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Completed

NCT Number: NCT00418704

Elderly Independent Patients With Non Small Cell Lung Cancer (NSCLC)

The purpose of this study is to determine duration before progression of first-line treatment chemotherapy following erlotinib in second-line comparing erlotinib in first-line following chemotherapy in second-line in old patients with none small cell lung cancer.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Site 12, Aix-en-Provence, France

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About this study

A multicenter phase II trial , prospective, randomized, open, non comparative

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age > 65 years
  • Comorbidities score,
  • PS frailty score**.according to(TABLE N°1)
  • No dementia, repeated falls, faecal or urinary incontinence, ADL=0, IADL=0
  • Life expectancy at least 12 weeks
  • Créatinine clearance de la créatinine > or =30cc/mn according to Cockrofts
  • Gault formula
  • Competency to give written informed consent
  • Haematological function as follows: absolute neutrophil count > 1.5 x 109/l and/or platelet> 100 x 109/l, hémoglobine > or = 9,5 g/dl
  • Hepatic function as followed :bilirubin <1,25 LNS SGOT/SGPT <5 x N,PAL <5N
  • PS < 3
  • No symptomatic cerebral metastasis
  • Histologically or cytologically confirmed NSCLC
  • Stage IV/IIIB4 (T4with pleural effusion)
  • No prior chemotherapy for NSCLC
  • Relapses of previous NSCLC treated by surgery or radiotherapy are eligible if the target is measurable out of initial radiotherapy field and if histological or cytological proof
  • At least one measurable target lesion by RECIST guidelines.

Exclusion criteria

  • Symptomatic cerebral metastasis
  • Any severe co-morbidity calculated by Charlson score (according to table 1), any kind of disorder that compromises the ability of the subject to give written informed and/or comply with the study procedure ADL > or = 1 et IADL > or =1 Dementia, repeated falls, faecal or urinary incontinence- Peripheral neuropathy grade 2 or more
  • Performance Status > 2 ( ECOG)- Contraindication to corticosteroids
  • Unwilling or unable to comply with study requirements for personal , family, sociologic, geographic or any reasons
  • Lack of liberty following administrative or judicial decision
  • Hypersensitivity to polysorbate
  • Hypersensitivity to erlotinib or any excipients of this product
  • Unusual hereditary disorders as galactosemia, deficit in lactase and malabsorption in glucose or galactose
  • Participation in concomitant clinical trial
  • Contraindication to a product of this study disease
  • Bronchioloalvéolar or neuroendocrine or composite carcinoma
  • Superior vena cava syndrome

Treatment and study plan

Erlotinib

Drug

Tarceva (150 mg) is a pill you take once a day -- every day

Taxotere

Drug

Taxotere® (docetaxel) is given intravenously (I.V.) into the vein. Taxotere® chemotherapy treatment takes about one hour, and usually people receive treatments every three weeks.

Other names: Docetaxel

Sponsors and collaborators

Lead sponsor

Groupe Francais De Pneumo-Cancerologie

Other

Collaborators

  • Chugai Pharma USA
  • Sanofi

Registry information

Official study title

A Multicenter Randomized Phase II Trial in NSCLC Stage IV and IIIB (T4 With Pleural Effusion) in Elderly Independent Patients the Schedule Docetaxel / Gemcitabine First Line Following by Erlotinib When Progression Versus Erlotinib First Line Following by/ Gemcitabine When Progression.

Important dates

Study start
2006
Primary completion
2006
Study completion
2009
First posted
Jan 5, 2007
Registry last updated
Oct 1, 2013

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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