Long-Term Outcomes of Stereotactic Radiosurgery for Pineocytomas: An International Multicenter Study
Status Publisher Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
39508591
DOI
10.1227/neu.0000000000003261
PII: 00006123-990000000-01429
Knihovny.cz E-zdroje
- Publikační typ
- časopisecké články MeSH
BACKGROUND AND OBJECTIVES: Pineocytomas are grade 1 tumors arising from the pineal parenchyma. Gross total resection can potentially cure these benign lesions but can be associated with morbidity. This study was designed to provide multi-institutional data to evaluate the results of stereotactic radiosurgery (SRS) for pineocytomas. METHODS: Centers participating in the International Radiosurgery Research Foundation were asked to review their database and provide data for patients who had SRS for histology confirmed grade 1 pineocytomas, for whom clinical and imaging follow-up of at least 6 months was available. RESULTS: In total, 38 patients underwent SRS as part of the management of a pineocytoma. The median age at SRS was 39 years (range 8-76). SRS was performed as primary approach in 68%, adjuvant after partial resection 19%, and at recurrence in 13% of patients. The median margin dose was 15 Gy (range 11-25 Gy). The median treatment volume was 3.35 cc (range 0.1-17.9 cc). Local tumor control was achieved in 92% of patients, with a mean actuarial progression-free survival of 21.6 years (median not reached). At last follow-up, 82% were still controlled, 8% had local recurrence, and 10% had cerebrospinal fluid dissemination. Tumor control was significantly better when SRS was used as primary care compared with the adjuvant or recurrent setting (P = .016). Five patients (13%) died during follow-up, all from tumor progression. The actuarial mean survival duration was 24.3 years, with a 5-year survival rate of 91%, and an estimated rate of 76% at 29 years. Larger tumor volume at SRS was found to be correlated to increased risk of death (P = .045). Transient symptomatic adverse radiation effects were observed in 4 patients (11%). CONCLUSION: SRS appears safe and effective for the management of pineocytomas. Long-term tumor control is achieved in most cases. SRS can be offered to selected patients as an alternative to surgical resection.
Department of Neurosurgery AOU Careggi Florence Italy
Department of Neurosurgery IRCCS Humanitas Research Hospital Milan Italy
Department of Neurosurgery New York University Langone New York New York USA
Department of Neurosurgery University of Alberta Edmonton Alberta Canada
Department of Neurosurgery University of Southern California Los Angeles California USA
Department of Neurosurgery University of Virginia Charlottesville Virginia USA
Department of Stereotactic and Radiation Neurosurgery Na Homolce Hospital Prague Czech Republic
Zobrazit více v PubMed
World Health Organization, International Agency for Research on Cancer; WHO Classification of Tumours Editorial Board. Central nervous system tumours. In WHO Classification of Tumours, Vol 6; 2021:241-258.
Reyns N, Hayashi M, Chinot O, et al. The role of Gamma Knife radiosurgery in the treatment of pineal parenchymal tumours. Acta Neurochir (Wien). 2006;148(1):5-11.
Iorio-Morin C, Kano H, Huang M, et al. Histology-stratified tumor control and patient survival after stereotactic radiosurgery for pineal region tumors: a report from the International Gamma Knife Research Foundation. World Neurosurg. 2017;107:974-982.
Clark AJ, Ivan ME, Sughrue ME, et al. Tumor control after surgery and radiotherapy for pineocytoma. J Neurosurg. 2010;113(2):319-324.
Deshmukh VR, Smith KA, Rekate HL, Coons S, Spetzler RF. Diagnosis and management of pineocytomas. Neurosurgery. 2004;55(2):349-357; discussion 355-357.
Bruce JN, Stein BM. Surgical management of pineal region tumors. Acta Neurochir (Wien). 1995;134(3-4):130-135.
Qi S, Fan J, Zhang X-an, Zhang H, Qiu B, Fang L. Radical resection of nongerminomatous pineal region tumors via the occipital transtentorial approach based on arachnoidal consideration: experience on a series of 143 patients. Acta Neurochir (Wien). 2014;156(12):2253-2262.
Hu X, Ren YM, Yang X, et al. Surgical treatment of pineal region tumors: an 18 year-experience at a single institution. World Neurosurg. 2023;172:e1-e11.
Hsieh CC, Chen JS. Radiotherapy after endoscopic biopsy in an adult with pineocytoma, the rare brain tumor in an adult: a case report and literature review. Int Med Case Rep J. 2022;15:307-311.
Motiei-Langroudi R, Sadeghian H, Soleimani MM, Seddighi AS, Shahzadi S. Treatment results for pineal region tumors: role of stereotactic biopsy plus adjuvant therapy vs. open resection. Turk Neurosurg. 2016;26(3):336-340.
Pople IK, Athanasiou TC, Sandeman DR, Coakham HB. The role of endoscopic biopsy and third ventriculostomy in the management of pineal region tumours. Br J Neurosurg. 2001;15(4):305-311.
Balossier A, Blond S, Touzet G, Sarrazin T, Lartigau E, Reyns N. Role of radiosurgery in the management of pineal region tumours: indications, method, outcome. Neurochirurgie. 2015;61(2-3):216-222.
Lekovic GP, Gonzalez LF, Shetter AG, et al. Role of Gamma Knife surgery in the management of pineal region tumors. Neurosurg Focus. 2007;23(6):e11.
Mori Y, Kobayashi T, Hasegawa T, Yoshida K, Kida Y. Stereotactic radiosurgery for pineal and related tumors. Prog Neurol Surg. 2009;23:106-118.
Wilson DA, Awad AW, Brachman D, et al. Long-term radiosurgical control of subtotally resected adult pineocytomas: clinical article. J Neurosurg. 2012;117(2):212-217.
Yianni J, Rowe J, Khandanpour N, et al. Stereotactic radiosurgery for pineal tumours. Br J Neurosurg. 2012;26(3):361-366.
Zeynal M, Karaaslan B, Dağli Ö, et al. Stereotactic radiosurgery for tumors of the pineal region: a single-center experience. Medicine (Baltimore). 2023;102(27):e34005.
Park TH, Kim SK, Phi JH, et al. Survival and malignant transformation of pineal parenchymal tumors: a 30-year retrospective analysis in a single-institution. Brain Tumor Res Treat. 2023;11(4):254-265.