Skip to main content
OpenTrials
Completed

NCT Number: NCT00658580

Randomized Study of Cisplatin-Etoposide Versus an Etoposide Regimen Without Cisplatin in Extensive Small-Cell Lung Cancer

The purpose of this study is to determine if a cisplatin-etoposide regimen improves survival in comparison to a regimen containing etoposide and without platinum derivative.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Department of Intensive Care Unit and Thoracic Oncology Institut Jules Bordet, Brussels, Belgium

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histological or cytological diagnosis of small-cell lung cancer
  • Extensive disease (i.e. a disease with distant metastases or that cannot be included in a single irradiation field incorporating primary tumour, mediastinum and supraclavicular lymph node(s))
  • Availability for participating in the detailed follow-up of the protocol
  • Presence of an evaluable or measurable lesion
  • Informed consent

Exclusion criteria

  • Prior treatment with chemotherapy, radiotherapy or surgery
  • Performance status < 60 on the Karnofsky scale
  • A history of prior malignant tumor, except non-melanoma skin cancer or in situ carcinoma of the cervix or a cured cancer (defined as a disease-free interval > 5 years)
  • White blood cells < 4000/mm3
  • Platelets < 100000/mm3
  • Serum bilirubin > 1.5 mg/100 ml
  • Serum creatinine > 1.3 mg/100 ml and creatinine clearance <60 ml/min
  • Recent myocardial infarction (less than 3 months prior to date of diagnosis)
  • Congestive cardiac failure or cardiac arrhythmia uncontrolled by medical treatment
  • Uncontrolled infectious disease
  • Serious medical or psychological factors which may prevent adherence to the treatment schedule

Treatment and study plan

Cisplatin + etoposide

Drug

Cisplatin 90 mg/m² day 1, every 3 weeks

Etoposide 100 mg/m² days 1-3, every 3 weeks

Epirubicin + ifosfamide + etoposide

Drug

Epirubicin 60 mg/m² day 1, every 3 weeks

Ifosfamide (+ uromitexan) 1.5 g/m² days 1-3, every 3 weeks

Etoposide 100 mg/m² days 1-3, every 3 weeks

Primary outcomes

  1. Survival

    Time frame: Survival will be dated from the day of randomisation until death or last follow up

Secondary outcomes

  1. Response rate

    Time frame: Every 3 cycles of chemotherapy

  2. Toxicity

    Time frame: After every cycle of chemotherapy

Sponsors and collaborators

Lead sponsor

European Lung Cancer Working Party

Other

Registry information

Official study title

A Phase III Randomized Study Comparing A Chemotherapy With Cisplatin And Etoposide To A Etoposide Regimen Without Cisplatin For Patients With Extensive Small-Cell Lung Cancer

Important dates

Study start
2000
Primary completion
2013
Study completion
2015
First posted
Apr 15, 2008
Registry last updated
Feb 12, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.