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1.
Urology ; 165: e39-e45, 2022 07.
Article in English | MEDLINE | ID: mdl-35123984

ABSTRACT

Inflammatory myofibroblastic tumor (IMT) is a tumor of unknown neoplastic potential that rarely arises in the genitourinary tract. We present the case of an otherwise healthy 16-year old boy with gross hematuria who underwent cystoscopy and transurethral resection of the bladder tumor without complication. Biopsy and immunohistochemistry were consistent with anaplastic lymphoma kinase-positive IMT. In addition to presenting this case of IMT, we review presentations, management and prognosis of bladder IMT.


Subject(s)
Granuloma, Plasma Cell , Urinary Bladder Neoplasms , Adolescent , Cystoscopy/adverse effects , Granuloma, Plasma Cell/surgery , Hematuria/complications , Humans , Male , Urinary Bladder/surgery , Urinary Bladder Neoplasms/complications , Urinary Bladder Neoplasms/diagnosis , Urinary Bladder Neoplasms/surgery
2.
Clin Adv Hematol Oncol ; 19(7): 460-467, 2021 Jul.
Article in English | MEDLINE | ID: mdl-34236345

ABSTRACT

Oligometastatic prostate cancer is a subtype of metastatic disease that generally is defined by the presence of 5 or fewer metastatic lesions. Metastatic prostate cancer currently is treated with androgen deprivation therapy and additional systemic therapy, such as novel antiandrogen medications or chemotherapy. The management of metastatic prostate cancer is evolving, however, with the notion that some patients with low-burden metastatic disease may benefit from both local and systemic therapy. Local therapy of the prostate in the setting of oligometastatic prostate cancer is a new concept. Evidence from retrospective studies suggests that cytoreductive therapy, including radical prostatectomy, can improve overall survival in these patients. Ongoing randomized trials are comparing cytoreductive therapy with standard-of-care treatment options. Local therapy in the form of radiation has also been investigated in phase 2 randomized trials. In this review, we discuss the biological and clinical rationales for local therapy, review the current evidence for local therapy, and compare the clinical designs of various ongoing trials.


Subject(s)
Prostatic Neoplasms/therapy , Androgen Antagonists/therapeutic use , Animals , Clinical Trials as Topic , Disease Management , Humans , Male , Neoplasm Metastasis/pathology , Neoplasm Metastasis/radiotherapy , Neoplasm Metastasis/therapy , Prostate/drug effects , Prostate/pathology , Prostate/radiation effects , Prostate/surgery , Prostatectomy , Prostatic Neoplasms/pathology , Prostatic Neoplasms/radiotherapy
3.
J Urol ; 206(5): 1157-1165, 2021 11.
Article in English | MEDLINE | ID: mdl-34181465

ABSTRACT

PURPOSE: We sought to evaluate whether bilateral prostate cancer detected at active surveillance (AS) enrollment is associated with progression to Grade Group (GG) ≥2 and to compare the efficacy of combined targeted biopsy plus systematic biopsy (Cbx) vs systematic biopsy (Sbx) or targeted biopsy alone to detect bilateral disease. MATERIALS AND METHODS: A prospectively maintained database of patients referred to our institution from 2007-2020 was queried. The study cohort included all AS patients with GG1 on confirmatory Cbx and followup of at least 1 year. Cox proportional hazard analysis identified baseline characteristics associated with progression to ≥GG2 at any point throughout followup. RESULTS: Of 579 patients referred, 103 patients had GG1 on Cbx and were included in the study; 49/103 (47.6%) patients progressed to ≥GG2, with 30/72 (41.7%) patients with unilateral disease progressing and 19/31 (61.3%) patients with bilateral disease progressing. Median time to progression was 68 months vs 52 months for unilateral and bilateral disease, respectively (p=0.006). Both prostate specific antigen density (HR 1.72, p=0.005) and presence of bilateral disease (HR 2.21, p=0.012) on confirmatory biopsy were associated with AS progression. At time of progression, GG and risk group were significantly higher in patients with bilateral versus unilateral disease. Cbx detected 16% more patients with bilateral disease than Sbx alone. CONCLUSIONS: Bilateral disease and prostate specific antigen density at confirmatory Cbx conferred greater risk of earlier AS progression. Cbx was superior to Sbx for identifying bilateral disease. AS risk-stratification protocols may benefit from including presence of bilateral disease and should use Cbx to detect bilateral disease.


Subject(s)
Prostate/diagnostic imaging , Prostate/pathology , Prostatic Neoplasms/diagnosis , Watchful Waiting/statistics & numerical data , Aged , Biopsy, Large-Core Needle/methods , Biopsy, Large-Core Needle/statistics & numerical data , Diffusion Magnetic Resonance Imaging/statistics & numerical data , Disease Progression , Humans , Image-Guided Biopsy/methods , Image-Guided Biopsy/statistics & numerical data , Kallikreins/blood , Magnetic Resonance Imaging, Interventional/statistics & numerical data , Male , Middle Aged , Multimodal Imaging/methods , Multimodal Imaging/statistics & numerical data , Neoplasm Grading , Prospective Studies , Prostate-Specific Antigen/blood , Prostatic Neoplasms/blood , Prostatic Neoplasms/pathology , Prostatic Neoplasms/therapy , Risk Assessment/methods , Risk Assessment/statistics & numerical data , Risk Factors , Ultrasonography, Interventional/statistics & numerical data
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