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安罗替尼成功治疗晚期卵巢癌 1 例报告。

Successful treatment of advanced ovarian cancer with anlotinib: a case report.

机构信息

Department of Oncology, Dezhou People's Hospital, Dezhou, P.R. China.

Department of Radiology, Dezhou People's Hospital, Dezhou, P.R. China.

出版信息

J Int Med Res. 2020 Dec;48(12):300060520976824. doi: 10.1177/0300060520976824.

DOI:10.1177/0300060520976824
PMID:33284728
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7724413/
Abstract

Ovarian cancer remains the most lethal gynecological malignant tumor, with relapse occurring in approximately 70% of advanced cases. Anlotinib is an oral small-molecule multi-targeted tyrosine kinase inhibitor that can resist neoangiogenesis and inhibit tumor growth. Previous research demonstrated clinical antitumor activity of anlotinib in various cancers. We report the case of an elderly woman with advanced ovarian cancer who received anlotinib after failure of multiple-line chemotherapy. A partial response was observed after six cycles of anlotinib monotherapy, with a reduction in the size of the metastases and significantly decreased serum CA125 levels from 1832.7 U/mL to 118.7 U/mL. She continued to take anlotinib, with a progression-free survival time of more than 4 months. Only mild hypertension was observed during the treatment. Anlotinib monotherapy may be a novel therapeutic option for patients with advanced ovarian cancer.

摘要

卵巢癌仍然是最致命的妇科恶性肿瘤,约 70%的晚期病例会出现复发。安罗替尼是一种口服小分子多靶点酪氨酸激酶抑制剂,能够抗血管生成并抑制肿瘤生长。先前的研究表明,安罗替尼在多种癌症中具有临床抗肿瘤活性。我们报告了一例老年晚期卵巢癌患者,在多次化疗失败后接受了安罗替尼治疗。在安罗替尼单药治疗的六个周期后观察到部分缓解,转移灶缩小,血清 CA125 水平从 1832.7 U/mL 显著降至 118.7 U/mL。她继续服用安罗替尼,无进展生存期超过 4 个月。在治疗过程中仅观察到轻度高血压。安罗替尼单药治疗可能是晚期卵巢癌患者的一种新的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d345/7724413/7504467fd8f9/10.1177_0300060520976824-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d345/7724413/cb176315f128/10.1177_0300060520976824-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d345/7724413/7504467fd8f9/10.1177_0300060520976824-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d345/7724413/cb176315f128/10.1177_0300060520976824-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d345/7724413/7504467fd8f9/10.1177_0300060520976824-fig2.jpg

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本文引用的文献

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Medicine (Baltimore). 2020 May;99(20):e20053. doi: 10.1097/MD.0000000000020053.
2
Knockdown of long non-coding RNA LINC00152 increases cisplatin sensitivity in ovarian cancer cells.长链非编码RNA LINC00152的敲低增加了卵巢癌细胞对顺铂的敏感性。
Exp Ther Med. 2019 Dec;18(6):4510-4516. doi: 10.3892/etm.2019.8066. Epub 2019 Sep 30.
3
Targeting autophagy potentiates the anti-tumor effect of PARP inhibitor in pediatric chronic myeloid leukemia.
尼拉帕利成功治疗一名BRCA野生型卵巢癌脑转移患者:病例报告及文献复习
Front Oncol. 2022 Apr 29;12:873198. doi: 10.3389/fonc.2022.873198. eCollection 2022.
靶向自噬可增强PARP抑制剂在小儿慢性粒细胞白血病中的抗肿瘤作用。
AMB Express. 2019 Jul 15;9(1):108. doi: 10.1186/s13568-019-0836-z.
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China National Medical Products Administration approval summary: anlotinib for the treatment of advanced non-small cell lung cancer after two lines of chemotherapy.中国国家药品监督管理局批准概要:安罗替尼用于二线化疗后治疗晚期非小细胞肺癌。
Cancer Commun (Lond). 2019 Jun 20;39(1):36. doi: 10.1186/s40880-019-0383-7.
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