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Effect of Genetic and Epigenetic Factors on the Clinical Response and Toxicity to Doxorubicin Among Egyptian Breast Cancer Patients

Effect of Genetic and Epigenetic Factors on the Clinical Response and Toxicity to Doxorubicin Among Egyptian Breast Cancer Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05733026
Enrollment
200
Registered
2023-02-17
Start date
2020-08-01
Completion date
2023-04-01
Last updated
2023-02-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

Doxorubcin, Breast cancer, Cardiotoxicity, Gene polymorphism

Brief summary

Recent advances in technologies, such as microarray and high-throughput sequencing, represented a deeper understanding of molecular biology, especially noncoding RNA (ncRNA). It was found that there are only \<2 % of the total genome sequence as protein-coding genes while at least 98 % of the genome are transcribed into ncRNA. In the past, non-protein-coding RNAs were known as transcription noise, but now it is obvious that ncRNAs play a crucial regulatory role in cell differentiation and organism growth and metabolism.

Interventions

None listed

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Metastatic and localized breast cancer patients treated with Doxorubicin among chemotherapeutic protocol. * Measurable disease. * Age of 18 years to 80 years. * The women of childbearing age must use an effective contraception for the duration of the study.

Exclusion criteria

* Breast cancer patients who had undergone radiotherapy or chemotherapy. * Pregnant and lactating females. * History of allergic reactions attributed to compounds of similar chemical or biologic composition to chemotherapeutic agents used. * Any other medical or psychiatric condition or severe or chronic laboratory abnormality making the inclusion of the patient in the study inappropriate in the opinion of the investigator.

Design outcomes

Primary

MeasureTime frameDescription
Cardiotoxicity6 monthsOccurrence of dilated cardiomyopathy

Secondary

MeasureTime frameDescription
Nephrotoxicity6 monthsOccurrence of nephrotoxicity

Countries

Egypt

Contacts

Primary ContactNeven Sarhan, PhD
sarhanneven@gmail.com+201021944422
Backup ContactMona Schaalan, PhD
mona.schaalan@miuegypt.edu.eg

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026