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Clinical impact of continued crizotinib administration after isolated central nervous system progression in patients with lung cancer positive for ALK rearrangement.ALK 基因重排阳性肺癌患者中枢神经系统孤立进展后继续克唑替尼治疗的临床影响。
J Thorac Oncol. 2013 May;8(5):654-7. doi: 10.1097/JTO.0b013e31828c28e7.
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Lapatinib with trastuzumab for HER2-positive early breast cancer (NeoALTTO): a randomised, open-label, multicentre, phase 3 trial.拉帕替尼联合曲妥珠单抗治疗人表皮生长因子受体 2 阳性早期乳腺癌(NeoALTTO):一项随机、开放标签、多中心、III 期临床试验。
Lancet. 2012 Feb 18;379(9816):633-40. doi: 10.1016/S0140-6736(11)61847-3. Epub 2012 Jan 17.
3
Continuous administration of EGFR-TKIs following radiotherapy after disease progression in bone lesions for non-small cell lung cancer.在非小细胞肺癌骨转移病灶疾病进展后,行放疗的同时持续给予 EGFR-TKIs 治疗。
Anticancer Res. 2011 Dec;31(12):4519-23.
4
A phase II study of lapatinib and bevacizumab as treatment for HER2-overexpressing metastatic breast cancer.拉帕替尼联合贝伐珠单抗治疗人表皮生长因子受体 2 过表达转移性乳腺癌的 II 期研究。
Breast Cancer Res Treat. 2012 Jul;134(1):13-20. doi: 10.1007/s10549-011-1918-z. Epub 2011 Dec 24.
5
Salivary duct carcinoma: targeting the phosphatidylinositol 3-kinase pathway by blocking mammalian target of rapamycin with temsirolimus.涎腺导管癌:通过替西罗莫司阻断雷帕霉素靶蛋白来靶向磷脂酰肌醇3激酶途径
J Clin Oncol. 2011 Sep 10;29(26):e727-30. doi: 10.1200/JCO.2011.36.2095. Epub 2011 Aug 15.
6
Continuous EGFR-TKI administration following radiotherapy for non-small cell lung cancer patients with isolated CNS failure.非小细胞肺癌患者孤立性中枢神经系统失败后行放疗并持续 EGFR-TKI 治疗。
Lung Cancer. 2011 Dec;74(3):457-61. doi: 10.1016/j.lungcan.2011.04.007. Epub 2011 May 14.
7
Sustained response of carcinoma ex pleomorphic adenoma treated with trastuzumab and capecitabine.曲妥珠单抗联合卡培他滨治疗多形性腺瘤癌变的持续缓解。
Head Neck Oncol. 2010 May 26;2:12. doi: 10.1186/1758-3284-2-12.
8
Randomized study of Lapatinib alone or in combination with trastuzumab in women with ErbB2-positive, trastuzumab-refractory metastatic breast cancer.拉帕替尼单药或联合曲妥珠单抗治疗 ErbB2 阳性、曲妥珠单抗耐药的转移性乳腺癌的随机研究。
J Clin Oncol. 2010 Mar 1;28(7):1124-30. doi: 10.1200/JCO.2008.21.4437. Epub 2010 Feb 1.
9
Lapatinib, a HER2 tyrosine kinase inhibitor, induces stabilization and accumulation of HER2 and potentiates trastuzumab-dependent cell cytotoxicity.拉帕替尼是一种HER2酪氨酸激酶抑制剂,可诱导HER2的稳定和积累,并增强曲妥珠单抗依赖性细胞毒性。
Oncogene. 2009 Feb 12;28(6):803-14. doi: 10.1038/onc.2008.432. Epub 2008 Dec 8.
10
Specific blockade of VEGF and HER2 pathways results in greater growth inhibition of breast cancer xenografts that overexpress HER2.对VEGF和HER2通路的特异性阻断导致对过表达HER2的乳腺癌异种移植瘤更强的生长抑制作用。
Cell Cycle. 2008 Dec;7(23):3747-58. doi: 10.4161/cc.7.23.7212. Epub 2008 Dec 16.

人表皮受体 2 扩增的唾液腺导管癌:双重人表皮受体 2 抑制和抗血管内皮生长因子联合治疗的消退。

Human epidermal receptor 2-amplified salivary duct carcinoma: regression with dual human epidermal receptor 2 inhibition and anti-vascular endothelial growth factor combination treatment.

机构信息

Department of Investigational Cancer Therapeutics, (Phase I Clinical Trials Program), The University of Texas MD Anderson Cancer Center, Houston, Texas.

出版信息

Head Neck. 2014 Mar;36(3):E25-7. doi: 10.1002/hed.23429. Epub 2013 Oct 19.

DOI:10.1002/hed.23429
PMID:23852769
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3893310/
Abstract

BACKGROUND

Salivary ductal carcinoma is a rare cancer with poor prognosis and limited treatment options. Human epidermal receptor 2 (HER2)-directed treatment has been attempted in HER2-amplified or overexpressed salivary gland malignancies with limited success.

METHODS

We report resolution of measurable disease and minimal residual disease in a patient with salivary duct cancer treated with trastuzumab, lapatinib, and bevacizumab, with treatment ongoing for more than 2 years.

RESULTS

This treatment has been tolerated well except for grade 2 diarrhea and mucositis, which required a dose reduction of lapatinib to 1000 mg daily. The response observed was achieved in spite of receiving extensive prior therapy, including trastuzumab and/or chemotherapy for 20 months on which his tumors progressed.

CONCLUSION

The combination of trastuzumab, lapatinib, and bevacizumab may warrant investigation as a non-cytotoxic alternative for treatment of HER2-amplified or overexpressed salivary duct carcinoma and other HER2-amplified or overexpressed salivary gland tumors, particularly those not responsive to trastuzumab monotherapy.

摘要

背景

唾液腺癌是一种罕见的癌症,预后较差,治疗选择有限。在 HER2 扩增或过表达的唾液腺癌中尝试了针对人表皮受体 2(HER2)的治疗,但效果有限。

方法

我们报告了一名患有唾液腺癌的患者接受曲妥珠单抗、拉帕替尼和贝伐珠单抗治疗后,可测量疾病和微小残留疾病得到缓解,且治疗已持续超过 2 年。

结果

除了 2 级腹泻和黏膜炎外,该治疗方案耐受性良好,需要将拉帕替尼的剂量减少至每天 1000mg。尽管患者接受了广泛的先前治疗,包括曲妥珠单抗和/或化疗 20 个月,肿瘤进展,但观察到的反应仍得以实现。

结论

曲妥珠单抗、拉帕替尼和贝伐珠单抗的联合应用可能值得研究,作为治疗 HER2 扩增或过表达的唾液腺癌和其他 HER2 扩增或过表达的唾液腺肿瘤的非细胞毒性替代方案,特别是那些对曲妥珠单抗单药治疗无反应的肿瘤。