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Updated: Aug 10, 2025

Modeling Spontaneous Metastatic Renal Cell Carcinoma mRCC in Mice Following Nephrectomy
Published on: April 29, 2014
An Update on the Treatment of Papillary Renal Cell Carcinoma
Neal S Chawla1, Nicolas Sayegh2, Sweta Prajapati1
1Department of Medical Oncology & Experimental Therapeutics, City of Hope Comprehensive Cancer Center, Duarte, CA 91010, USA.
Abstract:
Papillary renal cell carcinoma (pRCC) is the second-most common subtype of kidney cancer following clear cell renal cell carcinoma (ccRCC), representing 15% of kidney cancers. Despite advances in therapy, including combination strategies with targeted therapies and immune checkpoint inhibitors, progress has lagged behind that of ccRCC. This is in part due to the heterogenous nature of the various subtypes of pRCC. More recently, investigators have turned efforts towards histology and biology-based trials. In this review, we outline some of the distinct biological characteristics of pRCC and discuss the most impactful clinical trials to date. Finally, we look ahead to several highly anticipated ongoing trials in pRCC.
Insights
Papillary renal cell carcinoma (pRCC), a common kidney cancer, shows slower treatment progress than other subtypes due to its diverse nature. This review covers pRCC biology and clinical trials, highlighting future research directions.
Area of Science:
- Oncology
- Nephrology
- Cancer Biology
Background:
- Papillary renal cell carcinoma (pRCC) is the second most frequent kidney cancer subtype, accounting for 15% of cases.
- Therapeutic advancements in pRCC, including targeted therapies and immune checkpoint inhibitors, have lagged behind clear cell renal cell carcinoma (ccRCC).
- The heterogeneity among pRCC subtypes contributes to challenges in treatment development.
Purpose of the Study:
- To review the distinct biological characteristics of papillary renal cell carcinoma.
- To discuss the most impactful clinical trials conducted to date for pRCC.
- To provide an outlook on anticipated ongoing clinical trials in pRCC research.
Main Methods:
- Literature review of distinct biological features of pRCC.
- Analysis of key clinical trials in pRCC treatment.
- Synthesis of current research trends and future trial directions.
Main Results:
- pRCC exhibits significant biological heterogeneity, impacting therapeutic responses.
- Several clinical trials have explored targeted therapies and immunotherapies with varying success.
- Ongoing trials are focusing on histology and biology-driven approaches.
Conclusions:
- Understanding pRCC's unique biology is crucial for developing effective treatments.
- Clinical trial progress in pRCC necessitates tailored, subtype-specific strategies.
- Future research holds promise for improved outcomes in papillary renal cell carcinoma.
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