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OpenTrials
Completed

NCT Number: NCT00432315

Docetaxel in Non Small Cell Lung Cancer (NSCLC)

Primary objective:

• To assess the response rate to induction therapy with docetaxel/CDDP.

Secondary objectives:

To assess

* Resectability after induction therapy * Time to progression * Overall survival * Safety profile * Quality of Life

Completed

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Key information

Age range

19 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Sanofi-Aventis Administrative Office

Vienna, Austria

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Histology and staging of the disease
  • Histologically or cytologically confirmed NSCLC; histology may include: large cell, squamous cell or adenocarcinoma but no SCLC
  • Resectable or unresectable NSCLC stage II (T1-2 N1, T3 N0) or stage IIIa (T1-2 N2 or T3 N1-2) or stage IIIb (T1-3 N3 or T4 N0-3)
  • Measurable disease (bidimensionally or unidimensionally according to WHO criteria)
  • General conditions
  • Karnofsky Status > 70, if age > 70 years → PS > 70
  • Adequate hematological function (Hb > 10 g/dl, ANC > 2.0 x 109/L, platelets > 100 x 109/L)
  • Adequate renal and hepatic functions: total bilirubin < 1 x upper normal limit (UNL), serum creatinine < 1 x UNL, in case of limit value the creatinine clearance should be > 60 ml/min, ASAT and ALAT < 2.5 x UNL, alkaline phosphatase < 5 x UNL.

Exclusion criteria

  • Diagnosis
  • Evidence of brain metastases or other distant metastasis equivalent to stage IV disease
  • History of prior malignancies, except for curatively treated non-melanoma skin cancer or in situ carcinoma of the cervix or other curatively treated cancer with no evidence of disease for at least five years
  • Other serious concomitant illness or medical condition:
  • Congestive heart failure or angina pectoris, except if medically controlled, history of myocardial infarction within 1 year from study entry, uncontrolled hypertension or arrhythmia
  • History of significant neurologic or psychiatric disorders, including dementia or seizure
  • Active infection requiring i.v. Antibiotics
  • Active ulcer, unstable diabetes mellitus or other contraindications to corticotherapy
  • Hepatic function abnormality: ASAT and/or ALAT > 1.5 x UNL associated with alkaline phosphatase > 2.5 x UNL
  • Current peripheral neuropathy WHO grade > 2
  • Prior or concurrent therapy
  • Prior chemotherapy or immunotherapy for NSCLC, including neoadjuvant or adjuvant treatment
  • Prior surgery or radiotherapy for NSCLC
  • Concurrent treatment with other experimental drugs, unapproved medical procedures or other anticancer therapy
  • General conditions
  • Pregnant or lactating patients
  • Patients (M/F) with reproductive potential not implementing adequate contraceptive measurements

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Treatment and study plan

Docetaxel + CDDP

Drug
  • 3 cycles chemotherapy : docetaxel + CDDP
  • Surgery (if no histologically proven R0-resection could be achieved,additional adjuvant radiotherapy should be considered)
  • 3 cycles adjuvant chemotherapy docetaxel

Primary outcomes

  1. To assess the response rate to induction therapy with docetaxel in combination with CDDP

    Time frame: every 3 months until tumour progression and thereafter every 6 months until death

Secondary outcomes

  1. Resectability after induction therapy

    Time frame: every 3 months until tumour progression and thereafter every 6 months until death

  2. Time to progression

    Time frame: every 3 months until tumour progression and thereafter every 6 months until death

  3. Overall survival

    Time frame: every 3 months until tumour progression and thereafter every 6 months until death

  4. Safety profile

    Time frame: throughout the study

  5. Quality of life

    Time frame: every 3 months until tumour progression and thereafter every 6 months until death

Sponsors and collaborators

Lead sponsor

Sanofi

Industry

Registry information

Official study title

Multicenter Phase II Study Evaluating Docetaxel and CDDP as Induction Regimen Prior to Surgery or Radiochemotherapy With Docetaxel, Followed by Adjuvant Docetaxel Therapy in Chemonaive Patients With NSCLC Stage II, IIIa and IIIb

Important dates

Study start
2001
Primary completion
2009
Study completion
2009
First posted
Feb 7, 2007
Registry last updated
Sep 14, 2010

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.

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