Abstract
Patients with malignant glioma who are also diagnosed with one or more primary neoplasms of other organs present a unique challenge in both determining prognosis and clinical management. The overlapping impact of the malignancies and their treatment result in confounding variables that may adversely affect optimal management of such patients. Additionally, the glioma-related characteristics and survival outcome of these patients is not well-defined. In this retrospective chart and data review from our longitudinal database, we identified patients with malignant glioma including anaplastic glioma and glioblastoma, diagnosed between January 2005 and June 2011, who were also diagnosed with other non-CNS primary neoplasms. Patients with known genetic syndromes were excluded. The data was analyzed to determine the clinical characteristics and glioma-related survival. A total of 204 patients with malignant glioma (165 glioblastoma and 39 anaplastic glioma) were identified. There was no significant difference in the overall survival or progression-free survival between patients with malignant glioma plus non-CNS primary neoplasm when compared with patients with malignant glioma only. In patients with glioblastoma and non-CNS malignancy, the duration between diagnosis of glioblastoma and non-CNS neoplasms did not significantly alter glioma-related survival. Patients with malignant glioma who were diagnosed with other non-CNS malignancy have survival outcome comparable to those with malignant glioma only. The duration between diagnosis of glioblastoma and diagnosis of non-CNS neoplasms did not affect survival. Further prospective studies specifically addressing survival and molecular characteristics of patients with malignant glioma plus non-CNS cancers are recommended.
Similar content being viewed by others
References
Frodin JE, Ericsson J, Barlow L (1997) Multiple primary malignant tumors in a national cancer registry. Acta Oncol 36(5):465–469
Nagane M, Shibui S, Nishikawa R et al (1996) Triple primary malignant neoplasms including a malignant brain tumor: report of two cases and review of the literature. Surg Neurol 45(3):219–229
Piccirilli M, Salvati M, Bistazzoni S et al (2005) Glioblastoma multiforme and breast cancer: report on 11 cases and clinico-pathological remarks. Tumori 91(3):256–260
Pöyhönen L, Heikkinen J, Vehkalahti I (1979) Two different primary tumours of the brain in a patient with breast cancer. Eur J Nucl Med 4(6):483–484
Lamaida E, Caputi F, Rapanà A, Bracale C, Graziussi G (1996) Waldenström’s macroglobulinemia associated with glioblastoma. A case report. Rev Neurol 152(10):637–639
Freedman RA, Wirth LJ, Chirieac LR et al (2007) Glioblastoma in a patient with early-stage tonsil cancer. J Clin Oncol 25(19):2848–2850
Moertel CG (1964) Incidence and significance of multiple primary malignant neoplasms. Ann N Y Acad Sci 114:886–895
Mariotto AB, Rowland JH, Ries LA et al (2007) Multiple cancer prevalence: a growing challenge in long-term survivorship. Cancer Epidemiol Biomark Prev 16(3):566–571
Hayashi K, Ohtsuki Y, Sonobe H et al (1987) An autopsy case of triple primary cancers consisting of glioblastoma multiforme of the pons, colon cancer and rectal carcinoid–a statistical analysis of cases of brain tumor combined with other primary cancers in Japan autopsy annuals. Gan No Rinsho 33(14):1846–1853
Aung L, Gorlick RG, Shi W et al (2002) Second malignant neoplasms in long-term survivors of osteosarcoma: Memorial Sloan-Kettering Cancer Center experience. Cancer 95(8):1728–1734
Elkabets M, Gifford AM, Scheel C et al (2011) Human tumors instigate granulin-expressing hematopoietic cells that promote malignancy by activating stromal fibroblasts in mice. J Clin Invest 121:784–799
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
The authors declare that they do not have conflict of interest.
Electronic supplementary material
Below is the link to the electronic supplementary material.
11060_2015_1992_MOESM1_ESM.tif
Figure S1: Kaplan-Meier estimates of overall survival (OS) by anaplastic glioma with non-CNS neoplasms (grey line) and anaplastic glioma only (black line). Supplementary material 1 (TIFF 735 kb)
11060_2015_1992_MOESM2_ESM.tif
Figure S2: Kaplan-Meier estimates of progression-free survival (PFS) by glioblastoma with non-CNS neoplasms diagnosed within the period of 4 years before to 3 months after diagnosis with glioblastoma (broken line) and those who were diagnosed with non-CNS neoplasms more than 4 years before diagnosis of glioblastoma (black line). Supplementary material 2 (TIFF 645 kb)
Rights and permissions
About this article
Cite this article
Hamza, M.A., Kamiya-Matsuoka, C., Liu, D. et al. Outcome of patients with malignant glioma and synchronous or metachronous non-central nervous system primary neoplasms. J Neurooncol 126, 527–533 (2016). https://doi.org/10.1007/s11060-015-1992-x
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11060-015-1992-x