Long survival of a young patient with Xp11.2 translocation metastatic clear cell renal carcinoma: case report and review of the literature

2021 ◽  
pp. 030089162110492
Author(s):  
Stefania Pipitone ◽  
Maria Giuseppa Vitale ◽  
Cinzia Baldessari ◽  
Massimo Dominici ◽  
Roberto Sabbatini

Introduction: Xp11.2 translocation is a rare subtype of renal cell carcinoma (RCC), identified as a single entity only from 2004 by World Health Organization (WHO). These tumors involve pediatric age group and rarely patients over 40 years old. Children show indolent disease; adult population has invasive tumor at diagnosis with rapid progression. Case report: We describe a case report of a young woman affected by metastatic clear cell renal carcinoma with Xp11.2 translocation. She achieved a longer stable disease (SD) to first line treatment with atezolizumab plus bevacizumab, obtaining a progression free survival (PFS) of 21 months. After she received cabozantinib, sunitinib and then sorafenib. Conclusions: The patient had an overall survival (OS) of 51 months, which is much higher than that reported in literature data. Unfortunately, the biology of Xp11.2 translocation RCC and its therapeutic management are still unclear.

HPB ◽  
2016 ◽  
Vol 18 ◽  
pp. e442-e443
Author(s):  
A. Cury ◽  
A. Diniz ◽  
R. Brito ◽  
W. Costa ◽  
H. Ribeiro ◽  
...  

2020 ◽  
Vol 4 (1) ◽  
pp. 26-27
Author(s):  
Mart nez-Cordero Humberto ◽  
Salgado-Reyes Paula ◽  
Alcala-Lara Sebastian ◽  
Linares- Pati o ◽  
Maximo Mejia ◽  
...  

Author(s):  
Nabil Bel Feki. ◽  
Imed Ben Ghorbel. ◽  
Karim Mbarek. ◽  
Thouraya Ben Salem. ◽  
Mohamed Habib Houman.

2006 ◽  
Vol 1 ◽  
pp. 117727190600100 ◽  
Author(s):  
Albrecht Reichle ◽  
Jochen Grassinger ◽  
Klaus Bross ◽  
Jochen Wilke ◽  
Thomas Suedhoff ◽  
...  

Two consecutive multi-center phase II trials were designed to prove the hypothesis, whether therapeutic modeling of tumor-associated inflammatory processes could result in improved tumor response. Therapy in both trials consisted of low-dose capecitabine 1g/m2 twice daily p.o. for 14 days, every 3 weeks, day 1+, and rofecoxib 25 mg daily p.o., day 1+ (from 11/04 etoricoxib 60 mg daily instead) plus pioglitazone 60 mg daily p.o., day 1+. In study II low-dose IFN-α 4.5 MU sc. three times a week, week 1+, was added until disease progression. Eighteen, and 33 patients, respectively, with clear cell renal carcinoma and progressive disease were enrolled. Objective response (48%) was exclusively observed in study II (PR 35%, CR 13%), and paralleled by a strong CRP response after 4 weeks on treatment, p = 0.0005, in all 29 pts (100%) with elevated CRP levels. Median progression-free survival could be more than doubled from a median of 4.7 months (95% CI, 1.0 to 10.4) to 11.5 months (6.8 to 16.2) in study II, p = 0.00001. Median overall survival of population II was 26 months. Efficacious negative regulation of tumor-associated inflammation by transcription modulators may result in a steep increase of tumor response and survival.


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