Phase II Clinical Trial On Taxol As Single Agent In Locally Advanced And/Or Metastatic Or Recurrent Vulva Cancer Not Amenable For Surgery And/Or Radiotherapy

Inclusion Criteria

DISEASE CHARACTERISTICS:

- Histologically confirmed squamous cell carcinoma of the vulva

- Not suitable for radiotherapy or surgery as first-line treatment

- Measurable or evaluable disease

- At least 1 bidimensionally measurable target lesion

- Measurable metastatic disease outside previously irradiated areas OR

- Local recurrence within a previously treated area OR

- Local lesions showing progression while on treatment

- No brain metastasis

PATIENT CHARACTERISTICS:

Age:

- 18 and over

Performance status:

- WHO 0-2

- ECOG 0-2

Life expectancy:

- At least 3 months

Hematopoietic:

- Not specified

Hepatic:

- Bilirubin no greater than 1.5 mg/dL

- AST/ALT less than 2 times upper limit of normal

Renal:

- Creatinine clearance greater than 60 mL/min

Cardiovascular:

- No prior or concurrent cardiac disease (i.e., uncontrolled high blood pressure,
unstable angina, congestive heart failure, myocardial infarction within the past
year, cardiac ventricular arrhythmia requiring medication, or 2nd or 3rd degree heart
block)

Other:

- No peripheral neuropathy greater than grade 1

- No serious active infection

- No prior allergic reaction to drugs containing Cremophor EL

- No other serious medical, psychological, familial, or social condition that would
preclude study

- Not pregnant or nursing

- Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy:

- Not specified

Chemotherapy:

- No prior chemotherapy except as concurrent therapy with radiotherapy

Endocrine therapy:

- Not specified

Radiotherapy:

- See Disease Characteristics

- See Chemotherapy

- No concurrent radiotherapy

Surgery:

- Not specified