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高剂量紫杉醇联合粒细胞集落刺激因子治疗恶性间皮瘤:癌症和白血病B组(CALGB)II期研究9234

High-dose paclitaxel plus G-CSF for malignant mesothelioma: CALGB phase II study 9234.

作者信息

Vogelzang N J, Herndon J E, Miller A, Strauss G, Clamon G, Stewart F M, Aisner J, Lyss A, Cooper M R, Suzuki Y, Green M R

机构信息

University of Chicago, Department of Medicine, IL, USA.

出版信息

Ann Oncol. 1999 May;10(5):597-600. doi: 10.1023/a:1026438215309.

Abstract

BACKGROUND

New agents with activity in mesothelioma are sorely needed. The Cancer and Leukemia Group B (CALGB) therefore performed a phase II study of high-dose paclitaxel in patients with malignant mesothelioma who had no prior chemotherapy.

PATIENTS AND METHODS

Thirty-five patients accrued to this multi-institutional phase II study of paclitaxel given as a 24-hour infusion at 250 mg/m2 every three weeks plus filgrastim (G-CSF) 300 mcg subcutaneously days 3-18.

RESULTS

There were three (9%) regressions of evaluable disease. The median survival was five months (95% confidence interval (95% CI): 1.9-9.6 months), the one-year survival rate was 14% and the two-year survival rate was 6%. Toxicity was tolerable with one death from pneumonia (without neutropenia) on day 18 and a 23% rate of grade 4 granulocytopenia.

CONCLUSIONS

The level of activity seen with paclitaxel is similar to that seen in other CALGB trials of the single agents carboplatin, trimetrexate and 5-azacytidine. Future studies of of paclitaxel (at lower doses) in combination with synergistic agents could be considered.

摘要

背景

迫切需要有治疗间皮瘤活性的新型药物。因此,癌症与白血病B组(CALGB)对未接受过化疗的恶性间皮瘤患者进行了高剂量紫杉醇的II期研究。

患者与方法

35例患者纳入了这项多机构II期研究,该研究中紫杉醇采用每三周一次、250mg/m²、24小时静脉输注的给药方式,并于第3 - 18天皮下注射非格司亭(G - CSF)300μg。

结果

可评估疾病中有3例(9%)出现缓解。中位生存期为5个月(95%置信区间(95%CI):1.9 - 9.6个月),1年生存率为14%,2年生存率为6%。毒性是可耐受的,第18天有1例死于肺炎(无中性粒细胞减少),4级粒细胞减少发生率为23%。

结论

紫杉醇的活性水平与CALGB其他关于单一药物卡铂、三甲曲沙和5 - 氮杂胞苷的试验中观察到的相似。可以考虑未来进行紫杉醇(较低剂量)与协同药物联合的研究。

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