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用远距离钴源对大侵袭性垂体腺瘤进行外照射:一项对大多接受40-45Gy剂量照射患者的长期随访回顾性研究。

External irradiation of macroinvasive pituitary adenomas with telecobalt: a retrospective study with long-term follow-up in patients irradiated with doses mostly of between 40-45 Gy.

作者信息

Zaugg M, Adaman O, Pescia R, Landolt A M

机构信息

Department of Radiation Oncology, City Hospital Triemli, Zurich, Switzerland.

出版信息

Int J Radiat Oncol Biol Phys. 1995 Jun 15;32(3):671-80. doi: 10.1016/0360-3016(94)00620-Z.

Abstract

PURPOSE

Published dose recommendations for radiotherapy in patients with pituitary macroadenomas vary. Therefore, we retrospectively analyzed the results in our patients from the treatment period 1973-1992.

METHODS AND MATERIALS

From a total of 89 patients with macroinvasive adenomas, 66 received radiation therapy immediately following subtotal surgical removal (combined treatment modality), and 22 were irradiated as primary treatment or after surgical recurrence. Only one patient was reirradiated. The surgical interventions have been performed by the same surgeon. For the majority of patients (79 out of 89) with a mean follow-up of 8.1 years (0.5-19 years) the total tumor dose ranged between 40-45 Gy at a dose per fraction of 1.8-2.25 Gy. All patients had bilateral opposed fields with telecobalt. Eleven patients had an additional arc rotation.

RESULTS

The 10-year progression-free survival for all 89 patients independent of treatment modality was 88.1%. The 10-year progression-free survival for patients treated by surgery and adjuvant radiation therapy (40-45 Gy at 1.8-2.25 Gy, 60 out of 79) was 90.3%, and for radiation therapy alone (40-45 Gy at 1.8-2.25 Gy, 19 out of 79), 100% (p = 0.32). The prognostic factors for progression-free survival were the subtype of adenoma, the presence of visual symptoms at the time of diagnosis, the suprasellar extension, and the initial hormone levels. The presence of infiltration of adenoma cells in the basal dura or in the mucosa of the sinus sphenoidalis do not represent prognostic factors showing the special biological behavior of pituitary adenomas. Signs of x-ray-induced cerebral necrosis have not been observed in any patient. Long-term visual complications developed in four patients. This could be due to scar formation in the treated region, which can compress the optic nerve and provoke disturbance similar to an empty-sella syndrome. The latter occurred prevalently years after treatment, even though surgical methods of sellar plugging were used. The incidence of hypopituitarism after combined treatment modality at time of last follow-up (irradiated between 40-45 Gy at 1.8-2.25 Gy) was low (36%, 21 out of 60).

CONCLUSION

In patients with pituitary macroadenomas, radiotherapy with a total dose of 40-45 Gy at 1.8-2.25 Gy per fraction resulted in a high local tumor control without serious morbidity.

摘要

目的

已发表的垂体大腺瘤患者放射治疗剂量建议各不相同。因此,我们回顾性分析了1973年至1992年治疗期间我们患者的治疗结果。

方法和材料

在总共89例侵袭性大腺瘤患者中,66例在次全手术切除后立即接受放射治疗(联合治疗方式),22例作为初始治疗或手术复发后接受放疗。仅1例患者接受了再照射。手术均由同一位外科医生进行。对于大多数患者(89例中的79例),平均随访8.1年(0.5 - 19年),总肿瘤剂量在40 - 45 Gy之间,每次分割剂量为1.8 - 2.25 Gy。所有患者均采用双侧相对野钴远距离治疗。11例患者还进行了弧形旋转照射。

结果

89例患者无论治疗方式如何,10年无进展生存率为88.1%。接受手术及辅助放疗(1.8 - 2.25 Gy时40 - 45 Gy,79例中的60例)的患者10年无进展生存率为90.3%,单纯放疗(1.8 - 2.25 Gy时40 - 45 Gy,79例中的19例)的患者10年无进展生存率为100%(p = 0.32)。无进展生存的预后因素包括腺瘤亚型、诊断时是否存在视觉症状、鞍上扩展情况以及初始激素水平。腺瘤细胞浸润至硬脑膜基部或蝶窦黏膜并不代表垂体腺瘤特殊生物学行为的预后因素。未在任何患者中观察到X线诱导的脑坏死迹象。4例患者出现长期视觉并发症。这可能是由于治疗区域形成瘢痕,可压迫视神经并引发类似空蝶鞍综合征的紊乱。尽管采用了鞍内填塞手术方法,但后者多在治疗数年之后出现。联合治疗方式在最后一次随访时(1.8 - 2.25 Gy时照射40 - 45 Gy)垂体功能减退的发生率较低(36%,60例中的21例)。

结论

对于垂体大腺瘤患者,每次分割剂量为1.8 - 2.25 Gy、总剂量为40 - 45 Gy的放射治疗可实现较高的局部肿瘤控制率,且无严重并发症。

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