Clinical results of 24 pituitary macroadenomas with linac-based stereotactic radiosurgery

  • Sei Chul Yoon
  • , Tae Suk Suh
  • , Hong Seok Jang
  • , Su Mi Chung
  • , Yeon Shil Kim
  • , Mi Ryeong Ryu
  • , Kyu Ho Choi
  • , Ho Yong Son
  • , Moon Chan Kim
  • , Kyung Sub Shinn

Research output: Contribution to journalArticlepeer-review

92 Scopus citations

Abstract

Purpose: To determine the impact of stereotactic radiosurgery (SRS) on the clinical course, hormonal status, and follow-up CT/MRI scan of pituitary macroadenomas. Methods and Materials: From July 1988 to March 1996, 24 pituitary macroadenomas had been treated using 6 MV linear accelerator based SRS. They consisted of 11 (45.8%) prolactinomas, 2 (8.3%) growth hormone (GH)-secreting tumors, 1 (4.2%) Cushing's disease, 8 (33.3%) nonsecreting (nonfunctioning: NF) tumors, and 2 (8.3%) mixed prolactin-growth hormone (PRL-GH)-secreting tumors (M:F = 12:12; aged 21-61 years). Postoperative irradiation was performed in all cases except for the instance of Cushing's disease. The prescribed dose to tumor center varied from 10 to 27 Gy (mean 21.1 Gy) using a collimator size of 0.5 to 2.5 cm. The follow-up duration ranged from 13 to 89 months (mean 49.2 months). Results from these patients were compared to our results using conventional radiation. Results: Visual acuity and field defect were improved or became normal in 19 (79.2%) eases. Four (16.7%) remained unchanged after the treatment. One (4.1%) progressed 6 years after SRS and subsequently had repeat surgery with conventional boost irradiation. Of the 13 (46.4%) prolactinomas, including two mixed PRL-GH secreting tumors, 11 (84.1%) revealed normal hormonal levels within 1 year after SRS. In contrast, it took 2 years to become normal after conventional radiation therapy. In four GH-secreting tumors including two mixed PRL-GH secreting tumors, SRS and conventional methods showed similar responses. On follow-up imagings of the 21 patients, the mass was completely resolved in 4 (16.7%), including 3 PRLs and one NF, decreased in 11 (45.8%), and unchanged in 5 (16.7%) with central necrosis or cysts. One (4.2%) progressed and was reoperated 6 years after treatment. The complications related to SRS were comparable to those from conventional method. Conclusion: Radiosurgery can be used effectively in patients with pituitary adenoma. In this study, a more rapid hormonal and clinical response was achieved with radiosurgery than with conventional pituitary irradiation treatment.

Original languageEnglish
Pages (from-to)849-853
Number of pages5
JournalInternational Journal of Radiation Oncology Biology Physics
Volume41
Issue number4
DOIs
StatePublished - 1 Jul 1998

Bibliographical note

Funding Information:
This paper was supported by the 1997 Catholic Research Institute Medical Science Fund.

Keywords

  • Growth hormone
  • Linear accelerator
  • Pituitary adenoma
  • Prolactin
  • Stereotactic radiosurgery

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