Gale G B, D'Angio G J, Uri A, Chatten J, Koop C E
Pediatrics. 1982 Sep;70(3):409-13.
Among 22 neonates treated at the Children's Cancer Research Center of Philadelphia, 11 had neuroblastoma, which in two cases was widely metastatic. There were three infants with teratoma, three with sarcoma, three with leukemia, one with Wilms' tumor, and one with parotid carcinoma. Nine of eleven patients (82%) are long-term survivors following complete surgical excision of tumor, whereas only one of eight (13%) has survived following incomplete surgical excision. All three neonates with leukemia died. The overall two-year actuarial survival is 45% (10/22). The problems associated with treating neonates with chemotherapy, radiation therapy, or both are especially difficult because of the immaturity of the organs and structures. Surgical excision alone has been the treatment of choice for solid tumors. Chemotherapy or radiation therapy, when indicated, require careful monitoring for both acute toxicities and potential long-term morbidities.
在费城儿童癌症研究中心接受治疗的22名新生儿中,11名患有神经母细胞瘤,其中2例发生广泛转移。有3名婴儿患有畸胎瘤,3名患有肉瘤,3名患有白血病,1名患有肾母细胞瘤,1名患有腮腺癌。11名患者中有9名(82%)在肿瘤完全手术切除后成为长期幸存者,而8名患者中只有1名(13%)在手术切除不完全后存活。所有3名白血病新生儿均死亡。两年的总精算生存率为45%(10/22)。由于器官和结构不成熟,用化疗、放疗或两者治疗新生儿相关的问题尤其困难。对于实体瘤,单独手术切除一直是首选治疗方法。化疗或放疗在有指征时,需要对急性毒性和潜在的长期发病率进行仔细监测。