scholarly journals Management of metastatic renal cell carcinoma – mini review

2015 ◽  
Vol 2 (2) ◽  
pp. 75-83 ◽  
Author(s):  
Anubha Bharthuar ◽  
Himanshu Pandey ◽  
Swapan Sood

The management of metastatic renal cell carcinoma (mRCC) has evolved considerably in the last decade. A number of different systemic molecular targeted agents that have been recently approved have improved the survival of patients with mRCC. This mini-review focuses on the implementation of multi-modality therapy in the management of mRCC and the approved indications of the various available novel agents. These novel agents have expanded our armamentarium and improved clinical outcomes of this challenging disease that has considerable biological heterogeneity and clinical variability.  

2015 ◽  
Vol 11 (3) ◽  
pp. 329-335 ◽  
Author(s):  
Hideaki Miyake ◽  
Mototsugu Muramaki ◽  
Satoshi Imai ◽  
Ken-ichi Harada ◽  
Masato Fujisawa

2012 ◽  
Vol 2012 ◽  
pp. 1-3
Author(s):  
Takeshi Azuma ◽  
Yukihide Matayoshi ◽  
Yohsuke Sato ◽  
Yujiro Sato ◽  
Yasushi Nagase

Several molecular targeted agents have been approved for clinical use for metastatic renal cell carcinoma (mRCC). A case of a 32-year-old woman with mRCC is presented. These tumors could change vascularity by administration of molecular agents. We could select a drug timely based on findings of computed tomography. To our knowledge, this is the first report that tumor’s character change induced by molecular targeted agents can be detected and the efficacy of molecular targeted agents can be predicted.


Oncotarget ◽  
2017 ◽  
Vol 8 (45) ◽  
pp. 78825-78837 ◽  
Author(s):  
Jang Hee Han ◽  
Seung Hwan Lee ◽  
Won Sik Ham ◽  
Woong Kyu Han ◽  
Koon Ho Rha ◽  
...  

2021 ◽  
Vol 39 (6_suppl) ◽  
pp. 341-341
Author(s):  
Matthew D Tucker ◽  
Katy Beckermann ◽  
Kristin Kathleen Ancell ◽  
Kerry Schaffer ◽  
Renee McAlister ◽  
...  

341 Background: Neutrophilia is known to be associated with worse prognosis in metastatic renal cell carcinoma (mRCC); however, less is known about the role of eosinophils in the response to immunotherapy (IO). We investigated the association of the baseline neutrophil to eosinophil ratio (NER) with outcomes to IO-based combination treatment in mRCC. Methods: Patients with mRCC treated with ipilimumab plus nivolumab, pembrolizumab plus axitinib, or avelumab plus axitinib at the Vanderbilt-Ingram Cancer Center were retrospectively identified. Patients on >10mg prednisone and patients with prior IO were excluded. Baseline NER (at time of first IO) and association with progression free survival (PFS), overall survival (OS), and objective response rate (ORR) were investigated. Data cutoff was 9/1/2020. Analysis for PFS and OS was performed using the log-rank test and Mantel-Haenszel method, and analysis of the odds ratio for ORR was performed using Fischer’s exact test. Results: Sixty-one patients were identified: 89% clear cell histology, 74% prior nephrectomy, 69% IMDC intermediate risk, and 72% treatment-naïve. Patients with baseline NER < median (N=31) had improved clinical outcomes compared to patients with baseline NER > median (N=30) (Table). Improvement in PFS by NER was maintained when stratified by anti-PD-1/CTLA-4 and anti-PD(L)-1/VEGF (p= 0.0062 and p= 0.049); however, differences in OS and ORR were no longer significant. The median baseline NER among patients with partial response (PR) was significantly lower at 22.7 (95% CI 18.9-31.1) vs. 51.6 (95% CI 39.5-93.1) among those with progressive disease (PD) (p= 0.0054). For comparison, the median neutrophil to lymphocyte ratio was not significantly different between PR (2.60) and PD (3.84, p= 0.056). Conclusions: Patients with a low baseline NER treated with IO-based combinations had improved clinical outcomes compared to patients with a high baseline NER. Additional investigation of this parameter in larger cohorts is warranted. [Table: see text]


2014 ◽  
Vol 191 (3) ◽  
pp. 611-618 ◽  
Author(s):  
Bradley J. Atkinson ◽  
Sarathi Kalra ◽  
Xuemei Wang ◽  
Tharakeswara Bathala ◽  
Paul Corn ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document