Pattern of solid and hematopoietic second malignancy after local therapy for prostate cancer

Abstract Background and purpose Second malignancies (SM) after external beam radiotherapy (EBRT) or brachytherapy (BT) for prostate cancer (PCa) are rare but serious sequelae. Materials and methods The Surveillance, Epidemiology, and End Results (SEER) database was used to identify men diagnosed wit...

Full description

Saved in:
Bibliographic Details
Published inRadiotherapy and oncology Vol. 123; no. 1; pp. 133 - 138
Main Authors Wang, Chenyang, King, Christopher R, Kamrava, Mitchell, Iwamoto, Keisuke S, Chen, Allen M, Low, Daniel, Kupelian, Patrick A, Steinberg, Michael L
Format Journal Article
LanguageEnglish
Published Ireland Elsevier B.V 01.04.2017
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Abstract Background and purpose Second malignancies (SM) after external beam radiotherapy (EBRT) or brachytherapy (BT) for prostate cancer (PCa) are rare but serious sequelae. Materials and methods The Surveillance, Epidemiology, and End Results (SEER) database was used to identify men diagnosed with cT1-2N0M0 PCa between 1999 and 2005, who underwent EBRT, BT or radical prostatectomy (RP). Patients with time interval to second malignancy or follow-up shorter than five and two years were excluded for solid and hematopoietic SM analyses respectively. Risks for solid and hematopoietic SM were evaluated via the multivariate Fine and Gray proportional hazards model. Results EBRT and BT resulted in similar increases in solid and hematopoietic SM compared to RP. In subgroup analysis stratified by treatment modality, only the EBRT cohort demonstrated significantly decreased solid and hematopoietic SM in years 2002–2005 compared to years 1999–2001, with adjusted-hazard ratios of 0.752 ( p = 0.001) and 0.815 ( p = 0.018) respectively. Conclusions EBRT and BT resulted in statistically equivalent increase in both solid and hematopoietic SM compared to RP. EBRT in more recent years resulted in significantly decreased solid and hematopoietic SM, coinciding with increased utilization of IMRT.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0167-8140
1879-0887
DOI:10.1016/j.radonc.2017.01.009