Men's health supplement use and outcomes in men receiving definitive intensity-modulated radiation therapy for localized prostate cancer

被引:2
|
作者
Zaorsky, Nicholas G. [1 ]
Churilla, Thomas M. [1 ]
Ruth, Karen [2 ]
Hayes, Shelly B. [1 ]
Sobczak, Mark L. [1 ]
Hallman, Mark A. [1 ]
Smaldone, Marc C. [3 ]
Chen, David Y. T. [3 ]
Horwitz, Eric M. [1 ]
机构
[1] Fox Chase Canc Ctr, Dept Radiat Oncol, 7701 Burholme Ave, Philadelphia, PA 19111 USA
[2] Fox Chase Canc Ctr, Biostat & Bioinformat Facil, 7701 Burholme Ave, Philadelphia, PA 19111 USA
[3] Fox Chase Canc Ctr, Dept Surg Oncol, 7701 Burholme Ave, Philadelphia, PA 19111 USA
来源
AMERICAN JOURNAL OF CLINICAL NUTRITION | 2016年 / 104卷 / 06期
关键词
complementary and alternative medicine; dietary supplements; men's health; prostate cancer; radiation therapy vitamins; multivitamins; saw palmetto; supplements; multi-ingredient nutritional supplements (MINS); DIETARY-SUPPLEMENT; DOSE-ESCALATION; SELENIUM SUPPLEMENTATION; COMPLEMENTARY MEDICINE; CONTROLLED-TRIAL; COMPETING RISK; SERENOA-REPENS; RADIOTHERAPY; PREVENTION; VITAMIN;
D O I
10.3945/ajcn.115.119958
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Approximately 50% of newly diagnosed cancer patients start taking dietary supplements. Men's health supplements (MHSs), which we define as supplements that are specifically marketed with the terms men's health and prostate health (or similar permutations), are often mislabeled as having potential anticancer benefits. Objective: We evaluated the effects of MHSs on patient outcomes and toxicities in patients who were undergoing definitive intensity modulated radiation therapy (IMRT) for localized prostate cancer. Design: This retrospective analysis included patients who were being treated at a National Cancer Institute designated comprehensive cancer center and consented to have information stored in a prospective database. MHSs were queried online. Outcome measures were freedom from biochemical failure (FFBF) (biochemical failure was defined with the use of the prostate-specific antigen nadir + 2-ng/mL definition), freedom from distant metastasis (FFDM), cancer-specific survival (CSS), and overall survival (OS) as well as toxicities. Kaplan-Meier analysis, log-rank tests, Fine and Gray competing-risk regression (to adjust for patient and lifestyle factors), and Cox models were used. Results: From 2001 to 2012, 2207 patients were treated with IMRT with a median dose of 78 Gy, and a median follow-up of 46 mo. Of these patients, 43% were low risk, 37% were intermediate risk, and 20% were high risk; 10% used MHSs. MHSs contained a median of 3 identifiable ingredients (range: 0-78 ingredients). Patients who were taking an MHS compared with those who were not had improved 5-y OS (97% compared with 92%, respectively; P = 0.01), but there were no differences in the FFBF (94% compared with 89%, respectively; P = 0.12), FFDM (96% compared with 97%, respectively; P = 0.32), or CSS (100% compared with 99%, respectively; P = 0.22). The unadjusted association between MHS use and improved OS was attenuated after adjustment for patient lifestyle factors and comorbidities. There was no difference in toxicities between the 2 groups (late-grade 3-4 genitourinary <3%; gastrointestinal <4%). Conclusion: The use of MHSs is not associated with outcomes or toxicities.
引用
收藏
页码:1583 / 1593
页数:11
相关论文
共 50 条
  • [21] Impact of obesity on outcomes after definitive dose-escalated intensity-modulated radiotherapy for localized prostate cancer
    Wang, Lora S.
    Murphy, Colin T.
    Ruth, Karen
    Zaorsky, Nicholas G.
    Smaldone, Marc C.
    Sobczak, Mark L.
    Kutikov, Alexander
    Viterbo, Rosalia
    Horwitz, Eric M.
    CANCER, 2015, 121 (17) : 3010 - 3017
  • [22] Long-term clinical and toxicity outcomes of hypofractionated intensity-modulated radiation therapy for clinically localized prostate cancer
    Kotecha, Rupesh
    Weller, Michael A.
    Marwaha, Gaurav
    Hearn, Jason
    Kupelian, Patrick
    Reddy, Chandana A.
    Ciezki, Jay P.
    Stephans, Kevin L.
    Tendulkar, Rahul D.
    JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (04)
  • [23] Initial results of the intensity-modulated radiation therapy for localized and locally advanced prostate cancer (IMRT)
    Kim, Youngjoo
    BJU INTERNATIONAL, 2015, 116 : 5 - 5
  • [24] Intensity-Modulated Radiation Therapy for Elderly Patients with Prostate Cancer: Evaluation of Outcomes and Safety
    Tanaka, H.
    Ito, M.
    Yamaguchi, T.
    Hachiya, K.
    Hyodo, F.
    Matsuo, M.
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2018, 102 (03): : E145 - E145
  • [25] Intensity-modulated radiation therapy: Supportive data for prostate cancer
    Cahlon, Oren
    Hunt, Margie
    Zelefsky, Michael J.
    SEMINARS IN RADIATION ONCOLOGY, 2008, 18 (01) : 48 - 57
  • [26] ePRO Use in Men Receiving Radiotherapy for Localized Prostate Cancer
    Kudel, I.
    Curry, H. A.
    Pennanen, P.
    Lahelma, M.
    Shamsi, Z.
    Barlund, M.
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2023, 117 (02): : E225 - E225
  • [27] Serum Testosterone Levels in Men Treated With Intensity Modulated Radiation Therapy for Prostate Cancer
    Markovina, S.
    Gay, H.
    DeWees, T.
    Weschenfelder, D.
    McCandless, A.
    Michalski, J.
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2012, 84 (03): : S415 - S415
  • [28] Re: Urologists' Use of Intensity-Modulated Radiation Therapy for Prostate Cancer Editorial Comment
    Taneja, Samir S.
    JOURNAL OF UROLOGY, 2014, 192 (03): : 765 - 766
  • [29] RapidArc Volumetric Modulated Therapy for Localized Prostate Cancer: Comparison with Intensity-modulated Radiotherapy
    Csiki, I.
    Crass, J.
    Ding, G.
    Coffey, C.
    Hallahan, D. H.
    Malcolm, A. M.
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2009, 75 (03): : S731 - S731
  • [30] Uptake and outcomes of intensity-modulated radiation therapy for uterine cancer
    Wright, Jason D.
    Deutsch, Israel
    Wilde, Elizabeth T.
    Ananth, Cande V.
    Neugut, Alfred I.
    Lewin, Sharyn N.
    Siddiq, Zainab
    Herzog, Thomas J.
    Hershman, Dawn L.
    GYNECOLOGIC ONCOLOGY, 2013, 130 (01) : 43 - 48