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A randomised study of bolus vs continuous pump infusion of ifosfamide and doxorubicin with oral etoposide for small cell lung cancer.

机译:小剂量肺癌的推注与连续泵输异环磷酰胺和阿霉素与口服依托泊苷的随机对照研究。

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摘要

One hundred and fifty-nine previously untreated patients with small cell lung cancer (SCLC), who were not eligible for intensive chemotherapy, were entered into a randomised study of intravenous (i.v.) doxorubicin and ifosfamide (with mesna) and oral etoposide. The i.v. drugs were given either by bolus therapy or by a continuous infusion (CI) pump over 7 days via a central venous line. Therapy was given for 6 weeks only. On weeks 1, 3 and 5 IV doxorubicin 35 mg m-2 was given with 5 days of oral etoposide 100 mg m-2 daily. On weeks 2, 4 and 6 IV ifosfamide 5 g m-2 was given with equidose mesna. The overall median survival was 25 weeks for patients in the bolus arm and 30 weeks for the CI therapy (P = 0.45). The overall response rate was 64% (18% complete response-CR) and 69% (30% CR) respectively (P = 0.13). The median WHO score for haematological toxicity was 4 for bolus therapy and 3 for CI therapy (P = 0.0007). Despite a trend for less supportive care for patients on CI therapy there were no significant differences in the use of i.v. antibodies and blood or platelet transfusions. There were fewer treatment delays due to myelotoxicity in the CI arm (P = 0.04). The median WHO score for non-haematological toxicity was 2 in both treatment groups. There was significantly less nausea (P = 0.037) but more mucositis (P = 0.01) in the CI arm. Weekly chemotherapy using CI treatment was as effective as bolus therapy. It was well accepted by patients. The assessment of quality of life in a subgroup of patients showed a statistically significant reduction in anxiety and depression for both groups of patients during therapy.
机译:不接受强化化疗的159例先前未接受治疗的小细胞肺癌(SCLC)患者被纳入静脉内(i.v.)阿霉素和异环磷酰胺(与mesna联合使用)和口服依托泊苷的随机研究。 i.v.通过推注疗法或通过中心静脉线连续输注(CI)泵在7天内给予药物。治疗仅进行了6周。在第1、3和5周静脉注射阿霉素35 mg m-2,每天口服5次口服依托泊苷100 mg m-2。在第2、4和6周静脉给予异环磷酰胺5 g m-2,并给予等剂量的mesna。大剂量治疗组患者的总中位生存期为25周,CI疗法为30周(P = 0.45)。总体缓解率分别为64%(18%完全缓解-CR)和69%(30%CR)(P = 0.13)。推注疗法的血液学毒性世卫组织平均得分为4,而CI疗法的平均得分为3(P = 0.0007)。尽管对接受CI治疗的患者支持治疗的趋势有所减少,但i.v.的使用没有显着差异。抗体和血液或血小板输注。 CI臂的骨髓毒性导致的治疗延误较少(P = 0.04)。在两个治疗组中,非血液学毒性的WHO得分中位数均为2。 CI臂的恶心明显减少(P = 0.037),但粘膜炎较多(P = 0.01)。每周使用CI治疗的化疗与推注治疗一样有效。它被患者很好地接受。对亚组患者的生活质量评估显示,在治疗期间,两组患者的焦虑和抑郁情绪均有统计学意义的降低。

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