Synopsis
Keywords: Kidney, Tumor, Carcinoma, Renal Cell; Lymphatic Metastasis; Nephrectomy; Magnetic resonance imaging; Prognosis.
Motivation: The prognostic property of regional lymph node metastasis (RLNM) has been widely recognized, but the diagnostic workup has stagnated for renal cell carcinoma (RCC).
Goal(s): This study aimed to assess the diagnostic performance of MRI-based Node Reporting and Data System (Node-RADS) for RLNM and to explore its prognostic impact on patients with RCC.
Approach: A single-center retrospective comparative study.
Results: MRI-based Node-RADS presented better diagnostic performance for RLNM than the size criteria and previous clinical models (AUC, 0.91 vs 0.79–0.85; all P<.05), and exhibited a substantial prognostic value for RCCs regarding progress-free survival and overall survival (both P<.001).
Impact: Node-RADS,
a concept that combines size, texture, margin, and shape, is a promising
approach for lymph node metastasis in RCCs, which may contribute to improving
clinical node staging and guiding clinical decision making.
Introduction
Renal cell carcinoma (RCC) is the
predominant type of kidney cancer, accounting for about 90% of all cases [1]. Nephrectomy
is the main treatment option; however, whether to perform regional lymph node dissection
during surgery remains debatable due to the limited accuracy in detecting
regional lymph node metastasis (RLNM). [2–4]. Several
preoperative assessment methods are being explored for RLNM in patients with
RCC, but their diagnostic efficacy is suboptimal [5–8]. Node Reporting and Data
System (Node-RADS), a scoring system for standardized assessment of node
involvement in cancer, may be able to unlock the
deadlock [9]. In this study, we aimed to assess the
efficacy of MRI-based Node-RADS in diagnosing RLNM and to estimate its
prognostic significance in RCCs.Methods
This retrospective study included patients
with RCC who underwent nephrectomy and regional lymph node dissection between
January 2010 and October 2022. Using MRI-based Node-RADS with (eNode-RADS) and
without (uNode-RADS) reference to enhanced images, two senior radiologists
scored lymph nodes in consensus. The performance of RLNM detection was compared
with the size criteria and previous models constructed by Li, Kara, and
Umberto. Additionally, two radiologists and one urologist scored all lesions to
assess the interobserver agreement. Progress-free survival (PFS) and overall
survival (OS) were estimated and compared between patients with low (1–3) and
high (4–5) scores.Results
Overall, 201 patients with RCC (147 men; median age, 54 [46, 62] years) were enrolled, including 57
with RLNM. In diagnosing RLNM, eNode-RADS showed better performance than
uNode-RADS with higher specificity (96.53% vs. 92.36%, P=0.03) and superior
interobserver agreement (weighted κ = 0.74 vs. 0.67; P=0.003).
Furthermore, eNode-RADS outperformed the size criteria and previous clinical
models (area under the curves, 0.91 vs. 0.79–0.85; all P<0.001). During
a 57-month median follow-up, high-scoring patients experienced poorer PFS (median, 17
months vs. 116 months, P<0.001) and OS (median, 29 months vs. not reached, P<0.001) than low-scoring patients. According to multivariable Cox models adjusted for distant metastasis,
pathological T stage, RCC subtype, systemic therapy, and surgical methods,
eNode-RADS remained an independent predictor of PFS (hazard ratio [HR], 1.77; 95%
confidence interval [CI], 1.06–2.96; P=0.03) and OS (HR, 2.80; 95% CI, 1.56–5.02; P<0.001).Discussion
To date, few studies involved the
clinical node staging of RCCs based on various imaging modalities [10, 11], and
only three of them had a reasonable sample size (>10 with positive nodes)
and complete pathological evidence [12–14]. They showed a
sensitivity range of 63%–77% and a specificity
range of 75%–82% in detecting RLNM
using criteria such as a short diameter of ≥ 10 mm or an apparent diffusion
coefficient of <1.25×10-3 mm2/s. In
this context, Node-RADS, a concept that combines size, texture, margin, and
shape, may be a promising approach for node evaluation in RCCs. Our findings validated the hypothesis that Node-RADS had an impressive
performance compared with the short diameter and apparent diffusion coefficient.
In
the MRI algorithm of Node-RADS, unlike that of computed tomography (CT),
contrast agent use is not mandatory, given the superior soft-tissue contrast.
However, unenhanced MRI may be insufficient to assess the subtle architecture
of RCC-draining lymph nodes due to the retroperitoneal anatomical complexity,
small RLN size, and perifocal edema [15], particularly when accompanied by vein
thrombosis or sinus invasion. In this study, compared with uNode-RADS,
eNode-RADS yielded a favourable interobserver agreement and a superior
diagnostic efficacy of RLNs with higher specificity (96.53% vs. 92.36%),
reflecting the accurate exclusion of benign enlarged RLNs. Nevertheless, both
eNode-RADS (77.19%)
and uNode-RADS (70.18%)
yielded suboptimal sensitivity, which was attributed
to the inability to identify micro-metastases. Incorporating
other features, such as SI on T2WI, SI on DWI, and rim enhancement of RLNs, may
optimize Node-RADS and improve its sensitivity.
Unlike other
RADS algorithms used for lesion-specific risk assessment, Node-RADS presets a
clinical scenario of clinical node staging, that is, the accurate detection of
positive lymph nodes in the tumour-draining area. As a primary goal of tumour
staging, we evaluated the long-term prognosis of patients with RCC, and
eNode-RADS demonstrated excellent stratification capabilities for PFS and OS.
Especially after adjusting for recognized prognostic factors, Node-RADS still
had independent prognostic significance. As expected, the OS distribution based
on different eNode-RADS scores in this study roughly corresponded to that based
on different RLNM statuses in previous literature [16,17], confirming the
consistency between Node-RADS and RLNM. Conclusion
MRI-based
Node-RADS, especially contrast-enhanced MRI-based Node-RADS, demonstrated outstanding performance in
detecting RLNM
and distinct prognostic value for RCCs,
which may contribute to improving clinical node staging and guiding clinical
decision making.Acknowledgements
We
acknowledge the patients whose samples/data provided the foundation for this
study, and are grateful to the multidisciplinary team of urology in the Chinese
PLA General Hospital for their support and assistance. This work was
supported by the National Natural Science Foundation of China (Grant 81971580
and 82271951), Beijing Natural Science Foundation (Grant 7222167) and the Youth
Independent Innovation Science Foundation of Chinese PLA General Hospital
(Grant 22QNFC061).References
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