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磨玻璃影型肺腺癌对化疗无反应。

Ground-glass opacity-featured lung adenocarcinoma has no response to chemotherapy.

机构信息

Department of Thoracic Surgery, Fudan University Shanghai Cancer Center, 270 Dong-An Road, Shanghai, 200032, China.

Institute of Thoracic Oncology, Fudan University, Shanghai, 200032, China.

出版信息

J Cancer Res Clin Oncol. 2020 Sep;146(9):2411-2417. doi: 10.1007/s00432-020-03234-6. Epub 2020 Apr 30.

Abstract

PURPOSE

We aimed to investigate the treatment effect of chemotherapy on ground-glass opacity (GGO)-featured lung adenocarcinoma radiologically and pathologically.

METHODS

This retrospective study included patients who met the following criteria: (1) presence of lung GGO lesions before chemotherapy for other concurrent malignancies; (2) underwent surgical resection of GGO-featured primary lung adenocarcinoma. The last computed tomography images before chemotherapy (CT1) and the last images before GGO resection (CT2) were reviewed to assess radiologic response. Specimens of the resected tumors were reviewed to evaluate the histopathologic response. Immunohistochemical staining of ki-67, caspase-3 and β-gal was performed and compared between these tumors and a propensity score-matched (1:1) cohort of GGO-featured lung adenocarcinoma without prior chemotherapy.

RESULTS

Forty-four patients with 55 GGO lesions were included. There were 20 mixed GGOs and 22 invasive adenocarcinomas. These patients all received at least three cycles of chemotherapy for other concurrent malignancies in breast, lung, cervix, ovary or rectum. Thirty-four (77%) patients received chemotherapy regimens that contained platinum, pemetrexed, paclitaxel, docetaxel or gemcitabine. The median interval between CT1 and CT2 was 10 months. Radiologically, all the GGO lesions either remained unchanged or enlarged. There was no chemotherapy-induced histopathologic response (necrosis, fibrosis or inflammation) in any of these tumors. The protein expression of ki-67, caspase-3 and β-gal was comparable between GGO-featured lung adenocarcinoma with or without prior chemotherapy.

CONCLUSION

GGO-featured lung adenocarcinoma has no response to chemotherapy. For these patients, chemotherapy should not be a treatment option.

摘要

目的

本研究旨在探讨化疗对影像学和病理学上表现为磨玻璃密度(GGO)特征的肺腺癌的治疗效果。

方法

本回顾性研究纳入了符合以下标准的患者:(1)存在其他同时性恶性肿瘤化疗前的肺 GGO 病变;(2)接受 GGO 特征性原发性肺腺癌的手术切除。在化疗前的最后一次计算机断层扫描图像(CT1)和 GGO 切除前的最后一次图像(CT2)进行了评估,以评估放射学反应。评估切除肿瘤的标本,以评估组织病理学反应。对 Ki-67、半胱氨酸蛋白酶-3 和 β-半乳糖苷酶进行免疫组织化学染色,并与无先前化疗的 GGO 特征性肺腺癌的倾向评分匹配(1:1)队列进行比较。

结果

共纳入 44 例 55 个 GGO 病变患者,其中 20 个为混合性 GGO,22 个为浸润性腺癌。这些患者均因乳腺癌、肺癌、宫颈癌、卵巢癌或直肠癌等其他同时性恶性肿瘤接受了至少三个周期的化疗。34 例(77%)患者接受了包含铂类、培美曲塞、紫杉醇、多西他赛或吉西他滨的化疗方案。CT1 与 CT2 之间的中位间隔为 10 个月。影像学上,所有 GGO 病变要么保持不变,要么增大。这些肿瘤中均未发生化疗诱导的组织病理学反应(坏死、纤维化或炎症)。GGO 特征性肺腺癌无论是否有先前的化疗,Ki-67、半胱氨酸蛋白酶-3 和 β-半乳糖苷酶的蛋白表达无差异。

结论

GGO 特征性肺腺癌对化疗无反应。对于这些患者,化疗不应作为一种治疗选择。

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