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mTOR 抑制剂治疗转移性肾细胞癌患者相关性肺炎:发生率、影像学表现与临床结局的相关性。

Pneumonitis associated with mTOR inhibitors therapy in patients with metastatic renal cell carcinoma: incidence, radiographic findings and correlation with clinical outcome.

机构信息

Dana-Farber Cancer Institute/Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02215, United States.

出版信息

Eur J Cancer. 2012 Jul;48(10):1519-24. doi: 10.1016/j.ejca.2012.03.012. Epub 2012 Apr 5.

DOI:10.1016/j.ejca.2012.03.012
PMID:22483544
Abstract

BACKGROUND

Mammalian target of rapamycin (mTOR) inhibitors are approved for use in patients with metastatic renal cell carcinoma (mRCC) and are under investigation in several other malignancies. We assessed the incidence, clinical presentation and computed tomography (CT) findings of pneumonitis associated with mTOR inhibitors in mRCC. Correlation between radiological findings of pneumonitis and clinical outcome was also determined.

METHODS

We retrospectively reviewed the clinical data and serial CT scans from patients with mRCC treated with either temsirolimus or everolimus. Serial chest CT scans were reviewed in consensus, read by two independent radiologists for the presence of pneumonitis, and corresponding clinical data were reviewed for symptoms and clinical outcome. The baseline and follow up CTs were reviewed to assess outcome to therapy.

RESULTS

The study population consisted of 46 pts, 21 treated with temsirolimus and 25 with everolimus (M:F 2.5:1; median 63 years, range 31-79 years). CT evidence of pneumonitis was seen in 14/46 pts (30%), at a median of 56days on mTOR inhibitor treatment (range 31-214 days). Respiratory symptoms at the time of radiographically detected pneumonitis, were observed in 7pts. Stable disease (SD) by Response Evaluation Criteria in Solid Tumours (RECIST) was achieved in 12/14 pts (86%) who developed radiographic pneumonitis compared to 14/32 (44%) without pneumonitis (p=0.01) The mean change of tumour long axis size for target lesions by RECIST, normalised for 30 days on therapy was -2.9% in the pneumonitis group and +4.3% in the non-pneumonitis group (p=.002).

CONCLUSIONS

Preliminary data suggest that pneumonitis may be a marker of stable disease by RECIST and therefore, of therapeutic benefit. Careful patient assessment should be undertaken before the drug is discontinued.

摘要

背景

雷帕霉素靶蛋白(mTOR)抑制剂已被批准用于转移性肾细胞癌(mRCC)患者,并正在其他几种恶性肿瘤中进行研究。我们评估了 mTOR 抑制剂治疗 mRCC 患者相关的肺炎发生率、临床表现和计算机断层扫描(CT)结果。还确定了肺炎的影像学表现与临床结果之间的相关性。

方法

我们回顾性分析了接受替西罗莫司或依维莫司治疗的 mRCC 患者的临床数据和系列 CT 扫描。通过两名独立放射科医生对系列胸部 CT 扫描进行共识评估,以确定是否存在肺炎,并评估相应的临床数据以了解症状和临床结果。回顾了基线和随访 CT 以评估对治疗的反应。

结果

研究人群包括 46 例患者,21 例接受替西罗莫司治疗,25 例接受依维莫司治疗(M:F 2.5:1;中位年龄 63 岁,范围 31-79 岁)。在 mTOR 抑制剂治疗的中位数为 56 天(范围 31-214 天)时,46 例患者中有 14 例(30%)出现 CT 证据的肺炎。在影像学检测到肺炎时,有 7 例出现呼吸症状。与无肺炎的患者(14/32,44%)相比,14 例出现放射性肺炎的患者达到了实体瘤反应评估标准(RECIST)的疾病稳定(SD)(12/14,86%)(p=0.01)。按 RECIST 计算的靶病变长轴大小的肿瘤变化,经治疗 30 天归一化后,在肺炎组为-2.9%,在非肺炎组为+4.3%(p=.002)。

结论

初步数据表明,肺炎可能是 RECIST 疾病稳定的标志物,因此也是治疗获益的标志物。在停止药物治疗之前,应仔细评估患者。

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