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1973 - 1978年瑞典儿童急性淋巴细胞白血病

Acute lymphoblastic leukemia in Swedish children 1973-1978.

作者信息

Gustafsson G, Kreuger A, Dohlwitz A

出版信息

Acta Paediatr Scand. 1981 Sep;70(5):609-14. doi: 10.1111/j.1651-2227.1981.tb05754.x.

Abstract

Three hundred and sixty-seven children with acute lymphoblastic leukemia have been diagnosed in Sweden 1973-1978, 345 of whom were treated according to the national uniform regimens of the Swedish Child Leukemia Group (SCLG). The patients were classified into an SR (standard risk) and an IR (increased risk) group. Remission was obtained in 354 patients (96%). With 12-84 months observation time the total survival was 54% and the disease-free survival 44%. A more intensive cytostatic regimen in the induction period increased considerably the disease-free survival for the SR and to some extent also for the IR patients. Relapses were significantly more common in the IR group in spite of a more intensive cytostatic regimen. The most decisive IR criteria were B-LPK and age at diagnosis. Prognosis was significantly worse for boys in all groups. After 3 years in CCR treatment was discontinued in 95 out of 246 children (38%) of whom 19 later relapsed (20%).

摘要

1973年至1978年期间,瑞典共诊断出367例急性淋巴细胞白血病患儿,其中345例按照瑞典儿童白血病研究组(SCLG)的全国统一方案进行治疗。患者被分为SR(标准风险)组和IR(高风险)组。354例患者(96%)获得缓解。在12至84个月的观察期内,总生存率为54%,无病生存率为44%。诱导期采用更强的细胞抑制方案可显著提高SR组患者的无病生存率,对IR组患者也有一定程度的提高。尽管采用了更强的细胞抑制方案,但IR组的复发率明显更高。最关键的IR标准是B-LPK和诊断时的年龄。所有组中男孩的预后明显更差。246名儿童中有95名(38%)在持续完全缓解3年后停止治疗,其中19名后来复发(20%)。

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