed improved oncological outcomes in high-volume disease compared with the conventional ADT group, but not in low-volume disease.
[CONCLUSIONS] The oncological benefits of upfront doublet therapy are not diminished in mCSPC patients, even in the older population; but these benefits are limited when restricted to low-volume disease.
[METHODS] Subjects were mCSPC patients aged ≥ 75 years who received upfront doublet therapy (upfront doublet group) or ADT, either alone or in combination with bicalutamide (conventional ADT group) as a first-line systemic therapy. Castration-resistant prostate cancer-free survival (CRPC-FS), overall survival (OS), and cancer-specific survival (CSS) were analyzed. Propensity score matching (PSM) was used to adjust the clinicopathological features.
[RESULTS] After PSM, a total of 200 mCSPC patients, 100 in the upfront doublet group and 100 in the conventional ADT group, were included. In the PSM population, median CRPC-FS was 30.8 months in the upfront doublet group and 12.1 months in the conventional ADT group (p < 0.05). Median OS was N.A. in the upfront doublet group and 45.2 months in the conventional ADT group (p < 0.05). Median CSS was also statistically different between the two groups (N.A. vs. 61.6 months; p < 0.05). In subgroup analyses, the upfront doublet group showed improved oncological outcomes in high-volume disease compared with the conventional ADT group, but not in low-volume disease.
[CONCLUSIONS] The oncological benefits of upfront doublet therapy are not diminished in mCSPC patients, even in the older population; but these benefits are limited when restricted to low-volume disease.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
- Humans
- Male
- Aged
- Androgen Antagonists
- 80 and over
- Prostatic Neoplasms
- Castration-Resistant
- Retrospective Studies
- Nitriles
- Tosyl Compounds
- Anilides
- Androgen Receptor Antagonists
- Treatment Outcome
- Antineoplastic Combined Chemotherapy Protocols
- Propensity Score
- conventional androgen deprivation therapy
- metastatic castration‐sensitive prostate cancer
- older population
- upfront doublet therapy
같은 제1저자의 인용 많은 논문 (5)
- Overcoming Trastuzumab-Pertuzumab Resistance and Optimizing Sequential Anti-HER2 Therapy in HER2-Positive Metastatic Breast Cancer.
- Nephrotoxicity and associated risk factors in patients treated with pemetrexed.
- Utility of Laparoscopic Distal Pancreatectomy Following Esophagectomy With Gastric Roll Reconstruction Through the Retrosternal Route.
- Prognostic Impact of Pancreatic Body/Tail Cancer Involving the Portal Vein: A Project Study of the Japanese Society of Hepato-Biliary-Pancreatic Surgery.
- Impact of biliary drainage method before pancreaticoduodenectomy on short- and long-term outcomes in patients with periampullary carcinoma and obstructive jaundice: A multicenter retrospective analysis.
🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반
- A Phase I Study of Hydroxychloroquine and Suba-Itraconazole in Men with Biochemical Relapse of Prostate Cancer (HITMAN-PC): Dose Escalation Results.
- Self-management of male urinary symptoms: qualitative findings from a primary care trial.
- Clinical and Liquid Biomarkers of 20-Year Prostate Cancer Risk in Men Aged 45 to 70 Years.
- Diagnostic accuracy of Ga-PSMA PET/CT versus multiparametric MRI for preoperative pelvic invasion in the patients with prostate cancer.
- Comprehensive analysis of androgen receptor splice variant target gene expression in prostate cancer.
- Clinical Presentation and Outcomes of Patients Undergoing Surgery for Thyroid Cancer.