Overview

A Phase II Trial of Cabozantinib With Patients With Refractory GCTs

Status:
Recruiting
Trial end date:
2025-12-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of the CTO-IUSCCC-0752 study is to investigate the use of Cabozantinib for patients with incurable, refractory germ cell tumors. Patients will be treated until evidence of disease progression, non-compliance with study protocol, unacceptable major toxicity, at subject's own request for withdrawal, or if the study closes for any reason.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Nabil Adra
Collaborator:
Exelixis
Criteria
Inclusion Criteria:

1. Written informed consent and HIPAA authorization for release of personal health
information.

2. Capable of understanding and complying with the protocol requirements.

3. Age ≥ 18 years at the time of consent.

4. Histological or serological evidence of germ cell tumor, including seminoma,
non-seminoma, and women with ovarian GCTs.

5. Must have progressed after first-line cisplatin based combination chemotherapy AND
demonstrated progression following at least one salvage regimen for advanced germ cell
neoplasm and now considered incurable with standard therapies, including further
chemotherapy or surgery.

5.1. "Failure" of prior therapy is defined as: 5.1.1. A >25% increase in the products of
the perpendicular diameters of measurable tumor masses during prior therapy which are not
amenable to surgical resection.

5.1.2. The presence of new tumors that are not amenable to surgical resection 5.1.3. An
increase in AFP or beta-hcg (two separate determinations at least one week apart are
required if rising tumor markers are the only evidence of failure).

NOTE: Subjects with clinically growing teratoma (normal declining tumor markers and
radiographic or clinical progression) should be considered for surgery.

Subjects with relapsed primary mediastinal non-seminomatous germ cell tumor (PMNSGCT) are
eligible 7. Subjects with late relapse (>2 years from previous chemotherapy) not amenable
to resection are eligible if they have received first line platinum based chemotherapy and
are deemed not amenable to surgical resection (no need for 1 salvage regimen in late
relapse patients to be eligible).

8. Recovery to baseline or ≤ Grade 1 CTCAE v5 from toxicities related to any prior
treatments, unless AE(s) are clinically nonsignificant and/or stable on supportive therapy.

9. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.

10. Adequate laboratory values obtained within 10 days prior to registration for protocol
therapy and as defined below:

10.1. Hemoglobin ≥9g/dL

10.2. WBC ≥2500/μL

10.3. Absolute neutrophil count ≥1500/mm3

10.4. Platelet count ≥100,000/mm3

10.5. Total bilirubin ≤1.5 X ULN except patients with documented Gilbert's syndrome (≤3 X
ULN)

10.6. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline
phosphatase (ALP) ≤3 X ULN; for patients with hepatic metastases, ALT and AST ≤5 X ULN; ALP
≤5 X ULN with documented bone metastases.

10.7. Serum albumin ≥ 2.8 g/dl

10.8. (PT)/INR or partial thromboplastin time (PTT) test < 1.3x5x the laboratory ULN

- This applies only to patients who do not receive therapeutic anticoagulation; patients
receiving therapeutic anticoagulation (such as low-molecular-weight heparin or direct
factor Xa inhibitors) should be on a stable dose. 10.9. Serum creatinine ≤ 2.0 x ULN
or calculated creatinine clearance ≥ 30 mL/min (≥ 0.5 mL/sec) using the
Cockcroft-Gault equation:

1. Males: (140 - age) x weight (kg)/(serum creatinine [mg/dL] × 72)

2. Females: [(140 - age) x weight (kg)/(serum creatinine [mg/dL] × 72)] × 0.85

10.10. Urine protein/creatinine ratio (UPCR) ≤ 1 mg/mg (≤ 113.2 mg/mmol), or 24-h
urine protein ≤ 1 g

11. Female subjects of childbearing potential should have a negative urine or
serum pregnancy test within 72 hours prior to receiving the first dose of study
medication. If the urine test is positive or cannot be confirmed as negative, a
serum pregnancy test will be required.

12. Female subjects of childbearing potential should be willing to use 2 methods
of birth control or be surgically sterile, or abstain from heterosexual activity
for the course of the study through 120 days after the last dose of study
medication. Subjects of childbearing potential are those who have not been
surgically sterilized or have not been free from menses for > 1 year.

13. Male subjects should agree to use an adequate method of contraception
starting with the first dose of study therapy through 120 days after the last
dose of study therapy.

Exclusion Criteria:

1. Prior treatment with Cabozantinib.

2. Receipt of any type of small molecule kinase inhibitor (including
investigational kinase inhibitor) within 2 weeks before first dose of study
treatment.

3. Subjects who have not received ≥1 salvage treatment regimens (except late
relapse) or have further potentially curative treatment options.

4. Known brain metastases or cranial epidural disease unless adequately treated
and stable for at least 4 weeks prior to first dose of study treatment.
Subjects must have complete wound healing from major surgery or minor
surgery before first dose of study treatment. Eligible subjects must be
neurologically asymptomatic at the time of first dose of study treatment.

5. Radiation therapy for bone metastasis within 2 weeks, or any other radiation
therapy within 4 weeks prior to first dose of study treatment.

6. Expecting to father children within the projected duration of the trial,
starting with the pre-screening or screening visit through 120 days after
the last dose of trial treatment.

7. Treatment with investigational agent, any type of cytotoxic, biologic or
other systematic anticancer therapy within 28 days prior to registration for
protocol therapy.

8. Subjects with another active malignancy is not allowed except for adequately
treated basal cell or squamous cell skin cancer, in situ cervical cancer,
Gleason < Grade 7 prostate cancers, or other cancer for which the subject
has not received therapy for ≥1 year.

9. History of psychiatric illness or social situations that would limit
compliance with study requirements.

10. The subject has uncontrolled, significant intercurrent or recent illness
including, but not limited to, the following conditions:

10.1 Cardiovascular disorders:

1. Congestive heart failure New York Heart Association Class 3 or 4, unstable angina
pectoris, serious cardiac arrhythmias.

2. Uncontrolled hypertension defined as sustained blood pressure (BP) > 140 mm Hg
systolic or > 90 mm Hg diastolic despite optimal antihypertensive treatment.

3. Stroke (including transient ischemic attack [TIA]), myocardial infarction (MI),
or other ischemic event, or thromboembolic event (e.g., deep venous thrombosis,
pulmonary embolism) within 6 months before first dose of study treatment.

10.c.1. Subjects with a diagnosis of incidental, subsegmental PE or DVT within 6
months are allowed if stable, asymptomatic, and treated with a stable dose of
permitted anticoagulation (see exclusion criterion #6) for at least 1 week before
first dose of study treatment.

10.2 Gastrointestinal (GI) disorders associated with a high risk of perforation or fistula
formation:

a. The subject has evidence of tumor invading the GI tract, active peptic ulcer disease,
inflammatory bowel disease (e.g., Crohn's disease), diverticulitis, cholecystitis,
symptomatic cholangitis or appendicitis, acute pancreatitis, acute obstruction of the
pancreatic duct or common bile duct, or gastric outlet obstruction b. Abdominal fistula, GI
perforation, bowel obstruction, or intra-abdominal abscess within 6 months before first
dose of study treatment.

c. Note: Complete healing of an intra-abdominal abscess must be confirmed before first dose
of study treatment.

11. Clinically significant hematuria, hematemesis, or hemoptysis of > 0.5 teaspoon (2.5 ml)
of red blood, or other history of significant bleeding (e.g., pulmonary hemorrhage) within
12 weeks before first dose of study treatment.

12. Cavitating pulmonary lesion(s) or known endotracheal or endobronchial disease
manifestation.

13. Lesions invading or encasing any major blood vessels. 14. Other clinically significant
disorders that would preclude safe study participation per the investigator's opinion.

1. Serious non-healing wound/ulcer/bone fracture.

2. Uncompensated/symptomatic hypothyroidism.

3. Moderate to severe hepatic impairment (Child-Pugh B or C). 15. Major surgery (e.g.,
laparoscopic nephrectomy, GI surgery, removal or biopsy of brain metastasis) within 2
weeks before first dose of study treatment. Minor surgeries within 10 days before
first dose of study treatment. Subjects must have complete wound healing from major
surgery or minor surgery before first dose of study treatment. Subjects with
clinically relevant ongoing complications from prior surgery are not eligible.

16. Corrected QT interval calculated by the Fridericia formula (QTcF) > 500 ms per
electrocardiogram (ECG) within 14 days before first dose of study treatment.

Note: If a single ECG shows a QTcF with an absolute value > 500 ms, two additional
ECGs at intervals of approximately 3 min must be performed within 30 min after the
initial ECG, and the average of these three consecutive results for QTcF will be used
to determine eligibility.

17. Concomitant anticoagulation with coumarin agents (e.g., warfarin), direct thrombin
inhibitors (e.g., dabigatran), direct factor Xa inhibitor betrixaban, or platelet
inhibitors (e.g., clopidogrel). Allowed anticoagulants are the following:

a. Prophylactic use of low-dose aspirin for cardio-protection (per local applicable
guidelines) and low-dose low molecular weight heparins (LMWH).

b. Therapeutic doses of LMWH or anticoagulation with direct factor Xa inhibitors
rivaroxaban, edoxaban, or apixaban in subjects who are on a stable dose of the
anticoagulant for at least 1 week before first dose of study treatment without clinically
significant hemorrhagic complications from the anticoagulation regimen or the tumor.

18. Pregnant or lactating females.

19. Inability to swallow tablets.

20. Previously identified allergy or hypersensitivity to components of the study treatment
formulations.