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乳头状肾细胞癌的最新进展.pdf

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1、Updates in Papillary RCCBradley A McGregor,MDMarra Lochiatto Investigatorship in Kidney Cancer ResearchDirector of Clinical ResearchLank Center for GU Oncology,Dana Farber Cancer InstituteWhat is Papillary RCC?Papillary RCC Collecting Duct Carcinoma Tubulocystic RCC FH-Deficient RCC ALK-Translocated

2、 RCC TFE3-Transloated RCC Biphasic Hyalinizing Psammomatous RCC UnclassifiedAdapted from Michelle HirschMetastatic pRCC1 Histologically confirmed diagnosis of Papillary RCC Measurable disease 0-1 prior lines of therapy No prior therapy with sunitinib Zubrod 0-1CabozantinibCrizotinibPrimary Endpoint:

3、Progression-free survivalSecondary Endpoints:Overall survival Response rate Adverse events Exploratory evaluation of:MET mutational status MET expression SunitinibSavolitinibRandomization2Arms closed for futilityPal et al GU ASCO 2021,Lancet 2021PAPMETPAPMET-No OS benefitBarata,et al,JCO 20241.00.80

4、.60.40.20.0Probability of PFSSavolitinib(n=33)Sunitinib(n=27)03691215182124Time From Randomization(Months)332115843310271911741000SavolitinibSunitinibNumber of Patients at RiskNumber Randomized/Number of Events33/1727/20Median PFS by BICR in months(95%CI)Savolitinib 7.0(2.8,NC)Sunitinib 5.6(4.1,6.9)

5、HR(95%CI):0.71(0.37,1.36)Log-rank two-sided P-value:0.313Censored observations+Savolitinib(n=33)Sunitinib(n=27)Overall Response Rate(by BICR)9(27%)2(7%)Add Durvalumab 57%ORRChoueiri ASCO 2020,Rodriguez et al,ASCO 2021SAVOIR Genomic driven approachAWAIT SAMETAFH-Deficient RCC(N=43)Sporadic Papillary

6、RCC(N=40)ORR(95%CI)72(5783)(N=31)35(2251)(N=14)Best response no.(%)Complete response2(5)0Partial response29(67)14(35)Stable disease12(28)21(52)Unconfirmed partial response01(2)Progressive disease04(10)Median time to response(range)mo1.8(1.718.3)1.8(1.77.3)Median duration of respo

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根据报告的内容,全文主要内容概括如下: - **Papillary RCC类型**:包括多种亚型,如FH-Deficient RCC、ALK-Translocated RCC等。 - **治疗研究**: - **Savolitinib vs Sunitinib**:Savolitinib在无进展生存期(PFS)上优于Sunitinib(HR 0.71,P=0.313)。 - **Durvalumab联合治疗**:在FH-Deficient RCC中,Durvalumab联合治疗ORR为72%,中位PFS为21.1个月。 - **Ipilimumab/Nivolumab**:在所有Papillary RCC中,ORR为41%,完全缓解率为10%。 - **Genomic驱动研究**:如NFS2突变ORR为83%,FH突变ORR为80%。 - **结论**: - Papillary RCC异质性高。 - 靶向治疗和免疫治疗至关重要。 - 现有研究将确定最佳治疗途径。 - 基因驱动研究对提高治疗效果至关重要。
哪些最佳?" "免疫治疗在Papillary RCC中的应用" "基因驱动研究如何推动Papillary RCC治疗?"
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