Key result
Nivolumab and ipilimumab linked to improved hemorrhagic anemia and reduced tumor size in primary pleural angiosarcoma.
Why the study?
Primary pleural angiosarcoma is a rare and clinically fatal pleural tumor originating from vascular endothelial cells.
Does combined nivolumab and ipilimumab improve outcomes in a patient with primary pleural angiosarcoma?
Case Report (n=1)
Does combined nivolumab and ipilimumab improve outcomes in a patient with primary pleural angiosarcoma?
Answers are grounded in this paper and cite their sources.
Nivolumab and ipilimumab combination therapy may be a viable treatment option for primary pleural angiosarcoma, reducing tumor size and pleural effusion.
Primary pleural angiosarcoma (PPA) is a rare and clinically fatal pleural tumor originating from vascular endothelial cells. Herein, we presented the case of a 73-year-old man who was referred to our emergency room with complaints of right chest and back pain for a few days. Chest computed tomography revealed massive pleural effusion and a large mass in the right chest cavity. Thoracoscopic examination demonstrated a large hemorrhagic tumor on the parietal pleura whose pathological analysis indicated PPA. The patient received immunotherapy combined with nivolumab and ipilimumab. A cycle of nivolumab and ipilimumab improved his hemorrhagic anemia and reduced the pleural effusion and tumor size. This treatment outcome suggests that nivolumab and ipilimumab comprise a vital treatment option for PPA.
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Nakamura et al. (2023) conducted a case report in Primary pleural angiosarcoma (n=1). Nivolumab and ipilimumab was evaluated on Improvement in hemorrhagic anemia and reduction in pleural effusion and tumor size. A cycle of nivolumab and ipilimumab improved hemorrhagic anemia and reduced pleural effusion and tumor size in a patient with primary pleural angiosarcoma.
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