Gemcitabine in Treating Patients With Recurrent or Persistent Endometrial Cancer

Gynecologic Oncology Group (GOG)

Status and phase: Completed; Phase 2

Conditions: Endometrial Adenocarcinoma; Endometrial Clear Cell Adenocarcinoma; Recurrent Uterine Corpus Carcinoma; Endometrial Adenosquamous Carcinoma

Treatments: Drug: Gemcitabine Hydrochloride

Study type: Interventional

Funder types: NETWORK; NIH

Identifiers

NCT00820898

U10CA027469 (U.S. NIH Grant/Contract)

NCI-2009-01175 (Registry Identifier)

GOG-0129Q

CDR0000631591

Details and patient eligibility

About

This phase II trial is studying the side effects of gemcitabine and to see how well it works in treating patients with recurrent or persistent endometrial cancer. Drugs used in chemotherapy, such as gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing.

Full description

PRIMARY OBJECTIVES:

I. To estimate the antitumor activity of gemcitabine hydrochloride in patients with persistent or recurrent endometrial adenocarcinoma who have failed higher priority treatment protocols.

II. To determine the nature and degree of toxicity of this drug in these patients.

OUTLINE: This is a multicenter study.

Patients receive gemcitabine hydrochloride IV over 30 minutes on days 1 and 8. Courses repeat every 21 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.

Enrollment: 24 patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Histologically confirmed endometrial adenocarcinoma

  • Recurrent or persistent disease
  • Refractory to curative therapy or established treatments

• The following epithelial cell types are eligible:

  • Endometrioid adenocarcinoma
  • Serous adenocarcinoma
  • Undifferentiated carcinoma
  • Clear cell adenocarcinoma
  • Mixed epithelial carcinoma
  • Adenocarcinoma not otherwise specified
  • Mucinous adenocarcinoma
  • Squamous cell carcinoma
  • Transitional cell carcinoma
  • Mesonephric carcinoma

• Measurable disease, defined as ≥1 lesion that can be accurately measured in ≥ 1 dimension as ≥ 20 mm by conventional techniques, including palpation, plain x-ray, CT scan, or MRI OR as ≥ 10 mm by spiral CT scan

• Must have ≥ 1 target lesion

  • Tumors within a previously irradiated field are designated as target lesions provided there is documented disease progression or biopsy confirmed persistent disease ≥ 90 days after completion of radiotherapy

• Must have received 1 prior chemotherapeutic regimen for management of endometrial cancer

  • Initial treatment may have included non-cytotoxic agents or high-dose therapy, consolidation therapy, or extended therapy administered after surgical or non-surgical assessment

    • No more than one prior cytotoxic chemotherapy regimen (either with single or combination cytotoxic drug therapy)

      • One additional non-cytotoxic regimen for management of recurrent or persistent disease is allowed

• Not eligible for a higher priority GOG protocol, if one exists (i.e., any active Phase III GOG protocol for the same patient population)

• GOG performance status 0-2

• ANC ≥ 1,500/mm³

• Platelet count ≥ 100,000/mm³

• Creatinine ≤ 1.5 times upper limit of normal (ULN)

• Bilirubin ≤ 1.5 times ULN

• AST and ALT ≤ 2.5 times ULN

• Alkaline phosphatase ≤ 2.5 times ULN

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception during and for ≥ 3 months after completion of study treatment

• No neuropathy (sensory and motor) > grade 1, according to NCI CTCAE v3.0

• No active infection requiring antibiotics (except an uncomplicated urinary tract infection)

• No other invasive malignancies within the past 5 years except non-melanoma skin cancer

• No prior cancer treatment that contraindicates study therapy

• Recovered from prior surgery, radiotherapy, or chemotherapy

• At least 1 week since prior hormonal therapy for endometrial cancer

• At least 3 weeks since prior biological therapy, immunotherapy, or other therapy for endometrial cancer

• At least 4 weeks since prior radiotherapy

• More than 3 years since prior radiotherapy for localized breast cancer, head and neck cancer, or skin cancer and

  • No recurrent or persistent breast cancer, head and neck cancer, or skin cancer

• More than 3 years since prior adjuvant chemotherapy for localized breast cancer

  • No recurrent or metastatic breast cancer

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

• No prior chemotherapy for any abdominal or pelvic tumor except for the treatment of endometrial cancer

• No prior gemcitabine hydrochloride

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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24 participants in 1 patient group

Arm I

Experimental group

Description:

Patients receive gemcitabine hydrochloride IV over 30 minutes on days 1 and 8. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

Treatment:

Drug: Gemcitabine Hydrochloride