Primary resistance to nivolumab plus ipilimumab therapy in patients with metastatic renal cell carcinoma

被引:9
作者
Numakura, Kazuyuki [1 ,5 ]
Sekine, Yuya [1 ]
Hatakeyama, Shingo [2 ]
Muto, Yumina [1 ]
Sobu, Ryuta [1 ]
Kobayashi, Mizuki [1 ]
Sasagawa, Hajime [1 ]
Kashima, Soki [1 ]
Yamamto, Ryohei [1 ]
Nara, Taketoshi [1 ]
Akashi, Hideo [3 ]
Tabata, Ryuji [4 ]
Sato, Satoshi [4 ]
Saito, Mitsuru [1 ]
Narita, Shintaro [1 ]
Ohyama, Chikara [2 ]
Habuchi, Tomonori [1 ]
机构
[1] Akita Univ, Grad Sch Med, Dept Urol, Akita, Japan
[2] Hirosaki Univ, Grad Sch Med, Dept Urol, Hirosaki, Japan
[3] Akita Univ, Grad Sch Med, Dept Anat, Akita, Japan
[4] Ageo Cent Gen Hosp, Dept Urol, Ageo, Japan
[5] Akita Univ, Grad Sch Med, Dept Urol, 1-1-1 Hondo, Akita 0108543, Japan
关键词
ipilimumab; lymph node metastasis; neoplasm metastasis; nivolumab; renal cell carcinoma; survival rate; IMMUNOTHERAPY; TUMOR;
D O I
10.1002/cam4.6306
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Nivolumab plus ipilimumab (NIVO+IPI) is the first-line treatment for patients with metastatic renal cell carcinoma (mRCC). Approximately 40% of patients achieve a durable response; however, 20% develop primary resistant disease (PRD) to NIVO+IPI, about which little is known in patients with mRCC. Therefore, this investigation aimed to evaluate the clinical implication of PRD in patients with mRCC to select better candidates in whom NIVO+IPI can be initiated as first-line therapy.Methods: This multi-institutional retrospective cohort study used data collected between August 2015 and January 2023. In total, 120 patients with mRCC treated with NIVO+IPI were eligible. Associations between immune-related adverse events and progression-free survival, overall survival (OS), and objective response rate were analyzed. The relationship between other clinical factors and outcomes was also evaluated.Results: The median observation period was 16 months (interquartile range, 5-27). The median age at NIVO+IPI initiation was 68 years in the male-dominant population (n = 86, 71.7%), and most patients had clear cell histology (n = 104, 86.7%). PRD was recorded in 26 (23.4%) of 111 investigated patients during NIVO+IPI therapy. Patients who experienced PRD showed worse OS (hazard ratio: 4.525, 95% confidence interval [CI]: 2.315-8.850, p < 0.001). Multivariable analysis showed that lymph node metastasis (LNM) (odds ratio: 4.274, 95% CI: 1.075-16.949, p = 0.039) was an independent risk factor for PRD.Conclusions: PRD was strongly correlated with worse survival rates. LNM was independently associated with PRD in patients with mRCC receiving NIVO+IPI as first-line therapy and might indicate that a candidate will not benefit from NIVO+IPI.
引用
收藏
页码:16837 / 16845
页数:9
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