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A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
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Pattern of solid and hematopoietic second malignancy after local therapy for prostate cancer
Chenyang Wang1, Christopher R King1, Mitchell Kamrava1
1Department of Radiation Oncology, University of California, Los Angeles, Los Angeles, CA, United States.
Summary
Second malignancies (SM) are rare after prostate cancer (PCa) radiation. External beam radiotherapy (EBRT) and brachytherapy (BT) showed similar SM risks compared to radical prostatectomy (RP), but recent EBRT use decreased these risks.
Area of Science:
- Oncology
- Radiation Oncology
- Cancer Epidemiology
Background:
- Second malignancies (SM) are rare but serious risks following prostate cancer (PCa) treatment.
- External beam radiotherapy (EBRT) and brachytherapy (BT) are common PCa treatments with potential long-term sequelae.
Purpose of the Study:
- To evaluate the risk of SM after EBRT, BT, or radical prostatectomy (RP) for localized PCa.
- To compare SM incidence across different treatment modalities and over time.
Main Methods:
- Utilized the Surveillance, Epidemiology, and End Results (SEER) database for PCa patients diagnosed 1999-2005.
- Applied multivariate Fine and Gray proportional hazards models to assess risks for solid and hematopoietic SM.
- Excluded patients with short follow-up periods to ensure robust analysis.
Main Results:
- EBRT and BT demonstrated similar increased risks for both solid and hematopoietic SM compared to RP.
- A significant decrease in solid and hematopoietic SM was observed for EBRT in more recent years (2002-2005) versus earlier years (1999-2001).
- Adjusted hazard ratios indicated a protective effect of recent EBRT utilization against SM.
Conclusions:
- EBRT and BT carry statistically equivalent risks for SM compared to RP.
- The observed reduction in SM with recent EBRT use may be linked to advancements like Intensity-Modulated Radiation Therapy (IMRT).
- Further research into treatment evolution and its impact on long-term cancer survivorship is warranted.

