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Case Study |
Division of Neuro-Oncology, Department of Neurology, Brigham and Women's Hospital, Boston, MA (A.D.N., J.D., S.K., P.Y.W.); Center for Neuro-Oncology, Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA (A.D.N., J.D., A.S.C., L.D., D.C.L., S.K., P.Y.W.); Harvard Medical School, Boston, MA, (A.D.N., J.D., S.K., P.Y.W.); USA
Address correspondence to Andrew D. Norden, Center for Neuro-Oncology, Dana-Farber Cancer Institute, 44 Binney St., Boston, MA 02115, USA (anorden{at}partners.org).
Antiangiogenic drugs have emerged as effective treatment options for patients with recurrent malignant gliomas (MGs). Though this class of drugs is generally well tolerated, rare life-threatening complications, including thromboembolism, hemorrhage, and gastrointestinal (GI) perforation, are reported. We describe six cases of GI perforation among 244 glioma patients (2.5%) during treatment with antiangiogenic agents in combination with chemotherapy and corticosteroids. Two patients succumbed to this complication, and the others recovered. Because GI perforation is a life-threatening yet treatable complication, neurooncologists must have a low threshold to consider it in patients on antiangiogenic drug therapy who present with abdominal pain and other GI complaints.
Key Words: antiangiogenic drugs bevacizumab gastrointestinal perforation malignant glioma
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