2022
DOI: 10.3389/fonc.2022.1027696
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Case report: Unique FLT4 variants associated with differential response to anlotinib in angiosarcoma

Abstract: Angiosarcoma (AS) is a rare, clinically aggressive tumor with limited treatment options and a poor prognosis. Mutations involving the angiogenesis-related genesTP53, PTPRB, PLCG1, KDR as well as FLT4 amplification have been observed in AS. There is a potential therapeutic value of inhibition of the VEGF pathway against angiosarcoma. Our case first described a patient with two sites of cutaneous angiosarcomas (cASs) that responded differently to anlotinib. And genetic analysis revealed that those two sites had … Show more

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Cited by 4 publications
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“…The results of the postoperative pathological examination confirmed the presence of a malignant tumor originating from the blood vessels, which was consistent with the diagnosis of PCA with lung metastasis. Due to the rarity of this disease, the lack of established treatment protocols and the presence of hemoptysis, targeted therapies commonly used for PCA, such as anlotinib [9][10][11] or pazopanib, [12] were not administered to the patient. Instead, based on the patient's symptoms and a review of relevant literature, we initiated treatment with paclitaxel (with albumin) monotherapy.…”
Section: Discussionmentioning
confidence: 99%
“…The results of the postoperative pathological examination confirmed the presence of a malignant tumor originating from the blood vessels, which was consistent with the diagnosis of PCA with lung metastasis. Due to the rarity of this disease, the lack of established treatment protocols and the presence of hemoptysis, targeted therapies commonly used for PCA, such as anlotinib [9][10][11] or pazopanib, [12] were not administered to the patient. Instead, based on the patient's symptoms and a review of relevant literature, we initiated treatment with paclitaxel (with albumin) monotherapy.…”
Section: Discussionmentioning
confidence: 99%