Meningioma: analysis of recurrence and progression following neurosurgical resection.

The rates of survival, tumor recurrence, and tumor progression were analyzed in 225 patients with meningioma who underwent surgery as the only treatment modality between 1962 and 1980. Patients were considered to have a recurrence if their studies verified a mass effect in spite of a complete surgical removal, whereas they were defined as having progression if, after a subtotal excision, there was clear radiological documentation of an increase in the size of their tumor. There were 168 females and 57 males (a ratio of 2.9:1), with a peak incidence of tumor occurrence in the fifth (23%), sixth (29%), and seventh (23%) decades of life. Anatomical locations were the convexity (21%), parasagittal area (17%), sphenoid ridge (16%), posterior fossa (14%), parasellar region (12%), olfactory groove (10%), spine (8%), and orbit (2%). The absolute 5-, 10-, and 15-year survival rates were 83%, 77%, and 69%, respectively. Following a total resection, the recurrence-free rate at 5, 10, and 15 years was 93%, 80%, and 68%, respectively, at all sites. In contrast, after a subtotal resection, the progression-free rate was only 63%, 45%, and 9% during the same period (p less than 0.0001). The probability of having a second operation following a total excision after 5, 10, and 15 years was 6%, 15%, and 20%, whereas after a subtotal excision the probability was 25%, 44%, and 84%, respectively (p less than 0.0001). Tumor sites associated with a high percentage of total excisions had a low recurrence/progression rate. For example, 96% of convexity meningiomas were removed in toto, and the recurrence/progression rate at 5 years was only 3%. Parasellar meningiomas, with a 57% total excision rate, had a 5-year probability of recurrence/progression of 19%. Only 28% of sphenoid ridge meningiomas a second resection, the probability of a third operation at 5 and 10 years was 42% and 56%, respectively. There was no difference in the recurrence/progression rates according to the patients' age or sex, or the duration of symptoms. Implications for the potential role of adjunctive medical therapy or radiation therapy for meningiomas are discussed.

[1]  Elisa T. Lee,et al.  Statistical Methods for Survival Data Analysis , 1994, IEEE Transactions on Reliability.

[2]  K. Kiel,et al.  Radiation therapy in the treatment of aggressive fibromatoses (desmoid tumors) , 1984 .

[3]  R. Giuffrè Successful radical removal of an intracranial meningioma in 1835 by Professor Pecchioli of Siena. , 1984, Journal of neurosurgery.

[4]  M. Khan,et al.  The recurrence of intracranial meningiomas after surgical treatment. , 1983, Journal of neurosurgery.

[5]  J. Ransohoff,et al.  Role of radiation therapy in the management of meningioma. , 1982, Neurosurgery.

[6]  J. Evans,et al.  Steroid receptor proteins in human meningiomas , 1982, Cancer.

[7]  N. de Tribolet,et al.  Presence of sex steroid hormone receptors in meningioma tissue. , 1981, Surgical neurology.

[8]  R. Weichselbaum,et al.  Radiation therapy in the treatment of aggressive fibromatoses. , 1981, International journal of radiation oncology, biology, physics.

[9]  H. Handa,et al.  Recurrence of intracranial meningiomas, with special reference to radiotherapy. , 1980, Surgical neurology.

[10]  A. Buge,et al.  [Estrogen and progestin receptors in meningiomas: a study in 22 cases (author's transl)]. , 1980, Revue neurologique.

[11]  R. Ojemann Meningiomas of the basal parapituitary region: technical considerations. , 1980, Clinical neurosurgery.

[12]  W. Donegan,et al.  Estrogen-receptor protein in intracranial meningiomas. , 1979, Journal of neurosurgery.

[13]  A. Sahar,et al.  The recurrence of intracranial meningiomas , 1979, Neurochirurgia.

[14]  Bataini Jp,et al.  High energy radiotherapy in the treatment of meningiomas of the cavernous sinus. , 1979 .

[15]  M. Friedman Irradiation of meningioma: a prototype circumscribed tumor for planning high-dose irradiation of the brain. , 1977, International journal of radiation oncology, biology, physics.

[16]  J. Whisnant,et al.  Nervous system neoplasms and primary malignancies of other sites , 1975, Neurology.

[17]  H. Suit,et al.  Sarcoma of soft tissue: Clinical and histopathologic parameters and response to treatment , 1975, Cancer.

[18]  E. Boldrey,et al.  Radiation therapy of meningiomas. , 1975, The American journal of roentgenology, radium therapy, and nuclear medicine.

[19]  N. Gowing Tumors of the Central Nervous System (Atlas of Tumour Pathology, Second Series, Fascicle 6) , 1974 .

[20]  J. Moossy Tumors of the Central Nervous System, Atlas of Tumor Pathology, Second Series, Fascicle 6 , 1973, Neurology.

[21]  C. Fischer,et al.  [Surgical prognosis of meningiomas of the sphenoidal ridge]. , 1973, Neuro-Chirurgie.

[22]  L. J. Rubinstein,et al.  Tumors of the central nervous system , 1972 .

[23]  C. H. Chang,et al.  Radiotherapy in the management of meningiomas. , 2009, Acta radiologica: therapy, physics, biology.

[24]  W. Haenszel,et al.  Statistical aspects of the analysis of data from retrospective studies of disease. , 1959, Journal of the National Cancer Institute.

[25]  E. Bickerstaff,et al.  THE RELAPSING COURSE OF CERTAIN MENINGIOMAS IN RELATION TO PREGNANCY AND MENSTRUATION* , 1958, Journal of neurology, neurosurgery, and psychiatry.

[26]  H. Olivecrona,et al.  Report on 280 cases of verified parasagittal meningioma. , 1955, Journal of neurosurgery.

[27]  Harvey Cushing,et al.  Meningiomas : their classification, regional behaviour, life history, and surgical end results , 1938 .