Abstract:Pilocytic Astrocytoma (PA) is the most common low-level brain tumor in children, which is commonly found in optic nerve, optic chiasma, hypothalamus, brain stem, cerebellum and cerebrum. PA is often well-bounded, slow-growing and belongs to WHO I tumors, and surgical resection is the first choice for treatment. However, due to the importance of nerve functions of optic nerves, optic chiasma, hypothalamus, brain stem, total resection may not be possible. At present, there is no conclusion on the postoperative treatment of pediatric PA. The main treatment methods for postoperative pediatric PA patients include radiotherapy, chemotherapy, targeted therapy and follow-up observation. With the progress of imaging and radiation technology, in addition to traditional fractional radiotherapy, conformal radiotherapy, stereotactic radiotherapy and proton therapy are also included, aiming to reduce the toxic and side effects of radiotherapy and improve the efficacy of radiotherapy. However, most scholars currently do not recommend radiotherapy as the first-line treatment option for the patients after the surgery. Vincristine combined with carboplatin is the first-line treatment option for progressive PA. The combination of irinotecan and bevacizumab can be used as the second-line therapy. The development of target therapy is promising. Due to their less toxic side effects and excellent therapeutic effect, targeted therapy led by MEK inhibitors are expected to become the first-line drugs for the postoperative children suffered from PA in the future. However, there is still a lack of high-level clinical evidence. Follow-up observation is one of the postoperative options for children with PA. Some scholars have proposed hierarchical treatment for children with PA, and recommended postoperative follow-up observation for low-risk patients. This paper reviews the newly-published articles about the comprehensive treatment of the pediatric patients with PA.