Long-course temozolomide in aggressive pituitary adenoma: real-life experience in two tertiary care centers and review of the literature

被引:24
作者
Lizzul, Laura [1 ]
Lombardi, Giuseppe [2 ]
Barbot, Mattia [1 ]
Ceccato, Filippo [1 ]
Gardiman, Marina Paola [3 ]
Regazzo, Daniela [1 ]
Bellu, Luisa [2 ]
Mazza, Elena [5 ,6 ]
Losa, Marco [4 ]
Scaroni, Carla [1 ]
机构
[1] Padua Univ Hosp, Dept Med DIMED, Endocrinol Unit, I-35121 Padua, Italy
[2] Venetian Oncol Inst IOV, Neurooncol Unit, I-35121 Padua, Italy
[3] Padua Univ Hosp, Dept Med DIMED, Pathol Unit, I-35121 Padua, Italy
[4] San Raffaele Univ Hosp, Dept Neurosurg, Pituitary Unit, I-20132 Milan, Italy
[5] San Raffaele Univ Hosp, Dept Oncol, I-20132 Milan, Italy
[6] San Raffaele Univ Hosp, Pathol Unit, I-20132 Milan, Italy
关键词
Temozolomide; Aggressive pituitary adenoma; Pituitary carcinoma; Pituitary tumors; PitNETs; EUROPEAN-SOCIETY; TUMORS; CARCINOMAS; THERAPY;
D O I
10.1007/s11102-020-01040-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose Aggressive pituitary adenomas (APAs) and pituitary carcinomas (PCs) are challenging for their invasive nature, resistance to treatment and recurrences. Temozolomide (TMZ) is used with benefit and well-tolerated toxicity profile in APAs and PCs. In most studies patients received <= 12 cycles but the best length of treatment is debated since other options after discontinuation are scarce and a second course is mainly unsuccessful. Methods We report outcomes of 8 patients with APAs and PCs treated with TMZ for more than 12 continuous cycles with a literature review. Data were retrospectively collected from Padua and Milan University Hospitals. TMZ was used as a single agent (150-200 p.o. mg/m2 daily, 5/28 days) for 14 to 45 cycles. Results Eight patients (7 M), 7 APAs and 1 PC. Previous treatments included neurosurgery and radiotherapy in all cases except two giant masses (ACTH-silent APA and prolactinoma). No patient had progression disease (PD) during long-term treatment nor toxicities. No one had complete response (CR) but four had partial response (PR). Four ACTH+ tumors maintained stable disease (SD) but the secretion pattern improved in all. After drug withdrawal, three had delayed PD (2 after 18 and one after 29 months, all ACTH+); two are still in SD. Conclusions TMZ may be useful and well-tolerated in APAs and PCs as a long-term therapy. PR appears within the first cycles with no escape throughout the treatment; most patients achieve SD. We suggest extended protocols particularly in responsive ACTH+ PAs and PCs, when further therapies may be unsuccessful.
引用
收藏
页码:359 / 366
页数:8
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