Prognostic value of testosterone for the castration-resistant prostate cancer patients: a systematic review and meta-analysis
Jazyk angličtina Země Japonsko Médium print-electronic
Typ dokumentu časopisecké články, metaanalýza, systematický přehled
PubMed
32681382
PubMed Central
PMC7572350
DOI
10.1007/s10147-020-01747-1
PII: 10.1007/s10147-020-01747-1
Knihovny.cz E-zdroje
- Klíčová slova
- Androgen receptor-targeted agents, Castration-resistant, Meta-analysis, Prostate cancer, Testosterone,
- MeSH
- androgenní receptory metabolismus MeSH
- lidé MeSH
- nádory prostaty rezistentní na kastraci krev farmakoterapie mortalita MeSH
- prognóza MeSH
- testosteron krev MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- metaanalýza MeSH
- systematický přehled MeSH
- Názvy látek
- androgenní receptory MeSH
- AR protein, human MeSH Prohlížeč
- testosteron MeSH
INTRODUCTION: This systematic review and meta-analysis aimed to assess the prognostic value of testosterone in patients with castration-resistant prostate cancer (CRPC). MATERIALS AND METHODS: PubMed, Web of Science, and Scopus databases were systematically searched until December 2019, according to the Preferred Reporting Items for Systemic Review and Meta-analysis statement. The endpoints were progression-free survival (PFS) and overall survival (OS). RESULTS: We identified 11 articles with 4206 patients for systematic review and nine articles with 4136 patients for meta-analysis. Higher testosterone levels were significantly associated with better OS (pooled HR 0.74, 95% CI 0.58-0.95) and better PFS (pooled HR 0.51, 95% CI 0.30-0.87). Subgroup analyses based on the treatment type revealed that higher testosterone levels were significantly associated with better OS in CRPC patients treated with androgen receptor-targeted agents (ARTAs) (pooled HR 0.64, 95% CI 0.55-0.75), but not in those treated with chemotherapy (pooled HR 0.78, 95% CI 0.53-1.14). CONCLUSION: This meta-analysis demonstrated that the PFS and OS were significantly greater in patients with CRPC in those with higher testosterone levels than that of those with lower testosterone levels. In the subgroup analyses, lower testosterone levels were a consistently poor prognostic factor for OS in patients treated with ARTAs, but not in those treated with chemotherapy. Therefore, higher testosterone levels could be a useful biomarker to identify patient subgroups in which ARTAs should be preferentially recommended in the CRPC setting.
Department of Urology 2nd Faculty of Medicine Charles University Prague Czech Republic
Department of Urology Comprehensive Cancer Center Medical University of Vienna Vienna Austria
Department of Urology Ehime University Graduate School of Medicine Ehime Japan
Department of Urology King Fahad Specialist Hospital Dammam Saudi Arabia
Department of Urology The Jikei University School of Medicine Tokyo Japan
Department of Urology University Hospital of Tours Tours France
Department of Urology University of Texas Southwestern Dallas Texas USA
Department of Urology Weill Cornell Medical College New York NY USA
European Association of Urology Research Foundation Arnhem The Netherlands
Institute for Urology and Reproductive Health Sechenov University Moscow Russia
Karl Landsteiner Institute of Urology and Andrology Währinger Gürtel 18 20 1090 Vienna Austria
King Faisal Medical City Abha Saudi Arabia
Research Center for Evidence based Medicine Tabriz University of Medical Sciences Tabriz Iran
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Cornford P, Bellmunt J, Bolla M, et al. EAU-ESTRO-SIOG guidelines on prostate cancer. Part II: treatment of relapsing, metastatic, and castration-resistant prostate cancer. Eur Urol. 2017;71(4):630–642. doi: 10.1016/j.eururo.2016.08.002. PubMed DOI
Hoang DT, Iczkowski KA, Kilari D, et al. Androgen receptor-dependent and -independent mechanisms driving prostate cancer progression: Opportunities for therapeutic targeting from multiple angles. Oncotarget. 2017;8(2):3724–3745. doi: 10.18632/oncotarget.12554. PubMed DOI PMC
Beer TM, Armstrong AJ, Rathkopf D, et al. Enzalutamide in men with chemotherapy-naive metastatic castration-resistant prostate cancer: extended analysis of the phase 3 PREVAIL study. Eur Urol. 2017;71(2):151–154. doi: 10.1016/j.eururo.2016.07.032. PubMed DOI PMC
Ryan CJ, Smith MR, Fizazi K, et al. Abiraterone acetate plus prednisone versus placebo plus prednisone in chemotherapy-naive men with metastatic castration-resistant prostate cancer (COU-AA-302): final overall survival analysis of a randomised, double-blind, placebo-controlled phase 3 study. Lancet Oncol. 2015;16(2):152–160. doi: 10.1016/s1470-2045(14)71205-7. PubMed DOI
de Bono JS, Oudard S, Ozguroglu M, et al. Prednisone plus cabazitaxel or mitoxantrone for metastatic castration-resistant prostate cancer progressing after docetaxel treatment: a randomised open-label trial. Lancet. 2010;376(9747):1147–1154. doi: 10.1016/s0140-6736(10)61389-x. PubMed DOI
Hoskin P, Sartor O, O’Sullivan JM, et al. Efficacy and safety of radium-223 dichloride in patients with castration-resistant prostate cancer and symptomatic bone metastases, with or without previous docetaxel use: a prespecified subgroup analysis from the randomised, double-blind, phase 3 ALSYMPCA trial. Lancet Oncol. 2014;15(12):1397–1406. doi: 10.1016/s1470-2045(14)70474-7. PubMed DOI
Crawford ED, Heidenreich A, Lawrentschuk N, et al. Androgen-targeted therapy in men with prostate cancer: evolving practice and future considerations. Prostate Cancer Prostatic Dis. 2019;22(1):24–38. doi: 10.1038/s41391-018-0079-0. PubMed DOI PMC
Hashimoto K, Tabata H, Shindo T, et al. Serum testosterone level is a useful biomarker for determining the optimal treatment for castration-resistant prostate cancer. Urol Oncol. 2019;37(7):485–491. doi: 10.1016/j.urolonc.2019.04.026. PubMed DOI
Sakamoto S, Maimaiti M, Xu M, et al. higher serum testosterone levels associated with favorable prognosis in enzalutamide- and abiraterone-treated castration-resistant prostate cancer. J Clin Med. 2019 doi: 10.3390/jcm8040489. PubMed DOI PMC
Shiota M, Kashiwagi E, Murakami T, et al. Serum testosterone level as possible predictive marker in androgen receptor axis-targeting agents and taxane chemotherapies for castration-resistant prostate cancer. Urol Oncol. 2019;37(3):180.e119–180.e124. doi: 10.1016/j.urolonc.2018.10.020. PubMed DOI
Klap J, Schmid M, Loughlin KR. The relationship between total testosterone levels and prostate cancer: a review of the continuing controversy. J Urol. 2015;193(2):403–413. doi: 10.1016/j.juro.2014.07.123. PubMed DOI
Claps M, Petrelli F, Caffo O, et al. Testosterone levels and prostate cancer prognosis: systematic review and meta-analysis. Clin Genitourin Cancer. 2018;16(3):165–175.e162. doi: 10.1016/j.clgc.2018.01.005. PubMed DOI
Chi K, Hotte SJ, Joshua AM, et al. Treatment of mCRPC in the AR-axis-targeted therapy-resistant state. Ann Oncol. 2015;26(10):2044–2056. doi: 10.1093/annonc/mdv267. PubMed DOI
Liberati A, Altman DG, Tetzlaff J, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. PLoS Med. 2009;6(7):e1000100. doi: 10.1371/journal.pmed.1000100. PubMed DOI PMC
Bhasin S, Jasjua GK, Pencina M, et al. Sex hormone-binding globulin, but not testosterone, is associated prospectively and independently with incident metabolic syndrome in men: the framingham heart study. Diabetes Care. 2011;34(11):2464–2470. doi: 10.2337/dc11-0888. PubMed DOI PMC
Stang A. Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur J Epidemiol. 2010;25(9):603–605. doi: 10.1007/s10654-010-9491-z. PubMed DOI
Deeks JJ, Dinnes J, D’Amico R, Sowden AJ, et al. Evaluating non-randomised intervention studies. Health Technol Assess. 2003;7(27):iii-x. doi: 10.3310/hta7270. PubMed DOI
Altman DG, Bland JM. How to obtain the confidence interval from a P value. BMJ. 2011;343:d2090. doi: 10.1136/bmj.d2090. PubMed DOI
Altman DG, Bland JM. How to obtain the P value from a confidence interval. BMJ. 2011;343:d2304. doi: 10.1136/bmj.d2304. PubMed DOI
DerSimonian R, Kacker R. Random-effects model for meta-analysis of clinical trials: an update. Contemp Clin Trials. 2007;28(2):105–114. doi: 10.1016/j.cct.2006.04.004. PubMed DOI
DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials. 1986;7(3):177–188. doi: 10.1016/0197-2456(86)90046-2. PubMed DOI
Higgins JP, Thompson SG, Deeks JJ, Altman DG. Measuring inconsistency in meta-analyses. Bmj. 2003;327(7414):557–560. doi: 10.1136/bmj.327.7414.557. PubMed DOI PMC
Armstrong AJ, Halabi S, de Wit R, et al. The relationship of body mass index and serum testosterone with disease outcomes in men with castration-resistant metastatic prostate cancer. Prostate Cancer Prostatic Dis. 2009;12(1):88–93. doi: 10.1038/pcan.2008.36. PubMed DOI
Bertaglia V, Tucci M, Vignani F, et al. An exploratory analysis of the association between levels of hormones implied in steroid biosynthesis and activity of abiraterone in patients with metastatic castration-resistant prostate cancer. Minerva Urol Nefrol. 2017;69(4):349–358. doi: 10.23736/s0393-2249.16.02746-6. PubMed DOI
de Liano AG, Reig O, Mellado B, et al. Prognostic and predictive value of plasma testosterone levels in patients receiving first-line chemotherapy for metastatic castrate-resistant prostate cancer. Br J Cancer. 2014;110(9):2201–2208. doi: 10.1038/bjc.2014.189. PubMed DOI PMC
Halabi S, Ou SS, Vogelzang NJ, et al. Inverse correlation between body mass index and clinical outcomes in men with advanced castration-recurrent prostate cancer. Cancer. 2007;110(7):1478–1484. doi: 10.1002/cncr.22932. PubMed DOI
Hashimoto K, Masumori N, Hashimoto J, Takayanagi A, et al. Serum testosterone level to predict the efficacy of sequential use of antiandrogens as second-line treatment following androgen deprivation monotherapy in patients with castration-resistant prostate cancer. Jpn J Clin Oncol. 2011;41(3):405–410. doi: 10.1093/jjco/hyq193. PubMed DOI
Lolli C, De Lisi D, Conteduca V, et al. Testosterone levels and androgen receptor copy number variations in castration-resistant prostate cancer treated with abiraterone or enzalutamide. Prostate. 2019;79(11):1211–1220. doi: 10.1002/pros.23804. PubMed DOI
Montgomery B, Kheoh T, Molina A, et al. Impact of baseline corticosteroids on survival and steroid androgens in metastatic castration-resistant prostate cancer: exploratory analysis from COU-AA-301. Eur Urol. 2015;67(5):866–873. doi: 10.1016/j.eururo.2014.06.042. PubMed DOI
Lin GW, Yao XD, Ye DW, et al. The prognostic factors of effective ketoconazole treatment for metastatic castration-resistant prostate cancer: who can benefit from ketoconazole therapy? Asian J Androl. 2012;14(5):732–737. doi: 10.1038/aja.2012.57. PubMed DOI PMC
Kamada S, Sakamoto S, Ando K, et al. Nadir testosterone after long-term followup predicts prognosis in patients with prostate cancer treated with combined androgen blockade. J Urol. 2015;194(5):1264–1270. doi: 10.1016/j.juro.2015.03.120. PubMed DOI
Yamamoto S, Sakamoto S, Minhui X, et al. Testosterone reduction of >/= 480 ng/dL predicts favorable prognosis of Japanese men with advanced prostate cancer treated with androgen-deprivation therapy. Clin Genitourin Cancer. 2017;15(6):e1107–e1115. doi: 10.1016/j.clgc.2017.07.023. PubMed DOI
Saraon P, Jarvi K, Diamandis EP. Molecular alterations during progression of prostate cancer to androgen independence. Clin Chem. 2011;57(10):1366–1375. doi: 10.1373/clinchem.2011.165977. PubMed DOI
Efstathiou E, Titus M, Wen S, et al. Molecular characterization of enzalutamide-treated bone metastatic castration-resistant prostate cancer. Eur Urol. 2015;67(1):53–60. doi: 10.1016/j.eururo.2014.05.005. PubMed DOI PMC
Ryan CJ, Tindall DJ. Androgen receptor rediscovered: the new biology and targeting the androgen receptor therapeutically. J Clin Oncol. 2011;29(27):3651–3658. doi: 10.1200/jco.2011.35.2005. PubMed DOI
Shiota M, Kashiwagi E, Yokomizo A, et al. Interaction between docetaxel resistance and castration resistance in prostate cancer: implications of Twist1, YB-1, and androgen receptor. Prostate. 2013;73(12):1336–1344. doi: 10.1002/pros.22681. PubMed DOI
Wang C, Nieschlag E, Swerdloff R, et al. Investigation, treatment, and monitoring of late-onset hypogonadism in males: ISA, ISSAM, EAU, EAA, and ASA recommendations. Eur Urol. 2009;55(1):121–130. doi: 10.1016/j.eururo.2008.08.033. PubMed DOI
Bensalah K, Montorsi F, Shariat SF. Challenges of cancer biomarker profiling. Eur Urol. 2007;52(6):1601–1609. doi: 10.1016/j.eururo.2007.09.036. PubMed DOI