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培美曲塞在铂类一线治疗后的恶性胸膜间皮瘤中作为二线治疗。

Pemetrexed as second-line treatment in malignant pleural mesothelioma after platinum-based first-line treatment.

作者信息

Sørensen Jens Benn, Sundstrøm Stein, Perell Katharina, Thielsen Anne-Kathrine

机构信息

Department of Oncology, Finsen Centre/National University Hospital, Copenhagen, Denmark.

出版信息

J Thorac Oncol. 2007 Feb;2(2):147-52. doi: 10.1097/jto.0b013e31802f3813.

Abstract

INTRODUCTION

Pemetrexed is active as first-line treatment of malignant pleural mesothelioma. The objective was to evaluate its activity as second-line treatment.

METHODS

Patients had disease progression of malignant pleural mesothelioma after previous platinum-based regimens without pemetrexed. Treatment was pemetrexed alone or pemetrexed combined with carboplatin. Pemetrexed dosing was 500 mg/m and carboplatin was AUC (area under the curve) 5 once every 3 weeks.

RESULTS

Thirty-nine patients were included: 28 Danish patients received pemetrexed (three patients received pemetrexed as third-line treatment), whereas 11 Norwegian patients received pemetrexed plus carboplatin. Most patients were men (90%), had epithelial subtype (85%), and International Mesothelioma Interest Group stages III to IV (77%). Median age was 62 years (range, 30-77). The median number of treatment courses was six (range, 1-23). Common Toxicity Criteria grade 3 to 4 toxicity occurred only with respect to leukocytopenia (pemetrexed: 14% of patients; pemetrexed plus carboplatin: 9%) and thrombocytopenia (pemetrexed: 7%; pemetrexed plus carboplatin: 18%). One patient receiving pemetrexed died of sepsis. Partial response rates were 21% and 18%, the median time to progression was 21 weeks (range, 4-92) and 32 weeks (range, 4-128+), and the median survival was 42 weeks (range, 4-99) and 39 weeks (range, 10-128+) with pemetrexed and pemetrexed plus carboplatin, respectively.

CONCLUSIONS

Pemetrexed was generally well tolerated with noteworthy activity in malignant pleural mesothelioma after previous platinum-based treatment and may be considered for second-line treatment.

摘要

引言

培美曲塞作为恶性胸膜间皮瘤的一线治疗有效。目的是评估其作为二线治疗的活性。

方法

患者在先前未使用培美曲塞的铂类方案治疗后出现恶性胸膜间皮瘤疾病进展。治疗方案为单独使用培美曲塞或培美曲塞联合卡铂。培美曲塞剂量为500mg/m²,卡铂的曲线下面积(AUC)为5,每3周给药一次。

结果

纳入39例患者:28例丹麦患者接受培美曲塞治疗(3例患者接受培美曲塞作为三线治疗),而11例挪威患者接受培美曲塞加卡铂治疗。大多数患者为男性(90%),具有上皮亚型(85%),国际间皮瘤兴趣小组分期为III至IV期(77%)。中位年龄为62岁(范围30 - 77岁)。治疗疗程的中位数为6个(范围1 - 23个)。常见毒性标准3至4级毒性仅发生在白细胞减少方面(培美曲塞:14%的患者;培美曲塞加卡铂:9%)和血小板减少方面(培美曲塞:7%;培美曲塞加卡铂:18%)。1例接受培美曲塞治疗的患者死于败血症。部分缓解率分别为21%和18%,培美曲塞组和培美曲塞加卡铂组的中位进展时间分别为21周(范围4 - 92周)和32周(范围4 - 128 +周),中位生存期分别为42周(范围4 - 99周)和39周(范围)。

结论

培美曲塞耐受性总体良好,在先前铂类治疗后的恶性胸膜间皮瘤中具有显著活性,可考虑作为二线治疗。

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