Docetaxel Intermittent-Erlotinib (Tarceva®) In Metastatic Non Small Cell Lung Cancer (NSCLC)

Advanced Non-Small Cell Lung Cancer Clinical Trial

— DOPERLO  

Official title:

Docetaxel Combined With Pulsatile Erlotinib (Tarceva®) In Patients With Metastatic Non Small Cell Lung Cancer (NSCLC) (DOPERLO)

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00783471
• Other study ID #: HE 2D/07
• Status: Terminated
• Phase: Phase 2
• First received: October 30, 2008
• Last updated: June 15, 2010
• Start date: November 2008
• Est. completion date: June 2010

Study information

• Verified date: June 2010
• Source: Hellenic Cooperative Oncology Group
• Contact: n/a
• Is FDA regulated: No
• Health authority: Greece: Ethics CommitteeGreece: National Organization of Medicines
• Study type: Interventional

Clinical Trial Summary

To determine the more effective dosing sequence of intermittent erlotinib and docetaxel for treating patients with the diagnosis of advanced Non-Small-Lung-Cancer

Description:

The combination of chemotherapy [such as docetaxel] with continuous administration of targeted drugs which block the molecular machinery of cancer cell growth [such as erlotinib] have failed to improve their efficacy over only-chemotherapy in patients with metastatic lung cancer of the non-small cell histology type. It is not yet known whether administering targeted drugs intermittently could result in improved efficacy of the combinations. This is a multicenter randomized Phase II trial aiming to determine the more active dosing sequence between intermittent erlotinib and docetaxel for treating patients with advanced Non-Small-Lung-Cancer.Patients will be randomly assigned to one of two treatment arms: they will receive a 12-days course of erlotinib either before docetaxel [arm A] or after docetaxel administration [arm B].Treatment will be repeated every 21 days.Patients will be evaluated every 2 cycles (~6 weeks) for response using RECIST criteria. Those patients achieving stable disease or better will continue therapy up to a total 8 cycles. Those patients experiencing progressive disease will be taken off study. Biopsy material will be assessed for biomarkers.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 51
• Est. completion date: June 2010
• Est. primary completion date: May 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Male and female patients aged 18 to 75 years inclusive, with histologically confirmed metastatic NSCLC will be enrolled.

2. Patients must have not been previously treated with anticancer drugs for advanced disease.

3. ECOG performance status of 0 - 1.

4. Life expectancy of at least 12 weeks.

5. Patients must be able to take oral medication.

6. At least 4 weeks since any prior major surgery or extended-field radiotherapy. Patients who, in the opinion of the investigator, have fully recovered from limited surgery or have undergone limited-field radiotherapy within 2 weeks may also be considered eligible for the study

7. Granulocyte count > 1,500/mm3 and platelet count > 100,000/mm3. Haemoglobin ³ 9.0g/dl.

8. SGOT (AST) and SGPT (ALT) < 2,5 x ULN in the absence of liver metastases or up to 5 x ULN in case of liver metastases

9. Alkaline phosphatase (ALP) < 2,5 x ULN. If alkaline phosphatase is > 2.5 x ULN, SGOT (AST) and SGPT (ALT) must be < 1.5 x ULN. If alkaline phosphatase is ³ 2.5 x ULN in the presence of liver metastases, SGOT and SGPT must be < 5 x ULN

10. Serum creatinine <= 1.5 ULN or creatinine clearance > 60 ml/min.

11. Normal serum calcium.

12. For all females of childbearing potential a negative pregnancy test must be obtained within 48 hours before starting Tarceva/placebo treatment.

13. Patients with reproductive potential must use effective contraception.

14. Able to comply with study and follow-up procedures.

15. Written (signed) Informed Consent to participate in the study.

16. Written (signed) Informed Consent for use of tumour samples.

17. Presence of measurable or evaluable disease (lesions that are present but do not fulfil the criteria for measurable disease).

18. Formalin-fixed, paraffin-embedded tumour tissue samples representative of the tumour will be provided to sponsor within 3 weeks of the patient starting chemotherapy

Exclusion Criteria:

1. Prior exposure to agents directed at the HER axis (e.g. gefitinib, cetuximab, trastuzumab).

2. Prior chemotherapy or therapy with systemic anti-neoplastic therapy (e.g., monoclonal antibody therapy) for advanced disease. Prior surgery and/or localised irradiation is permitted.

3. Patients who have undergone complete tumour resection after responding to platinum based chemotherapy.

4. Any unstable systemic disease (including active infections, significant cardiovascular disease, [including myocardial infarction within the previous year], any significant hepatic, renal or metabolic disease) metabolic dysfunction, physical examination finding, or clinical laboratory finding that contraindicates the use of study medication(s) or that might affect the interpretation of the results or render the patient at high risk from treatment complications.

5. Any other malignancies within 5 years (except for adequately treated carcinoma in situ of the cervix or basal or squamous cell skin cancer).

6. Patients are excluded if they have symptomatic brain metastasis or spinal cord compression that has not yet been definitively treated with surgery and/or radiation; patients with CNS metastases with evidence of stable disease (clinically stable imaging) and stable neurologic function are allowed to enter the study.

7. Patients who are at risk (in the investigator's opinion) of transmitting human immunodeficiency virus (HIV) through blood or other body fluids are excluded.

8. Any inflammatory changes of the surface of the eye.

9. Patients who cannot take oral medication, who require intravenous alimentation, have had prior surgical procedures affecting absorption, or have active peptic ulcer disease.

10. Nursing and/or pregnant women.

11. Hypersensitivity to erlotinib (Tarceva) or to docetaxel or to any of the excipients.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Advanced Non-Small Cell Lung Cancer
• Carcinoma, Non-Small-Cell Lung
• Lung Neoplasms

Intervention

Drug:
• Erlotinib, Docetaxel
Drug: Erlotinib 150 mg po daily, days 1-12 Drug: Docetaxel 75 mg/m2 IV over 30 min on day 15 Treatment will be repeated every 21 days
• Docetaxel, Erlotinib
Drug: Docetaxel 75 mg/m2 IV over 30 min on day 1 Drug: Erlotinib 150 mg po daily, days 4-15 Treatment will be repeated every 21 days

Locations

Country	Name	City	State
Greece	"Alexandra" Hospital	Athens
Greece	"Attikon" University Hospital, 2nd Dept. of Internal Medicine, Propaedeutic, Oncology Section	Athens
Greece	Agii Anargiri Cancer Hospital, 3rd Dept. of Medical Oncology	Athens
Greece	Hygeia Hospital	Athens
Greece	Sotiria Hospital	Athens
Greece	University General Hospital of Ioannina, Medical Oncology Dept	Ioannina
Greece	Larissa University Hospital	Larissa
Greece	Metropolitan Hospital, Second Dept of Medical Oncology	Piraeus
Greece	Metropolitan Hospital, 1st Dept. of Medical Oncology	Pireaus
Greece	Patras University Hospital, Dept. of Internal Medicine, Oncology Section	Rio, Patras
Greece	"Papageorgiou" Hospital	Thessaloniki
Greece	Theagenio Cancer Hospital, 2nd Dept of Medical Oncology	Thessaloniki
Greece	Theagenio Cancer Hospital, 3rd Dept. of Medical Oncology	Thessaloniki

Sponsors (1)

Lead Sponsor	Collaborator
Hellenic Cooperative Oncology Group

Country where clinical trial is conducted

Greece, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression free survival (PFS)		Assessment every 6 weeks	No
Secondary	To compare the Overall Survival (OS),the Objective Response Rate (ORR) and duration of response		Assessment every 6 weeks while on treatment and every 3 months post completion of 8 cycles of treatment until progression	No
Secondary	Identify predictive signaling molecules of the EGFR pathway		Assessment every 6 weeks while on treatment and every 3 months post completion of 8 cycles of treatment until progression	No