[Clinical and Fundamental Approach for Chemotherapy-induced Adverse Effect Attenuation by Oncology Pharmacy Specialists]

Yakugaku Zasshi. 2020;140(12):1415-1419. doi: 10.1248/yakushi.20-00122.
[Article in Japanese]

Abstract

Management of chemotherapy-induced adverse effects and the associated pharmaceutical interventions as well as supportive care evidence creation are the most important responsibilities of oncology pharmacists. We have evaluated the (1) efficacy of long-term and successive pharmaceutical care in outpatient chemotherapy and (2) nephroprotective effects of magnesium (Mg) against cisplatin-induced nephrotoxicity (CIN). The results revealed that the adoption rate of pharmaceutical proposals was 98%, and that approximately 70% of the proposals attenuated painful symptoms. Moreover, approximately 60% of pharmaceutical interventions were established after the third visit; in particular, approximately 20% were suggested after the tenth visit. These results have shown that long-term and successive pharmaceutical care by oncology pharmacists in outpatient chemotherapy contributes to a safe and less onerous chemotherapy implementation. CIN frequency and serum creatinine elevation were significantly attenuated by Mg premedication during the cisplatin, docetaxel, and fluorouracil regimen, without changes in adverse effects and response rate. Mg premedication has been suggested to exert a protective effect against CIN without influencing on adverse effects and anti-tumor efficacy. The nephroprotective effect of Mg against CIN was evaluated using Wistar rats. Cisplatin (2.5 mg/kg) was administered once or three times weekly with or without 40 mg/kg MgSO4. The results revealed that Mg regulates the expression of organic cation transporter 2, multidrug and toxin extrusion protein 1, and copper transporter 1, leading to reduced renal platinum accumulation, which results in CIN attenuation. In conclusion, evaluation of pharmaceutical care and supportive care by oncology pharmacists is necessary for advanced care of cancer patients.

Keywords: cisplatin; magnesium; nephrotoxicity; outpatient chemotherapy; pharmaceutical care.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / adverse effects*
  • Antiporters / genetics
  • Antiporters / metabolism
  • Cisplatin / adverse effects
  • Docetaxel / adverse effects
  • Drug-Related Side Effects and Adverse Reactions / prevention & control*
  • Fluorouracil / adverse effects
  • Gene Expression / drug effects
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Magnesium Sulfate / administration & dosage*
  • Magnesium Sulfate / pharmacology
  • Medical Oncology*
  • Organic Cation Transport Proteins / genetics
  • Organic Cation Transport Proteins / metabolism
  • Organic Cation Transporter 2 / genetics
  • Organic Cation Transporter 2 / metabolism
  • Pharmacists*
  • Premedication*
  • Rats
  • Specialization*

Substances

  • Antineoplastic Agents
  • Antiporters
  • Organic Cation Transport Proteins
  • Organic Cation Transporter 2
  • Slc22a2 protein, rat
  • Slc47a1 protein, rat
  • Docetaxel
  • Magnesium Sulfate
  • Cisplatin
  • Fluorouracil