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多西他赛、吉西他滨和脂质体阿霉素三联化疗联合皮下注射氨磷汀和造血生长因子治疗晚期非小细胞肺癌。

Triplet chemotherapy with docetaxel, gemcitabine and liposomal doxorubicin, supported with subcutaneous amifostine and hemopoietic growth factors, in advanced non-small cell lung cancer.

作者信息

Patlakas George, Bouros Demosthenes, Tsantekidou-Pozova Sofia, Koukourakis Michael I

机构信息

Department of Pneumonology and Radiotherapy-Oncology, Democritus University of Thrace, Alexandroupolis, Greece.

出版信息

Anticancer Res. 2005 Mar-Apr;25(2B):1427-31.

Abstract

The activity of a triplet of chemotherapeutic drugs, namely docetaxel, gemcitabine and liposomal doxorubicin, was investigated in patients with advanced non-small cell lung cancer. The regimen was supported with amifostine cytoprotection (1000mg injected subcutaneously) and hemopoietic growth factors (rhuG-CSF and rhuEPO) in an attempt to minimize the substantial toxicity reported in previous studies investigating docetaxel/gemcitabine chemotherapy. Twenty chemotherapy- naïve patients with advanced non-small cell lung cancer (NSCLC) (18 with stage IV and 2 with stage IIIb) were recruited. None of the patients presented with grade 3-4 hematological or non-hematological toxicity. Palmar-plantar erythrodysesthesia grade 2 was noted in 6/20 (30%), mucositisloesophagitis grade 2 in 3/20 (15%) and mild alopecia in 6/20 (30%) patients. No case of interstitial pneumonia was noted. The overall response rate (complete and partial) in 18 evaluable patients was 33% (6/18), with 1/18 (5%) patients achieving complete response. The median survival was 11 months. The efficacy of the regimen was as high as the one reported in gemcitabine/docetaxel studies, but the toxicity was remarkably lower. Amifostine may have contributed to the better tolerance profile observed.

摘要

对多西他赛、吉西他滨和脂质体阿霉素这三种化疗药物联合使用的活性进行了研究,研究对象为晚期非小细胞肺癌患者。该方案辅以氨磷汀细胞保护(皮下注射1000mg)和造血生长因子(重组人粒细胞集落刺激因子和重组人促红细胞生成素),以尽量减少先前研究多西他赛/吉西他滨化疗时所报告的严重毒性。招募了20例初治的晚期非小细胞肺癌患者(18例IV期和2例IIIb期)。所有患者均未出现3 - 4级血液学或非血液学毒性。20例患者中有6例(30%)出现2级掌跖红斑感觉异常,3例(15%)出现2级黏膜炎/食管炎,6例(30%)出现轻度脱发。未观察到间质性肺炎病例。18例可评估患者的总缓解率(完全缓解和部分缓解)为33%(6/18),其中1例(5%)患者达到完全缓解。中位生存期为11个月。该方案的疗效与吉西他滨/多西他赛研究中报告的疗效一样高,但毒性明显更低。氨磷汀可能促成了所观察到的更好的耐受性。

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