This is the authors' abstract. We don't add key points for this paper.
Introduction The proportion of retroperitoneal malignant peripheral nerve sheath tumours (RMPNST) in retroperitoneal tumors is less than 5%, but the mortality rate is very high. However, there is no relevant research focused on RMPNST only. Methods We retrospectively analyzed data from the SEER database of patients with primary RMPNST from 2000 to 2019, by leveraging the advantages of the Seer database, we can explore the prognosis of such rare diseases. Kaplan-Meier method was used to construct the survival curve, and cox regression model was used to analyze the factors affecting the prognosis of patients. In addition, a model was developed to distinguish high-risk and low-risk patients. Results This study included a total of 52 patients, with a median survival time of 39 months (95% CI 12.740–65.260) and a 5-year survival rate of 44.2% (95% CI 0.299–0.565). Radiotherapy ( p = 0.004, OR: 1.475, 95% CI 0.718–3.033), metastasis disease ( p = 0.002, OR: 5.596, 95% CI 2.449–47.079) and surgery ( p = 0.003, OR: 5.003, 95% CI 0.011–0.409) were associated with overall survival (OS). The 5-year distant metastasis rate was 36% (95% CI 0.221–0.499). We used the above risk factors to separate patients into high and low groups and evaluate the results through the receiver operating characteristic (ROC) curve. This model is beneficial for guiding the selection of treatment strategies. Conclusion The majority of RMPNST patients have a good prognosis after surgery, and the establishment of high-low group is helpful for clinical decision-making.
Answers are grounded in this paper and cite their sources.
No takes yet. Share an insight, caveat, or question.
Xi et al. (2024) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: