AZD2171 in Treating Patients With Recurrent Ovarian, Peritoneal, or Fallopian Tube Cancer

National Cancer Institute (NCI)

Status and phase

Completed

Phase 2

Conditions

Stage I Ovarian Epithelial Cancer

Primary Peritoneal Serous Adenocarcinoma

Stage II Ovarian Epithelial Cancer

Recurrent Ovarian Epithelial Cancer

Fallopian Tube Cancer

Treatments

Drug: cediranib maleate

Study type

Interventional

Funder types

NIH

Identifiers

NCT00275028

NCI-2013-00036

U01CA062490 (U.S. NIH Grant/Contract)

05-170 (Other Identifier)

Details and patient eligibility

About

This phase II trial is studying how well AZD2171 works in treating patients with recurrent ovarian, peritoneal, or fallopian tube cancer. AZD2171 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor

Full description

PRIMARY OBJECTIVES:

I. To determine the efficacy of AZD2171 in platinum sensitive and platinum insensitive disease, based on either RECIST criteria (for patients with measurable cancer radiographically) or clinical response benefit (modified Gynecologic Cancer Intergroup [GCIG] CA-125 response or stable disease for at least 16 weeks).

SECONDARY OBJECTIVES:

I. To assess progression-free survival. II. To assess modified GCIG CA-125 response rate. III. To assess duration of modified GCIG CA-125 response. IV. To assess the safety of the recommended phase 2 dose of AZD2171 in this asymptomatic patient population.

V. To explore the pharmacodynamic effects of AZD2171 by correlating clinical outcomes with an angiogenic profile derived from serial assessments of soluble VEGFR2, circulating endothelial cell levels, and VEGFR phosphorylation in circulating endothelial cells.

VI. To explore pharmacogenetic differences in kdr/flk-1, HIF1alpha, p53, and endothelial nitric oxide synthase (eNOS) in PBMCs from subjects who consent separately for pharmacogenetic studies.

VII. To determine whether oncogenic mutations predict response to AZD2171.

OUTLINE: This is a multicenter study. Patients are stratified according to disease sensitivity (platinum-sensitive disease vs platinum-insensitive disease).

Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed periodically for up to 2 years.

PROJECTED ACCRUAL: A total of 71 patients will be accrued for this study.

Enrollment

47 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

must have histologically or cytologically confirmed epithelial ovarian cancer, primary peritoneal serous cancer, or fallopian tube cancer
must have either measurable cancer by RECIST criteria or an elevated CA125
Subjects must be asymptomatic or minimally symptomatic
Prior therapy:
- Prior chemotherapy must have included a first-line platinum-based regimen only
- Prior hormonal-based therapy for ovarian, primary peritoneal serous or fallopian tube cancer is acceptable
- Up to two prior lines of chemotherapy in the recurrent setting are allowed
- Toxic side effects related to prior chemotherapy or hormonal therapy must have resolved to less than or equal to grade 1 or to baseline (excluding alopecia), or for peripheral neuropathy to less than or equal to grade 2
- Subjects may begin AZD2171 at least 3 weeks after their last dose of chemotherapy or hormonal therapy
Life expectancy of greater than 6 months
ECOG performance status 0-1 (Karnofsky >= 70%)
must have lab values within normal institutional limits
eligibility of patients receiving any medications or substances known to affect or with the potential to affect the activity or PK of AZD2171 will be determined following review of their case by the Principal Investigator
Subjects with treated limited stage basal cell or squamous cell carcinoma of the skin or carcinoma in situ of the breast or cervix are eligible; subjects with stage I or II cancer treated with a curative intent are also eligible with no evidence of recurrent disease
No evidence of preexisting uncontrolled hypertension; if patient has hypertension, it must be medically controlled
AZD2171 has been shown to terminate fetal development in the rat, as expected for a process dependent on VEGF signaling; for this reason, women of child-bearing potential must have a negative pregnancy test prior to study entry; must agree to use adequate contraception; should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately
Ability to understand and the willingness to sign a written informed consent document- No therapeutic anticoagulation; the use of low dose warfarin (1 mg/day), intermittent doses of tPA (2 mg x 1), or heparin flushes to prophylax against central venous catheter-associated clots is permitted
Measurable or non-measurable disease on CT scan or MRI
Consider patients who have the following risk factors to be at increased risk; these patients should have increased monitoring:
- Prior treatment with anthracyclines
- Prior treatment with trastuzumab
- A New York Heart Association classification of II controlled with treatment
- Prior central thoracic radiation therapy (RT), including RT to the heart
- History of myocardial infarction within 12 months

Exclusion criteria

Patients who have had chemotherapy, radiotherapy, or major surgery within 3 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or those who have not recovered from adverse events due to agents administered more than 3 weeks earlier
Patients may not be receiving any other investigational agents nor have participated in an investigational trial within the past 3 weeks; subjects may not have received prior treatment affecting the VEGF pathway; subjects may not have received prior treatment with antibodies that may interfere with CA-125 measurements; subjects may not have received intraperitoneal therapy within the 4 weeks prior to starting AZD2171 and/or the treating physician must confirm the patient has recurrent disease
Patients may not be receiving any medication that may markedly affect renal function
Patients with known brain metastases should be excluded from this clinical trial because of their poor prognosis
History of allergic reactions attributed to compounds of similar chemical or biologic composition to AZD2171
Mean QTc > 500 msec (with Bazett's correction) in screening electrocardiogram or history of familial long QT syndrome
Uncontrolled intercurrent illness
Pregnant women are excluded from this study because AZD2171 is a VEGF inhibitor with known abortifacient effects; breastfeeding should be discontinued if the mother is treated with AZD2171
Major surgical procedure or medical interference with the peritoneum or pleura within 4 weeks of baseline CA-125 assessments
Subjects with a history of an active malignancy during the last 3 years except non-melanomatous skin cancer , in situ breast or cervical cancer or stage I or II cancer treated with a curative intent and no active cancer recurrence
HIV-positive patients on combination antiretroviral therapy are ineligible because of the potential for pharmacokinetic interactions with AZD2171
No therapeutic anti-coagulation; prophylaxis against central venous catheter-associated clots is permitted
A New York Heart Association classification of III or IV
Conditions requiring concurrent use of drugs or biologics with proarrhythmic potentiate