Integrating Systemic Therapies into the Multimodality Therapy of Patients with Craniopharyngioma

被引:1
|
作者
Gritsch, David [1 ]
Santagata, Sandro [2 ]
Brastianos, Priscilla K. [1 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp Canc Ctr, Canc Ctr, 55 Fruit St, Boston, MA 02114 USA
[2] Harvard Med Sch, Brigham & Womens Hosp, Dept Pathol, 75 Francis St, Boston, MA 02115 USA
关键词
Craniopharyngioma; Systemic therapies; Multimodality therapy; Targeted molecular therapies; DABRAFENIB PLUS TRAMETINIB; RADIATION-THERAPY; BETA-CATENIN; MEK INHIBITION; OPEN-LABEL; BRAF; SURGERY; MANAGEMENT; CHILDHOOD; MELANOMA;
D O I
10.1007/s11864-023-01156-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The integration of targeted therapy into the multimodal management of craniopharyngiomas represents a significant advancement in the field of neuro-oncology. Historically, the management of these tumors has been challenging due to their proximity to vital brain structures, necessitating a delicate balance between tumor control and the preservation of neurological function. Traditional treatment modalities, such as surgical resection and radiation, while effective, carry their own set of risks, including potential damage to surrounding healthy tissues and the potential for long-term side effects. Recent insights into the molecular biology of craniopharyngiomas, particularly the discovery of the BRAF V600E mutation in nearly all papillary craniopharyngiomas, have paved the way for a targeted systemic treatment approach. However, advances have been limited for adamantinomatous craniopharyngiomas. The success of BRAF/MEK inhibitors in clinical trials underscores the potential of these targeted therapies not only to control tumor growth but also to reduce the need for more invasive treatments, potentially minimizing treatment-related complications. However, the introduction of these novel therapies also brings forth new challenges, such as determining the optimal timing, sequencing, and duration of targeted treatments. Furthermore, there are open questions regarding which specific BRAF/MEK inhibitors to use, the potential need for combination therapy, and the strategies for managing intolerable adverse events. Finally, ensuring equitable access to these therapies, especially in healthcare systems with limited resources, is crucial to prevent widening healthcare disparities. In conclusion, targeted therapy with BRAF/MEK inhibitors holds great promise for improving outcomes and quality of life for patients with BRAF-mutated craniopharyngiomas. However, additional research is needed to address the questions that remain about its optimal use and integration into comprehensive treatment plans.
引用
收藏
页码:261 / 273
页数:13
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