Elesclomol Sodium and Paclitaxel in Treating Patients With Recurrent or Persistent Ovarian Epithelial Cancer, Fallopian Tube Cancer, or Primary Peritoneal Cancer



Status:Recruiting
Conditions:Ovarian Cancer, Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:4/2/2016
Start Date:December 2010

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A Phase II Evaluation of Elesclomol Sodium and Weekly Paclitaxel in the Treatment of Recurrent or Persistent Platinum-Resistant Ovarian,Fallopian Tube or Primary Peritoneal Cancer

This phase II trial studies how well giving elesclomol sodium together with paclitaxel works
in treating patients with recurrent or persistent ovarian epithelial cancer, fallopian tube
cancer, or primary peritoneal cancer. Drugs used in chemotherapy, such as elesclomol sodium
and paclitaxel, work in different ways to stop the growth of tumor cells, either by killing
the cells or by stopping them from dividing. Giving elesclomol together with paclitaxel may
kill more tumor cells.

PRIMARY OBJECTIVES:

I. To estimate the antitumor activity of elesclomol (elesclomol sodium) and paclitaxel in
patients with persistent or recurrent ovarian, fallopian tube, or primary peritoneal cancer
primarily through the frequency of objective tumor responses.

II. To determine the nature and degree of toxicity of elesclomol and paclitaxel in these
patients.

SECONDARY OBJECTIVES:

I. To estimate the progression-free survival and overall survival of patients treated with
elesclomol and paclitaxel.

OUTLINE:

Patients receive elesclomol sodium intravenously (IV) over 1 hour and paclitaxel IV over 1
hour on days 1, 8, and 15. 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.

Inclusion Criteria:

- Patients must have recurrent or persistent epithelial ovarian, fallopian tube or
primary peritoneal carcinoma; histologic documentation of the original primary tumor
is required via the pathology report

- Patients with the following histologic epithelial cell types are eligible:
serous adenocarcinoma, endometrioid adenocarcinoma, mucinous adenocarcinoma,
undifferentiated carcinoma, clear cell adenocarcinoma, mixed epithelial
carcinoma, transitional cell carcinoma, malignant Brenner's Tumor, or
adenocarcinoma not otherwise specified (N.O.S.)

- All patients must have measurable disease as defined by Response Evaluation Criteria
in Solid Tumors (RECIST) 1.1; measurable disease is defined as at least one lesion
that can be accurately measured in at least one dimension (longest diameter to be
recorded); each lesion must be >= 10 mm when measured by computed tomography (CT),
magnetic resonance imaging (MRI) or caliper measurement by clinical exam; or >= 20 mm
when measured by chest x-ray; lymph nodes must be >= 15 mm in short axis when
measured by CT or MRI

- Patients must have at least one "target lesion" to be used to assess response on this
protocol as defined by RECIST 1.1; tumors within a previously irradiated field will
be designated as "non-target" lesions unless progression is documented or a biopsy is
obtained to confirm persistence at least 90 days following completion of radiation
therapy

- Patients must not be eligible for a higher priority Gynecologic Oncology Group (GOG)
protocol, if one exists; in general, this would refer to any active GOG Phase III
protocol for the same patient population

- Patients must have a GOG performance status of 0, 1, or 2

- Patients must have baseline lactate dehydrogenase (LDH) levels =< 0.8 times upper
limit of normal (ULN)

- Recovered from prior surgery, radiotherapy, or chemotherapy

- Patients should be free of active infection requiring antibiotics (with the
exception of uncomplicated urinary tract infection [UTI])

- Any hormonal therapy directed at the malignant tumor must be discontinued at
least one week prior to registration

- Any other prior therapy directed at the malignant tumor, including biological
and immunologic agents, must be discontinued at least three weeks prior to
registration

- Prior therapy

- Patients must have had one prior platinum-based chemotherapeutic regimen for
management of primary disease containing carboplatin, cisplatin, or another
organoplatinum compound; this initial treatment may have included
intraperitoneal therapy, high-dose therapy, consolidation, non-cytotoxic agents
or extended therapy administered after surgical or non-surgical assessment

- Patients must have NOT received any additional cytotoxic chemotherapy for
management of recurrent or persistent disease, including retreatment with
initial chemotherapy regimens; (Note: optimal evaluation of the safety and
efficacy of new chemotherapy regimens is best performed in patients with minimal
prior therapy; non-investigational therapy, such as retreatment with platinum
and/or paclitaxel, is non-curative in the setting of recurrent disease, and can
generally be safely administered to patients following participation in a Phase
II trial)

- Patients are allowed to receive, but are not required to receive, one additional
non-cytotoxic regimen for management of recurrent or persistent disease
according to the following definition:

- Non-cytotoxic (biologic or cytostatic) agents include (but are not limited to)
hormones, monoclonal antibodies, cytokines, and small-molecule inhibitors of
signal transduction

- Patients must be considered platinum resistant or refractory according to
standard GOG criteria, i.e., have had a treatment-free interval following
platinum of less than 6 months, or have progressed during platinum-based therapy

- Absolute neutrophil count (ANC) greater than or equal to 1,500/mcl

- Platelets greater than or equal to 100,000/mcl

- Creatinine less than or equal to 1.5 x institutional upper limit normal (ULN)

- Bilirubin less than or equal to 1.5 x ULN

- Serum glutamic oxaloacetic transaminase (SGOT) (aspartate aminotransferase [AST])
less than or equal to 3 x ULN

- Alkaline phosphatase less than or equal to 2.5 x ULN

- Neurologic function: no neuropathy (sensory and motor) less than or equal to Common
Terminology Criteria for Adverse Events (CTCAE) grade 1

- Patients must have signed an approved informed consent and authorization permitting
release of personal health information

- Patients must meet pre-entry requirements

- Patients of childbearing potential must have a negative serum pregnancy test prior to
study entry and be practicing an effective form of contraception

- Cautions and prohibited medications/treatments

- Since elesclomol is a substrate for cytochrome P450 2C9 (CYP2C9), cytochrome
P450 2D6 (CYP2D6), cytochrome P450 2C19 (CYP2C19), and cytochrome P450 3A4
(CYP3A4) and an inducer of CYP3A4, cytochrome P450 1A2 (CYP1A2), cytochrome P450
2A6 (CYP2A6), and cytochrome P450 2E1 (CY2E1), it is recommended that the
following be used with caution: sensitive substrates of CYP3A4, CYP1A2, and
CY2E1, and strong inhibitors and inducers of CYP2C9, CYP2D6, CYP2C19, and CYP3A4

Exclusion Criteria:

- Patients who have had prior therapy with elesclomol or prior second-line cytotoxic
chemotherapy

- Patients who have received radiation to more than 25% of marrow-bearing areas

- Patients with a history of other invasive malignancies, with the exception of
non-melanoma skin cancer and other specific malignancies are excluded if there is any
evidence of other malignancy being present within the last three years; patients are
also excluded if their previous cancer treatment contraindicates this protocol
therapy

- Patients who have received prior radiotherapy to any portion of the abdominal cavity
or pelvis OTHER THAN for the treatment of ovarian, fallopian tube, or primary
peritoneal cancer are excluded; prior radiation for localized cancer of the breast,
head and neck, or skin is permitted, provided that it was completed more than three
years prior to registration, and the patient remains free of recurrent or metastatic
disease

- Patients who have received prior chemotherapy for any abdominal or pelvic tumor OTHER
THAN for the treatment of ovarian, fallopian tube, or primary peritoneal cancer are
excluded; patients may have received prior adjuvant chemotherapy for localized breast
cancer, provided that it was completed more than three years prior to registration,
and that the patient remains free of recurrent or metastatic disease

- Patients who are pregnant or breastfeeding
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