
Release date: 2024-08-16 17:50:36 Article From: Lucius Laos Recommended: 209
Selpercatinib is the first targeted drug specifically targeting RET gene mutations and was approved by the FDA in 2020; By inhibiting the activity of RET kinase and blocking the growth signal of tumor cells, it has achieved good efficacy in the treatment of a variety of cancers.
In terms of therapeutic efficacy, Selpercatinib has shown the following significant advantages.
Fourteen patients had a response to treatment of intracranial lesions, accounting for 88% of patients with CNS metastases at baseline or 6% of the total population. Thirty-nine percent of patients had intracranial remission for more than 12 months, demonstrating the durability of treatment.
The objective response rate was 63%, similar to that of the combination chemotherapy group, showing response to treatment. Of the 5 patients with brain metastases, 4 (80%) had a response to treatment, showing an effect of treatment. Thirty-eight percent of treatment-naïve patients had an intracranial remission of more than 12 months, comparable to that of the previous treatment group.
There may be some side effects associated with the use of Selpercatinib, and the following are the common adverse effects.
Hair loss is relatively common in treatment and can take a toll on the patient's psychological and social life. Hair loss is usually temporary, and patients can choose to wear a wig or use other cosmetic methods to cope with this change.
Symptoms of stomatitis, such as ulcers, pain, and redness of the oral mucosa, may make people feel uncomfortable when eating and talking. Patients should maintain oral hygiene, use non-irritating mouthwashes to reduce symptoms, and avoid spicy, acidic foods.
For the dosage and dosage of Selpercatinib, please understand the following dosage recommendations.
Selpercatinib is taken with meals at approximately the same time every day.
Swallow whole tablets without crushing, chewing, breaking or dissolving. If you miss taking the dose for more than 4 hours, or if you vomit after taking the medication, skip this dose and take the next dose as planned.
For patients with severe hepatic impairment whose total bilirubin exceeds 3 times the upper limit of normal and is accompanied by any elevated AST, the recommended dose is 9 mg, with a schedule of use (intermittent or continuous) specified according to the indication.
[Warm tips] Provide a comprehensive personal history and information about all medications you are taking, including prescription drugs, over-the-counter medications, and health supplements, to help your doctor make accurate treatment decisions.
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Lucius Pharmaceutical Co., Ltd., was established in 2020 in Vientiane, the capital of Laos. It aims to offer safe, effective, and affordable medicines globally. With a factory spanning 25,000 square meters, the company manufactures 200+ generic drugs in diverse therapeutic fields.
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