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铂类-长春瑞滨诱导化疗联合贝伐单抗在晚期非小细胞肺癌中应用或不应用培美曲塞序贯维持治疗

Platinum-Vinorelbine Induction Chemotherapy plus Bevacizumab With and Without Pemetrexed Switch Maintenance in Advanced NSCLC.

作者信息

Michelsen Linda, Sørensen Jens Benn

机构信息

Department of Oncology, Finsen Centre-National University Hospital, Copenhagen, Denmark

出版信息

Anticancer Res. 2015 Nov;35(11):6255-9.

Abstract

BACKGROUND

Little information is available until today regarding the effect of platinum-doublet chemotherapy with bevacizumab followed by pemetrexed as a sole maintenance treatment. Original data concerns different induction regimens plus bevacizumab with bevacizumab maintenance to progression in advanced non-squamous non-small cell lung cancer (NSCLC).

PATIENTS AND METHODS

Two consecutive groups of patients with advanced non-squamous NSCLC received carboplatin, vinorelbine and bevacizumab for four cycles. Group A (2010-2012) did not receive any maintenance therapy, whereas group B (2012-2013) received pemetrexed switch maintenance (500 mg/m(2)) every three weeks until disease progression.

RESULTS

The median progression-free survival (PFS) was 4.4 months and 7.3 months (p<0.001) and one-year survival was 42% and 52% for Group A (n=20) and B (n=22) patients, respectively. Disease control rates were 65% and 86% (p=0.104). Deep venous thrombosis and pulmonary embolism occurred in three (15%) and seven (32%) patients in group A and B, respectively.

CONCLUSION

The inferior PFS (p<0.001) without maintenance suggests that induction treatment including bevacizumab should not be planned without subsequent maintenance treatment. Whether it is better to use pemetrexed or bevacizumab, or a combination of both, as maintenance therapy is not yet established.

摘要

背景

迄今为止,关于铂类双联化疗联合贝伐单抗后培美曲塞作为单一维持治疗的效果,几乎没有可用信息。原始数据涉及晚期非鳞状非小细胞肺癌(NSCLC)中不同的诱导方案联合贝伐单抗以及贝伐单抗维持至疾病进展。

患者与方法

两组连续的晚期非鳞状NSCLC患者接受卡铂、长春瑞滨和贝伐单抗治疗四个周期。A组(2010 - 2012年)未接受任何维持治疗,而B组(2012 - 2013年)每三周接受一次培美曲塞转换维持治疗(500 mg/m²),直至疾病进展。

结果

A组(n = 20)和B组(n = 22)患者的中位无进展生存期(PFS)分别为4.4个月和7.3个月(p<0.001),一年生存率分别为42%和52%。疾病控制率分别为65%和86%(p = 0.104)。A组和B组分别有3例(15%)和7例(32%)患者发生深静脉血栓和肺栓塞。

结论

未进行维持治疗时较差的PFS(p<0.001)表明,不进行后续维持治疗不应计划包含贝伐单抗的诱导治疗。作为维持治疗,使用培美曲塞还是贝伐单抗,或两者联合是否更好尚未确定。

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