Treatment of Pituitary Carcinomas and Atypical Pituitary Adenomas: A Review

被引:14
作者
Hirohata, Toshio [1 ,2 ]
Ishii, Yudo [1 ]
Matsuno, Akira [1 ]
机构
[1] Teikyo Univ, Dept Neurosurg, Tokyo 173, Japan
[2] Univ Tokyo, Dept Neurosurg, Tokyo 1138655, Japan
关键词
atypical pituitary adenoma; pituitary carcinoma; temozolomide; DNA MISMATCH REPAIR; TEMOZOLOMIDE TREATMENT; NEUROENDOCRINE TUMORS; THERAPY; METASTASES; PROLACTINOMA; EXPERIENCE; EXPRESSION; MANAGEMENT; RESISTANT;
D O I
10.2176/nmc.ra.2014-0178
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Atypical pituitary adenomas (APAs) are aggressive tumors, harboring a Ki-67 (MIB-1) staining index of 3% or more, and positive immunohistochemical staining for p53 protein, according to the World Health Organization (WHO) classification in 2004. Pituitary carcinomas (PC) usually develop from progressive APAs and predominantly consist of hormone-generating tumors, defined by the presence of disseminations in the cerebrospinal system or systemic metastases. Most of the cases with these malignant pituitary adenomas underwent surgeries, irradiations and adjuvant medical treatments, nevertheless, the therapies are mainly palliative. Recently, the efficacy of temozolomide (TMZ), an orally administered alkylating agent, has been reported as an alternative medical treatment. However, some recent studies have demonstrated a significant recurrence rate after effective response to TMZ. Further clinical and pathological researches of malignant pituitary adenomas will be required to improve the outcome of patients with these tumors.
引用
收藏
页码:966 / 973
页数:8
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