Docetaxel Versus Intercalated Erlotinib-docetaxel in Patients With Relapsed EGFR Wild Type, ALK Negative Non Squamous Cell Carcinoma

• Status: Terminated
• Trial end date: 2019-04-01
• Target enrollment: 0
• Participant gender: All

Summary

The objective of this study is to investigate the effect of docetaxel monotherapy and the combination of docetaxel intercalated erlotinib in patients with relapsed EGFR wild type, ALK negative non squamous cell carcinoma.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: The Netherlands Cancer Institute
• Collaborator: Dutch Society of Physicians for Pulmonology and Tuberculosis
• Treatments: Docetaxel; Erlotinib Hydrochloride

Criteria

Inclusion Criteria:

1. Histologically or cytologically confirmed EGFR wild type, ALK negative, non-squamous cell carcinoma, locally advanced and metastatic disease stage IIIB and IV. Evidence of disease progression after one cytotoxic treatment platinum containing regimen. Immunotherapy pretreatment is allowed

2. Complete recovery from prior chemotherapy side effects to < Grade 2.

3. At least one unidimensionally measurable lesion meeting RECIST criteria.

4. ECOG PS 0-1.

5. Age ≥ 18 years.

6. Adequate organ function, including:

• Adequate bone marrow reserve: ANC > 1.5 x 109/L, platelets ≥ 100 x 109/L.

• Hepatic: bilirubin ≤1.5 x ULN (upper limit normal), AP, ALT, AST ≤ 1.5 x ULN. AP, ALT, and AST ≤5 x ULN is acceptable if the liver has tumor involvement.

• Renal: calculated creatinine clearance ≥ 40 ml/min based on the Cockcroft-Gault formula.

7. Male and female patients with reproductive potential must use an approved contraceptive method, if appropriate. Female patients with childbearing potential must have a negative serum pregnancy test within 7 days prior to study enrollment.

8. Signed informed consent.

9. Patient compliance and geographical proximity that allow adequate follow up.

10. Patients who have undergone cranial irradiation for brain metastases more than 4 weeks before inclusion in our protocol, provided that they are clinically fit to undergo second line treatment

Exclusion Criteria:

1. Pregnant or lactating women.

2. Patients with medical risks because of non-malignant disease as well as those with active uncontrolled infection.

3. Documented brain metastases unless the patient has completed local therapy for central nervous system metastases at least 4 weeks before enrollment and has been off corticosteroids for at least two weeks before enrollment. Prophylactic irradiation at least 4 weeks prior to enrollment is accepted.

4. Maintenance treatment with erlotinib or other TKI (Tyrosine Kinase Inhibitor), or docetaxel. Maintenance treatment with pemetrexed is allowed. Previous treatment with an EGFR-TKI or docetaxel within 6 months prior to enrollment.

5. Inability or unwillingness to take dexamethasone.

6. Concomitant treatment with any other experimental drug under investigation.

7. Patients experiencing disease progression within 2 months after the start of platinum based chemotherapy