Belotecan and Cisplatin Combination Chemotherapy for Previously Untreated Extensive-Disease Small Cell Lung Cancer

Jeong Eun Lee, K. Lee, H. Park, S. Jung, Ju Ock Kim, S. Kim
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Abstract

2 /day) on day 1 of a 3-week cycle. Results: Of the 19 assessable patients, 16 had an objective tumor response, including two complete responses, for an overall response rate of 84.2%. Toxicity was evaluated in all 20 patients who received a total of 106 cycles (median cycles/patient, 5.5; range, 1 ∼9). The major grade 3/4 hematologic toxicities were neutropenia (67.9% of cycles), anemia (19.8% of cycles) and thrombocytopenia (33.9% of cycles). No grade 3/4 non-hematologic toxicities were observed. No treatment-related deaths occurred. The median progression-free and overall survivals were 7.06 months (95% confidence interval (CI), 3.98 ∼10.14 months) and 9.96 months (95% CI, 6.12∼13.80 months), respectively. Conclusion: Combination chemotherapy with belotecan plus cisplatin is an effective treatment for ED-SCLC with acceptable hematologic and non-hematologic toxicities. (J Lung Cancer 2010;9(1):15 �� 19)
贝洛替康和顺铂联合化疗治疗未经治疗的广泛性小细胞肺癌
3周周期的第1天。结果:在19例可评估的患者中,16例有客观肿瘤缓解,包括2例完全缓解,总缓解率为84.2%。对所有接受106个疗程的20例患者的毒性进行评估(中位周期/患者,5.5;范围,1 ~ 9)。主要的3/4级血液学毒性是中性粒细胞减少(67.9%的周期)、贫血(19.8%的周期)和血小板减少(33.9%的周期)。未观察到3/4级非血液学毒性。无治疗相关死亡发生。中位无进展生存期和总生存期分别为7.06个月(95%可信区间(CI), 3.98 ~ 10.14个月)和9.96个月(95% CI, 6.12 ~ 13.80个月)。结论:贝罗替康联合顺铂化疗是治疗血液学和非血液学毒性均可接受的ED-SCLC的有效方法。[J] .肺癌杂志;2010;9(1):15 - 19。
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