Central nervous system tumors

Authors

DOI:

https://doi.org/10.46765/2675-374X.2025v6n1e284

Keywords:

Central Nervous System Tumors, Pediatrics, Children, High Dose Chemotherapy, Autologus Stem Cell Transplant

Abstract

Central nervous system (CNS) tumors represent one of the most prevalent groups of neoplasms in the pediatric population. Recent advances in molecular biology and neuro-oncology have led to continuous updates in the classification of these tumors, which poses significant diagnostic challenges, particularly in low- and middle-income countries, with limited access to advanced diagnostic tools. The therapeutic approach varies according to tumor subtype, often requiring complex and resource-intensive protocols. One such strategy involves the use of high-dose chemotherapy followed by autologous stem cell rescue, which has shown promise in improving outcomes for select pediatric patients with CNS tumors. However, implementation of this therapy in countries like Brazil faces logistical, financial, and clinical practice challenges. This article aimed to provide a brief overview and suggestions to use high-dose chemotherapy with autologous stem cell transplantation in the treatment of pediatric CNS tumors. We discussed practical considerations for patient selection, and conditioning regimens. Our objectives were to optimize and guide current practices by proposing strategies that maybe feasible in the Brazilian public and private healthcare systems.

References

1. Bale TA, Rosenblum MK. The 2021 WHO Classification of Tumors of the Central Nervous System: an update on pediatric low-grade gliomas and glioneuronal tumors. Brain Pathol. 2022;32(4):e13060. https://doi.org/10.1111/bpa.13060 DOI: https://doi.org/10.1111/bpa.13060

2. Gajjar A, Mahajan A, Abdelbaki M, Anderson C, Antony R, Bale T, Bindra R, Bowers DC, Cohen K, Cole B, Dorris K, Ermoian R, Franson A, Helgager J, Landi D, Lin C, Metrock L, Nanda R, Palmer J, Partap S, Plant A, Pruthi S, Reynolds R, Ruggieri P, Stearns D, Storm P, Wang A, Warren K, Whipple N, Zaky W, McMillian NR, Pluchino LA. Pediatric central nervous system cancers, version 2.2023, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Canc Netw. 2022;20(12):1339–62. https://doi.org/10.6004/jnccn.2022.0062

3. d’Amati A, Bargiacchi L, Rossi S, Carai A, Bertero L, Barresi V, Errico ME, Buccoliero AM, Asioli S, Marucci G, Del Baldo G, Mastronuzzi A, Miele E, D’Antonio F, Schiavello E, Biassoni V, Massimino M, Gessi M, Antonelli M, Gianno F. Pediatric CNS tumors and 2021 WHO classification: what do oncologists need from pathologists? Front Mol Neurosci. 2024;17:1268038. https://doi.org/10.3389/fnmol.2024.1268038. Erratum in: Front Mol Neurosci. 2024;17:1411360. https://doi.org/10.3389/fnmol.2024.1411360 DOI: https://doi.org/10.3389/fnmol.2024.1268038

4. Oztek MA, Noda SM, Romberg EK, Cole BL. Changes to pediatric brain tumors in 2021 WHO classification of CNS tumors. Pediatr Radiol. 2023;53(3):523–43. https://doi.org/10.1007/s00247-022 05546-w DOI: https://doi.org/10.1007/s00247-022-05546-w

5. Park YW, Vollmuth P, Foltyn-Dumitru M, Sahm F, Ahn SS, Chang JH, Kim SH. The 2021 WHO classification for gliomas and implications on imaging diagnosis: part 1-key points of the fifth edition and summary of imaging findings on adult-type diffuse gliomas. J Magn Reson Imaging. 2023;58(3):677 89. https://doi.org/10.1002/jmri.28743 DOI: https://doi.org/10.1002/jmri.28743

6. Horbinski C, Berger T, Packer RJ, Wen PY. Clinical implications of the 2021 edition of the WHO classification of central nervous system tumours. Nat Rev Neurol. 2022;18(9):515–29. https://doi.org/10.1038/s41582-022-00679-w DOI: https://doi.org/10.1038/s41582-022-00679-w

7. Soni N, Ora M, Bathla G, Desai A, Gupta V, Agarwal A. Ependymal tumors: overview of the recent World Health Organization histopathologic and genetic updates with an imaging characteristic. Am J Neuroradiol. 2024;45(11):1624–34. https://doi.org/10.3174/ajnr.a8237 DOI: https://doi.org/10.3174/ajnr.A8237

8. Lampros M, Alexiou GA. Brain and spinal cord tumors of embryonic origin. In: Rezaei N, Hanaei S, editors. Human brain and spinal cord tumors: from bench to bedside (vol. 2). Cham: Springer; 2023. p. 405–20. https://doi.org/10.1007/978-3-031-23705-8_15 DOI: https://doi.org/10.1007/978-3-031-23705-8_15

9. Pinheiro JAF, de Almeida JCM, Lopes JMPB. Embryonal tumors of the central nervous system: the WHO 2016 classification and new insights. J Pediatr Hematol Oncol. 2021;43(3):79–89. https://doi.org/10.1097/ MPH.0000000000001923 DOI: https://doi.org/10.1097/MPH.0000000000001923

10. Kamenova M, Kaneva R, Genova K, Gabrovsky N. Embryonal tumors of the central nervous system with multilayered rosettes and atypical teratoid/rhabdoid tumors. In: Rezaei N, Hanaei S, editors. Human brain and spinal cord tumors: from bench to bedside (vol. 2). Cham: Springer; 2023. p. 225–52. https://doi.org/10.1007/978-3-031-23705-8_8 DOI: https://doi.org/10.1007/978-3-031-23705-8_8

11. Wong TT, Tsai ML, Chang H, Hsieh KL, Ho DM, Lin SC, Yen HJ, Chen YW, Lee HL, Yang TF. Brain and spinal tumors originating from the germ line cells. Adv Exp Med Biol. 2023;1405:421–55. https://doi.org/10.1007/978-3-031-23705-8_16 DOI: https://doi.org/10.1007/978-3-031-23705-8_16

12. Woods JK, Lidov HG, Ligon KL, Santagata S, Chi SN, Yeo KK, Alexandrescu S. PD-L1 and PD-1 expression in pediatric central nervous system germ cell tumors. Mod Pathol. 2022;35(12):1770–4. https://doi.org/10.1038/s41379-022-01142-3 DOI: https://doi.org/10.1038/s41379-022-01142-3

13. Kong Z, Wang Y, Dai C, Yao Y, Ma W, Wang Y. Central nervous system germ cell tumors: a review of the literature. J Child Neurol. 2018;33(9):610–20. https://doi.org/10.1177/0883073818772470 DOI: https://doi.org/10.1177/0883073818772470

14. Yang B, Zhang N, Jiang T, Du J, Liu R, Yu S, Wang S, Li C. Intracranial choroid plexus carcinomas: report of 11 cases from a single institution. World Neurosurg. 2021;152:e45–e50. https://doi.org/10.1016/j.wneu.2021.04.049 DOI: https://doi.org/10.1016/j.wneu.2021.04.049

15. Jamshidi P, Brat DJ. The 2021 WHO classification of central nervous system tumors: what neurologists need to know. Curr Opin Neurol. 2022;35(6):764–71. https://doi.org/10.1097/WCO.0000000000001109 DOI: https://doi.org/10.1097/WCO.0000000000001109

16. Cruzeiro GAV, Salomão KB, de Biagi CAO Jr., Baumgartner M, Sturm D, Lira RCP, de Almeida Magalhães T, Baroni Milan M, da Silva Silveira V, Saggioro FP, de Oliveira RS, Dos Santos Klinger PH, Seidinger AL, Yunes JA, de Paula Queiroz RG, Oba-Shinjo SM, Scrideli CA, Nagahashi SMK, Tone LG, Valera ET. A simplified approach using Taqman low-density array for medulloblastoma subgrouping. Acta Neuropathol Commun. 2019;7(1):33. https://doi.org/10.1186/s40478-019-0681-y DOI: https://doi.org/10.1186/s40478-019-0681-y

17. Leal LF, Evangelista AF, de Paula FE, Caravina Almeida G, Carloni AC, Saggioro F, Stavale JN, Malheiros SMF, Mançano B, de Oliveira MA, Luu B, Neder L, Taylor MD, Reis RM. Reproducibility of the NanoString 22-gene molecular subgroup assay for improved prognostic prediction of medulloblastoma. Neuropathology. 2018;38(5):475–83. https://doi.org/10.1111/neup.12508 DOI: https://doi.org/10.1111/neup.12508

18. Bouffet E, Raquin M, Doz F, Gentet JC, Rodary C, Demeocq F, Chastagner P, Lutz P, Hartmann O, Kalifa C. Radiotherapy followed by high dose busulfan and thiotepa: a prospective assessment of high dose chemotherapy in children with diffuse pontine gliomas. Cancer. 2000;88(3):685–92. https://doi.org/10.1002/(sici)1097-0142(20000201)88:3<685::aid-cncr27>3.0.co;2-k DOI: https://doi.org/10.1002/(SICI)1097-0142(20000201)88:3<685::AID-CNCR27>3.0.CO;2-K

19. Osorio DS, Patel N, Ji L, Sposto R, Stanek J, Gardner SL, Allen JC, Cornelius A, McCowage GB, Termuhlen A, Dunkel IJ, Comito M, Garvin J, Finlay JL. Pre-irradiation intensive induction and marrow ablative consolidation chemotherapy in young children with newly diagnosed high-grade brainstem gliomas: report of the “Head-Start” I and II clinical trials. J Neurooncol. 2018;140(3):717–25. https://doi.org/10.1007/s11060-018-03003-z DOI: https://doi.org/10.1007/s11060-018-03003-z

20. Heideman RL, Douglass EC, Krance RA, Fontanesi J, Langston JA, Sanford RA, Kovnar EH, Ochs J, Kuttesch J, Jenkins JJ. High-dose chemotherapy and autologous bone marrow rescue followed by interstitial and external-beam radiotherapy in newly diagnosed pediatric malignant gliomas. J Clin Oncol. 1993;11(8):1458–65. https://doi.org/10.1200/jco.1993.11.8.1458 DOI: https://doi.org/10.1200/JCO.1993.11.8.1458

21. Bouffet E, Mottolese C, Jouvet A, Philip I, Frappaz D, Carrie C, Brunat-Mentigny M. Etoposide and thiotepa followed by autologous bone marrow transplantation in children and young adults with high-grade gliomas. Eur J Cancer. 1997;33(1):91–5. https://doi.org/10.1016/s0959-8049(96)00369-3 DOI: https://doi.org/10.1016/S0959-8049(96)00369-3

22. Zacharoulis S, Levy A, Chi SN, Gardner S, Dunkel IJ, Garvin JH, et al. Outcome for young children with intracranial ependymoma treated with the CCG-9921 and CCG-9942 protocols. Pediatr Blood Cancer. 2012;59(6):1144–50. https://doi.org/10.1002/pbc.24260 DOI: https://doi.org/10.1002/pbc.24260

23. Rajagopal R, Foo JC, Jawin V, Qaddoumi I, Bouffet E. High-dose chemotherapy with autologous stem cell transplantation in infants and young children with ependymoma: a 10-year experience with the Head Start II protocol. Pediatr Transplant. 2019;23(4):e13421. https://doi.org/10.1111/petr.13421 DOI: https://doi.org/10.1111/petr.13421

24. von Bueren AO, von Hoff K, Pietsch T, Gerber NU, Warmuth-Metz M, Deinlein F, Zwiener I, Faldum A, Fleischhack G, Benesch M, Krauss J, Kuehl J, Kortmann RD, Rutkowski S. Treatment of young children with localized medulloblastoma by chemotherapy alone: results of the prospective, multicenter trial HIT 2000 confirming the prognostic impact of histology. Neuro Oncol. 2011;13(6):669–79. https://doi.org/10.1093/neuonc/nor025 DOI: https://doi.org/10.1093/neuonc/nor025

25. PDQ Pediatric Treatment Editorial Board. Childhood medulloblastoma and other central nervous system embryonal tumors treatment (PDQ®): health professional version. PDQ Cancer Information Summaries. Bethesda: National Cancer Institute; 2024.

26. Dhall G, O’Neil SH, Ji L, Haley K, Whitaker AM, Nelson MD, Gilles F, Gardner SL, Allen JC, Cornelius AS, Pradhan K, Garvin JH, Olshefski RS, Hukin J, Comito M, Goldman S, Atlas MP, Walter AW, Sands S, Sposto R, Finlay JL. Excellent outcome of young children with nodular desmoplastic medulloblastoma treated on “Head Start” III: a multi-institutional, prospective clinical trial. Neuro Oncol. 2020;22(12):1862–72. https://doi.org/10.1093/neuonc/noaa102 DOI: https://doi.org/10.1093/neuonc/noaa102

27. Butturini AM, Jacob M, Aguajo J, Vander-Walde NA, Villablanca J, Jubran R, Erdreich-Epstein A, Marachelian A, Dhall G, Finlay JL. High-dose chemotherapy and autologous hematopoietic progenitor cell rescue in children with recurrent medulloblastoma and supratentorial primitive neuroectodermal tumors: the impact of prior radiotherapy on outcome. Cancer. 2009;115(13):2956–63. https://doi.org/10.1002/cncr.24341 DOI: https://doi.org/10.1002/cncr.24341

28. Dufour C, Foulon S, Geoffray A, Masliah-Planchon J, Figarella-Branger D, Bernier-Chastagner V, Padovani L, Guerrini-Rousseau L, Faure-Conter C, Icher C, Bertozzi AI, Leblond P, Akbaraly T, Bourdeaut F, André N, Chappé C, Schneider P, De Carli E, Chastagner P, Berger C, Lejeune J, Soler C, Entz-Werlé N, Delisle MB. Prognostic relevance of clinical and molecular risk factors in children with high-risk medulloblastoma treated in the phase II trial PNET HR+5. Neuro Oncol. 2021;23(7):1163–72. https://doi.org/10.1093/neuonc/noaa301 DOI: https://doi.org/10.1093/neuonc/noaa301

29. Consultar remédios. Bula do dipate [Internet]. [cited Apr. 3, 2025]. Available at: https://consultaremedios.com.br/dipate/bula

30. Rutkowski S, Cohen B, Finlay J, Luksch R, Ridola V, Valteau-Couanet D, Hara J, Garre ML, Grill J. Medulloblastoma in young children. Pediatr Blood Cancer. 2010;54(4):635–7. https://doi.org/10.1002/pbc.22372 DOI: https://doi.org/10.1002/pbc.22372

31. Chadda KR, Solano-Páez P, Khan S, Llempén-López M, Phyu P, Horan G, Trotman J, Tarpey P, Erker C, Lindsay H, Addy D, Jacques TS, Allinson K, Pizer B, Huang A, Murray MJ. Embryonal tumor with multilayered rosettes: Overview of diagnosis and therapy. Neurooncol Adv. 2023;5(1):vdad052. https://doi.org/10.1093/noajnl/vdad052 DOI: https://doi.org/10.1093/noajnl/vdad052

32. Hanson D, Hoffman LM, Nagabushan S, Goumnerova LC, Rathmann A, Vogel T, Ziegler DS, Chi S. A modified IRS-III chemotherapy regimen leads to prolonged survival in children with embryonal tumor with multilayer rosettes. Neurooncol Adv. 2020;2(1):vdaa120. https://doi.org/10.1093/noajnl/vdaa120 DOI: https://doi.org/10.1093/noajnl/vdaa120

33. Horwitz M, Dufour C, Leblond P, Bourdeaut F, Faure-Conter C, Bertozzi AI, Delisle MB, Palenzuela G, Jouvet A, Scavarda D, Vinchon M, Padovani L, Gaudart J, Branger DF, Andre N. Embryonal tumors with multilayered rosettes in children: the SFCE experience. Childs Nerv Syst. 2016;32(2):299–305. https://doi.org/10.1007/s00381-015-2920-2 DOI: https://doi.org/10.1007/s00381-015-2920-2

34. Juhnke BO, Gessi M, Gerber NU, Friedrich C, Mynarek M, von Bueren AO, Haberler C, Schüller U, Kortmann RD, Timmermann B, Bison B, Warmuth-Metz M, Kwiecien R, Pfister SM, Spix C, Pietsch T, Kool M, Rutkowski S, von Hoff K. Treatment of embryonal tumors with multilayered rosettes with carboplatin/etoposide induction and high-dose chemotherapy within the prospective P-HIT trial. Neuro Oncol. 2022;24(1): 127–37. https://doi.org/10.1093/neuonc/noab100 DOI: https://doi.org/10.1093/neuonc/noab100

35. Bandopadhayay P, Chi SN. The challenges in treating embryonal tumors with multilayered rosettes (ETMR) and other infant brain tumors. Neuro Oncol. 2022;24(1):138–40. https://doi.org/10.1093/neuonc/noab206 DOI: https://doi.org/10.1093/neuonc/noab206

36. Sugawa M, Fukuoka K, Mori M, Arakawa Y, Tanami Y, Nobusawa S, Hirato J, Nakazawa A, Kurihara J, Koh K. Prognostic impact of the multimodal treatment approach in patients with C19MC-altered embryonal tumor with multilayered rosettes. J Neurosurg Pediatr. 2022;30(2):232–8. https://doi.org/10.3171/2022.4.PEDS21542 DOI: https://doi.org/10.3171/2022.4.PEDS21542

37. Alva E, Rubens J, Chi S, Rosenberg T, Reddy A, Raabe EH, Margol A. Recent progress and novel approaches to treating atypical teratoid rhabdoid tumor. Neoplasia. 2023;37:100880. https://doi.org/10.1016/j.neo.2023.100880 DOI: https://doi.org/10.1016/j.neo.2023.100880

38. Tran S, Plant-Fox AS, Chi SN, Narendran A. Current advances in immunotherapy for atypical teratoid rhabdoid tumor (ATRT). Neurooncol Pract. 2023;10(4):322–34. https://doi.org/10.1093/nop/npad005 DOI: https://doi.org/10.1093/nop/npad005

39. Upadhyaya SA, Robinson GW, Onar-Thomas A, Orr BA, Johann P, Wu G, Billups CA, Tatevossian RG, Dhanda SK, Srinivasan A, Broniscer A, Qaddoumi I, Vinitsky A, Armstrong GT, Bendel AE, Hassall T, Partap S, Fisher PG, Crawford JR, Chintagumpala M, Bouffet E, Gururangan S, Mostafavi R, Sanders RP, Klimo P Jr, Patay Z, Indelicato DJ, Nichols KE, Boop FA, Merchant TE, Kool M, Ellison DW, Gajjar A. Relevance of molecular groups in children with newly diagnosed atypical teratoid rhabdoid tumor: results from prospective St. Jude multiinstitutional trials. Clin Cancer Res. 2021;27(10):2879–89. https://doi.org/10.1158/1078-0432.CCR-20-4731 DOI: https://doi.org/10.1158/1078-0432.CCR-20-4731

40. Reddy AT, Strother DR, Judkins AR, Burger PC, Pollack IF, Krailo MD, Buxton AB, Williams-Hughes C, Fouladi M, Mahajan A, Merchant TE, Ho B, Mazewski CM, Lewis VA, Gajjar A, Vezina LG, Booth TN, Parsons KW, Poss VL, Zhou T, Biegel JA, Huang A. Efficacy of high-dose chemotherapy and three-dimensional conformal radiation for atypical teratoid/rhabdoid tumor: a report from the children’s oncology group trial ACNS0333. J Clin Oncol. 2020;38(11):1175–85. https://doi.org/10.1200/JCO.19.01776 DOI: https://doi.org/10.1200/JCO.19.01776

41. Nemes K, Johann PD, Steinbügl M, Gruhle M, Bens S, Kachanov D, Teleshova M, Hauser P, Simon T, Tippelt S, Eberl W, Chada M, Lopez VS, Grigull L, Hernáiz-Driever P, Eyrich M, Pears J, Milde T, Reinhard H, Leipold A, van de Wetering M, Gil-da-Costa MJ, Ebetsberger-Dachs G, Kerl K, Lemmer A, Boztug H, Furtwängler R, Kordes U, Vokuhl C, Hasselblatt M, Bison B, Kröncke T, Melchior P, Timmermann B, Gerss J, Siebert R, Frühwald MC. Infants and newborns with atypical teratoid rhabdoid tumors (ATRT) and extracranial malignant rhabdoid tumors (eMRT) in the EU-RHAB Registry: a unique and challenging population. Cancers (Basel). 2022;14(9):2185. https://doi.org/10.3390/cancers14092185 DOI: https://doi.org/10.3390/cancers14092185

42. Abdelbaki MS, Abu-Arja MH, Davidson TB, Fangusaro JR, Stanek JR, Dunkel IJ, Dhall G, Gardner SL, Finlay JL. Pineoblastoma in children less than six years of age: The Head Start I, II, and III experience. Pediatr Blood Cancer. 2020;67(6):e28252. https://doi.org/10.1002/pbc.28252 DOI: https://doi.org/10.1002/pbc.28252

43. Friedrich C, von Bueren AO, von Hoff K, Gerber NU, Ottensmeier H, Deinlein F, Benesch M, Kwiecien R, Pietsch T, Warmuth-Metz M, Faldum A, Kuehl J, Kortmann RD, Rutkowski S. Treatment of young children with CNS-primitive neuroectodermal tumors/pineoblastomas in the prospective multicenter trial HIT 2000 using different chemotherapy regimens and radiotherapy. Neuro Oncol. 2013;15(2):224–34. https://doi.org/10.1093/neuonc/nos292 DOI: https://doi.org/10.1093/neuonc/nos292

44. Mynarek M, Pizer B, Dufour C, van Vuurden D, Garami M, Massimino M, Fangusaro J, Davidson T, Gilda-Costa MJ, Sterba J, Benesch M, Gerber N, Juhnke BO, Kwiecien R, Pietsch T, Kool M, Clifford S, Ellison DW, Giangaspero F, Wesseling P, Gilles F, Gottardo N, Finlay JL, Rutkowski S, von Hoff K. Evaluation of agedependent treatment strategies for children and young adults with pineoblastoma: analysis of pooled European Society for Paediatric Oncology (SIOP-E) and US Head Start data. Neuro Oncol. 2017;19(4): 576–85. https://doi.org/10.1093/neuonc/now234 DOI: https://doi.org/10.1093/neuonc/now234

45. Hansford JR, Huang J, Endersby R, Dodgshun AJ, Li BK, Hwang E, Leary S, Gajjar A, Von Hoff K, Wells O, Wray A, Kotecha RS, Raleigh DR, Stoller S, Mueller S, Schild SE, Bandopadhayay P, Fouladi M, Bouffet E, Huang A, Onar-Thomas A, Gottardo NG. Pediatric pineoblastoma: A pooled outcome study of North American and Australian therapeutic data. Neurooncol Adv. 2022;4(1):vdac056. https://doi.org/10.1093/noajnl/vdac056 DOI: https://doi.org/10.1093/noajnl/vdac056

46. Liu APY, Gudenas B, Lin T, Orr BA, Klimo P Jr, Kumar R, Bouffet E, Gururangan S, Crawford JR, Kellie SJ, Chintagumpala M, Fisher MJ, Bowers DC, Hassall T, Indelicato DJ, Onar-Thomas A, Ellison DW, Boop FA, Merchant TE, Robinson GW, Northcott PA, Gajjar A. Risk-adapted therapy and biological heterogeneity in pineoblastoma: integrated clinico-pathological analysis from the prospective, multi-center SJMB03 and SJYC07 trials. Acta Neuropathol. 2020;139(2):259–71. https://doi.org/10.1007/s00401-019-02106-9. Erratum in: Acta Neuropathol. 2020;139(2):273–75. https://doi.org/10.1007/s00401-019-02115-8 DOI: https://doi.org/10.1007/s00401-019-02115-8

47. Shih CS, Hale GA, Gronewold L, Tong X, Laningham FH, Gilger EA, Srivastava DK, Kun LE, Gajjar A, Fouladi M. High-dose chemotherapy with autologous stem cell rescue for children with recurrent malignant brain tumors. Cancer. 2008;112(6):1345–53. https://doi.org/10.1002/cncr.23305 DOI: https://doi.org/10.1002/cncr.23305

48. Leary SES, Onar-Thomas A, Fangusaro J, Gottardo NG, Cohen K, Smith A, Huang A, Haas-Kogan D, Fouladi M; COG Central Nervous System Committee. Children’s Oncology Group’s 2023 blueprint for research: Central nervous system tumors. Pediatr Blood Cancer. 2023;70(Suppl. 6):e30600. https://doi.org/10.1002/pbc.30600 DOI: https://doi.org/10.1002/pbc.30600

49. Murray MJ, Bailey S, Heinemann K, Mann J, Göbel UK, Saran F, Hale JP, Calaminus G, Nicholson JC. Treatment and outcomes of UK and German patients with relapsed intracranial germ cell tumors following uniform first-line therapy. Int J Cancer. 2017;141(3):621–35. https://doi.org/10.1002/ijc.30755 DOI: https://doi.org/10.1002/ijc.30755

50. Callec L, Lardy-Cleaud A, Guerrini-Rousseau L, Alapetite C, Vignon L, Chastagner P, Frappaz D, Faure-

Conter C. Relapsing intracranial germ cell tumours warrant retreatment. Eur J Cancer. 2020;136:186–94. https://doi.org/10.1016/j.ejca.2020.06.012 DOI: https://doi.org/10.1016/j.ejca.2020.06.012

51. Modak S, Gardner SL, Dunkel IJ, Balmaceda C, Finlay JL. Thiotepa-based high-dose chemotherapy with autologous stem-cell rescue in patients with recurrent or progressive CNS germ cell tumors. J Clin Oncol. 2004;22(10):1934–43. https://doi.org/10.1200/JCO.2004.11.053 DOI: https://doi.org/10.1200/JCO.2004.11.053

52. Finlay JL, Goldman S, Wong MC, Cairo M, Garvin J, August C, Cohen BH, Stanley P, Zimmerman RA, Bostrom B, Geyer JR, Harris RE, Sanders J, Yates AJ, Boyett JM, Packer RJ. Pilot study of high-dose thiotepa and etoposide with autologous bone marrow rescue in children and young adults with recurrent CNS tumors. The Children’s Cancer Group. J Clin Oncol. 1996;14(9):2495–503. https://doi.org/10.1200/JCO.1996.14.9.2495 DOI: https://doi.org/10.1200/JCO.1996.14.9.2495

53. Zaky W, Dhall G, Khatua S, Brown RJ, Ginn KF, Gardner SL, Yildiz VO, Yankelevich M, Finlay JL. Choroid plexus carcinoma in children: the Head Start experience. Pediatr Blood Cancer. 2015;62(5):784–9. https://doi.org/10.1002/pbc.25436 DOI: https://doi.org/10.1002/pbc.25436

54. Fisher PG, Needle MN, Cnaan A, Zhao H, Geyer JR, Molloy PT, Goldwein JW, Herman-Liu AB, Phillips PC. Salvage therapy after postoperative chemotherapy for primary brain tumors in infants and very young children. Cancer. 1998;83(3):566–74. https://doi.org/10.1002/(sici)1097-0142(19980801)83:3<566::aidcncr27>3.0.co;2-t DOI: https://doi.org/10.1002/(SICI)1097-0142(19980801)83:3<566::AID-CNCR27>3.0.CO;2-T

55. Mosleh O, Tabori U, Bartels U, Huang A, Schechter T, Bouffet E. Successful treatment of a recurrent choroid plexus carcinoma with surgery followed by high-dose chemotherapy and stem cell rescue. Pediatr Hematol Oncol. 2013;30(5):386–91. https://doi.org/10.3109/08880018.2012.756089 DOI: https://doi.org/10.3109/08880018.2012.756089

56. Tabori U, Shlien A, Baskin B, Levitt S, Ray P, Alon N, Hawkins C, Bouffet E, Pienkowska M, Lafay-Cousin L, Gozali A, Zhukova N, Shane L, Gonzalez I, Finlay J, Malkin D. TP53 alterations determine clinical subgroups and survival of patients with choroid plexus tumors. J Clin Oncol. 2010;28(12):1995–2001. https://doi.org/10.1200/JCO.2009.26.8169 DOI: https://doi.org/10.1200/JCO.2009.26.8169

57. Liu APY, Wu G, Orr BA, Lin T, Ashford JM, Bass JK, Bowers DC, Hassall T, Fisher PG, Indelicato DJ, Klimo P Jr, Boop F, Conklin H, Onar-Thomas A, Merchant TE, Ellison DW, Gajjar A, Robinson GW. Outcome and molecular analysis of young children with choroid plexus carcinoma treated with non-myeloablative therapy: results from the SJYC07 trial. Neurooncol Adv. 2020;3(1):vdaa168. https://doi.org/10.1093/noajnl/vdaa168 DOI: https://doi.org/10.1093/noajnl/vdaa168

58. Yankelevich M, Zaky W, Lafay-Cousin L, Osorio D, Adamski J, Kordes U, Finlay JL, Prados M, Mueller S. Marrow-ablative consolidation chemotherapy and molecular targeted therapy delivered in a risk-adapted manner for newly diagnosed children with choroid plexus carcinoma: A work in progress. Neurooncol Adv. 2024;6(1):vdae109. https://doi.org/10.1093/noajnl/vdae109 DOI: https://doi.org/10.1093/noajnl/vdae109

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10/18/2025

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Zamperlini, G., Klinger, P. H. dos S., Zanette, A., Kuwahara, C., Epelman, S., Seber, A., & Castro Junior, C. G. de. (2025). Central nervous system tumors. JOURNAL OF BONE MARROW TRANSPLANTATION AND CELLULAR THERAPY, 6(1). https://doi.org/10.46765/2675-374X.2025v6n1e284

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