pi3k突变的转移性成釉细胞瘤的持久疾病消退与coanlisib治疗:1例报告。

IF 0.9 Q4 ONCOLOGY Rare Tumors Pub Date : 2025-01-07 eCollection Date: 2025-01-01 DOI:10.1177/20363613241309961
Meghan M Lynch, Pedro Hermida-Viveiros, Sean Stencel, Hannah Knott, Rusul Al-Maryati, Farres Obeidin, Borislav A Alexiev, Susan Abbinanti, Senthil Damodaran, Mark Agulnik, Seth M Pollack
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引用次数: 0

摘要

成釉细胞瘤是一种罕见的由牙源性细胞引起的良性肿瘤,但具有局部侵袭性。转移性成釉细胞瘤(METAM)是一种极为罕见的成釉细胞瘤变体,其原发性和继发性肿瘤均具有良性成釉细胞瘤的组织学特征。这是一个病例报告的病人谁提出了颌骨肿块和随后的肺转移,后来诊断为METAM。最初的治疗包括卡铂、依托泊苷和紫杉烷为基础的化疗无效。分子分析显示突变包括PIK3CA H1047R和BRAF V600E。该患者参加了一项肿瘤不可知试验,并开始使用copanlisib(一种PI3K抑制剂)治疗,结果部分缓解,疾病持续消退。76个周期后,她继续耐受治疗,不良反应最小。该病例强调了靶向治疗如copanlisib治疗METAM的潜力,为PIK3CA突变患者提供了一个有希望的治疗选择。
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Durable disease regression with copanlisib treatment in PI3K-mutated metastasizing ameloblastoma: A case report.

Ameloblastoma is a rare tumor arising from odontogenic cells that is benign, yet locally aggressive. Metastasizing ameloblastoma (METAM) is an ultra-rare ameloblastoma variant in which both primary and secondary tumors have histological features of benign ameloblastoma. This is a case report of a patient who presented with a jaw mass and subsequent lung metastases, later diagnosed as METAM. Initial treatments, including carboplatin, etoposide, and taxane-based chemotherapy, were ineffective. Molecular profiling revealed mutations including PIK3CA H1047R and BRAF V600E. The patient was enrolled in a tumor-agnostic trial and began treatment with copanlisib, a PI3K inhibitor, which resulted in a partial response and durable disease regression. After 76 cycles, she continues to tolerate therapy well with minimal adverse events. This case highlights the potential of targeted therapies such as copanlisib for treating METAM, providing a promising therapeutic option for patients with PIK3CA mutations.

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来源期刊
Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
期刊最新文献
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