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髓母细胞瘤患儿管理中的问答历程。我们是如何走到这一步的?一项系统综述。

Questions and answers in the management of children with medulloblastoma over the time. How did we get here? A systematic review.

作者信息

Osuna-Marco Marta P, Martín-López Laura I, Tejera Águeda M, López-Ibor Blanca

机构信息

Pediatric Oncology Unit, Centro Integral Oncológico Clara Campal (CIOCC), Hospital Universitario HM Montepríncipe, HM Hospitales, Madrid, Spain.

Faculty of Experimental Sciences, Universidad Francisco de Vitoria, Madrid, Spain.

出版信息

Front Oncol. 2023 Jun 29;13:1229853. doi: 10.3389/fonc.2023.1229853. eCollection 2023.

Abstract

INTRODUCTION

Treatment of children with medulloblastoma (MB) includes surgery, radiation therapy (RT) and chemotherapy (CT). Several treatment protocols and clinical trials have been developed over the time to maximize survival and minimize side effects.

METHODS

We performed a systematic literature search in May 2023 using PubMed. We selected all clinical trials articles and multicenter studies focusing on MB. We excluded studies focusing exclusively on infants, adults, supratentorial PNETs or refractory/relapsed tumors, studies involving different tumors or different types of PNETs without differentiating survival, studies including <10 cases of MB, solely retrospective studies and those without reference to outcome and/or side effects after a defined treatment.

RESULTS

  1. The main poor-prognosis factors are: metastatic disease, anaplasia, MYC amplification, age younger than 36 months and some molecular subgroups. The postoperative residual tumor size is controversial.2. MB is a collection of diseases.3. MB is a curable disease at diagnosis, but survival is scarce upon relapse.4. Children should be treated by experienced neurosurgeons and in advanced centers.5. RT is an essential treatment for MB. It should be administered craniospinal, early and without interruptions.6. Craniospinal RT dose could be lowered in some low-risk patients, but these reductions should be done with caution to avoid relapses.7. Irradiation of the tumor area instead of the entire posterior fossa is safe enough.8. Hyperfractionated RT is not superior to conventional RT9. Both photon and proton RT are effective.10. CT increases survival, especially in high-risk patients.11. There are multiple drugs effective in MB. The combination of different drugs is appropriate management.12. CT should be administered after RT.13. The specific benefit of concomitant CT to RT is unknown.14. Intensified CT with stem cell rescue has no benefit compared to standard CT regimens.15. The efficacy of intraventricular/intrathecal CT is controversial.16. We should start to think about incorporating targeted therapies in front-line treatment.17. Survivors of MB still have significant side effects.

CONCLUSION

Survival rates of MB improved greatly from 1940-1970, but since then the improvement has been smaller. We should consider introducing targeted therapy as front-line therapy.

摘要

引言

髓母细胞瘤(MB)患儿的治疗包括手术、放射治疗(RT)和化学治疗(CT)。随着时间的推移,已经制定了多种治疗方案和临床试验,以最大限度地提高生存率并减少副作用。

方法

我们于2023年5月使用PubMed进行了系统的文献检索。我们选择了所有聚焦于MB的临床试验文章和多中心研究。我们排除了仅关注婴儿、成人、幕上原始神经外胚层肿瘤(PNET)或难治性/复发性肿瘤的研究,涉及不同肿瘤或不同类型PNET且未区分生存率的研究,纳入MB病例少于10例的研究,仅回顾性研究,以及那些未提及明确治疗后的结局和/或副作用的研究。

结果

  1. 主要的预后不良因素包括:转移性疾病、间变、MYC扩增、年龄小于36个月以及某些分子亚组。术后残留肿瘤大小存在争议。2. MB是一组疾病。3. MB在诊断时是可治愈的疾病,但复发时生存率很低。4. 儿童应由经验丰富的神经外科医生在先进的中心进行治疗。5. RT是MB的重要治疗方法。应进行全脑全脊髓照射,且要尽早且不间断地进行。6. 在一些低风险患者中,全脑全脊髓RT剂量可以降低,但这些降低应谨慎进行,以避免复发。7. 照射肿瘤区域而非整个后颅窝足够安全。8. 超分割RT并不优于传统RT。9. 光子RT和质子RT均有效。10. CT可提高生存率,尤其是在高风险患者中。11. 有多种药物对MB有效。联合使用不同药物是合适的治疗方法。12. CT应在RT后进行。13. 同步CT与RT的具体益处尚不清楚。14. 与标准CT方案相比,强化CT联合干细胞救援并无益处。15. 脑室内/鞘内CT的疗效存在争议。16. 我们应开始考虑在一线治疗中纳入靶向治疗。17. MB幸存者仍有明显的副作用。

结论

MB的生存率在1940 - 1970年有了很大提高,但从那时起改善幅度较小。我们应考虑将靶向治疗作为一线治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5064/10340518/15bb04a1ddff/fonc-13-1229853-g001.jpg

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