Department of Pediatric Neurosurgery, hôpital Femme-Mère-Enfant, 32, avenue du Doyen Jean-Lépine, 69677 Lyon Cedex, France.
Department of Pediatric Hematology and Oncology, Institut d'hématologie et d'oncologie pédiatrique, 69008 Lyon, France.
Neurochirurgie. 2021 Feb;67(1):52-60. doi: 10.1016/j.neuchi.2021.01.003. Epub 2021 Jan 19.
Modern approach for the treatment of posterior fossa medulloblastomas remains a challenge for pediatric neurosurgeons and pediatric oncologists and requires a multidisciplinary approach to optimize survival and clinical results.
We report the surgical principles of the treatment of posterior fossa medulloblastomas in children and how to avoid technical mistakes especially in very young patients. We also report our experience in a series of 64 patients operated from a medulloblastoma between 2000 and 2018 in Lyon.
All patients had a craniospinal MRI. Eighty-one percent of the patients (n=50) had strictly midline tumor while 19% (n=14) had lateralized one. Eleven percent (n=7) had metastasis at diagnosis on the initial MRI. Forty-one percent (n=29) had an emergency ETV to treat hydrocephaly and the intracranial hypertension. All patient underwent a direct approach and a complete removal was achieved in 78% (n=58) of the cases on the postoperative MRI realized within 48h postsurgery. Histological findings revealed classical medulloblastoma in 73% (n=46), desmoplastic medulloblastoma in 17% (n=11) and anaplastic/large cell medulloblastoma in 10% (n=7). Patients were classified as low risk in 7 cases, standard risk in 30 cases and high risk in 27 cases. Ninety-six percent (n=61) of the patient received radiotherapy. Seventy-six percent (n=48) received pre-irradiation or adjuvant chemotherapy. At last follow-up in December 2018, 65% (n=41) of the patient were in complete remission, 12% (n=8) were in relapse and 27% (n=15) had died from their disease. The overall survival at five , ten and fifteen years for all the series was of 76%, 73% and 65.7% respectively.
Medulloblastomas remain a chimiosensible and radiosensible disease and the complete surgical removal represents a favorable prognostic factor. The extension of surgery has also to be weighted in consideration of the new biomolecular and genetic knowledge that have to be integrated by surgeons to improve quality of life of patients.
对于儿童神经外科医生和儿科肿瘤学家来说,现代治疗后颅窝髓母细胞瘤的方法仍然是一个挑战,需要采用多学科方法来优化生存和临床结果。
我们报告了儿童后颅窝髓母细胞瘤治疗的手术原则,以及如何避免在非常年幼的患者中出现技术错误。我们还报告了我们在里昂 2000 年至 2018 年间对 64 例髓母细胞瘤患者的治疗经验。
所有患者均行颅脊髓 MRI 检查。81%(n=50)的患者肿瘤严格位于中线,而 19%(n=14)的患者肿瘤偏侧。11%(n=7)的患者在初始 MRI 上诊断时就有转移。41%(n=29)的患者因脑积水和颅内压升高而行紧急 ETV。所有患者均行直接入路,术后 48 小时内行 MRI 检查,78%(n=58)的患者完全切除肿瘤。术后病理发现经典髓母细胞瘤 73%(n=46),促纤维增生性髓母细胞瘤 17%(n=11),间变性/大细胞髓母细胞瘤 10%(n=7)。患者分为低危 7 例,中危 30 例,高危 27 例。96%(n=61)的患者接受放疗。76%(n=48)的患者接受放疗前或辅助化疗。2018 年 12 月最后一次随访时,65%(n=41)的患者完全缓解,12%(n=8)复发,27%(n=15)因疾病死亡。全组 5 年、10 年和 15 年总生存率分别为 76%、73%和 65.7%。
髓母细胞瘤仍然是一种对化疗和放疗敏感的疾病,完全手术切除是有利的预后因素。在考虑新的生物分子和遗传知识时,也必须权衡手术的范围,这些知识需要由外科医生来整合,以提高患者的生活质量。