Temsirolimus in Treating Patients With Refractory or Recurrent Ovarian Epithelial, Fallopian Tube, or Primary Peritoneal Cancer

National Cancer Institute (NCI)

Status and phase: Completed; Phase 2

Conditions: Primary Peritoneal Cavity Cancer; Recurrent Ovarian Epithelial Cancer; Fallopian Tube Cancer

Treatments: Drug: temsirolimus

Study type: Interventional

Funder types: NETWORK; NIH

Identifiers

NCT00429793

U10CA027469 (U.S. NIH Grant/Contract)

GOG-0170I (Other Identifier)

NCI-2012-02707 (Registry Identifier)

CDR0000528257

Details and patient eligibility

About

This phase II trial is studying the side effects and how well temsirolimus works in treating patients with refractory or recurrent ovarian epithelial cancer, fallopian tube cancer, or primary peritoneal cancer. Temsirolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

Full description

OBJECTIVES: Primary I. Determine the 6-month progression-free survival (PFS) or objective tumor response in patients with refractory or recurrent ovarian epithelial, fallopian tube, or primary peritoneal cavity cancer treated with temsirolimus.

II. Determine the toxicity of this drug in these patients.

Secondary I. Determine the duration of PFS and overall survival of these patients.

OUTLINE: This is a nonrandomized, multicenter study.

Patients receive temsirolimus IV over 30 minutes on days 1, 8, 15, and 22. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed every 3 months for 2 years and then every 6 months for 3 years.

PROJECTED ACCRUAL: A total of 52 patients will be accrued for this study.

Enrollment: 60 patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Histologically confirmed ovarian epithelial, fallopian tube or primary peritoneal cavity cancer

  • Recurrent or refractory

• Prior treatment with ≥ 1 platinum-based chemotherapeutic regimen for management of primary disease (containing carboplatin, cisplatin, or another organoplatinum compound) required

  • Initial treatment may have included any of the following:

    • High-dose therapy
    • Intraperitoneal therapy
    • Consolidation therapy
    • Noncytotoxic agents
    • Extended therapy administered after surgical or nonsurgical assessment

  • Patients must meet ≥ 1 of the following criteria:

    • Treatment-free interval after platinum therapy of < 12 months for patients who received only 1 platinum-based regimen
    • Progressed during platinum-based therapy
    • Refractory disease after a platinum-based regimen

• Measurable disease, defined as ≥ 1 unidimensionally measurable lesion ≥ 20 mm by conventional techniques OR ≥ 10 mm by spiral CT scan

  • Must have ≥ 1 target lesion

    • Tumors within a previously irradiated field will be designated as "non-target" lesions unless progression is documented or a biopsy is obtained ≥ 90 days after completion of radiotherapy

• Not eligible for a higher priority GOG protocol, if one exists

• GOG performance status (PS) 0-2 for patients who have receive one prior regimen OR GOG PS 0-1 for patients who have received 2-3 prior regimens

• Absolute neutrophil count ≥ 1,500/mm³

• Platelet count ≥ 100,000/mm³

• Creatinine ≤ 1.5 times upper limit normal (ULN)

• Bilirubin ≤ 1.5 times ULN

• AST ≤ 2.5 times ULN

• Alkaline phosphatase ≤ 2.5 times ULN

• No neuropathy (sensory and motor) > grade 2

• Fasting cholesterol < 350 mg/dL

• Fasting triglycerides < 400 mg/dL

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• No active infection requiring antibiotics (with the exception of uncomplicated UTI)

• No other invasive malignancies within the past 5 years, except for non-melanoma skin cancer, breast cancer, or head and neck cancer

• See Disease Characteristics

• Recovered from prior surgery, radiotherapy, or chemotherapy

• At least 1 week since prior hormonal therapy directed at the malignant tumor

• At least 3 years since prior radiotherapy for localized cancer of the breast, head and neck, or skin

  • Patient must remain free of recurrent or metastatic disease

• At least 3 years since prior adjuvant chemotherapy for localized breast cancer

  • Patient must remain free of recurrent or metastatic disease

• At least 3 weeks since other prior therapy directed at the malignant tumor, including immunologic agents

• No prior temsirolimus

• No prior cancer treatment that would preclude study therapy

• No prior radiotherapy to > 25% of marrow-bearing areas

• No prior radiotherapy to any portion of the abdominal cavity or pelvis, except for the treatment of ovarian cancer

• No prior non-cytotoxic therapy for management of recurrent or persistent ovarian disease, except for therapy that was part of the primary treatment regimen

• Two additional cytotoxic regimens (defined as any agent that targets the genetic and/or mitotic apparatus of dividing cells, resulting in dose-limiting toxicity to the bone marrow and/or gastrointestinal mucosa) for management of recurrent or persistent ovarian disease allowed

• Concurrent low molecular weight heparin allowed provided PT/INR ≤ 1.5

• Concurrent hormone replacement therapy allowed

• No concurrent amifostine or other protective reagents

• No concurrent prophylactic filgrastim (G-CSF)

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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60 participants in 1 patient group

Treatment (temsirolimus)

Experimental group

Description:

Patients receive temsirolimus IV over 30 minutes on days 1, 8, 15, and 22. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

Treatment:

Drug: temsirolimus