Abstract
Defining rational follow-up guidelines in patients treated for cancer is important, from both a medical and an economical perspective. Renal-cell carcinoma is reputed to be unpredictable in its course and only a few, and often contradictory, follow-up guidelines exist for patients treated for nonmetastatic renal-cell carcinoma. Recent advances in tumor biology have contributed to a better understanding of this cancer and have indicated that personalized follow-up regimens, based on tumor and host molecular characteristics, might be possible in the near future.
Key Points
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Conventional prognostic factors (e.g. TNM stage, histological subtype and grade) are robust parameters with appropriate validation but cannot entirely explain the complex natural history of renal-cell carcinoma
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Comprehensive nomograms that combine recognized outcome predictors seem to dramatically improve recurrence prognostication and should be widely used in the near future
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Many promising molecular markers with prognostic value have been described, but further validation is needed before they can be used in clinical practice
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Metastases usually appear within 2 years after radical nephrectomy, but 9–11% of the patients surviving at 10 years will experience late recurrence
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The promising preliminary results obtained with antiangiogenic treatments emphasize the need for early identification of recurrence and thus for rational follow-up protocols
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It is hoped that prognostic nomograms combining conventional and molecular markers will help to customize the follow-up strategy to the actual risk of recurrence for each patient
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Rouvière, O., Bouvier, R., Négrier, S. et al. Nonmetastatic renal-cell carcinoma: is it really possible to define rational guidelines for post-treatment follow-up?. Nat Rev Clin Oncol 3, 200–213 (2006). https://doi.org/10.1038/ncponc0479
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DOI: https://doi.org/10.1038/ncponc0479
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