Evidence map›Paper›PMID 36099876›Full record

Trial reportOncology2022

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.

Kodai Kawamura, Hidekazu Matsushima, Hiroshi Sakai, Akira Iwashima, Sukeyuki Nakamura, Tohru Kojima, Shinichi Sasaki, Takehiko Shigenaga, Ichiro Natsume, Takaaki Sasaki and 9 more

Open access · hybridAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 43% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 15 institutions in 1 country.

Kodai KawamuraDepartment of Respiratory Medicine, Saiseikai Kumamoto Hospital, Kumamoto, Japan.
Hidekazu MatsushimaDepartment of Respiratory Medicine, Saitama Red Cross Hospital, Saitama, Japan.
Hiroshi SakaiDepartment of Respiratory Medicine, Saitama Cancer Center, Saitama, Japan.
Akira IwashimaDepartment of Respiratory Medicine, Nagaoka Chuo General Hospital, Niigata, Japan.
Sukeyuki NakamuraDepartment of Respiratory Medicine, Funabashi Municipal Medical Center, Chiba, Japan.
Tohru KojimaDepartment of Respiratory Medicine, Fukui Prefectural Hospital, Fukui, Japan.
Shinichi SasakiDepartment of Respiratory Medicine, Juntendo University Urayasu Hospital, Chiba, Japan.
Takehiko ShigenagaDepartment of Respiratory Medicine, Oita Red Cross Hospital, Oita, Japan.
Ichiro NatsumeDepartment of Respiratory Medicine, Yokosuka Kyosai Hospital, Yokosuka, Japan.
Takaaki SasakiDepartment of Respiratory Center, Asahikawa Medical University Hospital, Asahikawa, Japan.
Yoshinobu OhsakiDepartment of Respiratory Center, Asahikawa Medical University Hospital, Asahikawa, Japan.
Kentaro IwanagaDepartment of Respiratory Medicine, Saga-Ken Medical Centre Koseikan, Saga, Japan.
Koichi NishiDepartment of Respiratory Medicine, Ishikawa Prefectural Central Hospital, Kanazawa, Japan.
Yoichiro MitsuishiDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Hirokazu TaniguchiDepartment of Respiratory Medicine, Toyama Prefectural Central Hospital, Toyama, Japan.
Kazuhiro SatoDepartment of Respiratory Medicine, Nagaoka Red Cross Hospital, Niigata, Japan.
Mitsugu YamauchiDepartment of Clinical Development, SBI Pharmaceuticals Co., Ltd., Tokyo, Japan.
Motowo NakajimaDepartment of Clinical Development, SBI Pharmaceuticals Co., Ltd., Tokyo, Japan.
Kazuhisa TakahashiDepartment of Respiratory Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Asahikawa Medical University · JPJuntendo University · JPSBI Pharmaceuticals (Japan) · JPFukui Prefectural Hospital · JPFunabashi Municipal Medical Center · JPIshikawa Prefectural Central Hospital · JPJuntendo University Urayasu Hospital · JPNagaoka Red Cross Hospital · JPOita Red Cross Hospital · JPSaga-Ken Medical Centre Koseikan · JPSaiseikai Kumamoto Hospital · JPSaitama Cancer Center · JPSaitama Red Cross Hospital · JPToyama Prefectural Central Hospital · JPYokosuka Kyosai Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCisplatin-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.

methodsWe 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.

resultsThe 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 m2, 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 m2, respectively, p = 0.013).

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

Indexed as

Aminolevulinic AcidLung NeoplasmsAdultAgedCisplatinCitric AcidFemaleFerrous CompoundsHumansMaleMiddle AgedAminolevulinic AcidCisplatinCitric Acidferrous citrateFerrous Compounds5-Aminolevulinic acidChemotherapyCisplatinLung cancerNephrotoxicityShort hydrationSodium ferrous citrate

Identifiers

PMID36099876
PMCPMC9808709
OpenAlexW4295759952

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.