Comparison of Two Combination Chemotherapy Regimens Plus Radiation Therapy in Treating Patients With Stage III or Stage IV Endometrial Cancer

Gynecologic Oncology Group (GOG)

Status and phase: Completed; Phase 3

Conditions: Endometrial Adenocarcinoma; Endometrial Endometrioid Adenocarcinoma, Variant With Squamous Differentiation; Endometrial Serous Adenocarcinoma; Endometrial Clear Cell Adenocarcinoma; Stage III Uterine Corpus Cancer; Endometrial Adenosquamous Carcinoma

Treatments: Drug: Cisplatin; Drug: Doxorubicin Hydrochloride; Biological: Pegfilgrastim; Drug: Paclitaxel; Biological: Filgrastim

Study type: Interventional

Funder types: NETWORK; NIH

Identifiers

NCT00006011

U10CA027469 (U.S. NIH Grant/Contract)

ECOG-G0184

NCI-2012-02350 (Registry Identifier)

GOG-0184 (Other Identifier)

RTOG-EN0130

CDR0000068020

Details and patient eligibility

About

Randomized phase III trial to compare the effectiveness of two combination chemotherapy regimens plus radiation therapy in treating patients who have stage III or stage IV endometrial cancer. Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one chemotherapy drug with radiation therapy may kill more tumor cells. It is not yet known which combination chemotherapy regimen plus radiation therapy is more effective for endometrial cancer.

Full description

OBJECTIVES:

I. Compare survival and progression-free survival in patients with stage III endometrial carcinoma treated with tumor volume-directed pelvic radiotherapy with or without paraaortic radiotherapy followed by cisplatin and doxorubicin with or without paclitaxel.

II. Compare short and long-term toxic effects of these treatment regimens in this patient population.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to radiotherapy field (pelvic vs extended field). Within 8 weeks after surgery, patients receive tumor volume-directed pelvic radiotherapy with or without paraaortic nodal radiotherapy once daily for 5 consecutive days for up to 16 weeks after surgery. Within 8 weeks of completing radiotherapy, patients are randomized to 1 of 2 chemotherapy treatment arms.

Arm I: Patients receive doxorubicin IV over 30 minutes immediately followed by cisplatin IV over 1 hour on day 1. Patients also receive filgrastim (G-CSF) subcutaneously (SC) or pegfilgrastim on days 2-11.

Arm II: Patients receive doxorubicin and cisplatin as in arm I, paclitaxel IV over 3 hours on day 2, and G-CSF SC or pegfilgrastim on days 3-12. Treatment repeats every 3 weeks for a maximum of 6 courses in the absence of disease progression or unacceptable toxicity.

Patients are followed every 3 months for 2 years, every 6 months for 3 years, and then annually thereafter.

PROJECTED ACCRUAL: A total of 614 patients (307 per treatment arm) will be accrued for this study within 5.2 years.

Enrollment: 659 patients

Sex: Female

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Histologically confirmed advanced endometrial carcinoma with any histology, including:

  • Clear cell and serous papillary carcinoma

• Surgical stage III disease, including:

  • Positive adnexa
  • Tumor invading the serosa
  • Positive pelvic and/or paraaortic nodes
  • Involvement of bowel mucosa
  • Intraabdominal metastases
  • Positive pelvic washings
  • Vaginal involvement within the radiation port

• Must have had prior surgery, including hysterectomy and bilateral salpingo-oophorectomy

  • Tumor maximally debulked to a maximum residual diameter of no greater than 2 cm

  • Paraaortic lymph node sampling allowed

    • If positive, must have negative chest CT scan

• No recurrent disease

• No parenchymal liver metastases

• No disease outside the abdomen

• Performance status - GOG 0-2

• At least 3 months

• Absolute neutrophil count at least 1,500/mm^3

• Platelet count at least 100,000/mm^3

• Bilirubin no greater than 1.5 times normal

• SGOT/SGPT no greater than 3 times normal

• Alkaline phosphatase no greater than 3 times normal

• Creatinine no greater than 1.6 mg/dL

• LVEF at least 50% within 6 months of study entry

• No other prior or concurrent malignancy within the past 5 years except adequately treated nonmelanoma skin cancer

• No serious comorbid illness that would preclude study participation

• No prior chemotherapy

• See Disease Characteristics

• No prior pelvic or abdominal radiotherapy

• No prior radiotherapy for prior malignancy

• See Disease Characteristics

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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659 participants in 2 patient groups

Arm I (doxorubicin, cisplatin, filgrastim, pegfilgrastim)

Experimental group

Description:

Patients receive doxorubicin IV over 30 minutes immediately followed by cisplatin IV over 1 hour on day 1. Patients also receive filgrastim (G-CSF) SC or pegfilgrastim on days 2-11.

Treatment:

Drug: Cisplatin

Drug: Doxorubicin Hydrochloride

Biological: Filgrastim

Biological: Pegfilgrastim

Arm II (doxorubicin, cisplatin, paclitaxel, filgrastim)

Experimental group

Description:

Patients receive doxorubicin and cisplatin as in arm I, paclitaxel IV over 3 hours on day 2, and G-CSF SC or pegfilgrastim on days 3-12. Treatment repeats every 3 weeks for a maximum of 6 courses in the absence of disease progression or unacceptable toxicity.

Treatment:

Drug: Cisplatin

Drug: Doxorubicin Hydrochloride

Drug: Paclitaxel

Biological: Filgrastim

Biological: Pegfilgrastim