Literature DB >> 7200263

Renal and metabolic toxicities of cancer chemotherapy.

R L Schilsky.   

Abstract

This paper has outlined the varied renal and metabolic abnormalities which may occur as complications of antineoplastic chemotherapy. Rapid tumor lysis leading to acute uric acid nephropathy, hyperkalemia and hyperphosphatemia may complicate the treatment of patients with chemotherapy-responsive tumors. Aggressive management with intravenous hydration, urinary alkalinization and administration of allopurinol can ameliorate these complications of therapy. Many commonly used antineoplastic agents, particularly cisplatin, methotrexate, streptozotocin, and nitrosoureas, are nephrotoxic. Careful monitoring of renal function and serum electrolytes are essential during administration of these agents. In addition, intravascular volume depletion, urinary tract infection, and obstructive uropathy must always be considered when renal function deteriorates in patients with cancer. With foresight and aggressive management, many of these derangements can be ameliorated or avoided entirely and the toxicity of effective cancer chemotherapy can be minimized. Patients with established renal failure who require chemotherapy pose a particularly difficult clinical problem. Though a complete discussion of this subject is beyond the scope of this paper, Table 3 is included to provide some guidelines for dose modification in patients with altered renal function.

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Year:  1982        PMID: 7200263

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  6 in total

Review 1.  Chemotherapy-associated renal dysfunction.

Authors:  Vaibhav Sahni; Devasmita Choudhury; Ziauddin Ahmed
Journal:  Nat Rev Nephrol       Date:  2009-06-30       Impact factor: 28.314

Review 2.  Therapeutic drug monitoring in oncology. Problems and potential in antineoplastic therapy.

Authors:  M J Moore; C Erlichman
Journal:  Clin Pharmacokinet       Date:  1987-10       Impact factor: 6.447

3.  [The iodine 131-hippurate clearance for the determination of the nephrotoxic effect of cis-dichlorodiamino-platin (II) (cis-platin, cis-DDP)].

Authors:  T G Wendt; R Hartenstein; U Büll; K Schlechtweg; E A Moser
Journal:  Klin Wochenschr       Date:  1983-06-01

4.  Analysis of risk factors for cisplatin-induced ototoxicity in patients with testicular cancer.

Authors:  C Bokemeyer; C C Berger; J T Hartmann; C Kollmannsberger; H J Schmoll; M A Kuczyk; L Kanz
Journal:  Br J Cancer       Date:  1998-04       Impact factor: 7.640

Review 5.  Systemic treatment-induced gastrointestinal toxicity: incidence, clinical presentation and management.

Authors:  Stergios Boussios; George Pentheroudakis; Konstantinos Katsanos; Nicholas Pavlidis
Journal:  Ann Gastroenterol       Date:  2012

6.  Feasibility study of short hydration using oral rehydration solution in cisplatin including chemotherapy of lung cancer.

Authors:  Junya Sato; Naoto Morikawa; Hiroo Nitanai; Hiromi Nagashima; Satoru Nihei; Kohei Yamauti; Kenzo Kudo
Journal:  J Pharm Health Care Sci       Date:  2016-03-05
  6 in total

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