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新辅助化疗对上尿路尿路上皮癌的影响:一项基于人群的分析。

Impact of Neoadjuvant Chemotherapy for Upper Tract Urothelial Carcinoma: A Population Based Analysis.

作者信息

Venkat Siv, Lewicki Patrick J, Basourakos Spyridon P, Scherr Douglas S

机构信息

Weill Cornell Medicine/NewYork-Presbyterian Hospital, New York, NY, USA.

出版信息

Bladder Cancer. 2021 Dec 13;7(4):401-412. doi: 10.3233/BLC-211515. eCollection 2021.

Abstract

BACKGROUND AND OBJECTIVES

We examined pathologic complete response (pCR) and pathologic downstaging (pDS) rates after neoadjuvant chemotherapy (NAC) in high-risk upper tract urothelial carcinoma, as well as their predictors. We further sought to determine their effects on overall survival and examine prognosticators of survival after NAC.

METHODS

The National Cancer Database was used to identify all patients from 2004 to 2016 with nonmetastatic high grade upper tract urothelial carcinoma who received NAC followed by nephroureterectomy. pCR and pDS rates were examined, and univariate and multivariate logistic regression was performed to identify clinical predictors. Kaplan-Meier and Cox proportional hazard methods were used to estimate overall survival.

RESULTS

309 patients met inclusion criteria. 27 patients (8.74%) had pCR, and 92 (29.77%) had pDS. pCR and pDS rates for N+ subgroup were 6.82% and 47.73% respectively, and for N0 subgroup, 9.50% and 22.62%. Female sex (OR 2.94,  = 0.010) was the only predictor of pCR. Node-positive disease (cN1 vs. cN0: OR 6.40,  < 0.001; cN2 vs. cN0: OR 7.46,  < 0.001) was a positive predictor of pDS, and the presence of lymphovascular invasion (LVI) (OR 0.14,  < 0.001) was a negative predictor of pDS. The median OS for all patients was 45.5 months. pCR and pDS were both associated with improved OS, ( < 0.001 for both); median was 99.1 months for both. LVI was the strongest negative prognostic factor for OS (HR 2.85,  < 0.001).

CONCLUSIONS

Overall pathological complete response and downstaging rates were 8.74% and 29.77% respectively after multi-agent neoadjuvant chemotherapy. Node-negative and node-positive disease had equivalent rates of complete response, but node-positive disease had a significantly higher rate of downstaging. The presence of LVI was associated with worse overall survival.

摘要

背景与目的

我们研究了新辅助化疗(NAC)后高危上尿路尿路上皮癌的病理完全缓解(pCR)率和病理降期(pDS)率及其预测因素。我们进一步试图确定它们对总生存期的影响,并研究NAC后生存的预后因素。

方法

利用国家癌症数据库识别2004年至2016年所有接受NAC后行肾输尿管切除术的非转移性高级别上尿路尿路上皮癌患者。检查pCR和pDS率,并进行单因素和多因素逻辑回归以识别临床预测因素。采用Kaplan-Meier法和Cox比例风险法估计总生存期。

结果

309例患者符合纳入标准。27例(8.74%)达到pCR,92例(29.77%)达到pDS。N+亚组的pCR率和pDS率分别为6.82%和47.73%,N0亚组分别为9.50%和22.62%。女性(OR 2.94,P=0.010)是pCR的唯一预测因素。淋巴结阳性疾病(cN1 vs. cN0:OR 6.40,P<0.001;cN2 vs. cN0:OR 7.46,P<0.001)是pDS的阳性预测因素,而存在淋巴管浸润(LVI)(OR 0.14,P<0.001)是pDS的阴性预测因素。所有患者的中位总生存期为45.5个月。pCR和pDS均与总生存期改善相关(两者P<0.001);两者的中位生存期均为99.1个月。LVI是总生存期最强的阴性预后因素(HR 2.85,P<0.001)。

结论

多药新辅助化疗后总体病理完全缓解率和降期率分别为8.74%和29.77%。淋巴结阴性和阳性疾病的完全缓解率相当,但淋巴结阳性疾病的降期率显著更高。LVI的存在与较差的总生存期相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3882/11181789/07781dc767c7/blc-7-blc211515-g001.jpg

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