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Docetaxel in Non Small Cell Lung Cancer (NSCLC)

Primary Purpose

Carcinoma, Squamous Cell

Status
Completed
Phase
Phase 2
Locations
Austria
Study Type
Interventional
Intervention
Docetaxel + CDDP
docetaxel + CDDP
Sponsored by
Sanofi
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Carcinoma, Squamous Cell

Eligibility Criteria

19 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. 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)
  2. 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:

  1. 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
  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
  3. 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.

Sites / Locations

  • Sanofi-Aventis Administrative Office

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

1

2

Arm Description

Resectable NSCLC

Unresectable NSCSC

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

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

Full Information

First Posted
February 6, 2007
Last Updated
September 13, 2010
Sponsor
Sanofi
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1. Study Identification

Unique Protocol Identification Number
NCT00432315
Brief Title
Docetaxel in Non Small Cell Lung Cancer (NSCLC)
Official 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
Study Type
Interventional

2. Study Status

Record Verification Date
September 2010
Overall Recruitment Status
Completed
Study Start Date
May 2001 (undefined)
Primary Completion Date
October 2009 (Actual)
Study Completion Date
October 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Sanofi

4. Oversight

5. Study Description

Brief Summary
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

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carcinoma, Squamous Cell

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Resectable NSCLC
Arm Title
2
Arm Type
Experimental
Arm Description
Unresectable NSCSC
Intervention Type
Drug
Intervention Name(s)
Docetaxel + CDDP
Intervention Description
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
Intervention Type
Drug
Intervention Name(s)
docetaxel + CDDP
Intervention Description
3 cycles chemotherapy: docetaxel + CDDP Radiochemotherapy 3 cycles adjuvant chemotherapy docetaxel
Primary Outcome Measure Information:
Title
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 Outcome Measure Information:
Title
Resectability after induction therapy
Time Frame
every 3 months until tumour progression and thereafter every 6 months until death
Title
Time to progression
Time Frame
every 3 months until tumour progression and thereafter every 6 months until death
Title
Overall survival
Time Frame
every 3 months until tumour progression and thereafter every 6 months until death
Title
Safety profile
Time Frame
throughout the study
Title
Quality of life
Time Frame
every 3 months until tumour progression and thereafter every 6 months until death

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alexandra Edlmayer, Dr.
Organizational Affiliation
Sanofi
Official's Role
Study Director
Facility Information:
Facility Name
Sanofi-Aventis Administrative Office
City
Vienna
Country
Austria

12. IPD Sharing Statement

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Docetaxel in Non Small Cell Lung Cancer (NSCLC)

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