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Original Research

The prognostic value and clinicopathological features of sarcomatoid differentiation in patients with renal cell carcinoma: a systematic review and meta-analysis

, , , &
Pages 1687-1703 | Published online: 22 Jun 2018
 

Abstract

Background and purpose

Numerous studies have demonstrated that sarcomatoid differentiation is linked to the risk of renal cell carcinoma (RCC). However, its actual clinicopathological impact remains inconclusive. Therefore, we undertook a meta-analysis to evaluate the pathologic and prognostic impacts of sarcomatoid differentiation in patients with RCC by assessing cancer-specific survival, overall survival, recurrence-free survival, progression-free survival, and cancer-specific mortality.

Materials and methods

In accordance with the preferred reporting items for systematic reviews and meta-analysis statement, relevant studies were collected systematically from PubMed, Embase, and Web of Science to identify relevant studies published prior to January 2018. The pooled effects (hazard ratios, odds ratios, and standard mean differences) and 95% confidence intervals were calculated to investigate the association of sarcomatoid differentiation with cancer prognosis and clinicopathological features.

Results

Thirty-five studies (N=11,261 patients [n=59–1,437 per study]) on RCC were included in this meta-analysis. Overall, the pooled analysis suggested that sarcomatoid differentiation was significantly associated with unfavorable cancer-specific survival (HR=1.46, 95% CI: 1.26–1.70, p<0.001), overall survival (HR=1.59, 95% CI: 1.42–1.78, p<0.001), progression-free survival (HR=1.61, 95% CI: 1.35–1.91, p<0.001), recurrence-free survival (HR=1.60, 95% CI: 1.29–1.99, p<0.001), and cancer-specific mortality (HR=2.36, 95% CI: 1.64–3.41, p<0.001) in patients with RCC. Moreover, sarcomatoid differentiation was closely correlated with TNM stage (III/IV vs I/II: OR=1.84, 95% CI: 1.12–3.03, p=0.017), Fuhrman grade (III/IV vs I/II: OR=8.37, 95% CI: 2.92–24.00, p<0.001), lymph node involvement (N1 vs N0: OR=1.88, 95% CI: 1.08–3.28, p=0.026), and pathological types (clear cell RCC-only vs mixed type: OR=0.48, 95% CI: 0.29–0.80, p=0.005), but was not related to gender (male vs female, OR=0.86, 95% CI: 0.58–1.28, p=0.464) and average age (SMD=−0.02, 95% CI: −0.20–0.17, p=0.868).

Conclusion

This study suggests that sarcomatoid differentiation in histopathology is associated with poor clinical outcome and advanced clinicopathological features in RCC and could serve as a poor prognostic factor for RCC patients.

Author contributions

LJZ and BW designed the research. ZLZ and HZ undertook the literature search. HZ and YJF analyzed the data and interpreted the results. LJZ wrote the paper. All authors contributed toward data analysis, drafting and revising the paper and agree to be accountable for all aspects of the work.

Disclosure

The authors report no conflicts of interest in this work.