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恶性胸膜疾病与IV期非小细胞肺癌患者随后的腹膜转移高度相关,且与癌基因状态无关。

Malignant pleural disease is highly associated with subsequent peritoneal metastasis in patients with stage IV non-small cell lung cancer independent of oncogene status.

作者信息

Patil Tejas, Aisner Dara L, Noonan Sinead A, Bunn Paul A, Purcell William T, Carr Laurie L, Camidge D Ross, Doebele Robert C

机构信息

Department of Medicine, University of Colorado School of Medicine, Aurora, CO, United States.

Department of Pathology, University of Colorado School of Medicine, Aurora, CO, United States.

出版信息

Lung Cancer. 2016 Jun;96:27-32. doi: 10.1016/j.lungcan.2016.03.007. Epub 2016 Mar 26.

Abstract

INTRODUCTION

Peritoneal metastasis from lung cancer is an uncommon clinical event and there are limited data on what factors predict peritoneal progression. This study retrospectively investigated whether patterns of metastatic spread and oncogene status in patients with advanced non-small cell lung cancer (NSCLC) are associated with peritoneal metastasis.

METHODS

Patients with metastatic non-squamous NSCLC (n=410) were identified at the University of Colorado Cancer Center. Sites of metastatic disease and baseline oncogene status (EGFR, ALK, KRAS, or triple negative) were documented via a retrospective chart review. In patients with EGFR mutations who developed peritoneal disease, we documented the presence of known resistance mechanisms. Median time to peritoneal metastasis, time from peritoneal disease to death, and overall survival were collected.

RESULTS

Eight percent (33/410) patients in this study developed peritoneal metastasis. Malignant pleural disease at baseline was significantly associated with subsequent peritoneal spread. There was no association between oncogene status and peritoneal metastasis. Three patients with EGFR mutations who developed peritoneal metastasis had documented resistance to tyrosine kinase inhibitors (TKIs) in the ascitic fluid. Median time from stage IV disease to peritoneal metastasis was 16.5 months (range 0.6-108 months). There were no differences in overall survival between patients who developed peritoneal metastasis and those who did not.

CONCLUSIONS

Malignant pleural disease is highly associated with peritoneal metastasis in patients with advanced NSCLC. The underlying mechanism is not clear. The presence of resistance mutations in ascitic fluid implies that poor drug penetration is unlikely to be the dominant mechanism. Despite being a late clinical finding, there were no differences in overall survival between patients who developed peritoneal metastasis and those who did not. Additional studies exploring treatment related factors in patients with malignant pleural disease that can reduce risk of peritoneal metastasis are warranted.

摘要

引言

肺癌的腹膜转移是一种不常见的临床情况,关于哪些因素可预测腹膜进展的数据有限。本研究回顾性调查了晚期非小细胞肺癌(NSCLC)患者的转移扩散模式和癌基因状态是否与腹膜转移相关。

方法

在科罗拉多大学癌症中心确定了转移性非鳞状NSCLC患者(n = 410)。通过回顾性病历审查记录转移疾病的部位和基线癌基因状态(EGFR、ALK、KRAS或三阴性)。在发生腹膜疾病的EGFR突变患者中,我们记录了已知耐药机制的存在情况。收集了至腹膜转移的中位时间、从腹膜疾病到死亡的时间以及总生存期。

结果

本研究中8%(33/410)的患者发生了腹膜转移。基线时的恶性胸膜疾病与随后的腹膜扩散显著相关。癌基因状态与腹膜转移之间无关联。3例发生腹膜转移的EGFR突变患者在腹水中记录到对酪氨酸激酶抑制剂(TKIs)耐药。从IV期疾病到腹膜转移的中位时间为16.5个月(范围0.6 - 108个月)。发生腹膜转移的患者与未发生腹膜转移的患者在总生存期方面无差异。

结论

恶性胸膜疾病与晚期NSCLC患者的腹膜转移高度相关。潜在机制尚不清楚。腹水中存在耐药突变意味着药物穿透性差不太可能是主要机制。尽管腹膜转移是晚期临床发现,但发生腹膜转移的患者与未发生腹膜转移的患者在总生存期方面无差异。有必要进行更多研究,探索可降低恶性胸膜疾病患者腹膜转移风险的治疗相关因素。

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