Journal of Clinical Pediatrics ›› 2023, Vol. 41 ›› Issue (10): 708-714.doi: 10.12372/jcp.2023.22e1112
• Literature Review • Previous Articles Next Articles
Reviewer: ZHANG Zaiyu, WU Yuxin, Reviser: LIANG Ping
Received:2022-08-15
Published:2023-10-15
Online:2023-10-08
ZHANG Zaiyu, WU Yuxin, LIANG Ping. Research progress on characterization and therapeutics for recurrent medulloblastoma in children[J].Journal of Clinical Pediatrics, 2023, 41(10): 708-714.
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| 临床试验名称 | 年龄 | 放射治疗方案 | 化学治疗方案 | 复发率/% | 复发中位 时间/a |
|---|---|---|---|---|---|
| HIT-SKK’2000[ | <4岁 | 化疗后完全缓解则不接受放疗 | CTX+VCR+MTX+CBP+VP-16+ i.vc.MTX | 37.5 | 1.3 |
| Head Start I-II[ | <3岁 | 不接受放疗 | 诱导:CTX+VCR+VP-16+CDDP 巩固:CBP+VP-16+Thiotepa | 33.3 | NA |
| HIT-SIOP-PNET4[ | 4~21岁 | 标准方案:全脑脊髓23.4 Gy+后颅窝54 Gy 超分割方案:全脑脊髓36 Gy+后颅窝60 Gy+瘤床68 Gy | CDDP+CCNU+VCR | 19.5 | 2.2 |
| SJMB96[ | 3~21岁 | 标危组:全脑脊髓23.4 Gy+后颅窝36 Gy+瘤床55.8 Gy 高危组:全脑脊髓36~39.6 Gy+瘤床55.8 Gy+转移病灶50.4 Gy | VCR+CTX+CDDP | 标危组/高危组: 15.1/29.21) | 标危组/高危组: 2.0/1.62) |
| SJMB03[ | 3~21岁 | 标危组:全脑脊髓23.4 Gy+瘤床55.8 Gy 高危组:全脑脊髓36~39.6 Gy+瘤床55.8~59.4 Gy | VCR+CTX+CDDP | 标危组/高危组: 16.3/34.01) | 标危组/高危组: 2.0/1.32) |
| SJYC07[ | <3岁 | 不接受放疗 | 诱导:MTX+VCR+CTX+CDDP 巩固:CTX+CBP+VP-16 维持:CTX+Topotecan+Erlotinib | 65.83) | 0.7 |
| COG-P9934[ | 8月龄~3岁 | 化疗后完全缓解则不接受放疗 | 诱导:CTX+VCR+VP-16+CDDP 巩固:CBP+Thiotepa | 39.23) | NA |
| [1] |
Ostrom QT, Cioffi G, Waite K, et al. CBTRUS statistical report: primary brain and other central nervous system tumors diagnosed in the United States in 2014-2018[J]. Neuro Oncol, 2021, 23(12 Suppl 2): iii1-iii105.
doi: 10.1093/neuonc/noab200 |
| [2] |
Louis DN, Perry A, Wesseling P, et al. The 2021 WHO Classification of Tumors of the Central Nervous System: a summary[J]. Neuro Oncol, 2021, 23(8): 1231-1251.
doi: 10.1093/neuonc/noab106 |
| [3] |
Mynarek M, von Hoff K, Pietsch T, et al. Nonmetastatic medulloblastoma of early childhood: results from the prospective clinical trial HIT-2000 and an extended validation cohort[J]. J Clin Oncol, 2020, 38(18): 2028-2040.
doi: 10.1200/JCO.19.03057 pmid: 32330099 |
| [4] |
Sabel M, Fleischhack G, Tippelt S, et al. Relapse patterns and outcome after relapse in standard risk medulloblastoma: a report from the HIT-SIOP-PNET4 study[J]. J Neurooncol, 2016, 129(3): 515-524.
doi: 10.1007/s11060-016-2202-1 |
| [5] |
Kumar R, Smith KS, Deng M, et al. Clinical outcomes and patient-matched molecular composition of relapsed medulloblastoma[J]. J Clin Oncol, 2021, 39(7): 807-821.
doi: 10.1200/JCO.20.01359 pmid: 33502920 |
| [6] |
Müller K, Mynarek M, Zwiener I, et al. Postponed is not canceled: role of craniospinal radiation therapy in the management of recurrent infant medulloblastoma--an experience from the HIT-REZ 1997 & 2005 studies[J]. Int J Radiat Oncol Biol Phys, 2014, 88(5): 1019-1024.
doi: 10.1016/j.ijrobp.2014.01.013 |
| [7] |
Levy AS, Krailo M, Chi S, et al. Temozolomide with irinotecan versus temozolomide, irinotecan plus bevacizumab for recurrent medulloblastoma of childhood: report of a COG randomized phase II screening trial[J]. Pediatr Blood Cancer, 2021, 68(8): e29031.
doi: 10.1002/pbc.v68.8 |
| [8] |
Gaab C, Adolph JE, Tippelt S, et al. Local and systemic therapy of recurrent medulloblastomas in children and adolescents: results of the P-HIT-REZ 2005 study[J]. Cancers (Basel), 2022, 14(3):471.
doi: 10.3390/cancers14030471 |
| [9] |
Gajjar A, Chintagumpala M, Ashley D, et al. Risk-adapted craniospinal radiotherapy followed by high-dose chemotherapy and stem-cell rescue in children with newly diagnosed medulloblastoma (St Jude Medulloblastoma-96): long-term results from a prospective, multicentre trial[J]. Lancet Oncol, 2006, 7(10): 813-820.
doi: 10.1016/S1470-2045(06)70867-1 pmid: 17012043 |
| [10] |
Lannering B, Rutkowski S, Doz F, et al. Hyperfractionated versus conventional radiotherapy followed by chemo-therapy in standard-risk medulloblastoma: results from the randomized multicenter HIT-SIOP PNET 4 trial[J]. J Clin Oncol, 2012, 30(26): 3187-3193.
doi: 10.1200/JCO.2011.39.8719 pmid: 22851561 |
| [11] |
Dhall G, Grodman H, Ji L, et al. Outcome of children less than three years old at diagnosis with non-metastatic medulloblastoma treated with chemotherapy on the “head start” I and II protocols[J]. Pediatr Blood Cancer, 2008, 50(6): 1169-1175.
doi: 10.1002/(ISSN)1545-5017 |
| [12] |
von Bueren AO, von Hoff K, Pietsch T, et al. Treatment of young children with localized medulloblastoma by chemotherapy alone: results of the prospective, multicenter trial HIT 2000 confirming the prognostic impact of histology[J]. Neuro Oncol, 2011, 13(6): 669-679.
doi: 10.1093/neuonc/nor025 |
| [13] |
Ashley DM, Merchant TE, Strother D, et al. Induction chemotherapy and conformal radiation therapy for very young children with nonmetastatic medulloblastoma: children’s oncology group study P9934[J]. J Clin Oncol, 2012, 30(26): 3181-3186.
doi: 10.1200/JCO.2010.34.4341 pmid: 22851568 |
| [14] |
Robinson GW, Rudneva VA, Buchhalter I, et al. Risk-adapted therapy for young children with medulloblastoma (SJYC07): therapeutic and molecular outcomes from a multicentre, phase 2 trial[J]. Lancet Oncol, 2018, 19(6): 768-784.
doi: S1470-2045(18)30204-3 pmid: 29778738 |
| [15] |
Johnston DL, Keene D, Strother D, et al. Survival following tumor recurrence in children with medullo-blastoma[J]. J Pediatr Hematol Oncol, 2018, 40(3): e159-e163.
doi: 10.1097/MPH.0000000000001095 |
| [16] | Nobre L, Zapotocky M, Khan S, et al. Pattern of relapse and treatment response in WNT-activated medulloblastoma[J]. Cell Rep Med, 2020, 1(3):100038 |
| [17] |
Huybrechts S, Le Teuff G, Tauziède-Espariat A, et al. Prognostic clinical and biologic features for overall survival after relapse in childhood medulloblastoma[J]. Cancers (Basel), 2020, 13(1):53.
doi: 10.3390/cancers13010053 |
| [18] |
Koschmann C, Bloom K, Upadhyaya S, et al. Survival after relapse of medulloblastoma[J]. J Pediatr Hematol Oncol, 2016, 38(4): 269-273.
doi: 10.1097/MPH.0000000000000547 pmid: 26907655 |
| [19] |
Huang PI, Lin SC, Lee YY, et al. Large cell/anaplastic medulloblastoma is associated with poor prognosis-a retrospective analysis at a single institute[J]. Childs Nerv Syst, 2017, 33(8): 1285-1294.
doi: 10.1007/s00381-017-3435-9 |
| [20] |
Aboian MS, Kline CN, Li Y, et al. Early detection of recurrent medulloblastoma: the critical role of diffusion-weighted imaging[J]. Neurooncol Pract, 2018, 5(4): 234-240.
doi: 10.1093/nop/npx036 pmid: 30402262 |
| [21] |
Grassberger C, Shinnick D, Yeap BY, et al. Circulating lymphocyte counts early during radiation therapy are associated with recurrence in pediatric medulloblastoma[J]. Int J Radiat Oncol Biol Phys, 2021, 110(4): 1044-1052.
doi: 10.1016/j.ijrobp.2021.01.035 |
| [22] |
Du S, Yang S, Zhao X, et al. Clinical characteristics and outcome of children with relapsed medulloblastoma: a retrospective study at a single center in China[J]. J Pediatr Hematol Oncol, 2018, 40(8): 598-604.
doi: 10.1097/MPH.0000000000001241 pmid: 29927794 |
| [23] |
Hill RM, Kuijper S, Lindsey JC, et al. Combined MYC and P53 defects emerge at medulloblastoma relapse and define rapidly progressive, therapeutically targetable disease[J]. Cancer cell, 2015, 27(1): 72-84.
doi: 10.1016/j.ccell.2014.11.002 pmid: 25533335 |
| [24] |
Richardson S, Hill RM, Kui C, et al. Emergence and maintenance of actionable genetic drivers at medulloblastoma relapse[J]. Neuro Oncol, 2022, 24(1): 153-165.
doi: 10.1093/neuonc/noab178 |
| [25] |
Gajjar A, Robinson GW, Smith KS, et al. Outcomes by clinical and molecular features in children with medulloblastoma treated with risk-adapted therapy: results of an international phase III trial (SJMB03)[J]. J Clin Oncol, 2021, 39(7): 822-835.
doi: 10.1200/JCO.20.01372 pmid: 33405951 |
| [26] |
Hill RM, Richardson S, Schwalbe EC, et al. Time, pattern, and outcome of medulloblastoma relapse and their association with tumour biology at diagnosis and therapy: a multicentre cohort study[J]. Lancet Child Adolesc Health, 2020, 4(12): 865-874.
doi: 10.1016/S2352-4642(20)30246-7 pmid: 33222802 |
| [27] |
Ricklefs FL, Fritzsche F, Winkler B, et al. Relapse of a group 4 medulloblastoma after 18 years as proven by histology and DNA methylation profiling[J]. Childs Nerv Syst, 2019, 35(6): 1029-1033.
doi: 10.1007/s00381-019-04086-3 |
| [28] | Tsang DS, Sarhan N, Ramaswamy V, et al. Re-irradiation for children with recurrent medulloblastoma in Toronto, Canada: a 20-year experience[J]. Neuro-oncol, 2019, 145(1): 107-114. |
| [29] |
Baroni LV, Freytes C, Fernández Ponce N, et al. Craniospinal irradiation as part of re-irradiation for children with recurrent medulloblastoma[J]. J Neurooncol, 2021, 155(1): 53-61.
doi: 10.1007/s11060-021-03842-3 |
| [30] |
Phi JH, Park AK, Lee S, et al. Genomic analysis reveals secondary glioblastoma after radiotherapy in a subset of recurrent medulloblastomas[J]. Acta Neuropathol, 2018, 135(6): 939-953.
doi: 10.1007/s00401-018-1845-8 pmid: 29644394 |
| [31] | Zhao M, Wang X, Fu X, et al. Bevacizumab and stereotactic radiosurgery achieved complete response for pediatric recurrent medulloblastoma[J]. J Cancer Res Ther, 2018, 14(Supplement): S789-S792. |
| [32] |
Rao AD, Rashid AS, Chen Q, et al. Reirradiation for recurrent pediatric central nervous system malignancies: a multi-institutional review[J]. Int J Radiat Oncol Biol Phys, 2017, 99(3): 634-641.
doi: 10.1016/j.ijrobp.2017.07.026 |
| [33] |
Napieralska A, Brąclik I, Radwan M, et al. Radiosurgery or hypofractionated stereotactic radiotherapy after craniospinal irradiation in children and adults with medulloblastoma and ependymoma[J]. Childs Nerv Syst, 2019, 35(2): 267-275.
doi: 10.1007/s00381-018-4010-8 |
| [34] | Osorio DS, Dunkel IJ, Cervone KA, et al. Tandem thiotepa with autologous hematopoietic cell rescue in patients with recurrent, refractory, or poor prognosis solid tumor malignancies[J]. Pediatr Blood Cancer, 2018, 65(1). doi: 10.1002/pbc.26776. |
| [35] | Slavc I, Peyrl A, Gojo J, et al. MMbcl-43. recurrent medulloblastoma - long-term survival with a “memmat” based antiangiogenic approach[J]. Neuro-oncology, 2020, 22(Supplement_3): iii397-iii397. |
| [36] |
Pajtler KW, Tippelt S, Siegler N, et al. Intraventricular etoposide safety and toxicity profile in children and young adults with refractory or recurrent malignant brain tumors[J]. J Neurooncol, 2016, 128(3): 463-471.
doi: 10.1007/s11060-016-2133-x |
| [37] |
Bonney PA, Santucci JA, Maurer AJ, et al. Dramatic response to temozolomide, irinotecan, and bevacizumab for recurrent medulloblastoma with widespread osseous metastases[J]. J Clin Neurosci, 2016, 26: 161-163.
doi: 10.1016/j.jocn.2015.10.022 pmid: 26777082 |
| [38] |
Schiavetti A, Varrasso G, Mollace MG, et al. Bevaci-zumab-containing regimen in relapsed/progressed brain tumors: a single-institution experience[J]. Childs Nerv Syst, 2019, 35(6): 1007-1012.
doi: 10.1007/s00381-019-04117-z |
| [39] |
Robinson GW, Orr BA, Wu G, et al. Vismodegib exerts targeted efficacy against recurrent sonic hedgehog-subgroup medulloblastoma: results from phase II pediatric brain tumor consortium studies PBTC-025B and PBTC-032[J]. J Clin Oncol, 2015, 33(24): 2646-2654.
doi: 10.1200/JCO.2014.60.1591 pmid: 26169613 |
| [40] |
Kieran MW, Chisholm J, Casanova M, et al. Phase I study of oral sonidegib (LDE225) in pediatric brain and solid tumors and a phase II study in children and adults with relapsed medulloblastoma[J]. Neuro Oncol, 2017, 19(11): 1542-1552.
doi: 10.1093/neuonc/nox109 |
| [41] | Pereira V, Torrejon J, Kariyawasam D, et al. Clinical and molecular analysis of smoothened inhibitors in sonic hedgehog medulloblastoma[J]. Neurooncol Adv, 2021, 3(1): vdab097. |
| [42] |
Cook Sangar ML, Genovesi LA, Nakamoto MW, et al. Inhibition of CDK4/6 by palbociclib significantly extends survival in medulloblastoma patient-derived xenograft mouse models[J]. Clin Cancer Res, 2017, 23(19): 5802-5813.
doi: 10.1158/1078-0432.CCR-16-2943 pmid: 28637687 |
| [43] |
Shapiro GI. Cyclin-dependent kinase pathways as targets for cancer treatment[J]. J Clin Oncol, 2006, 24(11): 1770-1783.
doi: 10.1200/JCO.2005.03.7689 pmid: 16603719 |
| [44] |
Burkhart DL, Sage J. Cellular mechanisms of tumour suppression by the retinoblastoma gene[J]. Nat Rev Cancer, 2008, 8(9): 671-682.
doi: 10.1038/nrc2399 pmid: 18650841 |
| [45] |
Bockmayr M, Mohme M, Klauschen F, et al. Subgroup-specific immune and stromal microenvironment in medulloblastoma[J]. Oncoimmunology, 2018, 7(9): e1462430.
doi: 10.1080/2162402X.2018.1462430 |
| [46] |
Diao S, Gu C, Zhang H, et al. Immune cell infiltration and cytokine secretion analysis reveal a non-inflammatory microenvironment of medulloblastoma[J]. Oncol Lett, 2020, 20(6): 397.
doi: 10.3892/ol.2020.12260 pmid: 33193857 |
| [47] |
Pham CD, Flores C, Yang C, et al. Differential immune microenvironments and response to immune checkpoint blockade among molecular subtypes of murine medulloblastoma[J]. Clin Cancer Res, 2016, 22(3): 582-595.
doi: 10.1158/1078-0432.CCR-15-0713 pmid: 26405194 |
| [48] |
Donovan LK, Delaidelli A, Joseph SK, et al. Locoregional delivery of CAR T cells to the cerebrospinal fluid for treatment of metastatic medulloblastoma and ependymoma[J]. Nat Med, 2020, 26(5): 720-731.
doi: 10.1038/s41591-020-0827-2 pmid: 32341580 |
| [49] |
Castriconi R, Dondero A, Negri F, et al. Both CD133+ and CD133- medulloblastoma cell lines express ligands for triggering NK receptors and are susceptible to NK-mediated cytotoxicity[J]. Eur J Immunol, 2007, 37(11): 3190-3196.
doi: 10.1002/eji.200737546 pmid: 17918205 |
| [50] |
Khatua S, Cooper LJN, Sandberg DI, et al. Phase I study of intraventricular infusions of autologous ex vivo expanded NK cells in children with recurrent medulloblastoma and ependymoma[J]. Neuro Oncol, 2020, 22(8): 1214-1225.
doi: 10.1093/neuonc/noaa047 |
| [51] | Kramer K, Pandit-Taskar N, Humm JL, et al. A phase II study of radioimmunotherapy with intraventricular (131) I-3F8 for medulloblastoma[J]. Pediatr Blood Cancer, 2018, 65(1):10.1002. |
| [52] |
Liu Y, Yuelling LW, Wang Y, et al. Astrocytes promote medulloblastoma progression through hedgehog secretion[J]. Cancer Res, 2017, 77(23): 6692-6703.
doi: 10.1158/0008-5472.CAN-17-1463 pmid: 28986380 |
| [53] |
Zhang L, He X, Liu X, et al. Single-Cell transcriptomics in medulloblastoma reveals tumor-initiating progenitors and oncogenic cascades during tumorigenesis and relapse[J]. Cancer Cell, 2019, 36(3): 302-318.
doi: S1535-6108(19)30336-8 pmid: 31474569 |
| [54] |
Yao M, Ventura PB, Jiang Y, et al. Astrocytic trans-differentiation completes a multicellular paracrine feedback loop required for medulloblastoma tumor growth[J]. Cell, 2020, 180(3): 502-520.
doi: S0092-8674(19)31386-8 pmid: 31983537 |
| [55] |
Singh SK, Hawkins C, Clarke ID, et al. Identification of human brain tumour initiating cells[J]. Nature, 2004, 432(7015): 396-401.
doi: 10.1038/nature03128 |
| [56] |
Garg N, Bakhshinyan D, Venugopal C, et al. CD133(+) brain tumor-initiating cells are dependent on STAT3 signaling to drive medulloblastoma recurrence[J]. Oncogene, 2017, 36(5): 606-617.
doi: 10.1038/onc.2016.235 pmid: 27775079 |
| [57] |
Bakhshinyan D, Adile AA, Liu J, et al. Temporal profiling of therapy resistance in human medulloblastoma identifies novel targetable drivers of recurrence[J]. Sci Adv, 2021, 7(50): eabi5568.
doi: 10.1126/sciadv.abi5568 |
| [58] |
Leung C, Lingbeek M, Shakhova O, et al. Bmi1 is essential for cerebellar development and is overexpressed in human medulloblastomas[J]. Nature, 2004, 428(6980): 337-341.
doi: 10.1038/nature02385 |
| [59] |
Bakhshinyan D, Venugopal C, Adile AA, et al. BMI1 is a therapeutic target in recurrent medulloblastoma[J]. Oncogene, 2019, 38(10): 1702-1716.
doi: 10.1038/s41388-018-0549-9 pmid: 30348991 |
| [60] |
Guo D, Wang Y, Cheng Y, et al. Tumor cells generate astrocytelike cells that contribute to SHH-driven medulloblastoma relapse[J]. J Exp Med, 2021, 218(9): e20202350.
doi: 10.1084/jem.20202350 |
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