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High dose-rate Intra-Operative Radiation Therapy During High Risk Genitourinary Surgery: Initial Observations and a Proposal for its Study in Bladder Cancer.

作者信息

Kates Max, Chappidi Meera R, Brant Aaron, Milbar Niv, Sopko Nikolai A, Meyer Christian, Terezakis Stephanie A, Herman Joseph M, Efron Jonathan E, Safar Bashar, Tran Phuoc T, Ahuja Nita, Pierorazio Phillip M, Bivalacqua Trinity J

机构信息

The James Buchanan Brady Urological Institute and Department of Urology, The Johns Hopkins School of Medicine, Baltimore, MD, USA.

出版信息

Bladder Cancer. 2017 Jul 27;3(3):191-199. doi: 10.3233/BLC-170104.

DOI:10.3233/BLC-170104
PMID:28824947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5545919/
Abstract

BACKGROUND

High dose-rate Intra-Operative Radiation Therapy (HD-IORT) is used to provide effective local control for patients with high-risk locally advanced or recurrent tumors. However, the utility of HD-IORT for patients with bladder cancer has not been studied.

OBJECTIVE

To characterize our institutional experience with HD-IORT in patients with cancer requiring genitourinary surgery, in an effort to identify patients with bladder cancer that may benefit from HD-IORT.

METHODS

We performed a retrospective review of all patients who have undergone HD-IORT during genitourinary surgery at our institution. Patients were stratified by surgical margin status, and primary outcomes assessed were overall survival, recurrence free survival and 90-day complications. Patients undergoing cystectomy and HD-IORT with sarcomatoid urothelial cancer were compared to a similar cohort undergoing cystectomy alone. A sample case of one such patient is discussed in detail.

RESULTS

84 patients at our institution have undergone HD-IORT with genitourinary surgery. Positive surgical margin status was the greatest predictor of both OS (HR = 3.42) and RFS (HR = 2.61). The overall 90-day complication rate was 61%, with wound infections (43%) and GI complications (21%) being most common. 4 of these patients had sarcomatoid urothelial histology, and all are still alive with >2 yrs follow up. This compares to a 52% 1 yr survival in our sarcomatoid urothelial cohort (25 pts) that did not undergo HD-IORT.

CONCLUSIONS

Our institutional experience with HD-IORT has been promising, particularly among patients with locally advanced disease and sarcomatoid histology. We are currently enrolling patients in a multi-institutional registry to assess the utility of HD-IORT in high risk bladder cancer.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/f7317a500cb6/blc-3-blc170104-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/56d0229bd0d2/blc-3-blc170104-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/bcededa8d21d/blc-3-blc170104-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/359738abc99b/blc-3-blc170104-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/45bec99d7b41/blc-3-blc170104-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/d9d7fbb10956/blc-3-blc170104-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/8d115d331c91/blc-3-blc170104-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/f7317a500cb6/blc-3-blc170104-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/56d0229bd0d2/blc-3-blc170104-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/bcededa8d21d/blc-3-blc170104-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/359738abc99b/blc-3-blc170104-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/45bec99d7b41/blc-3-blc170104-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/d9d7fbb10956/blc-3-blc170104-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/8d115d331c91/blc-3-blc170104-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc73/5545919/f7317a500cb6/blc-3-blc170104-g007.jpg

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本文引用的文献

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Current clinical trials testing the combination of immunotherapy with radiotherapy.目前正在进行临床试验,以测试免疫疗法与放射疗法相结合的效果。
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Sarcomatoid Urothelial Carcinoma of the Bladder: Analysis of 28 Cases With Emphasis on Clinicopathologic Features and Markers of Epithelial-to-Mesenchymal Transition.
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Arch Pathol Lab Med. 2016 Jun;140(6):543-51. doi: 10.5858/arpa.2015-0085-OA. Epub 2016 Mar 31.
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The future of immune checkpoint therapy.免疫检查点疗法的未来。
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Cancer statistics, 2015.癌症统计数据,2015 年。
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Novel wound management system reduction of surgical site morbidity after ventral hernia repairs: a critical analysis.新型伤口管理系统降低腹疝修补术后手术部位发病率的批判性分析
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