节拍化疗治疗BRAFV600E突变的低级别浆液性卵巢癌1例报告及文献复习

IF 0.3 Q4 ONCOLOGY
Maria Rozpłoch-Sapa, Patrycja Mrowczyk, Łukasz Kwinta, Mateusz Łobacz, Paweł M. Potocki
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引用次数: 0

摘要

介绍。卵巢癌(OC)是全球癌症死亡的主要原因。在波兰,它是妇女因肿瘤死亡的第四大原因。OC是一种异质性疾病,低级别病例的特点是预后较好,但化疗敏感性差。节律化疗(MC)可能是一种有益的方法。案例演示。我们报告了一例低级别浆液性卵巢癌(LGSOC)患者,尽管对紫杉醇和卡铂的标准剂量化疗有耐药性,但通过MC获得了长期的疾病控制。总生存期(OS)为65个月。大部分时间都进行了MC。患者接受两种节律治疗方案:拓扑替康加环磷酰胺和长春瑞滨加甲氨蝶呤,两者均与激素治疗联合使用。该癌症被发现含有BRAF V600E突变(v-raf鼠肉瘤病毒癌基因同源物B1,在600位缬氨酸到谷氨酸的替代),但这并不影响治疗。结论。LGSOC与高级别浆液性卵巢癌(HGSOC)具有不同的特征。MC可能是LGSOC的一个有价值的选择,尽管还没有得到充分的研究。BRAF V600E突变发生在2-33%的低级别浆液性卵巢肿瘤中。这在LGSOC中比在HGSOC中更常见。抑制BRAF可能是一种新的治疗选择。一些BRAF抑制剂已经被注册用于这种突变的实体瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low-grade serous ovarian cancer with BRAFV600E mutation treated with metronomic chemotherapy — a case report and literature review
Introduction. Ovarian cancer (OC) is the leading cause of cancer death worldwide. In Poland, it is the fourth leading cause of death from neoplasms in women. OC is a heterogeneous disease with low-grade cases characterized by a better prognosis, but poor chemosensitivity. Metronomic chemotherapy (MC) may be a beneficial approach. Case presentation. We present a patient with low-grade serous ovarian cancer (LGSOC) with long-term disease control achieved with MC despite being resistant to standard-dose chemotherapy with paclitaxel and carboplatin. Overall survival (OS) of the patient was 65 months. MC was administered most of the time. The patient was treated with two metronomic regimens: topotecan plus cyclophosphamide and vinorelbine plus methotrexate, both in combination with hormone therapy. The cancer was found to harbor the BRAF V600E mutation (v-raf murine sarcoma viral oncogene homolog B1, a valine-to-glutamic acid substitution at position 600), but that did not impact the treatment. Conclusions. LGSOC has distinct features from high-grade serous ovarian cancer (HGSOC). MC may be a valuable option in LGSOC despite being understudied. The BRAF V600E mutation occurs in 2–33% of low-grade serous ovarian tumors. It is a more common finding in LGSOC than in HGSOC. BRAF inhibition in OC may be a new therapeutic option. Some BRAF inhibitors have already been registered for solid tumors with this mutation.
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来源期刊
CiteScore
0.90
自引率
20.00%
发文量
46
审稿时长
15 weeks
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