Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Seagen Inc.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Patients with pathologically confirmed NSCLC which is metastatic or recurrent (non-resectable), who have failed at least one but no more than two prior therapies for advanced stage disease or have a recurrence within 6 months of completing adjuvant chemotherapy.
Lewis-y antigen expression documented by immunohistochemistry for all patients.
Patients must have:
Bidimensionally or unidimensionally measurable disease on the basis of physical exam or imaging studies, or
Evaluable disease: bone metastases defined on bone scan or malignant pleural effusion
Performance status ≤ 2 (ECOG scale) with a life expectancy of at least 3 months
Patients must be at least four weeks from prior treatment (chemotherapy, hormonal therapy, or definitive radiotherapy)
You may not be if
Prior therapy with TAXOTERE (docetaxel)
Cumulative anthracycline exposure \> 300 mg/m2.
More than one primary malignancy with the exception of:
Non-melanoma skin cancer
In situ carcinoma of the cervix
Localized prostate cancer
Completely resected stage I or II disease with no evidence of recurrent cancer from which the patient has remained disease free for more than 3 years.
Concomitant therapy with other anti-neoplastic agents or experimental agents except for small volume radiation to a solitary bony metastasis.
Active viral, bacterial or systemic fungal infections including known HIV or Hepatitis B or C.
Women who are pregnant or breastfeeding
Any serious underlying medical condition, which would impair the ability of the patient to receive the planned treatment including prior allergic reactions to recombinant human or murine proteins.
Dementia or altered mental status that would prohibit the understanding and rendering of informed consent.
Patients with uncontrolled peptic ulcer disease will be excluded.
