Linear muscle segmentation for metastatic renal cell carcinoma.

Authors

null

Edouard Nicaise

Department of Urology, Emory University School of Medicine, Atlanta, GA

Edouard Nicaise , Benjamin Schmeusser , Adil Ali , Eric Midenberg , Arnold Raul Palacios , Ethan Kearns , Sriram Ambadi , Dattatraya H. Patil , Shreyas S. Joshi , Vikram M Narayan , Sarah P. Psutka , Bassel Nazha , Jacqueline T Brown , Kenneth Ogan , Mehmet Asim Bilen , Viraj A. Master

Organizations

Department of Urology, Emory University School of Medicine, Atlanta, GA, Department of Urology, Emory University, Atlanta, GA, Department of Urology, Creighton University School of Medicine, Omaha, NE, University of Washington, Fred Hutchinson Cancer Center, Seattle, WA, Winship Cancer Institute of Emory University, Atlanta, GA

Research Funding

No funding sources reported

Background: Baseline sarcopenia and postoperative changes in muscle mass are independently associated with overall survival in patients with metastatic renal cell carcinoma (mRCC) undergoing cytoreductive nephrectomy (CN). Here we examine the relationship between preoperative (baseline) and postoperative changes in muscle quantity with survival outcomes following CN as determined by linear segmentation, a fast and clinic-friendly tool. Methods: Our nephrectomy database was reviewed for patients with clear cell, papillary, or chromophobe mRCC who underwent CN. Linear segmentation of bilateral psoas/paraspinal muscles was completed for baseline imaging within 60 days of surgery and imaging up to 1 year postoperatively. ANOVA for numerical and chi-square for categorical variables were used to test for differences according to change in linear muscle index (LMI, cm2/m2). Multivariable models estimated COX hazard ratios for cancer-specific survival (CSS) and overall survival (OS). Kaplan Meier curves estimated CSS and OS. Results: From 2004-2020, 190 patients were identified 48 stable LMI (25.3%; <5% change [0Δ]), 54 increase LMI (28.4%; +5% change [+Δ]), and 88 decrease LMI (46.3%; -5% change [-Δ]). Median time from baseline imaging to surgery was 18 days, while time from surgery to postoperative imaging was 119 days. Patients with +Δ had lower baseline LMI than -Δ or 0Δ (28.5 vs. 32.4 vs.32.5 cm2/m2; p=0.003). 0Δ LMI had lower rates of pN1 disease than other groups (27.1% [0Δ] vs. 42.6% [+Δ] vs. 45.5% [-Δ]; p=0.019). No other differences in pathology were noted. Median CSS and OS were highest among patients with 0Δ LMI (CSS: not reached [0Δ] vs. 61.9 [+Δ] vs. 37.4 [-Δ] months; p=0.0018 || OS: 67.2 [0Δ] vs. 48.5 [+Δ] vs. 26.4 [-Δ] months; p=0.0007). Median follow-up was 56 months for survivors. The table lists factors associated with increased risk of cancer-specific mortality. Conclusions: 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 demonstrated greatest survival, potentially secondary to high baseline muscle mass.

Multivariable model estimating COX hazard CSS according to percent change LMI.
CovariateN (%)HR (95% CI)p-value
∆ LMI (cm2/m2)
0∆ LMI48 (25.3)0.42 (0.21-0.82)0.011
-5% LMI88 (46.3)1.69 (1.01-2.83)0.046
+5% LMI54 (28.4)Ref
Age 60+104 (54.7)1.40 (0.91-2.16)0.127
Obesity (BMI ≥30kg/m2)67 (35.3)0.86 (0.54-1.38)0.538
Male144 (75.8)1.01 (0.59-1.71)0.978
Black Race30 (15.8)2.23 (1.21-4.11)0.01
ECOG ≥147 (24.7)2.70 (1.66-4.41)<0.001
Tumor Size (cm)0.99 (0.93-1.05)0.672
Clear Cell Histology150 (78.9)1.18 (0.61-2.31)0.619
Nuclear High Grade175 (95.1)5.75 (1.26-26.38)0.024
pT Stage
T424 (12.6)0.94 (0.45-1.96)0.876
T1-3166 (87.4)Ref
pN Stage
N060 (31.6)0.65 (0.35-1.20)0.17
N176 (40)1.33 (0.72-2.47)0.361
NX54 (28.4)Ref
pM1154 (81.1)2.72 (1.38-5.34)0.004

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Abstract Details

Meeting

2024 ASCO Genitourinary Cancers Symposium

Session Type

Poster Session

Session Title

Poster Session C: Renal Cell Cancer; Adrenal, Penile, and Testicular Cancers

Track

Renal Cell Cancer,Adrenal Cancer,Penile Cancer,Testicular Cancer

Sub Track

Diagnostics and Imaging

Citation

J Clin Oncol 42, 2024 (suppl 4; abstr 380)

DOI

10.1200/JCO.2024.42.4_suppl.380

Abstract #

380

Poster Bd #

F4

Abstract Disclosures

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