Cabozantinib (Cabometyx, Exelixis) has shown efficacy in the first-line treatment of radioactive iodine (RAI)–refractory differentiated thyroid carcinoma (DTC) and could offer an option in addition to the drugs approved for this indication, such as sorafenib (Nexavar, Bayer) and lenvatinib (Lenvima, Eisai).
New data from a phase 2 study showed that patients with thyroid cancer that progressed after surgery and RAI achieved an objective response rate of 54% with cabozantinib, and tumor shrinkage was seen in 34 of the 35 enrolled patients.
These data were highlighted at a press conference before their presentation at the 2018 Multidisciplinary Head and Neck Cancers Symposium, to be held in Scottsdale, Arizona, on February 15 to 17.
Presenter Marcia S. Brose, MD, PhD, an associate professor at the Perelman School of Medicine at the University of Pennsylvania in Philadelphia, noted that while RAI is curative for most patients, in about 5% to 15% of patients with thyroid cancer, the disease becomes refractory to treatment.
“Our positive results indicate that cabozantinib offers an additional option to shrink patients’ tumors and provide an additional progression-free period,” Brose said.
Cabozantinib is a multikinase tyrosine kinase inhibitors targeting VEGFR, RET, MET, and AXL and is already approved for use in patients with advanced thyroid cancer and renal cell carcinoma.
The manufacturer is exploring other indications. “Based on these promising results and data from other studies of cabozantinib in previously treated DTC, Exelixis plans to initiate a pivotal phase 3 study with cabozantinib in patients with advanced DTC later this year,” Gisela Schwab, MD, company president and chief medical officer, said in a statement.
Shows “Good Activity”
Brose presented data from the UPCC 28313 (NCT 02041260) study, which enrolled 35 patients with metastatic, RAI-refractory thyroid cancer who had not received prior treatment with VEGFR inhibitors. Median age at enrollment was 65 years, and three fourths of the patients had papillary thyroid cancer.
Patients received cabozantinib, 60 mg daily.
The study was powered to detect an overall response rate of 15%, which translates to responses in at least 5 of the 35 patients.
Although no patient showed a complete response, partial responses were seen in 19 of 35 (54%) patients and stable disease was reported for 15 of 35 (43%) patients. Duration of partial response ranged from 11 weeks to more than 174 weeks.
–GDMeds, an India Pharmacy Service company
[Disclaimer]The Site is operated by GDMeds and all rights thereto are owned and reserved by GDMeds. The contents and works on these pages compiled by GDMeds are subject to copyright law. Copying, processing, distribution and any kind of use outside the limits of copyright law require the written consent of GDMeds In case the content is not created by GDMeds the copyrights of third parties are being observed. However, if a user becomes aware of a copyright infringement, GDMeds asks the user for notification. Upon notification of such violations, GDMeds will remove the content immediately.
[免责声明]本网站由印度极得美运营。印度极得美拥有和保留一切权利。印度极得美的网页内容及文档受版权法保护。复制、加工、传播及任何超出版权法限制的任何使用行为均必须得到印度极得美书面许可。如相关内容如非由印度极得美创作,需遵守第三方的版权,特别是标示为第三方内容的。如用户发现侵犯版权的行为,请通知极得美。一旦收到违反通知,极得美将立刻移除相关内容。
[отказ]Сайт управляется GDMeds, и все права на него принадлежат и зарезервированы GDMeds. Содержание и работы на этих страницах, составленные GDMeds, защищены законом об авторском праве. Копирование, обработка, распространение и любое использование вне пределов авторского права требуют письменного согласия GDMeds. Если контент не создан GDMeds, то соблюдаются авторские права третьих лиц. Однако, если пользователь узнает о нарушении авторских прав, GDMeds запрашивает у пользователя уведомление. После уведомления о таких нарушениях GDMeds немедленно удалит контент.