TY - JOUR
T1 - Risk evaluation, prophylaxis, and treatment of tumor lysis syndrome
T2 - Consensus of an italian expert panel
AU - Pession, Andrea
AU - Masetti, Riccardo
AU - Gaidano, Gianluca
AU - Tosi, Patrizia
AU - Rosti, Giovanni
AU - Aglietta, Massimo
AU - Specchia, Giorgina
AU - Porta, Fulvio
N1 - Funding Information:
A. Pession is the guarantor for this article, and takes responsibility for the integrity of the work as a whole. The authors declare that they have no conflicts of interest. A. Pession has received honoraria for lectures and advisory work from sanofi-aventis. G. Gaidano has been involved involved in advisory boards for Celgene, Novartis, Roche, Onyx, sanofi-aventis, and received research funding from Celgene. M. Aglietta is involved in research projects with the following companies: Novartis Farma Spa, sanofi-aventis Spa, Roche Spa, Merck Serono Spa, Bayer Spa, and Pfizer Spa. G. Specchia has been involved in advisory boards for Novartis, BMS, Roche, Celgene, and received research funding from Roche and Celgene.
PY - 2011/8
Y1 - 2011/8
N2 - Tumor lysis syndrome (TLS) is a life-threatening complication in patients with hematological disease and/or solid tumors that results from rapid, large-scale tumor necrosis occurring spontaneously, or more commonly, as a result of chemotherapy. TLS is characterized by metabolic and electrolyte imbalances that include hyperuricemia, hyperkalemia, hyperphosphatemia, and hypocalcemia. Identification of risk groups as well as early detection of TLS is crucial for the establishment of appropriate strategies of prophylaxis and treatment. Methods: A review of the peerreviewed literature on TLS between 1990 and 2011 was conducted via a systematic search of the PubMed database using the keywords 'TLS' [AND] 'management,' 'risk evaluation,' 'prophylaxis,' and 'treatment.' An expert opinion-based approach was used to review the national and international recommendations and guidelines on the topic. Results: The PubMed search produced 90 results, all of which were evaluated. These studies, together with a recent international consensus panel provided recommendations for evaluating the risk of TLS and providing prophylaxis. Five algorithms are presented that consider all of the factors when assessing the risk for neoplastic disease in general, and specifically for leukemia and lymphoma. Conclusion: The present report provides clinicians with an easily consultable tool to guide the evidence-based management of this oncohematological emergency.
AB - Tumor lysis syndrome (TLS) is a life-threatening complication in patients with hematological disease and/or solid tumors that results from rapid, large-scale tumor necrosis occurring spontaneously, or more commonly, as a result of chemotherapy. TLS is characterized by metabolic and electrolyte imbalances that include hyperuricemia, hyperkalemia, hyperphosphatemia, and hypocalcemia. Identification of risk groups as well as early detection of TLS is crucial for the establishment of appropriate strategies of prophylaxis and treatment. Methods: A review of the peerreviewed literature on TLS between 1990 and 2011 was conducted via a systematic search of the PubMed database using the keywords 'TLS' [AND] 'management,' 'risk evaluation,' 'prophylaxis,' and 'treatment.' An expert opinion-based approach was used to review the national and international recommendations and guidelines on the topic. Results: The PubMed search produced 90 results, all of which were evaluated. These studies, together with a recent international consensus panel provided recommendations for evaluating the risk of TLS and providing prophylaxis. Five algorithms are presented that consider all of the factors when assessing the risk for neoplastic disease in general, and specifically for leukemia and lymphoma. Conclusion: The present report provides clinicians with an easily consultable tool to guide the evidence-based management of this oncohematological emergency.
KW - Allopurinol
KW - Expert panel
KW - Hyperuricemia
KW - Rasburicase
KW - Tumor lysis syndrome
UR - http://www.scopus.com/inward/record.url?scp=82455187894&partnerID=8YFLogxK
U2 - 10.1007/s12325-011-0041-1
DO - 10.1007/s12325-011-0041-1
M3 - Article
SN - 0741-238X
VL - 28
SP - 684
EP - 697
JO - Advances in Therapy
JF - Advances in Therapy
IS - 8
ER -