Gemcitabine in Treating Patients With Recurrent or Persistent Endometrial Cancer
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| ClinicalTrials.gov Identifier: NCT00820898 |
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Recruitment Status :
Completed
First Posted : January 12, 2009
Results First Posted : December 5, 2017
Last Update Posted : December 29, 2017
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Endometrial Adenocarcinoma Endometrial Adenosquamous Carcinoma Endometrial Clear Cell Adenocarcinoma Recurrent Uterine Corpus Carcinoma | Drug: Gemcitabine Hydrochloride | Phase 2 |
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.
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 24 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | A Phase II Evaluation of Gemcitabine (Gemzar®, LY188011) in the Treatment of Recurrent or Persistent Endometrial Carcinoma |
| Study Start Date : | February 2009 |
| Actual Primary Completion Date : | January 2011 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Arm I
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.
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Drug: Gemcitabine Hydrochloride
Given IV
Other Names:
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- Proportion of Patients With Objective Tumor Response Rate (Complete Response [CR] or Partial Response [PR]) Using RECIST Version 1.0 [ Time Frame: CT scan or MRI if used to follow lesion for measurable disease every other cycle until disease progression for up to 5 years. ]RECIST 1.0 defines complete response as the disappearance of all target lesions and non-target lesions and no evidence of new lesions documented by two disease assessments at least 4 weeks apart. Partial response is defined as at least a 30% decrease in the sum of longest dimensions (LD) of all target measurable lesions taking as reference the baseline sum of LD. There can be no unequivocal progression of non-target lesions and no new lesions. Documentation by two disease assessments at least 4 weeks apart is required. In the case where the ONLY target lesion is a solitary pelvic mass measured by physical exam, which is not radiographically measurable, a 50% decrease in the LD is required. These patients will have their response classified according to the definitions stated above. Complete and partial responses are included in the objective tumor response rate.
- Incidence of Adverse Effects as Assessed by Common Terminology Criteria for Adverse Events Version 3.0 [ Time Frame: Assessed every cycle while on treatment, 30 days after the last cycle of treatment, and up to 5 years in follow-up ]
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
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Histologically confirmed endometrial adenocarcinoma
- Recurrent or persistent disease
- Refractory to curative therapy or established treatments
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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
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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
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Must have received 1 prior chemotherapeutic regimen for management of endometrial cancer
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Initial treatment may have included non-cytotoxic agents or high-dose therapy, consolidation therapy, or extended therapy administered after surgical or non-surgical assessment
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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
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- 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
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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
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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
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00820898
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| Principal Investigator: | David Tait | Gynecologic Oncology Group |
| Responsible Party: | Gynecologic Oncology Group |
| ClinicalTrials.gov Identifier: | NCT00820898 |
| Other Study ID Numbers: |
GOG-0129Q NCI-2009-01175 ( Registry Identifier: CTRP (Clinical Trial Reporting Program) ) GOG-0129Q CDR0000631591 GOG-0129Q ( Other Identifier: Gynecologic Oncology Group ) GOG-0129Q ( Other Identifier: CTEP ) U10CA027469 ( U.S. NIH Grant/Contract ) |
| First Posted: | January 12, 2009 Key Record Dates |
| Results First Posted: | December 5, 2017 |
| Last Update Posted: | December 29, 2017 |
| Last Verified: | May 2015 |
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Carcinoma Adenocarcinoma Adenocarcinoma, Clear Cell Carcinoma, Adenosquamous Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms Neoplasms, Complex and Mixed Gemcitabine Antimetabolites, Antineoplastic |
Antimetabolites Molecular Mechanisms of Pharmacological Action Antineoplastic Agents Antiviral Agents Anti-Infective Agents Enzyme Inhibitors Immunosuppressive Agents Immunologic Factors Physiological Effects of Drugs |