Non-clear cell renal cell carcinoma: does the mammalian target of rapamycin represent a rational therapeutic target?

Laurence Albiges1, Vincent Molinie, Bernard Escudier

  • 1Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France.

The Oncologist
|July 19, 2012
PubMed

Insights

Non-clear cell renal cell carcinomas (nccRCCs) are a diverse group of tumors with limited treatment options. Mammalian target of rapamycin (mTOR) inhibitors show promise for nccRCC treatment, but further clinical trials are needed to confirm efficacy.

Area of Science:

  • Oncology
  • Genetics
  • Pharmacology

Background:

  • Non-clear cell renal cell carcinomas (nccRCCs) represent a heterogeneous group of kidney cancers with few approved treatments.
  • Patients with nccRCC have often been excluded from clinical trials, leading to a lack of robust evidence for targeted therapies.

Purpose of the Study:

  • To review nccRCC subtypes, diagnostic criteria, and prognoses.
  • To evaluate the potential of mammalian target of rapamycin (mTOR) inhibitors in treating nccRCC.
  • To assess current evidence and future directions for targeted therapies in nccRCC.

Main Methods:

  • Review of existing literature on nccRCC subtypes and prognoses.
  • Analysis of genetic data and preclinical research on mTOR's role in nccRCC.
  • Evaluation of recent clinical studies on targeted therapies, including mTOR inhibitors.

Main Results:

  • mTOR plays a central role in nccRCC, suggesting its inhibition could be efficacious across subtypes.
  • Early studies indicate potential efficacy of targeted therapies, including mTOR inhibitors (everolimus, temsirolimus), as monotherapy and combination therapy.
  • Current guidelines recommend mTOR inhibitors for nccRCC, but evidence levels are low.

Conclusions:

  • Further randomized, controlled clinical trials are essential to establish optimal therapies for nccRCC.
  • Ongoing trials of mTOR inhibitors and other agents are anticipated to significantly impact the nccRCC treatment landscape.

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