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Subramanian, Megha

https://orcid.org/0000-0002-4416-5128

Mayo Clinic

Massachusetts General Hospital

Citations 2

RARE-04. TARGETED TREATMENT OF PAPILLARY CRANIOPHARYNGIOMAS HARBORING BRAFV600E MUTATIONS
Jones, Pamela S. , Subramanian, Megha , Aylwin, Simon , Gudjonsson, Olafur, Shaw, Brian , Uhm, Joon H. , Barker, Fred G., Juratli, Tareq A. , Wang, Nancy , Odia, Yazmín , Rostami, Elham , Cahill, Daniel P. , Galanis, Evanthia , Santagata, Sandro , Brastianos, Priscilla K.

Neuro-Oncology | November 11, 2019 | Volume: 21 | Issue: Supplement_6 | Pages: vi222-vi222

10.1093/neuonc/noz175.927 Get It

Abstract Craniopharyngiomas are surgically challenging brain tumors. Postoperatively, quality of life is often significantly impaired due to neurological and endocrinological complications. Currently, FDA approved systemic treatments are not available for patients in whom craniopharyngiomas recur after surgery and radiation. Papillary craniopharyngiomas are characterized by the presence of BRAFV600E mutations. To date, five case reports have been published on the treatment of BRAFV600E mutant papillary craniopharyngiomas with BRAF and/or MEK inhibitors. In this presentation, authors from all five previously published reports share their collective experience and provide updated follow-up on their patients, thus generating an overview of all currently available information on targeted therapy in patients with BRAFV600E mutant papillary craniopharyngiomas. We have also included information on an additional patient with a papillary craniopharyngioma recently treated with BRAF and MEK inhibitors after tumor biopsy alone, in the absence of recurrence, highlighting the potential for a neo-adjuvant therapeutic approach. All six cases in our series showed dramatic responses to targeted treatment with BRAF (and MEK) inhibitors. Collectively, our cases are highly promising and informative for patient treatment, although uncertainty remains with regards to the optimal timing, the specific agents (single agent or dual therapy) to be used and the duration of treatment. The ongoing multicenter phase II Alliance A071601 trial (NCT03224767) of vemurafenib and cobimetinib for patients with biopsy-proven residual or recurrent papillary craniopharyngiomas should provide additional information to help guide patient management.
Targeted treatment of papillary craniopharyngiomas harboring BRAF V600E mutations
Juratli, Tareq A. , Jones, Pamela S. , Subramanian, Megha , Aylwin, Simon , Odia, Yazmín , Rostami, Elham , Gudjonsson, Olafur, Shaw, Brian , Barker, Fred G., Santagata, Sandro , Galanis, Evanthia , Santagata, Sandro , Odia, Yazmin , Wang, Nancy , Cahill, Daniel P. , Galanis, Evanthia , Brastianos, Priscilla K.

Cancer | July 17, 2019 | Volume: 125 | Issue: 17 | Pages: 2910-2914

10.1002/cncr.32197 Get It

Papillary craniopharyngiomas (PCPs) are characterized by the presence of BRAF V600E mutations, which are emerging as a useful guide for diagnosis and treatment decision making. The ongoing multicenter phase 2 Alliance A071601 trial is evaluating the efficacy of BRAF and mitogen‐activated protein kinase kinase (MEK) inhibitors for patients with PCPs. With continued successful responses, it is proposed that BRAF (and MEK) inhibitors be evaluated for the neoadjuvant treatment of patients with PCPs.