Renal surgery following HIF-2α antagonist therapy: Surgical indications, outcomes and growth kinetics.

IF 2.3 3区 医学 Q3 ONCOLOGY
Daniel Nethala, Braden Millan, Jason Hyman, Nityam Rathi, Jessica Hsueh, Christopher Koller, Charles Hesswani, Alexander P Kenigsberg, Neil Mendhiratta, Keith Lawson, Matthew Miller, Sahil Parikh, William Azar, Kyle Schuppe, Maria J Merino, Cathy D Vocke, Christopher J Ricketts, Ramaprasad Srinivasan, Sandeep Gurram, W Marston Linehan, Mark W Ball
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引用次数: 0

Abstract

Background: The development of HIF-2α antagonists marked an advancement in the treatment of localized VHL-deficient kidney cancer; however, their impact on subsequent surgical interventions remains unexplored. This study investigated the indications for and outcomes of patients undergoing renal surgery after exposure to HIF-2α antagonists and the growth rates (GR) of their index renal tumors.

Design, setting, and participants: We performed a retrospective analysis of patients who underwent renal surgery at a single institution following or during treatment with a HIF-2α antagonist. Data regarding the clinicopathologic characteristics, therapy management, and surgical outcomes were collected. Index tumor GRs before, during and after drug administration were calculated and compared.

Results and limitations: Twenty-seven patients underwent 28 surgeries after exposure to a HIF-2α antagonist from 2015 to 2023, with a total of 82 tumors removed. About 24 patients were treated with Belzutifan, and 3 patients were treated with PT2385, with 26 patients having a diagnosis of VHL syndrome. The median time on therapy prior to surgery was 14.7 months, with a median washout time of drug to surgery of 10 days. Median preoperative hemoglobin prior to surgery was 11.6 g/dL. Two blood transfusions were administered, 1 intraoperatively and 1 postoperatively. Seven postoperative complications were noted, 2 of which were ≥ Grade 3. The median index tumor GR prior to treatment was 0.37 cm/y, 0.46 cm/y during treatment, and 0.54 cm/y post-treatment. There was no significant difference in GRs between the groups. Median time to restart HIF-2α antagonist after surgery was 43 days. Limitations of this study include retrospective nature, single center, and lack of control group.

Conclusions: Renal surgery after or during exposure to a HIF-2α antagonist is safe and feasible, with rates of both transfusions and complications commensurate with the reported literature from standard renal surgery. GRs of index renal tumors that eventually needed surgical intervention did not show a significant difference before, during, and after therapy. Tumors exhibiting a positive GR on drug may represent the indication that drives early surgical intervention prior to the tumor reaching the 3 cm threshold. A median washout time of 10 days from last dose of HIF-2α antagonist to surgery was safe and well tolerated.

HIF-2α拮抗剂治疗后的肾脏手术:手术指征,结果和生长动力学。
背景:HIF-2α拮抗剂的开发标志着局部vhl缺陷肾癌治疗的进展;然而,它们对后续手术干预的影响仍未被探索。本研究探讨了HIF-2α拮抗剂暴露后肾手术患者的适应证和预后及其指标肾肿瘤的生长速率(GR)。设计、环境和参与者:我们对在单一机构接受HIF-2α拮抗剂治疗后或治疗期间接受肾脏手术的患者进行了回顾性分析。收集了有关临床病理特征、治疗管理和手术结果的数据。计算给药前、给药中、给药后指标肿瘤GRs并进行比较。结果和局限性:2015年至2023年,27例患者在暴露于HIF-2α拮抗剂后接受了28次手术,共切除了82个肿瘤。贝尔祖替芬治疗24例,PT2385治疗3例,其中26例诊断为VHL综合征。手术前治疗的中位时间为14.7个月,从药物到手术的中位洗脱时间为10天。术前血红蛋白中位数为11.6 g/dL。两次输血,一次术中输血,一次术后输血。7例术后并发症,其中2例≥3级。治疗前肿瘤GR中位指数为0.37 cm/y,治疗期间为0.46 cm/y,治疗后为0.54 cm/y。两组间GRs无显著差异。术后重新使用HIF-2α拮抗剂的中位时间为43天。本研究的局限性包括回顾性、单中心和缺乏对照组。结论:暴露于HIF-2α拮抗剂后或期间的肾脏手术是安全可行的,输血和并发症的发生率与文献报道的标准肾脏手术相当。最终需要手术干预的肾肿瘤的GRs在治疗前、治疗中和治疗后无显著差异。表现出GR阳性的肿瘤可能是在肿瘤达到3cm阈值之前进行早期手术干预的指征。从最后一剂HIF-2α拮抗剂到手术的中位洗脱时间为10天,是安全且耐受性良好的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.80
自引率
3.70%
发文量
297
审稿时长
7.6 weeks
期刊介绍: Urologic Oncology: Seminars and Original Investigations is the official journal of the Society of Urologic Oncology. The journal publishes practical, timely, and relevant clinical and basic science research articles which address any aspect of urologic oncology. Each issue comprises original research, news and topics, survey articles providing short commentaries on other important articles in the urologic oncology literature, and reviews including an in-depth Seminar examining a specific clinical dilemma. The journal periodically publishes supplement issues devoted to areas of current interest to the urologic oncology community. Articles published are of interest to researchers and the clinicians involved in the practice of urologic oncology including urologists, oncologists, and radiologists.
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