دورية أكاديمية

Upgrading on Per Protocol versus For Cause surveillance prostate biopsies: An opportunity to decreasing the burden of active surveillance.

التفاصيل البيبلوغرافية
العنوان: Upgrading on Per Protocol versus For Cause surveillance prostate biopsies: An opportunity to decreasing the burden of active surveillance.
المؤلفون: Wang M; Department of Urology, Wayne State University, Detroit, Michigan, USA., Lange A; Department of Urology, Wayne State University, Detroit, Michigan, USA., Perlman D; Department of Urology, Wayne State University, Detroit, Michigan, USA., Qi J; University of Michigan Medical School, Ann Arbor, Michigan, USA., George AK; University of Michigan Medical School, Ann Arbor, Michigan, USA., Ferrante S; University of Michigan Medical School, Ann Arbor, Michigan, USA., Semerjian A; IHA Urology, St. Joseph Mercy Hospital, Ann Arbor, Michigan, USA., Sarle R; Department of Urology, Sparrow Point Hospitals, Lansing, Michigan, USA., Cher ML; Department of Urology, Wayne State University, Detroit, Michigan, USA., Ginsburg KB; Department of Urology, Wayne State University, Detroit, Michigan, USA.
مؤلفون مشاركون: Michigan Urological Surgery Improvement Collaborative; University of Michigan Medical School, Ann Arbor, Michigan, USA.
المصدر: The Prostate [Prostate] 2023 Sep; Vol. 83 (12), pp. 1141-1149. Date of Electronic Publication: 2023 May 12.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8101368 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0045 (Electronic) Linking ISSN: 02704137 NLM ISO Abbreviation: Prostate Subsets: MEDLINE
أسماء مطبوعة: Publication: <2005-> : Hoboken, NJ : Wiley-Liss
Original Publication: New York : Alan R. Liss, c1980-
مواضيع طبية MeSH: Prostate*/diagnostic imaging , Prostate*/pathology , Prostatic Neoplasms*/diagnostic imaging , Prostatic Neoplasms*/pathology, Male ; Humans ; Prostate-Specific Antigen ; Retrospective Studies ; Watchful Waiting/methods ; Image-Guided Biopsy/methods ; Biopsy ; Magnetic Resonance Imaging/methods ; Neoplasm Grading
مستخلص: Background: Most prostate cancer (PC) active surveillance (AS) protocols recommend "Per Protocol" surveillance biopsy (PPSBx) every 1-3 years, even if clinical and imaging parameters remained stable. Herein, we compared the incidence of upgrading on biopsies that met criteria for "For Cause" surveillance biopsy (FCSBx) versus PPSBx.
Methods: We retrospectively reviewed men with GG1 PC on AS in the Michigan Urological Surgery Improvement Collaborative (MUSIC) registry. Surveillance prostate biopsies obtained 1 year after diagnosis were classified as either PPSBx or FCSBx. Biopsies were retrospectively deemed FCSBx if any of these criteria were met: PSA velocity > 0.75 ng/mL/year; rise in PSA > 3 ng from baseline; surveillance magnetic resonance imaging (MRI) (sMRI) with a PIRADS ≥ 4; change in DRE. Biopsies were classified PPSBx if none of these criteria were met. The primary outcome was upgrading to ≥GG2 or ≥GG3 on surveillance biopsy. The secondary objective was to assess for the association of reassuring (PIRADS ≤ 3) confirmatory or surveillance MRI findings and upgrading for patients undergoing PPSBx. Proportions were compared with the chi-squared test.
Results: We identified 1773 men with GG1 PC in MUSIC who underwent a surveillance biopsy. Men meeting criteria for FCSBx had more upgrading to ≥GG2 (45%) and ≥GG3 (12%) compared with those meeting criteria for PPSBx (26% and 4.9%, respectively, p < 0.001 and p < 0.001). Men with a reassuring confirmatory or surveillance MRI undergoing PPSBx had less upgrading to ≥GG2 (17% and 17%, respectively) and ≥GG3 (2.9% and 1.8%, respectively) disease compared with men without an MRI (31% and 7.4%, respectively).
Conclusions: Patients undergoing PPSBx had significantly less upgrading compared with men undergoing FCSBx. Confirmatory and surveillance MRI seem to be valuable tools to stratify the intensity of surveillance biopsies for men on AS. These data may help inform the development of a risk-stratified, data driven AS protocol.
(© 2023 Wiley Periodicals LLC.)
References: Eeles R, Goh C, Castro E, et al. The genetic epidemiology of prostate cancer and its clinical implications. Nat Rev Urol. 2014;11(1):18-31. doi:10.1038/nrurol.2013.266.
Schröder FH, Hugosson J, Roobol MJ, et al. Screening and prostate cancer mortality: results of the European Randomised Study of Screening for Prostate Cancer (ERSPC) at 13 years of follow-up. Lancet. 2014;384(9959):2027-2035. doi:10.1016/S0140-6736(14)60525-0.
Tosoian JJ, Mamawala M, Epstein JI, et al. Intermediate and longer-term outcomes from a prospective active-surveillance program for favorable-risk prostate cancer. J Clin Oncol. 2015;33(30):3379-3385. doi:10.1200/JCO.2015.62.5764.
Klotz L, Vesprini D, Sethukavalan P, et al. Long-term follow-up of a large active surveillance cohort of patients with prostate cancer. J Clin Oncol. 2015;33(3):272-277. doi:10.1200/JCO.2014.55.1192.
Arcot R, Cher ML, Qi J, et al. Delayed radical prostatectomy after a period of active surveillance is not associated with the use of secondary treatments compared with immediate prostatectomy. Prostate. 2022;82(3):323-329. doi:10.1002/pros.24277.
Ahmed HU, Arya M, Freeman A, Emberton M. Do low-grade and low-volume prostate cancers bear the hallmarks of malignancy. Lancet Oncol. 2012;13(11):e509-e517. doi:10.1016/S1470-2045(12)70388-1.
Newcomb LF, Thompson IM, Boyer HD, et al. Outcomes of active surveillance for clinically localized prostate cancer in the prospective, multi-institutional Canary PASS cohort. J Urol. 2016;195(2):313-320. doi:10.1016/j.juro.2015.08.087.
Bokhorst LP, Valdagni R, Rannikko A, et al. A decade of active surveillance in the PRIAS study: an update and evaluation of the criteria used to recommend a switch to active treatment. Eur Urol. 2016;70(6):954-960. doi:10.1016/j.eururo.2016.06.007.
Inoue LYT, Lin DW, Newcomb LF, et al. Comparative analysis of biopsy upgrading in four prostate cancer active surveillance cohorts. Ann Intern Med. 2018;168(1):1. doi:10.7326/M17-0548.
Wang JH, Downs TM, Jason Abel E, Richards KA, Jarrard DF. Prostate biopsy in active surveillance protocols: immediate re-biopsy and timing of subsequent biopsies. Curr Urol Rep. 2017;18(7):48. doi:10.1007/s11934-017-0702-y.
Klotz L, Pond G, Loblaw A, et al. Randomized study of systematic biopsy versus magnetic resonance imaging and targeted and systematic biopsy in men on active surveillance (ASIST): 2-year postbiopsy follow-up. Eur Urol. 2020;77(3):311-317. doi:10.1016/j.eururo.2019.10.007.
Newman TH, Stroman L, Hadjipavlou M, et al. EXIT from TRansrectal prostate biopsies (TREXIT): sepsis rates of transrectal biopsy with rectal swab culture guided antimicrobials versus freehand transperineal biopsy. Prostate Cancer Prostatic Dis. Published online August 19, 2021. doi:10.1038/s41391-021-00438-w.
Mallapareddi A, Ruterbusch J, Reamer E, Eggly S, Xu J. Active surveillance for low-risk localized prostate cancer: what do men and their partners think? Fam Pract. 2017;34(1):90-97. doi:10.1093/fampra/cmw123.
Ellis SD, Hwang S, Morrow E, et al. Perceived barriers to the adoption of active surveillance in low-risk prostate cancer: a qualitative analysis of community and academic urologists. BMC Cancer. 2021;21(1):649. doi:10.1186/s12885-021-08386-3.
Ginsburg KB, Cher ML, Montie JE. Defining quality metrics for active surveillance: the Michigan Urological Surgery Improvement Collaborative Experience. J Urol. 2020;204(6):1119-1121. doi:10.1097/JU.0000000000001308.
Auffenberg GB, Lane BR, Linsell S, et al. A roadmap for improving the management of favorable risk prostate cancer. J Urol. 2017;198(6):1220-1222. doi:10.1016/j.juro.2017.07.085.
Ploussard G, Beauval JB, Lesourd M, et al. Active surveillance eligibility of MRI-positive patients with grade group 2 prostate cancer: a pathological study. World J Urol. 2020;38(7):1735-1740. doi:10.1007/s00345-019-02973-7.
Cher ML, Dhir A, Auffenberg GB, et al. Appropriateness criteria for active surveillance of prostate cancer. J Urol. 2017;197(1):67-74. doi:10.1016/j.juro.2016.07.005.
Gross MD, Alshak MN, Shoag JE, et al. Healthcare costs of post-prostate biopsy sepsis. Urology. 2019;133:11-15. doi:10.1016/j.urology.2019.06.011.
Kang SK, Mali RD, Prabhu V, Ferket BS, Loeb S. Active surveillance strategies for low-grade prostate cancer: comparative benefits and cost-effectiveness. Radiology. 2021;300(3):594-604. doi:10.1148/radiol.2021204321.
Chesnut GT, Vertosick EA, Benfante N, et al. Role of changes in magnetic resonance imaging or clinical stage in evaluation of disease progression for men with prostate cancer on active surveillance. Eur Urol. 2020;77(4):501-507. doi:10.1016/j.eururo.2019.12.009.
Luiting HB, Remmers S, Boevé ER, et al. A multivariable approach using magnetic resonance imaging to avoid a protocol-based prostate biopsy in men on active surveillance for prostate Cancer-data from the International Multicenter Prospective PRIAS Study. Eur Urol Oncol. 2022;5(6):651-658. doi:10.1016/j.euo.2022.03.007.
Kaye DR, Qi J, Morgan TM, et al. Pathological upgrading at radical prostatectomy for patients with grade group 1 prostate cancer: implications of confirmatory testing for patients considering active surveillance. BJU Int. 2019;123(5):846-853. doi:10.1111/bju.14554.
Ginsburg KB, Jacobs JC, Qi J, et al. Impact of early confirmatory tests on upgrading and conversion to treatment in prostate cancer patients on active surveillance. Urology. 2021;147:213-222. doi:10.1016/j.urology.2020.07.067.
Lange JM, Laviana AA, Penson DF, et al. Prostate cancer mortality and metastasis under different biopsy frequencies in North American active surveillance cohorts. Cancer. 2020;126(3):583-592. doi:10.1002/cncr.32557.
فهرسة مساهمة: Keywords: MRI; active surveillance; genomic classifier; prostate biopsy; prostate cancer
المشرفين على المادة: EC 3.4.21.77 (Prostate-Specific Antigen)
تواريخ الأحداث: Date Created: 20230512 Date Completed: 20230724 Latest Revision: 20230725
رمز التحديث: 20230725
DOI: 10.1002/pros.24556
PMID: 37173808
قاعدة البيانات: MEDLINE
الوصف
تدمد:1097-0045
DOI:10.1002/pros.24556