A case series was recently published in CNS Oncology that investigated whether adult pilocytic astrocytoma—a rare and highly vascular tumor—is responsive to bevacizumab treatment.
A case series was recently published in CNS Oncology that investigated whether adult pilocytic astrocytoma (APA)—a rare and highly vascular tumor—is responsive to bevacizumab treatment.
Bevacizumab, a monoclonal antibody that blocks vascular endothelial growth factor (VEGF) pathways, has been previously found to decrease the permeability of vasculature as well as perilesional edema in glioblastoma. Researchers hypothesized that APA may be uniquely receptive to treatments that block VEGF, such as bevacizumab, given the vascularity of the tumor.
Though juvenile pilocytic astrocytoma are curable with complete surgical resection, relatively few studies have researched APA. However, some retrospective studies and anecdotal reports suggest that APAs have a more aggressive clinical course compared with juvenile cases, with a higher incidence of recurrence and progression. Recurrence rates for APA have been reported as high as 30% to 42%, and currently no standard of care exists for the treatment of APA.
Researchers reported on 4 adult patients, aged 23 years to 66 years, with pathologically diagnosed World Health Organization grade 1 pilocytic astrocytoma and who had durable, robust response to bevacizumab at the time of recurrence. Three of the tumors were located in the cerebellum, tectum, and brainstem, with the last appearing in the lateral ventricle.
All patients were treated with bevacizumab at a dose of 10 mg every 14 days for 6 cycles at the time of recurrence. The treatment was well tolerated, and no patients experienced adverse events. Following bevacizumab administration, steroids were weaned and eventually discontinued in all patients.
At the conclusion of treatment, all patients had achieved a significant clinical and radiographic response. Magnetic resonance imaging (MRI) studies of each patient’s brain after 6 cycles of bevacizumab showed significant decrease or resolution of tumor contrast enhancement. In addition, all patients experienced a significant reduction in tumor size following treatment. Two of the patients experienced complete responses, with no radiographic evidence of tumor upon follow-up MRI.
The sustained decrease in tumor size and contrast enhancement after treatment suggest that bevacizumab may be an important agent to achieve durable disease control in APA. To date, there are no prospective studies evaluating the use of such treatments in APA, however. Due to the low incidence of the tumor, the authors say, future studies are warranted to further assess efficacy of bevacizumab treatment in APA.
Reference
Wasilewski A, Mohile N. Durable response to bevacizumab in adults with recurrent pilocytic astrocytoma [Published online April 9, 2018]. CNS Oncol. doi: 10.2217/cns-2017-0039.
Breaking Down Biosimilar Barriers: Payer and PBM Policies
November 13th 2024Part 2 of this series for Global Biosimilars Week dives into the complexities of payer and pharmacy benefit manager (PBM) policies, how they impact biosimilar accessibility, and how addressing these issues may look under a second Trump term.
Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
Biosimilars Oncology Roundup for June 2024—Podcast Edition
July 7th 2024On this episode of Not So Different, we review biosimilar news coming out of June, with clinical trial results from conferences and a study showcasing how to overcome economic and noneconomic barriers to oncology biosimilars.
Competitive Pricing in Biosimilars: How Adalimumab Could Shape the Industry
Published: October 29th 2024 | Updated: October 29th 2024Sophia Humphreys, PharmD, MHA, BCBBS, of Sutter Health notes that although initial adoption of adalimumab biosimilars remained low in 2023, competitive pricing pressures have already benefited patients and the health care sector.