Related Experiment Video
Updated: Jul 10, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Intermittent versus continuous androgen suppression for prostatic cancer.
Intermittent androgen suppression (IAS) shows similar effectiveness to continuous androgen suppression (CAS) for prostate cancer, with potentially fewer adverse events like impotence. However, data are limited by small sample sizes and short study durations.
Area of Science:
- Urology
- Oncology
- Clinical Trials
Background:
- Prostate cancer is a leading cause of cancer death in men.
- Androgen suppression therapy (AST) is a standard treatment for advanced prostate cancer.
- The use of AST for early-stage disease is increasing despite limited evidence.
Purpose of the Study:
- To evaluate the effectiveness and safety of intermittent androgen suppression (IAS) compared to continuous androgen suppression (CAS) in prostate cancer treatment.
- To analyze outcomes including biochemical progression and adverse events.
Main Methods:
- Systematic review of randomized or quasi-randomized controlled trials.
- Searched databases: Cochrane Central Register of Controlled Trials, EMBASE, and LILACS.
- Two reviewers assessed study quality and extracted data.
Main Results:
- Five trials with 1382 patients were included, all focusing on advanced prostate cancer.
- No significant difference in biochemical progression for Gleason scores 4-10, but favored IAS for Gleason > 6.
- IAS showed a significant reduction in impotence compared to CAS, with no difference in other adverse events.
Conclusions:
- Limited data from small, short-duration trials restrict definitive conclusions on IAS vs. CAS effectiveness for survival or disease progression.
- IAS may offer a slight reduction in adverse events, particularly impotence.
- IAS appears as effective as CAS for potency, with superiority noted during treatment intervals.
Related Concept Videos
Drug Accumulation During Multiple Dosing: Intermittent IV Infusions
Oral Drug Delivery Systems: Continuous-Release Systems
Continuous Renal Replacement Therapy
Extracorporeal Removal of Drugs: Continuous Renal Replacement Therapy
Treatment Resistent Cancers
Treatment Resistant Cancers
