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多模式疗法在局部和区域性神经母细胞瘤患者中的作用。

The role of multimodal therapy in patients with local and regional neuroblastoma.

作者信息

Evans A E, D'Angio G J, Koop C E

出版信息

J Pediatr Surg. 1984 Feb;19(1):77-80. doi: 10.1016/s0022-3468(84)80021-4.

DOI:10.1016/s0022-3468(84)80021-4
PMID:6366182
Abstract

The records of 49 patients with local and regional neuroblastoma treated at The Children's Hospital of Philadelphia between 1972-1981 were reviewed to determine the contribution of radiation therapy and chemotherapy to their management. All 11 state I patients were treated with surgery alone and 10 (91%) survived for periods ranging from 3 to 10 years. Half of the 24 stage II patients received radiation therapy with or without chemotherapy and 8/12 (67%) survive. Ten of the 12 remaining stage II patients survive (83%) following surgery alone. All stage II patients had residual disease and 13 had involvement in lymph nodes. 7 in the combined treatment group and 6 in the surgery alone group. All 14 stage III patients received postoperative chemotherapy and radiation therapy (RT) and 7 or 50% remain disease free. We conclude that surgery alone is sufficient for patients with stage I NBL, that RT and chemotherapy do not appear to alter the outcome in stage II patients, and better methods of therapy are needed for patients with stage III disease.

摘要

回顾了1972年至1981年间在费城儿童医院接受治疗的49例局部和区域神经母细胞瘤患者的记录,以确定放射治疗和化疗在其治疗中的作用。所有11例I期患者仅接受手术治疗,10例(91%)存活3至10年。24例II期患者中有一半接受了放疗,无论是否联合化疗,8/12例(67%)存活。其余12例II期患者中,10例(83%)仅接受手术后存活。所有II期患者均有残留病灶,13例有淋巴结受累。联合治疗组7例,单纯手术组6例。所有14例III期患者均接受术后化疗和放疗(RT),7例(50%)仍无疾病。我们得出结论,对于I期神经母细胞瘤患者,单纯手术就足够了;放疗和化疗似乎不会改变II期患者的预后;对于III期疾病患者,需要更好的治疗方法。

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The role of multimodal therapy in patients with local and regional neuroblastoma.多模式疗法在局部和区域性神经母细胞瘤患者中的作用。
J Pediatr Surg. 1984 Feb;19(1):77-80. doi: 10.1016/s0022-3468(84)80021-4.
2
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Radiotherapy improves the outlook for patients older than 1 year with Pediatric Oncology Group stage C neuroblastoma.放射治疗改善了1岁以上患有儿童肿瘤学组C期神经母细胞瘤患者的预后。
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Hyperfractionated low-dose radiotherapy for high-risk neuroblastoma after intensive chemotherapy and surgery.强化化疗和手术后高危神经母细胞瘤的超分割低剂量放疗
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N-Myc gene amplification is a major prognostic factor in localized neuroblastoma: results of the French NBL 90 study. Neuroblastoma Study Group of the Société Francaise d'Oncologie Pédiatrique.N-Myc基因扩增是局限性神经母细胞瘤的主要预后因素:法国NBL 90研究结果。法国儿科肿瘤学会神经母细胞瘤研究组。
J Clin Oncol. 1997 Mar;15(3):1171-82. doi: 10.1200/JCO.1997.15.3.1171.

引用本文的文献

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Second malignancies in patients with neuroblastoma: the effects of risk-based therapy.神经母细胞瘤患者的二次恶性肿瘤:基于风险的治疗效果。
Pediatr Blood Cancer. 2015 Jan;62(1):128-33. doi: 10.1002/pbc.25249. Epub 2014 Sep 23.
2
Intensive chemotherapy in children with stage IV neuroblastoma.
Indian J Pediatr. 1999 Nov-Dec;66(6):867-72. doi: 10.1007/BF02723857.
3
Unresectable localized neuroblastoma: improved survival after primary chemotherapy including carboplatin-etoposide. Neuroblastoma Study Group of the Société Française d'Oncologie Pédiatrique (SFOP).不可切除的局限性神经母细胞瘤:含卡铂-依托泊苷的初始化疗后生存率提高。法国儿科肿瘤学会(SFOP)神经母细胞瘤研究组
Br J Cancer. 1998 Jun;77(12):2310-7. doi: 10.1038/bjc.1998.384.
4
Prognostic value of different staging systems in neuroblastomas and completeness of tumour excision.不同分期系统在神经母细胞瘤中的预后价值及肿瘤切除的完整性
Arch Dis Child. 1986 Sep;61(9):832-42. doi: 10.1136/adc.61.9.832.
5
Surgical management of thoracic malignancy in childhood: eight years' experience in Leeds.儿童胸部恶性肿瘤的外科治疗:利兹八年经验
Ann R Coll Surg Engl. 1988 Mar;70(2):109-12.