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Kardioprotektiv effekt av melatonin kontra vitamin D hos pasienter med brystkreft som får doksorubicin

22. oktober 2026 oppdatert av: Majed Essa Alharbi, Tanta University

Klinisk studie som evaluerer kardioprotektiv effekt av melatonin versus vitamin D hos pasienter med brystkreft som mottar doxorubicin

This study aims to assess the cardioprotective effect of melatonin and vitamin D in breast cancer patients who receive doxorubicin.

Studieoversikt

Detaljert beskrivelse

Doxorubicin is one of the most potent chemotherapeutic agents and is widely used for the treatment of various cancers and hematological malignancies . Although Doxorubicin has a potential beneficial effect in cancer treatment, its dose-dependent cardio toxicity is considered a major challenge.

Doxorubicin is known to generate free radicals either by redox cycling between a semiquinone form and a quinone form or by forming a Doxorubicin-Fe3+ complex . In both pathways, molecular oxygen is reduced to superoxide ion , which is converted to other forms of reactive oxygen species such as hydrogen peroxide and hydroxyl radical . These free radicals could then cause membrane and macromolecule damage, both of which lead to injury to the heart, an organ that has a relatively low level of antioxidant enzymes such as superoxide dismutase and catalase .

Furthermore, it was revealed that Doxorubicin may enhance the death of cardiomyocytes by affecting the tumor necrosis factor signaling pathway via increasing the expression and levels of inflammatory genes interleukin and interleukin -6 .

To alleviate DOX-induced toxicity, researchers have tested a number of strategies, including the administration of antioxidants and/or antiapoptotic agents, in both in vitro and in vivo models of Doxorubicin induced cytotoxicity, but most of these trials have failed to translate into clinical benefits . As a result, there are no effective approaches for alleviating Doxorubicin induced cytotoxicity despite intensive research over recent decades .

Melatonin is a natural hormone that is primarily secreted by the pineal gland and functions as a major regulator of circadian rhythms in humans . Melatonin also plays a variety of biological roles as a modulator of mood, sexual behavior and sleep; low levels or a deficiency of melatonin are also associated with Parkinson's disease, Alzheimer's disease, epilepsy, ischemic injury, diabetes, and even cancer .

Melatonin has emerged as a promising adjuvant that protects against doxorubicin-induced cytotoxicity, as highlighted by various studies and clinical trials that have demonstrated cardioprotective effects against several chemotherapeutic agents . Moreover, melatonin exhibits low toxicity and easily enters cells owing to its good solubility in both aqueous and organic phases and its highly lipophilic properties . Vitamin D plays an important role in the regulation of body function including the cardiovascular system .

Vitamin D deficiency results in the decrease of active calcitriol leading to inhibition of proliferation of cardiomyocytes and vascular smooth muscles .

This study aims to assess the cardioprotective effect of melatonin and vitamin D in breast cancer patients who receive doxorubicin.

Studietype

Intervensjonell

Registrering (Faktiske)

90

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

      • Tanta, Egypt
        • Tanta University

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 65 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Hunn

Beskrivelse

Inclusion Criteria:

  • Age from 18 to 65 years old.
  • Gender: female.
  • Positive breast cancer women who are scheduled to receive Doxorubicin.
  • Have a good performance status according to the eastern cooperative oncology group with a score of 0-2.
  • Normal baseline Echocardiography with left ventricular ejection fraction ≥ 50%.
  • Normal renal and liver function tests.

Exclusion Criteria:

  • Pregnant or breastfeeding women.
  • Women with HER-2 positive of breast cancer.
  • Formerly treated with Doxorubicin.
  • Patients with a known hypersensitivity to any of the used drugs.
  • On other concomitant vitamins or food supplements.
  • Valvular heart disease, coronary artery disease, history of congestive heart failure or cardiomyopathy.
  • Impaired Left ventricular systolic function in which the Left Ventricular Ejection Fraction < 50%.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Forebygging
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: Group 1 (Doxorubicin group)

30 patients will receive a traditional chemotherapeutic agent (Doxorubicin group) for 12 weeks.

30 patients will receive a traditional chemotherapeutic agent (Doxorubicin group) for 12 weeks.

Eksperimentell: Group 2 (Vitamin D group)

patients with Vitamin D supplementation (1000 iu/day) plus Doxorubicin for 12 weeks

patients with Vitamin D supplementation (1000 iu/day) plus traditional therapy for 12 weeks

Eksperimentell: Group 3 (melatonin group)

30 patients with 10 mg of melatonin orally, once daily plus Doxorubicin for 12 weeks.

patients with 10 mg of melatonin orally, once daily plus traditional therapy for 12 weeks

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Decreasing incidence and severity of cardiotoxicity
Tidsramme: 12 weeks

Assessment of decreasing incidence and severity of cardiotoxicity by echocardiogram and ejection fraction is associated with doxorubicin treatment.

12 weeks

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in Plasma B-Type Natriuretic Peptide (BNP) Concentration
Tidsramme: Baseline and 12 weeks.

Change in plasma B-type natriuretic peptide (BNP) concentration from baseline to 12 weeks, measured using a chemiluminescent microparticle immunoassay (CMIA) on the Abbott Alinity i analyzer. Changes will be calculated as the 12-week concentration minus the baseline concentration and expressed in pg/mL.

Baseline and 12 weeks.
Change in N-Terminal Pro-B-Type Natriuretic Peptide (NT-proBNP) Concentration
Tidsramme: Baseline and 12 weeks.

Change in serum/plasma N-terminal pro-B-type natriuretic peptide (NT-proBNP) concentration from baseline to 12 weeks, measured using a chemiluminescent microparticle immunoassay (CMIA) on the Abbott Alinity i analyzer. Changes will be calculated as the 12-week concentration minus the baseline concentration and expressed in pg/mL.

Baseline and 12 weeks.
Change in High-Sensitivity Cardiac Troponin I (hs-cTnI) Concentration
Tidsramme: Baseline and 12 weeks.

Change in serum/plasma high-sensitivity cardiac troponin I (hs-cTnI) concentration from baseline to 12 weeks, measured using the Alinity i STAT High Sensitive Troponin-I chemiluminescent microparticle immunoassay (CMIA). Changes will be calculated as the 12-week concentration minus the baseline concentration and expressed in ng/L.

Baseline and 12 weeks.
Change in Myeloperoxidase (MPO) Concentration
Tidsramme: Baseline and 12 weeks.

Change in myeloperoxidase (MPO) concentration from baseline to 12 weeks, measured using a human MPO double-antibody sandwich enzyme-linked immunosorbent assay (ELISA; SunRed Biological Technology Co., Ltd.). Changes will be calculated as the 12-week concentration minus the baseline concentration and expressed in ng/mL.

Baseline and 12 weeks.
Change in Interleukin-6 (IL-6) Concentration
Tidsramme: Baseline and 12 weeks.

Change in interleukin-6 (IL-6) concentration from baseline to 12 weeks, measured using a human IL-6 double-antibody sandwich enzyme-linked immunosorbent assay (ELISA; SunRed Biological Technology Co., Ltd.). Changes will be calculated as the 12-week concentration minus the baseline concentration and expressed in ng/L.

Baseline and 12 weeks.
Change in Creatine Kinase-MB (CK-MB) Concentration
Tidsramme: Baseline and 12 weeks.

Change in serum/plasma creatine kinase-MB (CK-MB) concentration from baseline to 12 weeks, measured using the Alinity i STAT CK-MB chemiluminescent microparticle immunoassay (CMIA). Changes will be calculated as the 12-week concentration minus the baseline concentration and expressed in ng/mL.

Baseline and 12 weeks.

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

1. april 2025

Primær fullføring (Faktiske)

30. mai 2026

Studiet fullført (Faktiske)

30. mai 2026

Datoer for studieregistrering

Først innsendt

9. januar 2026

Først innsendt som oppfylte QC-kriteriene

9. januar 2026

Først lagt ut (Faktiske)

16. januar 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

26. oktober 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

22. oktober 2026

Sist bekreftet

1. oktober 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • 36265MD408/5/25

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

JA

IPD-planbeskrivelse

All data will be available when needed

IPD-deling Støtteinformasjonstype

  • STUDY_PROTOCOL
  • ICF

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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