PMID- 22235142 OWN - NLM STAT- MEDLINE DCOM- 20120306 LR - 20220310 IS - 1460-2105 (Electronic) IS - 0027-8874 (Linking) VI - 104 IP - 2 DP - 2012 Jan 18 TI - Targeted therapies for renal cell carcinoma: review of adverse event management strategies. PG - 93-113 LID - 10.1093/jnci/djr511 [doi] AB - With the advent of targeted agents for the treatment of renal cell carcinoma (RCC), overall survival has improved, and patients are being treated continuously for increasingly long periods of time. This has raised challenges in the management of adverse events (AEs) associated with the six targeted agents approved in RCC-sorafenib, sunitinib, pazopanib, bevacizumab (in combination with interferon alpha), temsirolimus, and everolimus. Suggestions for monitoring and managing AEs have been published, but there are few consensus recommendations. In addition, there is a risk that patients will be subjected to multiple unnecessary investigations. In this review, we aimed to identify the level of supporting evidence for suggested AE management strategies to provide practical guidance on essential monitoring and management that should be undertaken when using targeted agents. Five databases were systematically searched for relevant English language articles (including American Society of Clinical Oncology abstracts) published between January 2007 and March 2011; European Society of Medical Oncology congress abstracts were hand searched. Strategies for AE management were summarized and categorized according to the level of recommendation. A total of 107 articles were identified that describe a large number of different investigations for monitoring AEs and interventions for AE management. We identify and summarize clear recommendations for the management of dermatologic, gastrointestinal, thyroid, cardiovascular, and other AEs, based predominantly on expert opinion. However, because the evidence for the suggested management strategies is largely anecdotal, there is a need for further systematic investigation of management strategies for AEs related to targeted therapies for RCC. FAU - Eisen, Tim AU - Eisen T AD - Cambridge University Health Partners, Cambridge, UK. tim.eisen@medschl.cam.ac.uk FAU - Sternberg, Cora N AU - Sternberg CN FAU - Robert, Caroline AU - Robert C FAU - Mulders, Peter AU - Mulders P FAU - Pyle, Lynda AU - Pyle L FAU - Zbinden, Stephan AU - Zbinden S FAU - Izzedine, Hassan AU - Izzedine H FAU - Escudier, Bernard AU - Escudier B LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Review DEP - 20120110 PL - United States TA - J Natl Cancer Inst JT - Journal of the National Cancer Institute JID - 7503089 RN - 0 (Antibodies, Monoclonal, Humanized) RN - 0 (Antineoplastic Agents) RN - 0 (Benzenesulfonates) RN - 0 (Indazoles) RN - 0 (Indoles) RN - 0 (Phenylurea Compounds) RN - 0 (Protein Kinase Inhibitors) RN - 0 (Pyridines) RN - 0 (Pyrimidines) RN - 0 (Pyrroles) RN - 0 (Sulfonamides) RN - 0 (Vascular Endothelial Growth Factor A) RN - 25X51I8RD4 (Niacinamide) RN - 2S9ZZM9Q9V (Bevacizumab) RN - 624KN6GM2T (temsirolimus) RN - 7RN5DR86CK (pazopanib) RN - 9HW64Q8G6G (Everolimus) RN - 9ZOQ3TZI87 (Sorafenib) RN - EC 2.7.1.1 (MTOR protein, human) RN - EC 2.7.10.1 (Protein-Tyrosine Kinases) RN - EC 2.7.11.1 (TOR Serine-Threonine Kinases) RN - V99T50803M (Sunitinib) RN - W36ZG6FT64 (Sirolimus) SB - IM EIN - J Natl Cancer Inst. 2012 Apr 18;104(8):638 MH - Anorexia/chemically induced/therapy MH - Antibodies, Monoclonal, Humanized/adverse effects MH - Antineoplastic Agents/administration & dosage/*adverse effects/pharmacology MH - Antineoplastic Combined Chemotherapy Protocols/adverse effects MH - Benzenesulfonates/adverse effects MH - Bevacizumab MH - Carcinoma, Renal Cell/*drug therapy/*metabolism MH - Cardiovascular System/drug effects MH - Drug Eruptions/therapy MH - Europe MH - Everolimus MH - Evidence-Based Medicine MH - Gastrointestinal Tract/drug effects MH - Humans MH - Hypothyroidism/chemically induced/therapy MH - Indazoles MH - Indoles/adverse effects MH - Kidney Neoplasms/*drug therapy/*metabolism MH - *Molecular Targeted Therapy/methods MH - Niacinamide/analogs & derivatives MH - Phenylurea Compounds MH - Pneumonia/chemically induced/therapy MH - Protein Kinase Inhibitors/adverse effects MH - Protein-Tyrosine Kinases/antagonists & inhibitors MH - Pyridines/adverse effects MH - Pyrimidines/adverse effects MH - Pyrroles/adverse effects MH - Sirolimus/adverse effects/analogs & derivatives MH - Sorafenib MH - Sulfonamides/adverse effects MH - Sunitinib MH - TOR Serine-Threonine Kinases/antagonists & inhibitors MH - Vascular Endothelial Growth Factor A/antagonists & inhibitors MH - Weight Loss/drug effects MH - Wound Healing/drug effects EDAT- 2012/01/12 06:00 MHDA- 2012/03/07 06:00 CRDT- 2012/01/12 06:00 PHST- 2012/01/12 06:00 [entrez] PHST- 2012/01/12 06:00 [pubmed] PHST- 2012/03/07 06:00 [medline] AID - djr511 [pii] AID - 10.1093/jnci/djr511 [doi] PST - ppublish SO - J Natl Cancer Inst. 2012 Jan 18;104(2):93-113. doi: 10.1093/jnci/djr511. Epub 2012 Jan 10.