Survival rates 来自妙佑医疗国际员工 What is the survival rate for the different grades of astrocytoma? Grade 1, also called pilocytic, is usually cured with surgery. The five-year survival rate is around 96%. Grade 2, also called diffuse, astrocytomas have a median survival of about 7 to 8 years. Grade 3, also called anaplastic, astrocytomas have a median survival of about five years. Grade 4, also called glioblastoma, astrocytomas have a median survival of about 14 to 15 months. How does IDH-mutant status change life expectancy? An IDH mutation is linked with longer survival and better response to therapy compared with IDH-wild-type tumors. For grade 2 disease, a change to the IDH1 gene is specifically linked with longer survival and has a better outlook than IDH wild type. What is the prognosis for pilocytic astrocytoma in children?Pilocytic astrocytoma (grade 1) in children is slow growing and often cured with surgery. The five-year survival rate is about 96%. Anaplastic astrocytoma (grade 3): Factors linked to longer survivalSome people with anaplastic astrocytoma, also called grade 3, live much longer than the average five-year survival. In general, people with IDH-mutant tumors, who are younger, recover well from surgery, and receive both chemotherapy and radiation, are the most likely to have long-term survival. Several factors can help improve outcomes: More complete tumor removal. When surgeons can safely remove most or all the tumor, people tend to live longer. The exact amount removed often makes a big difference. Combined treatment. Using surgery followed by both radiation and chemotherapy gives the best survival rates for high-grade tumors. Favorable tumor genetics. Tumors with certain gene changes, such as an IDH or MGMT gene change, tend to grow more slowly and respond better to treatment. Younger age and good overall health. Younger people and those with fewer neurological symptoms at diagnosis tend to do better. Astrocytoma treatment is personalized. Surgery is usually first, followed by radiation or chemotherapy or both based on the tumor's grade and genes. Some people also may receive targeted therapy. Supportive care, also called palliative care, can start early to control symptoms and protect quality of life. New options, such as gene-targeted medicines and immunotherapy, are being tested in clinical trials and may expand choices over time. 申请预约 诊断与治疗医生与科室 Nov. 07, 2025 Living with 星形细胞瘤? Connect with others like you for support and answers to your questions in the Brain Tumor support group on Mayo Clinic Connect, a patient community. Brain Tumor Discussions Meningioma: Anyone else? I'm frightened 581 Replies Tue, Nov 11, 2025 chevron-right Anyone had Proton Beam Therapy for Meningioma? 53 Replies Sun, Nov 09, 2025 chevron-right Pituitary tumor symptoms: joint, muscle and body aches 178 Replies Sat, Nov 08, 2025 chevron-right See more discussions 显示参考文献 Central nervous system cancers. National Comprehensive Cancer Network. https://www.nccn.org/guidelines/guidelines-detail?category=1&id=1425. Accessed Sept. 27, 2025. Elsevier Point of Care. Clinical Overview: Astrocytoma. https://www.clinicalkey.com. Accessed Sept. 27, 2025. Adult central nervous system tumors treatment (PDQ) — Patient version. National Cancer Institute. https://www.cancer.gov/types/brain/patient/adult-brain-treatment-pdq. Accessed Sept. 27, 2025. Salari N, et al. Patients' survival with astrocytoma after treatment: A systematic review and meta‑analysis of clinical trial studies. Indian Journal of Surgical Oncology. 2022; doi:10.1007/s13193-022-01533-7. Tonn JC, et al. Astrocytomas of the spinal cord. Neuro-Oncology Advances. 2024; doi:10.1093/noajnl/vdad166. Shehaj A, et al. Genetic biomarkers in astrocytoma: Diagnostic, prognostic, and therapeutic potential. World Neurosurgery. 2024; doi:10.1016/j.wneu.2024.06.009. Ostrom QT, et al. CBTRUS statistical report: Primary brain and other central nervous system tumors diagnosed in the United States in 2016-2020. Neuro-Oncology. 2023; doi:10.1093/neuonc/noad149. Jankovic J, et al., eds. Structural imaging using magnetic resonance imaging and computed tomography. In: Bradley and Daroff's Neurology in Clinical Practice. 8th ed. Elsevier; 2022. https://www.clinicalkey.com. Accessed Sept. 28, 2025. Astrocytoma tumors. American Association of Neurological Surgeons. https://www.aans.org/patients/conditions-treatments/astrocytoma-tumors/. Accessed Sept. 28, 2025. Elsevier Point of Care. Clinical Overview: Brain neoplasm, glioblastoma. https://www.clinicalkey.com. Accessed Oct. 9, 2025. Kessler T, et al. Conventional and emerging treatments of astrocytomas and oligodendrogliomas. Journal of Neuro-Oncology. 2023; doi:10.1007/s11060-022-04216-z. Rudà R, et al. DH inhibition in gliomas: From preclinical models to clinical trials. Nature Review Neurology. 2024; doi:10.1038/s41582-024-00967-7. Recht LD, et al. Treatment and prognosis of IDH-mutant astrocytomas in adults. https://www.uptodate.com/contents/search. Accessed Oct. 9, 2025. Khagi S, et al. Recent advances in Tumor Treating Fields (TTFields) therapy for glioblastoma. The Oncologist. 2025; doi:10.1093/oncolo/oyae227. Yu A, et al. Theory and application of TTFields in newly diagnosed glioblastoma. CNS Neuroscience & Therapeutics. 2023; doi:10.1111/cns.14563. Wen PY, et al. The 2021 WHO Classification of Tumors of the Central Nervous System: clinical implications. Neuro-Oncology. 2021. doi:10.1093/neuonc/noab120. 星形细胞瘤症状与病因诊断与治疗Survival rates医生与科室在 Mayo Clinic 治疗 CON-20117611 疾病与状况 星形细胞瘤