Key result
Chemotherapy administration was associated with significantly improved overall survival compared to no chemotherapy in patients with stage III soft tissue sarcoma (adjusted HR 0.85).
Why the study?
Does chemotherapy improve overall survival in patients with stage III soft tissue sarcoma?
Observational (n=16,370)
Yes
Does chemotherapy improve overall survival in patients with stage III soft tissue sarcoma?
Hazard Ratio: 0.85 (95% CI 0.76–0.96)
Absolute Event Rate: 67.1% vs 55.1%
p-value: p=0.004
In patients with stage III soft tissue sarcoma, chemotherapy administration is associated with improved overall survival, especially in those with undifferentiated pleomorphic sarcoma.
Should not yet change practice in stage III soft tissue sarcoma; hypothesis-generating pending randomized confirmation.
BACKGROUND: Conflicting data exist on the benefit of chemotherapy in the management of high-risk soft tissue sarcoma (STS). Use of chemotherapy may be dependent on patient, tumor, and facility characteristics. This study sought to identify these factors and compare survival between treatment groups. PATIENTS AND METHODS: Patients with stage III STS were identified from the National Cancer Data Base (NCDB) from 1998 to 2012. Multiple logistic regression analysis was used to determine factors that influenced the probability of receiving chemotherapy. In a subset of patients, we determined the relationship between chemotherapy use and overall survival, using Kaplan-Meier curves and Cox regression analysis with propensity score adjustment. We also examined the effect of chemotherapy by histologic subgroup using interaction models. RESULTS: A total of 16,370 patients were included (N=5,377 for survival analysis). Patients who were younger than 40 years; male; privately insured; earned a higher income; had no comorbidities; had synovial sarcoma, angiosarcoma or "other" histology; and whose tumors were high-grade, greater than 10 cm, or from the lower extremity were significantly more likely to receive chemotherapy. Median unadjusted overall survival (OS) in the nonchemotherapy and chemotherapy groups was 51.3 and 82.7 months, respectively (P<.001). On adjusted analysis, the survival benefit remained significant (hazard ratio [HR], 0.85; P=.004). The benefit was particularly strong in the undifferentiated pleomorphic sarcoma (UPS) group on adjustment, with a median OS of 49.1 and 77.8 months for nonchemotherapy versus chemotherapy, respectively (HR, 0.77; P=.02). CONCLUSIONS: In addition to expected tumor and patient factors, histology, location of primary tumor, and socioeconomic status are associated with receipt/nonreceipt of chemotherapy in stage III STS. Chemotherapy use was associated with improved OS in the overall population, and specifically in the UPS subgroup.
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Movva et al. (2015) conducted an observational in Stage III soft tissue sarcoma (n=16,370). Chemotherapy vs. No chemotherapy was evaluated on Overall survival (HR 0.85, 95% CI 0.76-0.96, p=0.004). Chemotherapy administration was associated with significantly improved overall survival compared to no chemotherapy in patients with stage III soft tissue sarcoma (adjusted HR 0.85).
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