CC BY-NC-ND 4.0 · Indian J Med Paediatr Oncol 2017; 38(03): 311-315
DOI: 10.4103/ijmpo.ijmpo_154_16
Original Article

Poor Risk Advanced Renal Cell Carcinoma: Outcomes from a Registry in a Tertiary Cancer Center

Anant Ramaswamy
Department of Medical Oncology, Radiology,Nuclear Medicine and Pathology, Tata Memorial Hospital, Mumbai, Maharashtra, India
,
Amit Joshi
Department of Medical Oncology, Radiology,Nuclear Medicine and Pathology, Tata Memorial Hospital, Mumbai, Maharashtra, India
,
Vanita Noronha
Department of Medical Oncology, Radiology,Nuclear Medicine and Pathology, Tata Memorial Hospital, Mumbai, Maharashtra, India
,
Vijay Patil
Department of Medical Oncology, Radiology,Nuclear Medicine and Pathology, Tata Memorial Hospital, Mumbai, Maharashtra, India
,
Arvind Sahu
Department of Medical Oncology, Radiology,Nuclear Medicine and Pathology, Tata Memorial Hospital, Mumbai, Maharashtra, India
,
Deepan R Manickam
Department of Medical Oncology, Radiology,Nuclear Medicine and Pathology, Tata Memorial Hospital, Mumbai, Maharashtra, India
,
Rushabh Kothari
Department of Medical Oncology, Radiology,Nuclear Medicine and Pathology, Tata Memorial Hospital, Mumbai, Maharashtra, India
,
Nilesh Sable
Department of Medical Oncology, Radiology,Nuclear Medicine and Pathology, Tata Memorial Hospital, Mumbai, Maharashtra, India
,
Archi Agrawal
Department of Medical Oncology, Radiology,Nuclear Medicine and Pathology, Tata Memorial Hospital, Mumbai, Maharashtra, India
,
Santosh Menon
Department of Medical Oncology, Radiology,Nuclear Medicine and Pathology, Tata Memorial Hospital, Mumbai, Maharashtra, India
,
Kumar Prabhash
Department of Medical Oncology, Radiology,Nuclear Medicine and Pathology, Tata Memorial Hospital, Mumbai, Maharashtra, India
› Author Affiliations
Financial support and sponsorship Nil.

Abstract

Background: Poor-risk advanced Renal cell carcinoma (RCC) are an under-evaluated and difficult to treat subset of patients with poor prognosis. While Temsirolimus is the approved first line therapy for this category, Tyrosine kinase inhibitors (TKIs) are also commonly uses as initial treatment. We present an analysis of poor-risk advanced RCC treated in our institute. Materials and Methods: Patients diagnosed as poor-risk (as per Heng criteria) advanced RCC from June 2008 to December 2015 were analysed for baseline demographics, treatment received, toxicity (primarily Grade 3 and Grade 4), response rates (RR) and survival. Results: 60 patients (43 males, 17 females) with a median age of 53 years were included for final analysis. Median ECOG PS was 1, clear cell was the predominant histology (63.3%), and 46.7% of patients had greater than 2 sites of metastases. Sorafenib, Sunitinib, Temsirolimus and Pazopanib were used to treat 43.3%, 36.7%, 8.3% and 6.7% of patients respectively, while 3 patients were offered upfront best supportive care. Common adverse events included skin rash (31.5%), HFS (Grade 2 and 3 - 30.8%), mucositis (26.3%), hypertension (24.5%), and dyslipidaemias (22.8%). 41 patients were available for response - overall response rate observed was 15%, while clinical benefit rate was 50%. Median progression free survival was 5.78 months (4.67-6.89) and median overall survival (OS) was 10.05 months (7.31-12.79). Conclusion: A majority of poor-risk metastatic RCC patients in our study were treated with TKIs and the survival outcomes appear to suggest that this strategy is a feasible alternative to Temsirolimus in the Indian setting.



Publication History

Article published online:
04 July 2021

© 2017. Indian Society of Medical and Paediatric Oncology. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/.)

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