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马拉维儿童肾母细胞瘤的 SIOP 术前化疗的疗效和毒性。

The efficacy and toxicity of SIOP preoperative chemotherapy in Malawian children with a Wilms tumour.

机构信息

Department of Paediatric Oncology, Emma Children's Hospital/AMC, Amsterdam, The Netherlands.

出版信息

Pediatr Blood Cancer. 2012 Oct;59(4):636-41. doi: 10.1002/pbc.24088. Epub 2012 Jan 23.

Abstract

BACKGROUND

In Malawi, preoperative chemotherapy for Wilms tumour is a logical strategy, but detailed information on toxicity and efficacy in such a resource limited setting has been unavailable.

PROCEDURE

Patients diagnosed with a unilateral Wilms tumour received preoperative chemotherapy-a two-drug 4-week regimen for localized disease and 6 weeks of a three-drug regimen for metastatic disease. Estimated maximum tumour diameter, decrease in tumour size, resectability, stage distribution and haematological toxicity during therapy were documented.

RESULTS

At diagnosis, 28% of 72 patients had an estimated maximum tumour diameter of more than 25 cm; 29% of patients had metastases. Eight children (11%) died during preoperative chemotherapy. More than half (59%) of the patients developed moderate neutropenia (neutrophils <1.0 × 10(9) /L; CTC grade 3) and 27% severe neutropenia (CTC grade 4 neutrophils <0.5 × 10.9/L). Grade 4 neutropenia occurred significantly more frequently in children receiving the three-drug regimen compared to the two-drug regimen; 50% (10/20) versus 15% (6/40) (P = 0.004). Fifty-seven percent of all patients had CTC grade 4 anaemia (Hb < 6.5 g/dL) during treatment. Most tumours (92%, 56/61) showed a response to chemotherapy but 14% (8/58) remained unresectable.

CONCLUSION

Preoperative chemotherapy for Wilms tumour causes considerable haematological toxicity and treatment-related mortality in malnourished Malawian children. A significant number of children have unresectable disease despite preoperative chemotherapy. To reduce treatment related mortality, consideration should be given to starting treatment with reduced doses in acutely malnourished patients.

摘要

背景

在马拉维,术前化疗治疗肾母细胞瘤是一种合理的策略,但在资源有限的情况下,有关毒性和疗效的详细信息尚不清楚。

方法

经诊断患有单侧肾母细胞瘤的患者接受术前化疗——局部疾病采用两药 4 周方案,转移性疾病采用 6 周三药方案。记录了肿瘤最大估计直径、肿瘤大小缩小、可切除性、分期分布以及治疗期间的血液学毒性。

结果

在诊断时,72 名患者中有 28%的患者肿瘤最大估计直径超过 25 厘米;29%的患者有转移。8 名儿童(11%)在术前化疗期间死亡。超过一半(59%)的患者出现中度中性粒细胞减少症(中性粒细胞<1.0×10(9)/L;CTC 分级 3),27%的患者出现严重中性粒细胞减少症(CTC 分级 4,中性粒细胞<0.5×10.9/L)。接受三药方案的儿童比接受两药方案的儿童更频繁地发生 4 级中性粒细胞减少症;50%(10/20)比 15%(6/40)(P=0.004)。57%的患者在治疗期间出现 CTC 分级 4 贫血(Hb<6.5g/dL)。大多数肿瘤(92%,56/61)对化疗有反应,但 14%(8/58)仍无法切除。

结论

术前化疗治疗马拉维营养不良的肾母细胞瘤患儿会导致严重的血液学毒性和治疗相关死亡率。尽管接受了术前化疗,但仍有相当数量的儿童无法切除肿瘤。为了降低治疗相关死亡率,应考虑在急性营养不良的患者中减少剂量开始治疗。

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