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Effect of Genetic and Epigenetic Factors on the Clinical Response and Toxicity to Cisplatin Among Egyptian Non-small Cell Lung Cancer Patients

A

Ain Shams University

Status

Enrolling

Conditions

Cardiotoxicity
Nephropathy
Non Small Cell Lung Cancer

Treatments

Drug: Cisplatin injection

Study type

Observational

Funder types

Other

Identifiers

NCT05746598
NSCLC-Genetics

Details and patient eligibility

About

Lung cancer is the leading cause of death worldwide, with non-small-cell lung cancer (NSCLC) being the most common histotype according to the global cancer observatory 2022. A variety of therapeutic options for advanced/metastatic non-oncogene-addicted NSCLC have recently been approved based on their impact on patient outcomes in terms of survival and safety profile. Current guidelines advocate for personalized treatment options based on molecular and immunologic characteristics, which drives the physician's decision toward tailored oncology.

In the last two to three decades, hundreds of cancer biological prognostic markers for non-small cell lung cancer have been proposed. Although they have shown a potential in this field, validation studies are still required and, to date, there is in sufficient evidence to recommend the routine clinical use of any of these putative biomarkers. Therefore, the discovery of robust prognostic and/or predictive biomarkers in patients with non-small cell lung cancer is imperative for advancing treatment strategies for the disease and improving patient care.

Enrollment

178 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • NSCLC cancer patients treated with Cisplatin-containing chemotherapy.
  • Measurable disease.
  • Age of 18 years to 80 years.

Exclusion criteria

  • Non-small cell lung 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 oxaliplatin.
  • 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.

Trial design

178 participants in 2 patient groups

1
Description:
NSCLC patients Who developed Toxicity to Chemotherapeutic agents
Treatment:
Drug: Cisplatin injection
2
Description:
NSCLC patients Who did not developToxicity to Chemotherapeutic agents
Treatment:
Drug: Cisplatin injection

Trial contacts and locations

1

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Central trial contact

Mona Schaalan, PhD; Neven Sarhan, PhD

Data sourced from clinicaltrials.gov

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