Linear Muscle Segmentation for Metastatic Renal Cell Carcinoma: Changes in Clinic-Friendly Estimation Predict Survival Following Cytoreductive Nephrectomy

IF 2.3 3区 医学 Q3 ONCOLOGY Clinical genitourinary cancer Pub Date : 2024-06-01 DOI:10.1016/j.clgc.2024.02.007
Edouard H. Nicaise , Benjamin N. Schmeusser , Adil Ali , Eric Midenberg , Arnold R. Palacios , Blaise Hartsoe , Ethan Kearns , Sriram Ambadi , Dattatraya H. Patil , Shreyas S. Joshi , Vikram M. Narayan , Sarah P. Psutka , Bassel Nazha , Jacqueline T. Brown , Kenneth Ogan , Mehmet A. Bilen , Viraj A. Master
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Abstract

Introduction

Baseline sarcopenia and postoperative changes in muscle mass are independently associated with overall survival (OS) in patients with metastatic renal cell carcinoma (mRCC) undergoing cytoreductive nephrectomy (CN). Here we examine the relationships between preoperative (baseline), postoperative changes in muscle quantity, and survival outcomes following CN as determined by linear segmentation, a clinic-friendly tool that rapidly estimates muscle mass.

Materials and Methods

Our nephrectomy database was reviewed for patients with metastatic disease who underwent CN for RCC. Linear segmentation of the bilateral psoas/paraspinal muscles was completed for baseline imaging within 60 days of surgery and imaging 30 to 365 days postoperatively. Kruskal-Wallis for numerical and Fisher's exact test for categorical variables were used to test for differences between groups according to percent change in linear muscle index (LMI, cm2/m2). Multivariable Cox proportional hazards models evaluated associations between LMI percent change and cancer-specific (CSM) and all-cause mortality (ACM). Kaplan Meier curves estimated cancer-specific (CSS) and overall survival (OS).

Results

From 2004-2020, 205 patients were included of whom 52 demonstrated stable LMI (25.4%; LMI change < 5% [0Δ]), 60 increase (29.3%; LMI +5% [+Δ]), and 92 decrease (44.9%; LMI -5% [-Δ]). Median time from baseline imaging to surgery was 18 days, and time from surgery to postoperative imaging was 133 days. Median CSS and OS were highest among patients with 0Δ LMI (CSS: 133.6 [0Δ] vs. 61.9 [+Δ] vs. 37.4 [-Δ] months; P = .0018 || OS: 67.2 [0Δ] vs. 54.8 [+Δ] vs. 29.5 [-Δ] months; P = .0007). Stable LMI was a protective factor for CSM (HR 0.48; P = .024) and ACM (HR 0.59; P = .040) on multivariable analysis.

Discussion

Change in muscle mass after CN, as measured by the linear muscle segmentation technique, is independently associated with OS and CSS in patients following CN. Of note, lack of change was associated with longer survival.

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转移性肾细胞癌的线性肌肉分割:临床友好估计值的变化可预测肾切除术后的存活率
接受细胞切除肾切除术(CN)的转移性肾细胞癌(mRCC)患者的基线肌肉疏松症和术后肌肉量变化与总生存期(OS)有独立关联。在此,我们研究了术前(基线)、术后肌肉量变化与CN术后生存结果之间的关系,这些变化是通过线性分割法确定的,这是一种方便临床使用的工具,可快速估算肌肉量。我们对肾切除术数据库中因 RCC 而接受 CN 治疗的转移性疾病患者进行了审查。在手术后 60 天内的基线成像和术后 30-365 天的成像中完成了双侧腰肌/脊柱旁肌的线性分割。数字变量采用 Kruskal-Wallis 检验,分类变量采用费雪精确检验,根据线性肌肉指数(LMI,cm/m)的百分比变化检验组间差异。多变量考克斯比例危险模型评估了线性肌肉指数百分比变化与癌症特异性死亡率(CSM)和全因死亡率(ACM)之间的关系。卡普兰-麦尔曲线估算了癌症特异性生存率(CSS)和总生存率(OS)。2004-2020 年间,共纳入 205 例患者,其中 52 例患者的 LMI 保持稳定(25.4%;LMI 变化 <5% [0Δ]),60 例患者的 LMI 增加(29.3%;LMI +5% [+Δ]),92 例患者的 LMI 减少(44.9%;LMI -5% [-Δ])。从基线成像到手术的中位时间为 18 天,从手术到术后成像的时间为 133 天。LMI 为 0Δ 的患者的 CSS 中位数和 OS 中位数最高(CSS:133.6 [0Δ] vs. 61.9 [+Δ] vs. 37.4 [-Δ] 个月;P=0.0018 || OS:67.2 [0Δ] vs. 54.8 [+Δ] vs. 29.5 [-Δ] 个月;p=0.0007)。在多变量分析中,稳定的 LMI 是 CSM(HR 0.48;p=0.024)和 ACM(HR 0.59;p=0.040)的保护因素。通过线性肌肉分割技术测量的CN术后肌肉质量变化与CN术后患者的OS和CSS独立相关。值得注意的是,无变化与更长的生存期相关。微摘要:评估和选择患者是确定最有可能从细胞肾切除术中获益的患者的关键。我们假设,根据横断面成像评估术前至术后肌肉量的临床友好型工具,肌肉量的动态变化可预测存活率。肌肉量增加或稳定的患者总生存期和癌症特异性生存期更长,这是一个重要的考虑因素。
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来源期刊
Clinical genitourinary cancer
Clinical genitourinary cancer 医学-泌尿学与肾脏学
CiteScore
5.20
自引率
6.20%
发文量
201
审稿时长
54 days
期刊介绍: Clinical Genitourinary Cancer is a peer-reviewed journal that publishes original articles describing various aspects of clinical and translational research in genitourinary cancers. Clinical Genitourinary Cancer is devoted to articles on detection, diagnosis, prevention, and treatment of genitourinary cancers. The main emphasis is on recent scientific developments in all areas related to genitourinary malignancies. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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