Influence of androgen suppression therapy for prostate cancer on the frequency and timing of fatal myocardial infarctions

被引:410
作者
D'Amico, Anthony V.
Denham, James W.
Crook, Juanita
Chen, Ming-Hui
Goldhaber, Samuel Z.
Lamb, David S.
Joseph, David
Tai, Keen-Hun
Malone, Shawn
Ludgate, Charles
Steigler, Allison
Kantoff, Philip W.
机构
[1] Brigham & Womens Hosp, Dept Radiat Oncol, Boston, MA 02215 USA
[2] Brigham & Womens Hosp, Dept Med, Div Cardiol, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Lank Ctr Genitourinary Oncol, Boston, MA 02115 USA
[4] Univ Connecticut, Dept Radiat Oncol, Storrs, CT USA
[5] Univ Connecticut, Dept Stat, Storrs, CT 06269 USA
[6] Newcastle Mater Hosp, Trans Tasman Radiat Oncol Grp, Newcastle, NSW, Australia
[7] Peter MacCallum Canc Inst, Dept Radiat Oncol, Melbourne, Vic 3000, Australia
[8] Princess Margaret Hosp, Toronto, ON M4X 1K9, Canada
[9] Ottawa Reg Canc Ctr, Dept Radiat Oncol, Ottawa, ON K1Y 4K7, Canada
[10] Vancouver Isl Canc Ctr, Dept Radiat Oncol, Vancouver, BC, Canada
[11] Wellington Hosp, Dept Radiat Oncol, Wellington, New Zealand
关键词
D O I
10.1200/JCO.2006.09.3369
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose We evaluated whether the timing of fatal myocardial infarction (MI) was influenced by the administration of androgen suppression therapy (AST). Patients and Methods The study cohort comprised 1,372 men who were enrolled onto three randomized trials between February 1995 and June 2001. In the three trials, the men were randomly assigned to receive radiation therapy with 0 versus 3 versus 6, 3 versus 8, or 0 versus 6 months of AST. Fine and Gray's regression was used to determine the clinical factors associated with the time to fatal MI, and estimates of time to fatal MI were calculated using a cumulative incidence method. When comparing the cumulative incidence estimates using Gray's k-sample P values, increased weight was ascribed to the earlier data because recovery of testosterone is expected for most men within 2 years after short-course AST. Results Men age 65 years or older who received 6 months of AST experienced shorter times to fatal MIs compared with men in this age group who did not receive AST (P = .017) and men younger than 65 years (P = .016). No significant difference (P = .97) was observed in the time to fatal MIs in men age 65 years or older who received 6 to 8 months of AST compared with 3 months of AST. Conclusion The use of AST is associated with earlier onset of fatal MIs in men age 65 years or older who are treated for 6 months compared with men who are not treated with AST.
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页码:2420 / 2425
页数:6
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