Trial Information

A Phase II Study of the Association of Glivec® (Imatinib Mesylate, Formerly Known as STI 571) Plus Gemzar® (Gemcitabine) in Patients With Unresectable, Refractory, Malignant Mesothelioma Expressing Either PDGFR-Beta or C-Kit

TITLE "A phase II study of the association of Glivec® (Imatinib mesylate, formerly known as
STI 571) plus Gemzar® (Gemcitabine) in patients with unresectable, refractory, malignant
mesothelioma expressing either PDGFR-beta or C-Kit"

PURPOSE Primary objective of the phase II

➢ Efficacy, i.e., response rate to study drugs

Secondary objectives of the phase II

- Duration of response

- Time to progression

- Toxicity profile

- Overall survival

PRIMARY VARIABLE The primary efficacy variable for the phase II part of the study is Best
Overall Tumor Response, evaluated using the "Modified RECIST criteria for assessment of
response in malignant pleural mesothelioma"

SECONDARY VARIABLES

- Progression-free survival (PFS) form 1st administration onwards

- Overall survival

- Safety criteria, according to NCI-CTC criteria version 3.0

EFFICACY Objective tumor response assesed using the "Modified RECIST criteria for assessment
of response in malignant pleural mesothelioma" SAFETY

- Adverse events

- Vital signs

- Clinical and biohumoral findings

TREATMENT SCHEDULE

- Gemzar 500 mg/m2, i.v., days 1 and 8 of a 21-days schedule, plus

- Glivec 400 mg/die., per os

STATISTICAL DESIGN The study follows a two-stage design, according to the Simon model. We
assume that with a response rate of 5% (H0) or less the drug is likely to be ineffective,
and also, that, for the drug to be effective, a target response rate of 15% (H1) is
required. With a probability errors alfa of 5% and beta 20%, the calculated sample size is
as reported in "PLANNED NUMBER OF PTS."

PLANNED NUMBER OF PTS. 23 or 56 patients, evaluable for efficacy. The number depends on the
response rate. When 2 or more objective responses, i.e., CR or PR, are observed in the first
23 patients, the total number of patients will be increased to 56, otherwise the study will
be stopped

STATISTICAL EVALUATION Efficacy and safety variables will be evaluated descriptively.
Indeed, ORR estimates and its exact 95% confidence interval will be calculated. Kaplan-Meier
method will be used to estimate duration of response, PFS and OS

DURATION OF TREATMENT All patients are scheduled to receive at least two cycles of
chemotherapy unless there is unacceptable toxicity, progressive disease, or the patient
requires or asks for withdrawal from the study Responding patients will receive treatment
for 6 cycles or earlier if progression or unbearable toxicity Disease status will be
re-evaluated every two cycles, using the same imaging procedures used at baseline, i.e., CT
or NMR

INCLUSION CRITERIA

- Age of > 18 years and < 72 years

- Patients with a histologically proven malignant mesothelioma of the pleura or of the
peritoneum, expressing either PDFGR-beta or C-Kit by immunochemistry (ICH)

- Locally advanced disease, unsuitable for curative surgical resection, or metastatic
disease

- Confirmed progression of the disease according to modified REcist-criteria, documented
after a first-line, systemic (premetrex+cisplatin regimen) or local treatment (i.e.,
intrapleuric)

- ECOG Performance Status of 0, 1 or 2

- Life expectancy of at least 3 months

- Capability of understanding the objectives of the study and giving written informed
consent

- Willingness and ability to comply with study requirements

- Sufficient caloric and fluid intake, including patients under enteral or parenteral
nutrition

EXCLUSION CRITERIA

- Co-existing tumors of different histologic origin, except non melanomatous localized
skin cancer and/or in situ cervical carcinoma

- A history of earlier tumors of different histologic origin being in complete remission
since less than 5 years

- Unresolved toxicity from prior antitumor treatment(s)

- Primary peritoneal mesothelioma

- Any of the following abnormal baseline hematological values:

- Hb < 9 g/dL

- WBC < 3 x 109/L

- Neutrophils < 1.5 x 109/L

- Platelets < 100 x 109/L

- Serum bilirubin > 2.5 mg/dL

- ALAT and ASAT > 3 x UNL (unless due to liver metastases)

- Serum creatinine > 1.5 mg/dL

- Clinically relevant cardiovascular disease, i.e., myocardial infarction or other severe
coronary artery diseases within the prior 6 months, cardiac arrythmia requiring
medication, uncontrolled hypertension, overt cardiac failure or non compensated chronic
heart disease in NYHA class II or more

- History of psychiatric disabilities, potentially interfering with the capability of
giving adequate informed consent

- Pregnant or lactating women or inability/unwillingness to practice a medically approved
method of contraception during study period (including 3 months following the end of
treatment)

- Uncontrolled active infections

- Any condition which, in the judgement of the Investigator, would place the patient at
undue risk or interfere with the results of the study