BRAF-MEK Inhibition in Newly Diagnosed Papillary Craniopharyngiomas

被引:50
作者
Brastianos, Priscilla K. [1 ]
Twohy, Erin [4 ]
Geyer, Susan [4 ]
Gerstner, Elizabeth R. [1 ]
Kaufmann, Timothy J. [5 ]
Tabrizi, Shervin [1 ]
Kabat, Brian [4 ]
Thierauf, Julia [1 ]
Ruff, Michael W. [5 ]
Bota, Daniela A. [6 ]
Reardon, David A. [2 ]
Cohen, Adam L. [7 ]
De La Fuente, Macarena I. [8 ]
Lesser, Glenn J. [9 ]
Campian, Jian [10 ]
Agarwalla, Pankaj K. [11 ]
Kumthekar, Priya
Mann, Bhupinder
Vora, Shivangi [12 ]
Knopp, Michael [12 ]
Iafrate, A. John [1 ]
Curry, William T., Jr.
Cahill, Daniel P. [1 ]
Shih, Helen A. [1 ]
Brown, Paul D. [5 ]
Santagata, Sandro [3 ]
Barker, Fred G., II [1 ]
Galanis, Evanthia [5 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp, Canc Ctr, Boston, MA USA
[2] Dana Farber Canc Inst, Boston, MA USA
[3] Brigham & Womens Hosp, Harvard Program Therapeut Sci, DanaFarber Partners CancerCare, Boston, MA USA
[4] Alliance Stat & Data Management Ctr, Rochester, MN USA
[5] Mayo Clin, Rochester, MN USA
[6] UC Irvine, Chao Family Comprehens Canc Ctr, Orange, CA USA
[7] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT USA
[8] Univ Miami, Miller Sch Med, Sylvester Comprehens Canc Ctr, Miami, FL USA
[9] Wake Forest Univ, Sch Med, Winston Salem, NC USA
[10] Washington Univ, Sch Med, St Louis, MO USA
[11] Rutgers Canc Inst, New Brunswick, NJ USA
[12] Ohio State Univ, Columbus, OH USA
基金
美国国家卫生研究院;
关键词
RADIATION-THERAPY; MELANOMA; SURVIVAL; VEMURAFENIB; CONFIDENCE; OUTCOMES; DISEASE; SURGERY;
D O I
10.1056/NEJMoa2213329
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Craniopharyngiomas, primary brain tumors of the pituitary-hypothalamic axis, can cause clinically significant sequelae. Treatment with the use of surgery, radiation, or both is often associated with substantial morbidity related to vision loss, neuroendocrine dysfunction, and memory loss. Genotyping has shown that more than 90% of papillary craniopharyngiomas carry BRAF V600E mutations, but data are lacking with regard to the safety and efficacy of BRAF-MEK inhibition in patients with papillary craniopharyngiomas who have not undergone previous radiation therapy. METHODS Eligible patients who had papillary craniopharyngiomas that tested positive for BRAF mutations, had not undergone radiation therapy previously, and had measurable disease received the BRAF-MEK inhibitor combination vemurafenib-cobimetinib in 28-day cycles. The primary end point of this single-group, phase 2 study was objective response at 4 months as determined with the use of centrally determined volumetric data. RESULTS Of the 16 patients in the study, 15 (94%; 95% confidence interval [CI], 70 to 100) had a durable objective partial response or better to therapy. The median reduction in the volume of the tumor was 91% (range, 68 to 99). The median follow-up was 22 months (95% CI, 19 to 30) and the median number of treatment cycles was 8. Progression-free survival was 87% (95% CI, 57 to 98) at 12 months and 58% (95% CI, 10 to 89) at 24 months. Three patients had disease progression during followup after therapy had been discontinued; none have died. The sole patient who did not have a response stopped treatment after 8 days owing to toxic effects. Grade 3 adverse events that were at least possibly related to treatment occurred in 12 patients, including rash in 6 patients. In 2 patients, grade 4 adverse events (hyperglycemia in 1 patient and increased creatine kinase levels in 1 patient) were reported; 3 patients discontinued treatment owing to adverse events. CONCLUSIONS In this small, single-group study involving patients with papillary craniopharyngiomas, 15 of 16 patients had a partial response or better to the BRAF-MEK inhibitor combination vemurafenib-cobimetinib.
引用
收藏
页码:118 / 126
页数:9
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