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英国儿童癌症研究小组恶性生殖细胞肿瘤研究结果。

Results of the United Kingdom Children's Cancer Study Group's malignant germ cell tumor studies.

作者信息

Mann J R, Pearson D, Barrett A, Raafat F, Barnes J M, Wallendszus K R

机构信息

Oncology Department, Children's Hospital, Birmingham, England.

出版信息

Cancer. 1989 May 1;63(9):1657-67. doi: 10.1002/1097-0142(19900501)63:9<1657::aid-cncr2820630902>3.0.co;2-8.

Abstract

The United Kingdom Children's Cancer Study Group's malignant germ cell tumor studies were undertaken to establish standard protocols for investigating, staging, and treating children, and to study the efficacy of new drug combinations and the value of serial measurement of serum alphafetoprotein (AFP) and human chorionic gonadotrophin (HCG). Boys with Stage I testicular tumors were treated by orchidectomy alone, whereas, after appropriate surgery, chemotherapy was recommended for children with more advanced testicular tumors or with tumors at other sites. From 1979 to 1987, 126 children aged 0 to younger than 16 years with malignant germ cell tumors were registered. They were similar to patients in other large pediatric series with respect to sites of origin, age at presentation in relationship to primary site, histology, female predominance for sacrococcygeal site, and presence of associated malformations (present in 17%). Serum AFP was measured in 123 patients and was elevated in 115, whereas HCG was raised in 19 of 77. Monitoring by serial AFP measurement proved valuable in assessing response to therapy and in early detection of tumor recurrence. When treatment results were assessed in February 1988, 101 of 122 patients were alive (four who received nonprotocol chemotherapy were excluded). Forty-four patients had been cured by surgery alone (41 with testicular tumors, two with ovarian tumors, and one with sacrococcygeal tumor). All of the remaining 78 children received chemotherapy. The initial low dose vincristine, actinomycin, and cyclophosphamide (LDVAC) regimen proved ineffective, actuarial survival at 5 years followup being 8% (12 patients), and a regimen of cisplatin, vinblastine, and bleomycin (PVB) caused unacceptable toxicity, with actuarial survival at 5 years follow-up being 67% (nine patients). Five-year actuarial survival was 87% for 17 children given high dose VAC with or without doxorubicin and 84% for 33 given bleomycin, etoposide, and cisplatin (BEP). All 7 children given various combinations of these regimens survived. Excluding the 12 LDVAC cases, patient survival by site was as follows: testis (59 patients, 100%); vagina, uterus, and prostate (four patients, 100%); ovary (25 patients, 88%); thorax (five patients, 40%), and other (four patients, 67%). Similarly, patient survival by stage was Stage I (62,97%), Stage II (14,86%); Stage III (18,83%); and Stage IV (16,72%). Survival by histology was analysed only in cases for which histologic review had been done the LDVAC cases were excluded.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

英国儿童癌症研究小组开展了恶性生殖细胞瘤研究,旨在建立针对儿童进行调查、分期和治疗的标准方案,研究新药组合的疗效以及血清甲胎蛋白(AFP)和人绒毛膜促性腺激素(HCG)系列测量的价值。I期睾丸肿瘤男孩仅接受睾丸切除术治疗,而对于更晚期睾丸肿瘤或其他部位肿瘤的儿童,在进行适当手术后推荐化疗。1979年至1987年,登记了126名0至未满16岁的患有恶性生殖细胞瘤的儿童。他们在肿瘤起源部位、与原发部位相关的就诊年龄、组织学、骶尾部肿瘤以女性为主以及存在相关畸形(17%存在)方面与其他大型儿科系列中的患者相似。123例患者检测了血清AFP,115例升高,而77例中的19例HCG升高。通过系列AFP测量进行监测在评估治疗反应和早期发现肿瘤复发方面被证明有价值。1988年2月评估治疗结果时,122例患者中有101例存活(排除4例接受非方案化疗的患者)。44例患者仅通过手术治愈(41例睾丸肿瘤、2例卵巢肿瘤和1例骶尾部肿瘤)。其余78名儿童均接受了化疗。最初的低剂量长春新碱、放线菌素和环磷酰胺(LDVAC)方案被证明无效,5年随访的精算生存率为8%(12例患者),顺铂、长春碱和博来霉素(PVB)方案导致不可接受的毒性,5年随访的精算生存率为67%(9例患者)。17例接受高剂量VAC(含或不含阿霉素)的儿童5年精算生存率为87%,33例接受博来霉素、依托泊苷和顺铂(BEP)的儿童5年精算生存率为84%。接受这些方案各种组合治疗的所有7例儿童均存活。排除12例LDVAC病例后,各部位患者生存率如下:睾丸(59例患者,100%);阴道、子宫和前列腺(4例患者,100%);卵巢(25例患者,88%);胸部(5例患者,40%),其他(4例患者,67%)。同样,按分期的患者生存率为I期(62例,97%),II期(14例,86%);III期(18例,83%);IV期(16例,72%)。仅对进行了组织学复查的病例(排除LDVAC病例)分析了按组织学的生存率。(摘要截短为400字)

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