司美替尼
生产厂家：英国阿斯利康
功能主治：1型神经纤维瘤病（NF1）与无法手术的盆状神经纤维瘤。
用法用量：用法用量 1、建议剂量为每天2次(约每12小时)口服25mg/㎡，直至疾病进展或出现不可接受的毒性。 2、空腹服用司美替尼(Selumetinib)。 3、每次服药前2小时或每次服药后1小时不要食用食物。 4、用水吞服整个司美替尼(Selumetinib)胶囊。 5、不要咀嚼，溶解或打开胶囊。 基于体表面积的推荐剂量： 体表面积推荐剂量 0.55–0.69m2早上20mg，晚上10mg 0.70–0.89m220mg，每天两次 0.90–1.09m225mg，每天两次 1.10–1.2930mg，每天两次 1.30–1.4935mg，每天两次 1.50–1.6940mg，每天两次 1.70–1.8945mg，每天两次 ≥1.90m250mg，每天两次
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Selumetinib, also known by its brand name, Koselugo, is a targeted therapy drug developed by AstraZeneca. It belongs to a class of drugs called MEK inhibitors, which work by blocking an enzyme called MEK1 and MEK2. This enzyme is part of the MAPK signaling pathway that plays a crucial role in regulating cell growth, differentiation, and survival. By inhibiting this enzyme, selumetinib can stop the growth and spread of cancer cells.
Selumetinib was first approved by the U.S. Food and Drug Administration (FDA) in 2020 for the treatment of neurofibromatosis type 1 (NF1) associated plexiform neurofibromas (PNs) in children aged 2 years and older. NF1 is a genetic disorder that affects the development and growth of nerve cells, leading to the formation of tumors called neurofibromas. PNs are a type of neurofibroma that grows along the nerves and can cause pain, disfigurement, and other complications.The approval of selumetinib for NF1-associated PNs was based on the results of a phase II clinical trial that showed significant improvement in tumor response and patient-reported outcomes. In the trial, 70% of patients treated with selumetinib had a partial response or better, compared with 20% of those receiving a placebo. Moreover, patients treated with selumetinib reported a reduction in pain and disability, and improved quality of life.
Apart from its use in NF1, selumetinib is also being studied for the treatment of other types of cancer, such as melanoma, lung cancer, and pancreatic cancer. In particular, selumetinib has shown promising results in combination with other chemotherapy or targeted therapy drugs. For example, a phase II clinical trial of selumetinib and dacarbazine (DTIC) in patients with metastatic melanoma showed an overall response rate of 49%, compared with 24% for patients treated with DTIC alone.
Another phase II trial of selumetinib and docetaxel in patients with advanced non-small cell lung cancer (NSCLC) showed an increase in progression-free survival (PFS) from 2.7 to 5.3 months, compared with docetaxel alone. Similarly, a phase Ib/II study of selumetinib and gemcitabine in patients with advanced pancreatic cancer showed an increase in PFS from 2.1 to 3.9 months, compared with gemcitabine alone.
The side effects of selumetinib are generally mild to moderate, and include diarrhea, rash, acneiform dermatitis, nausea, vomiting, fatigue, and peripheral edema. However, selumetinib can also cause serious adverse effects, such as cardiomyopathy, interstitial lung disease, retinal pigment epithelial detachment, and hepatitis. Therefore, selumetinib should only be used under the supervision of a qualified healthcare professional.
In conclusion, selumetinib is a promising targeted therapy drug that has shown efficacy in the treatment of NF1-associated PNs, as well as other types of cancer. Its ability to block the MEK enzyme and inhibit the MAPK signaling pathway makes it a valuable addition to the armamentarium of anti-cancer drugs. However, more research is needed to optimize its use, determine its long-term safety, and identify patients who are most likely to benefit from it.
