Adjuvant Radiation Therapy With Ifosfamide in Patients With Mixed Mesodermal Tumors of the Uterus

Uterine sarcomas account for only 2-4% of uterine malignancies, yet they are responsible for
26% of uterine cancer deaths. Mixed mesodermal tumors (MMT), previously known as
carcinosarcoma, are the most common of the uterine sarcomas in the United States. Prognosis
for these patients is generally grim due to the propensity for early metastatic disease.
Patterns of spread are by both hematogenous and lymphatic dissemination. It has been noted
that 66% of patients with disease clinically confined to the uterus have nodal metastasis at
the time of diagnosis. The majority of patients will die with both wide spread
intra-abdominal and pelvic disease within two years of diagnosis.

Adjuvant pelvic radiation therapy has been advantageous in controlling local recurrence. One
study reports 26% local recurrence in patients treated with surgery alone versus 14%
recurrence in patients treated with surgery and adjuvant pelvic radiation. Although adjuvant
radiation shows a benefit in improving local control, it has not been found to impact
survival. This finding is likely attributed to the high incidence of distant metastasis (85%)
known to occur with disease recurrence.

Multiple chemotherapeutic agents have been evaluated in the management of advanced,
persistent or recurrent uterine MMT. Response to single agent therapy has been less than 35%
with the most active agents identified being ifosfamide (response rate = 34.8%) and cisplatin
(response rate 17.9%. The use of chemotherapy in the adjuvant setting has been explored as a
means of attempting to impact the incidence of distant metastasis.

Inclusion Criteria:

- Histologically documented mixed mesodermal tumor (MMT) of uterus with no visible
residual disease.

- Surgical staging to include total abdominal hysterectomy, bilateral
salpingo-oophorectomy, peritoneal washings, and lymph node sampling.

- Surgical staging should be completed 6 weeks ± 7 days prior to enrollment.

- Age >= 18 years.

- Written voluntary informed consent.

Exclusion Criteria:

- Patient has impairment of hepatic, renal or hematologic function as defined by the
following baseline laboratory values:

- Total serum bilirubin >1.5mg/dl

- History of chronic or active hepatitis

- Serum creatinine >2.0 mg/dl

- Platelets <100,000/mm3

- Absolute neutrophil count (ANC) <1500/mm3

- Hemoglobin <8.0 g/dl (the patient may be transfused prior to study entry)

- Patient has severe or uncontrolled medical disease (eg. uncontrolled diabetes,
unstable angina, myocardial infarction within 6 months, congestive heart failure,
etc.)

- Patient has been treated with myelosuppressive chemotherapy within three weeks prior
to study entry.

- Patients with any prior chemotherapy or radiotherapy for pelvic malignancy.

- Patients with dementia or altered mental status that would prohibit the giving and
understanding of informed consent at time of study entry.

- Patient has a uterine sarcoma other then mixed mesodermal tumor (MMT).