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Evaluation of the Effect of Rosuvastatin on Cisplatin-induced Nephrotoxicity and Ototoxicity

Primary Purpose

Cisplatin Adverse Reaction

Status
Unknown status
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
Rosuvastatin 10mg
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cisplatin Adverse Reaction focused on measuring cisplatin, rosuvastatin, nephrotoxicity, ototoxicity

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Histologically proven lung and breast cancer patients indicated for cisplatin (4-6 cycles)
  • Normal baseline serum creatinine levels
  • Normal baseline audiometry
  • Age between 18-70 years

Exclusion Criteria:

  • Patients with more than one type of cancer
  • Patients with prior chemotherapy treatment
  • Treatment with statins within 12 months before assignment
  • Treatment with fibrates within 4 weeks before assignment
  • Pregnancy and Lactation
  • Abnormal liver function tests or blood count

Sites / Locations

  • Kasr El-Aini Center of Radiation Oncology and Nuclear MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Statin-Treated

Statin-Free

Arm Description

This arm will be receiving: Cisplatin along with conventional nephroprotective interventions (IV hydration with 3 liters with electrolyte replacement administered on the same day of cisplatin) Rosuvastatin 10 mg/day

This arm will be receiving: -Cisplatin along with conventional nephroprotective interventions only (IV hydration with 3 liters with electrolyte replacement administered on the same day of cisplatin)

Outcomes

Primary Outcome Measures

Incidence of cisplatin-induced nephrotoxicity
Increase in serum creatinine by ≥0.3 mg/dL or 1.5-2 fold increase from baseline

Secondary Outcome Measures

Difference in biological research markers between both arms
Measurement of total antioxidant capacity and malondialdehyde levels
Difference in sensory-neural hearing impairment in both arms
Audiometry assessment
Incidence of electrolyte imbalance in both arms
Reduction in magnesium level ˂1.8 mg/dL and potassium level ˂3.5 mmol/L

Full Information

First Posted
March 21, 2021
Last Updated
July 26, 2021
Sponsor
Cairo University
Collaborators
German University in Cairo
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1. Study Identification

Unique Protocol Identification Number
NCT04817904
Brief Title
Evaluation of the Effect of Rosuvastatin on Cisplatin-induced Nephrotoxicity and Ototoxicity
Official Title
Evaluation of the Effect of Rosuvastatin on Cisplatin-induced Nephrotoxicity and Ototoxicity
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Unknown status
Study Start Date
November 17, 2020 (Actual)
Primary Completion Date
August 2021 (Anticipated)
Study Completion Date
August 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University
Collaborators
German University in Cairo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes

5. Study Description

Brief Summary
Cisplatin is an effective anti-cancer drug for the treatment of many solid tumors in humans. Although the clinical response to cisplatin chemotherapy is encouraging, the nephrotoxicity and ototoxicity of the drug makes it difficult to continue its administration in many cases. Cisplatin nephrotoxicity occurs through several mechanisms, mainly through the transport and accumulation of cisplatin into renal epithelial cells, injury to nuclear and mitochondrial DNA, activation of multiple cell death pathways and initiation of inflammatory response. Accordingly, several experimental strategies were developed to prevent this toxicity. For example, drugs that reduced renal cisplatin accumulation such as organic cation transporter 2 (OCT2) and copper transporter (Ctr1) inhibitors, antioxidants, antiapoptotic and anti-inflammatory agents were investigated. However, many of these drugs interfered with the cytotoxic effects of cisplatin. Statins are agents used for reducing plasma cholesterol through the inhibition of the enzyme 3- hydroxy-3- methylglutaryl coenzyme A (HMG-CoA) reductase. In addition, statins are also proven to have pleiotropic, non-lipid dependent effects. These effects include anti-inflammatory actions and reduction of oxidative stress. Based on animal studies performed, statins have been shown to reduce the nephrotoxic effects of cisplatin in rats. In addition, ongoing clinical trials are aiming to investigate the role of statins in the protection against the ototoxicity of cisplatin as well. Our aim is to assess the protective effect of statins on cisplatin-induced nephrotoxicity and ototoxicity in humans.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cisplatin Adverse Reaction
Keywords
cisplatin, rosuvastatin, nephrotoxicity, ototoxicity

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Care ProviderInvestigator
Allocation
Randomized
Enrollment
65 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Statin-Treated
Arm Type
Experimental
Arm Description
This arm will be receiving: Cisplatin along with conventional nephroprotective interventions (IV hydration with 3 liters with electrolyte replacement administered on the same day of cisplatin) Rosuvastatin 10 mg/day
Arm Title
Statin-Free
Arm Type
No Intervention
Arm Description
This arm will be receiving: -Cisplatin along with conventional nephroprotective interventions only (IV hydration with 3 liters with electrolyte replacement administered on the same day of cisplatin)
Intervention Type
Drug
Intervention Name(s)
Rosuvastatin 10mg
Intervention Description
The statin-treated arm will receive Rosuvastatin tablets 10 mg/day starting from the point of cisplatin initiation through the entire duration of therapy
Primary Outcome Measure Information:
Title
Incidence of cisplatin-induced nephrotoxicity
Description
Increase in serum creatinine by ≥0.3 mg/dL or 1.5-2 fold increase from baseline
Time Frame
4 months
Secondary Outcome Measure Information:
Title
Difference in biological research markers between both arms
Description
Measurement of total antioxidant capacity and malondialdehyde levels
Time Frame
4 months
Title
Difference in sensory-neural hearing impairment in both arms
Description
Audiometry assessment
Time Frame
4 months
Title
Incidence of electrolyte imbalance in both arms
Description
Reduction in magnesium level ˂1.8 mg/dL and potassium level ˂3.5 mmol/L
Time Frame
4 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically proven lung and breast cancer patients indicated for cisplatin (4-6 cycles) Normal baseline serum creatinine levels Normal baseline audiometry Age between 18-70 years Exclusion Criteria: Patients with more than one type of cancer Patients with prior chemotherapy treatment Treatment with statins within 12 months before assignment Treatment with fibrates within 4 weeks before assignment Pregnancy and Lactation Abnormal liver function tests or blood count
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Aya T Moustafa, BSc
Phone
+201022666179
Email
ayatarek623@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohamed H Solayman, PhD
Organizational Affiliation
German University in Cairo
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Loay Kassem, PhD
Organizational Affiliation
Cairo University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Dalia S Elhelw, PhD
Organizational Affiliation
German University in Cairo
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Aya T Moustafa, BSc
Organizational Affiliation
German University in Cairo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kasr El-Aini Center of Radiation Oncology and Nuclear Medicine
City
Cairo
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Loay Kassem, PhD
Phone
+201003022907
Email
loay.kassem@cairocure.com
First Name & Middle Initial & Last Name & Degree
Loay Kassem, PhD
First Name & Middle Initial & Last Name & Degree
Aya T Moustafa, BSc

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
20060696
Citation
An Y, Xin H, Yan W, Zhou X. Amelioration of cisplatin-induced nephrotoxicity by pravastatin in mice. Exp Toxicol Pathol. 2011 Mar;63(3):215-9. doi: 10.1016/j.etp.2009.12.002. Epub 2010 Jan 8.
Results Reference
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PubMed Identifier
20650967
Citation
Fujieda M, Morita T, Naruse K, Hayashi Y, Ishihara M, Yokoyama T, Toma T, Ohta K, Wakiguchi H. Effect of pravastatin on cisplatin-induced nephrotoxicity in rats. Hum Exp Toxicol. 2011 Jul;30(7):603-15. doi: 10.1177/0960327110376551. Epub 2010 Jul 22.
Results Reference
background
PubMed Identifier
28240967
Citation
Seckl MJ, Ottensmeier CH, Cullen M, Schmid P, Ngai Y, Muthukumar D, Thompson J, Harden S, Middleton G, Fife KM, Crosse B, Taylor P, Nash S, Hackshaw A. Multicenter, Phase III, Randomized, Double-Blind, Placebo-Controlled Trial of Pravastatin Added to First-Line Standard Chemotherapy in Small-Cell Lung Cancer (LUNGSTAR). J Clin Oncol. 2017 May 10;35(14):1506-1514. doi: 10.1200/JCO.2016.69.7391. Epub 2017 Feb 27.
Results Reference
background
PubMed Identifier
18272962
Citation
Pabla N, Dong Z. Cisplatin nephrotoxicity: mechanisms and renoprotective strategies. Kidney Int. 2008 May;73(9):994-1007. doi: 10.1038/sj.ki.5002786. Epub 2008 Feb 13.
Results Reference
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Evaluation of the Effect of Rosuvastatin on Cisplatin-induced Nephrotoxicity and Ototoxicity

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