2022
DOI: 10.1016/j.annonc.2022.05.003
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Durable response to crizotinib in metastatic angiomatoid fibrous histiocytoma with EWSR1–CREB1 fusion and ALK overexpression

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Cited by 9 publications
(6 citation statements)
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“…Treatment with crizotinib has shown efficacy in a variety of ALK mutant and rearranged tumors including non‐small‐cell lung cancer (NSCLC), inflammatory myofibroblastic tumors, and neuroblastoma, 8 , 9 , 10 and now, there is emerging evidence of the effectiveness of ALK inhibitors in the treatment of tumors with ALK overexpression without mutation or fusion. 11 , 12 While PNET is a distinct entity from neuroblastoma, there are shared biological and molecular characteristics that make the finding of oncogenic ALK expression less surprising in the case presented here. It has been shown that embryonic neuroblasts and neural crest cells rely on ALK‐ and MYC‐pathway activation to maintain differentiation during embryonic development.…”
Section: Discussionmentioning
confidence: 74%
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“…Treatment with crizotinib has shown efficacy in a variety of ALK mutant and rearranged tumors including non‐small‐cell lung cancer (NSCLC), inflammatory myofibroblastic tumors, and neuroblastoma, 8 , 9 , 10 and now, there is emerging evidence of the effectiveness of ALK inhibitors in the treatment of tumors with ALK overexpression without mutation or fusion. 11 , 12 While PNET is a distinct entity from neuroblastoma, there are shared biological and molecular characteristics that make the finding of oncogenic ALK expression less surprising in the case presented here. It has been shown that embryonic neuroblasts and neural crest cells rely on ALK‐ and MYC‐pathway activation to maintain differentiation during embryonic development.…”
Section: Discussionmentioning
confidence: 74%
“…This is the first report of a PNET treated with targeted tyrosine kinase inhibitor (TKI) therapy. Treatment with crizotinib has shown efficacy in a variety of ALK mutant and rearranged tumors including non‐small‐cell lung cancer (NSCLC), inflammatory myofibroblastic tumors, and neuroblastoma, 8–10 and now, there is emerging evidence of the effectiveness of ALK inhibitors in the treatment of tumors with ALK overexpression without mutation or fusion 11,12 . While PNET is a distinct entity from neuroblastoma, there are shared biological and molecular characteristics that make the finding of oncogenic ALK expression less surprising in the case presented here.…”
Section: Discussionmentioning
confidence: 76%
“…In the head and neck area, performing a wide excision is often clinically impossible and is associated with disease recurrence in the future. However, local recurrence of the lesion depends on the size and depth of tissue invasion[ 11 ] and occurs in 15%[ 13 ] or, according to another source, in 2%-12% of cases[ 5 ].…”
Section: Discussionmentioning
confidence: 99%
“…This is the first report of a PNET treated with targeted tyrosine kinase inhibitor (TKI) therapy. Treatment with crizotinib has shown efficacy in a variety of ALK mutant and rearranged tumors including non-small cell lung cancer (NSCLC), inflammatory myofibroblastic tumors, and neuroblastoma [7][8][9] and, now there is emerging evidence of the effectiveness of ALK-inhibitors in the treatment of tumors with ALK overexpression without mutation or fusion [10,11]. While PNET is a distinct entity from neuroblastoma, there are shared biologic and molecular characteristics that make the finding of oncogenic ALK expression less surprising in the case presented here.…”
Section: Discussionmentioning
confidence: 99%