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      A Randomized Phase 2 Study of 5-Aminolevulinic Acid Hydrochloride and Sodium Ferrous Citrate for the Prevention of Nephrotoxicity Induced by Cisplatin-Based Chemotherapy of Lung Cancer

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          Abstract

          Introduction

          Cisplatin-based chemotherapy was established in the 1980s, and it has been improved by the development of a short hydration protocol in lung cancer therapy. However, cisplatin-based chemotherapy is still associated with renal toxicity. Because 5-aminolevulinic acid (5-ALA) with sodium ferrous citrate (SFC) is known to be a mitochondrial activator and a heme oxygenase-1 (HO-1) inducer, 5-ALA with SFC is speculated to mitigate cisplatin-induced renal inflammation.

          Methods

          We investigated the effects of oral administration of 5-ALA with SFC for preventing cisplatin-based nephrotoxicity in patients with lung cancer and evaluated its benefits for patients who received cisplatin-based chemotherapy. The primary endpoint was the significance of the difference between the serum creatinine (sCr) levels of the patients administered 5-ALA with SFC and those given placebo after course 1 of chemotherapy. The difference in the estimated glomerular filtration rate (eGFR) between the two groups was also evaluated as the secondary endpoint.

          Results

          The double-blind, randomized two-arm studies were conducted at 15 medical facilities in Japan; 54 male and 20 female patients with lung cancer who received cisplatin-based chemotherapy between the ages of 42 and 75 years were included in the study. The compliance rate was greater than 94% in the primary assessment and subsequent drug administration periods. All enrolled patients completed the four cycles of cisplatin-based chemotherapy with short hydration. The average level of sCr on day 22 of course 1 was 0.707 mg/dL in the group treated with 5-ALA and SFC and 0.735 mg/dL in the placebo group, respectively, and the sCr in the test group was significantly lower than that in the placebo group ( p = 0.038). In addition, the eGFR was significantly higher in the SPP-003 group than in the placebo group up to day 1 of course 3 (84.66 and 75.68 mL/min/1.73 m<sup>2</sup>, respectively, p = 0.02) and kept better even after the last administration of the study drug (82.37 and 73.49 mL/min/1.73 m<sup>2</sup>, respectively, p = 0.013).

          Conclusions

          The oral administration of 5-ALA with SFC is beneficial to patients undergoing cisplatin-based chemotherapy for lung cancer with short hydration.

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          Most cited references35

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          Mechanisms of Cisplatin Nephrotoxicity

          Cisplatin is a widely used and highly effective cancer chemotherapeutic agent. One of the limiting side effects of cisplatin use is nephrotoxicity. Research over the past 10 years has uncovered many of the cellular mechanisms which underlie cisplatin-induced renal cell death. It has also become apparent that inflammation provoked by injury to renal epithelial cells serves to amplify kidney injury and dysfunction in vivo. This review summarizes recent advances in our understanding of cisplatin nephrotoxicity and discusses how these advances might lead to more effective prevention.
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            Cisplatin nephrotoxicity: mechanisms and renoprotective strategies.

            N Pabla, Z Dong (2008)
            Cisplatin is one of the most widely used and most potent chemotherapy drugs. However, side effects in normal tissues and organs, notably nephrotoxicity in the kidneys, limit the use of cisplatin and related platinum-based therapeutics. Recent research has shed significant new lights on the mechanism of cisplatin nephrotoxicity, especially on the signaling pathways leading to tubular cell death and inflammation. Renoprotective approaches are being discovered, but the protective effects are mostly partial, suggesting the need for combinatorial strategies. Importantly, it is unclear whether these approaches would limit the anticancer effects of cisplatin in tumors. Examination of tumor-bearing animals and identification of novel renoprotective strategies that do not diminish the anticancer efficacy of cisplatin are essential to the development of clinically applicable interventions.
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              Heme oxygenase-1/carbon monoxide: from basic science to therapeutic applications.

              The heme oxygenases, which consist of constitutive and inducible isozymes (HO-1, HO-2), catalyze the rate-limiting step in the metabolic conversion of heme to the bile pigments (i.e., biliverdin and bilirubin) and thus constitute a major intracellular source of iron and carbon monoxide (CO). In recent years, endogenously produced CO has been shown to possess intriguing signaling properties affecting numerous critical cellular functions including but not limited to inflammation, cellular proliferation, and apoptotic cell death. The era of gaseous molecules in biomedical research and human diseases initiated with the discovery that the endothelial cell-derived relaxing factor was identical to the gaseous molecule nitric oxide (NO). The discovery that endogenously produced gaseous molecules such as NO and now CO can impart potent physiological and biological effector functions truly represented a paradigm shift and unraveled new avenues of intense investigations. This review covers the molecular and biochemical characterization of HOs, with a discussion on the mechanisms of signal transduction and gene regulation that mediate the induction of HO-1 by environmental stress. Furthermore, the current understanding of the functional significance of HO shall be discussed from the perspective of each of the metabolic by-products, with a special emphasis on CO. Finally, this presentation aspires to lay a foundation for potential future clinical applications of these systems.
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                Author and article information

                Journal
                Oncology
                Oncology
                OCL
                Oncology
                S. Karger AG (Allschwilerstrasse 10, P.O. Box · Postfach · Case postale, CH–4009, Basel, Switzerland · Schweiz · Suisse, Phone: +41 61 306 11 11, Fax: +41 61 306 12 34, karger@karger.com )
                0030-2414
                1423-0232
                December 2022
                13 September 2022
                13 September 2022
                : 100
                : 11
                : 620-632
                Affiliations
                [1] aDepartment of Respiratory Medicine, Saiseikai Kumamoto Hospital, Kumamoto, Japan
                [2] bDepartment of Respiratory Medicine, Saitama Red Cross Hospital, Saitama, Japan
                [3] cDepartment of Respiratory Medicine, Saitama Cancer Center, Saitama, Japan
                [4] dDepartment of Respiratory Medicine, Nagaoka Chuo General Hospital, Niigata, Japan
                [5] eDepartment of Respiratory Medicine, Funabashi Municipal Medical Center, Chiba, Japan
                [6] fDepartment of Respiratory Medicine, Fukui Prefectural Hospital, Fukui, Japan
                [7] gDepartment of Respiratory Medicine, Juntendo University Urayasu Hospital, Chiba, Japan
                [8] hDepartment of Respiratory Medicine, Oita Red Cross Hospital, Oita, Japan
                [9] iDepartment of Respiratory Medicine, Yokosuka Kyosai Hospital, Yokosuka, Japan
                [10] jDepartment of Respiratory Center, Asahikawa Medical University Hospital, Asahikawa, Japan
                [11] kDepartment of Respiratory Medicine, Saga-Ken Medical Centre Koseikan, Saga, Japan
                [12] lDepartment of Respiratory Medicine, Ishikawa Prefectural Central Hospital, Kanazawa, Japan
                [13] mDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan
                [14] nDepartment of Respiratory Medicine, Toyama Prefectural Central Hospital, Toyama, Japan
                [15] oDepartment of Respiratory Medicine, Nagaoka Red Cross Hospital, Niigata, Japan
                [16] pDepartment of Clinical Development, SBI Pharmaceuticals Co., Ltd., Tokyo, Japan
                Author notes
                Article
                ocl-0100-0620
                10.1159/000526977
                9808709
                36099876
                82b8184a-4250-4f92-a4fa-6a236ef61a14
                The Author(s). Published by S. Karger AG, Basel

                This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC). Usage and distribution for commercial purposes requires written permission.

                History
                : 30 June 2022
                : 2 September 2022
                : 2022
                Page count
                Figures: 4, Tables: 5, References: 38, Pages: 13
                Funding
                The study was fully supported by a grant from SBI Pharmaceuticals.
                Categories
                Research Article

                5-aminolevulinic acid,sodium ferrous citrate,lung cancer,cisplatin,chemotherapy,nephrotoxicity,short hydration

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