Key result
Adjuvant treatment is linked to better overall survival in primary cardiac sarcoma, particularly angiosarcoma.
Why the study?
Primary cardiac sarcomas are rare and heterogeneous, with intimal sarcoma posing diagnostic challenges, prompting investigation into their incidence, types, and the prognostic significance of MDM2 reclassification and adjuvant therapy.
Does adjuvant treatment and MDM2 expression impact overall survival in patients with primary cardiac sarcomas?
Observational (n=48)
No
Does adjuvant treatment and MDM2 expression impact overall survival in patients with primary cardiac sarcomas?
p-value: p=<0.001
Adjuvant treatment improves survival in primary cardiac sarcomas, particularly angiosarcomas, and MDM2 testing aids in accurate diagnosis and prognostication of intimal sarcomas.
Adjuvant therapy may warrant consideration in cardiac angiosarcoma; leaves open randomized trials and MDM2-guided prognostication for intimal subtypes.
BACKGROUND: Primary cardiac sarcomas are rare and their clinicopathologic features are heterogeneous. Among them, particularly intimal sarcoma is a diagnostic challenge due to nonspecific histologic features. Recently, MDM2 amplification reported to be a characteristic genetic event in the intimal sarcoma. In this study, we aimed to identify the types and incidence of primary cardiac sarcomas that occurred over 25 years in tertiary medical institutions, and to find clinicopatholgical significance through reclassification of diagnoses using additional immunohistochemistry (IHC). METHODS: We reviewed the primary cardiac sarcoma cases between January 1993 and June 2018 at Asan Medical Center, South Korea, with their clinicopathologic findings, and reclassified the subtypes, especially using IHC for MDM2 and then, analyzed the significance of prognosis. RESULTS: Forty-eight (6.8%) cases of a primary cardiac sarcoma were retrieved. The tumors most frequently involved the right atrium (n = 25, 52.1%), and the most frequent tumor subtype was angiosarcoma (n = 23, 47.9%). Seven cases (53.8%) were newly reclassified as an intimal sarcoma by IHC for MDM2. Twenty-nine (60.4%) patients died of disease (mean, 19.8 months). Four patients underwent a heart transplantation and had a median survival of 26.8 months. This transplantation group tended to show good clinical outcomes in the earlier stages, but this was not statistically significant (p = 0.318). MDM2 positive intimal sarcoma showed the better overall survival (p = 0.003) than undifferentiated pleomorphic sarcoma. Adjuvant treatment is beneficial for patient survival (p < 0.001), particularly in angiosarcoma (p < 0.001), but not in intimal sarcoma (p = 0.154). CONCLUSION: Our study supports the use of adjuvant treatment in primary cardiac sarcoma, as it was associated with a significantly better overall survival rate. Further consideration of tumor histology may be important in determining the optimal use of adjuvant treatment for different types of sarcomas. Therefore, accurate diagnosis by MDM2 test is important condsidering patient's prognosis and treatment.
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Cho et al. (2023) conducted an observational in Primary cardiac sarcomas (n=48). Adjuvant treatment was evaluated on Overall survival (p=<0.001). Adjuvant treatment was associated with significantly better overall survival in primary cardiac sarcoma (p<0.001), particularly in angiosarcoma (p<0.001), but not in intimal sarcoma (p=0.154).
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