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Children's Oncology Group's 2013 blueprint for research: stem cell transplantation.儿童肿瘤学组 2013 年研究蓝图:干细胞移植。
Pediatr Blood Cancer. 2013 Jun;60(6):1044-7. doi: 10.1002/pbc.24437. Epub 2012 Dec 19.
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Children's Oncology Group's 2013 blueprint for research: neuroblastoma.儿童肿瘤学组 2013 年研究蓝图:神经母细胞瘤。
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Children's Oncology Group's 2013 blueprint for research: acute myeloid leukemia.儿童肿瘤学组 2013 年研究蓝图:急性髓系白血病。
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EXERCISE in pediatric autologous stem cell transplant patients: a randomized controlled trial protocol.运动在儿科自体干细胞移植患者中的应用:一项随机对照试验方案。
BMC Cancer. 2012 Sep 10;12:401. doi: 10.1186/1471-2407-12-401.
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Stem cell transplantation for neuroblastoma.神经母细胞瘤的干细胞移植
Bone Marrow Transplant. 2008 Jan;41(2):159-65. doi: 10.1038/sj.bmt.1705929. Epub 2007 Nov 26.
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Recommendations for donor human leukocyte antigen assessment and matching for allogeneic stem cell transplantation: consensus opinion of the Blood and Marrow Transplant Clinical Trials Network (BMT CTN).异基因干细胞移植供者人类白细胞抗原评估与配型建议:血液与骨髓移植临床试验网络(BMT CTN)的共识意见
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Reduced-intensity allogeneic stem cell transplantation for children with neuroblastoma who failed tandem autologous stem cell transplantation.对串联自体干细胞移植失败的神经母细胞瘤患儿行减轻强度异基因干细胞移植。
Pediatr Blood Cancer. 2011 Oct;57(4):660-5. doi: 10.1002/pbc.23035. Epub 2011 Jun 16.
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Improved survival of children with advanced neuroblastoma treated by intensified therapy including myeloablative chemotherapy with stem cell transplantation: a retrospective analysis from the Tohoku Neuroblastoma Study Group.通过强化治疗(包括采用干细胞移植的清髓性化疗)治疗晚期神经母细胞瘤患儿的生存率提高:来自东北神经母细胞瘤研究组的一项回顾性分析
Tohoku J Exp Med. 2001 Oct;195(2):73-83. doi: 10.1620/tjem.195.73.

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Fertility preservation in female patients with hematological disorders.血液系统疾病患者的生育力保存。
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The Potential of Mesenchymal Stromal Cells in Neuroblastoma Therapy for Delivery of Anti-Cancer Agents and Hematopoietic Recovery.间充质基质细胞在神经母细胞瘤治疗中递送抗癌药物及促进造血恢复的潜力
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Outcomes of matched sibling donor bone marrow transplantation in children using single-agent calcineurin inhibitors as prophylaxis for graft versus host disease.使用单剂钙调神经磷酸酶抑制剂预防移植物抗宿主病的儿童匹配同胞供体骨髓移植的结果
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Challenges and opportunities for international cooperative studies in pediatric hematopoeitic cell transplantation: priorities of the Westhafen Intercontinental Group.儿科造血细胞移植国际合作研究的挑战与机遇:威斯特法伦洲际组的优先事项。
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本文引用的文献

1
Treatment of advanced leukemia in mice with mRNA engineered T cells.用 mRNA 工程化 T 细胞治疗小鼠晚期白血病。
Hum Gene Ther. 2011 Dec;22(12):1575-86. doi: 10.1089/hum.2011.070. Epub 2011 Sep 23.
2
T cells with chimeric antigen receptors have potent antitumor effects and can establish memory in patients with advanced leukemia.嵌合抗原受体 T 细胞具有强大的抗肿瘤作用,并能在晚期白血病患者中建立记忆。
Sci Transl Med. 2011 Aug 10;3(95):95ra73. doi: 10.1126/scitranslmed.3002842.
3
Chimeric antigen receptor-modified T cells in chronic lymphoid leukemia.嵌合抗原受体修饰的 T 细胞治疗慢性淋巴细胞白血病。
N Engl J Med. 2011 Aug 25;365(8):725-33. doi: 10.1056/NEJMoa1103849. Epub 2011 Aug 10.
4
Adoptive cellular therapy.过继性细胞疗法。
Curr Top Microbiol Immunol. 2011;344:149-72. doi: 10.1007/82_2010_94.
5
A phase I/II study of the safety and efficacy of the addition of sirolimus to tacrolimus/methotrexate graft versus host disease prophylaxis after allogeneic haematopoietic cell transplantation in paediatric acute lymphoblastic leukaemia (ALL).一项关于西罗莫司联合他克莫司/甲氨蝶呤预防异基因造血细胞移植后儿童急性淋巴细胞白血病(ALL)移植物抗宿主病的 I/II 期安全性和有效性的研究。
Br J Haematol. 2009 Dec;147(5):691-9. doi: 10.1111/j.1365-2141.2009.07889.x. Epub 2009 Sep 10.
6
Chimeric receptors containing CD137 signal transduction domains mediate enhanced survival of T cells and increased antileukemic efficacy in vivo.含有CD137信号转导结构域的嵌合受体介导T细胞在体内的存活率提高及抗白血病疗效增强。
Mol Ther. 2009 Aug;17(8):1453-64. doi: 10.1038/mt.2009.83. Epub 2009 Apr 21.
7
Mammalian target of rapamycin inhibitors and their potential role in therapy in leukaemia and other haematological malignancies.雷帕霉素哺乳动物靶点抑制剂及其在白血病和其他血液系统恶性肿瘤治疗中的潜在作用。
Br J Haematol. 2009 Jun;145(5):569-80. doi: 10.1111/j.1365-2141.2009.07657.x. Epub 2009 Mar 16.
8
Novel molecular and cellular therapeutic targets in acute lymphoblastic leukemia and lymphoproliferative disease.急性淋巴细胞白血病和淋巴增殖性疾病中的新型分子与细胞治疗靶点。
Immunol Res. 2008;42(1-3):84-105. doi: 10.1007/s12026-008-8038-9.
9
The impact of soluble tumor necrosis factor receptor etanercept on the treatment of idiopathic pneumonia syndrome after allogeneic hematopoietic stem cell transplantation.可溶性肿瘤坏死因子受体依那西普对异基因造血干细胞移植后特发性肺炎综合征治疗的影响。
Blood. 2008 Oct 15;112(8):3073-81. doi: 10.1182/blood-2008-03-143412. Epub 2008 Jul 29.
10
mTOR inhibitors are synergistic with methotrexate: an effective combination to treat acute lymphoblastic leukemia.雷帕霉素靶蛋白抑制剂与甲氨蝶呤具有协同作用:一种治疗急性淋巴细胞白血病的有效联合疗法。
Blood. 2008 Sep 1;112(5):2020-3. doi: 10.1182/blood-2008-02-137141. Epub 2008 Jun 10.

儿童肿瘤学组 2013 年研究蓝图:干细胞移植。

Children's Oncology Group's 2013 blueprint for research: stem cell transplantation.

机构信息

Children's Hospital of Philadelphia, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104-4318, USA.

出版信息

Pediatr Blood Cancer. 2013 Jun;60(6):1044-7. doi: 10.1002/pbc.24437. Epub 2012 Dec 19.

DOI:10.1002/pbc.24437
PMID:23255402
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4064788/
Abstract

The role of SCT in pediatric oncology has continued to evolve with the introduction of new therapeutic agents and immunological insights into cancer. COG has focused its efforts on the study of hematopoietic stem cell transplantation in the treatment of pediatric malignancies in several major multi-institutional Phase II and Phase III studies. These studies include addressing the impact of allogenicity in ALL (ASCT0431), and establishing autologous stem cell transplant as the standard of care in neuroblastoma. Reducing transplant-associated toxicity was addressed in the ASCT0521 study, where the TNFα inhibitor etanercept was tested for the treatment of idiopathic pneumonia syndrome. Impact of cell dose was explored in the single versus tandem umbilical cord blood study CTN-0501, in close collaboration with the BMT-CTN.

摘要

SCT 在儿科肿瘤学中的作用随着新的治疗药物和对癌症的免疫学认识的引入而不断发展。COG 专注于在几项主要的多机构 II 期和 III 期研究中研究造血干细胞移植治疗儿科恶性肿瘤。这些研究包括解决 ALL 中的异体性影响(ASCT0431),并将自体干细胞移植确立为神经母细胞瘤的标准治疗方法。ASCT0521 研究解决了与移植相关的毒性问题,其中 TNFα 抑制剂依那西普被测试用于治疗特发性肺炎综合征。与 BMT-CTN 密切合作,在单脐血与双脐血研究 CTN-0501 中探讨了细胞剂量的影响。