Linsitinib in Treating Patients With Gastrointestinal Stromal Tumors

• Register: ClinicalTrials.gov
• Last refreshed on: 12 December 2020
• Main ID: NCT01560260
• Date of registration: 20/03/2012
• Prospective Registration: No
• Primary sponsor: National Cancer Institute (NCI)
• Public title: Linsitinib in Treating Patients With Gastrointestinal Stromal Tumors
• Scientific title: A Phase 2 Study of Linsitinib (OSI-906) in Pediatric and Adult Wild Type Gastrointestinal Stromal Tumors
• Date of first enrolment: March 2012
• Target sample size: 20
• Recruitment status: Completed
• URL: https://clinicaltrials.gov/show/NCT01560260
• Study type: Interventional
• Study design: Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Treatment. Masking: None (Open Label).
• Phase: Phase 2

Countries of recruitment

United States

Contacts

• Name: Margaret von Mehren
• Affiliation: Sarcoma Alliance for Research through Collaboration

Key inclusion & exclusion criteria

Inclusion Criteria:

- Patients must have histologically confirmed gastrointestinal stromal tumor (GIST) with
confirmed genotype of wild-type in a Clinical Laboratory Improvement Amendments (CLIA)
certified laboratory

- Patients will be stratified into pediatric and adult cohorts; patients in the
pediatric cohort (age at diagnosis =< 18 years OR diagnosis of Carney Triad or
Carney-Stratakis Diad (paraganglioma, pulmonary chondroma) must have received at least
sunitinib and have had progression on or intolerance to progression on therapy;
patients in the adult cohort (age at diagnosis > 18 years AND no diagnosis of
diagnosis of Carney Triad or Carney-Stratakis Diad) have had progression on or
intolerance to imatinib therapy as documented by treating physician

- Performance status: Eastern Cooperative Oncology Group (ECOG) 0-2

- Patients must have measurable disease defined as lesions that can be measured in 2
dimensions by medical imaging techniques such as CT or magnetic resonance imaging
(MRI); ascites, pleural fluid, and lesions seen on PET scan only are not considered
measurable

- White blood cells count (WBC) >= 2.0 x 10^9/L (being >= 14 days off growth factors) OR

- Absolute neutrophil count (ANC) >= 1.5 x 10^9/L (being >= 14 days off growth factors)

- Platelet count >= 75 x 10^9/L

- Total bilirubin =< 1.5 times the upper limit of normal for age

- Alanine aminotransferase (ALT)/aspartate aminotransferase (AST) (serum glutamate
pyruvate transaminase [SGPT]/serum glutamic oxaloacetic transaminase [SGOT]) =< 3 x
the upper limit of normal (ULN) for the reference lab (=< 5 x the ULN for the
reference lab in the presence of known hepatic metastasis, adjusted for age)

- Creatinine clearance > 70 ml/min/1.73m^2 or

- Serum creatinine < 1.5 x ULN per age and gender

- QT interval corrected using Frederica formula (QTcF) interval average of < 450 msec at
baseline using the Frederica formula (QTcF)

- No concomitant drugs that prolong the QT corrected (QTc) interval

- No significant cardiac disease

- Fasting blood glucose < 150 mg/dL at baseline

- Hemoglobin A1C (HbA1c) < 7% at screening

- Patients or their legal representative must be able to read, understand and provide
written informed consent to participate in the trial

- Women of child-bearing potential and men must agree to use adequate contraception
(hormonal or barrier method of birth control; abstinence) prior to study entry and for
the duration of study participation; should a woman become pregnant or suspect she is
pregnant while she or her partner is participating in this study, she should inform
her treating physician immediately; women of childbearing potential must provide a
negative pregnancy test (serum or urine) within 7days prior to registration

- Patients with diabetes mellitus should have controlled disease on oral medications,
defined as: no diabetic ketoacidosis (hyperglycemia, ketonuria, pH < 7.3 and
bicarbonate < 15mEq/L) at the time of enrollment or within 30 days prior to enrollment
and; no change in oral medications greater than 10% within 30 days prior to enrollment

- Patient must be able to swallow to participate in the study

- Signed informed consent

Exclusion Criteria:

- Time elapsed from previous therapy must be >= 3 weeks except for prior tyrosine kinase
inhibitor therapy which can be >= 7 days; patients must be recovered from the effects
of any prior surgery, radiotherapy or systemic therapy

- Patients who are receiving any other investigational agents or other anti-cancer
therapies other than those administered in this study during protocol treatment

- Patients with diabetes mellitus requiring insulin for control of their diabetes

- Patients with a history of liver cirrhosis

- Patients with known brain metastases should be excluded from this clinical trial

- History of allergic reactions attributed to compounds of similar chemical or biologic
composition to linsitinib (OSI-906)

- While cytochrome P450 1A2 (CYP1A2) inhibitors/inducers are not specifically excluded,
investigators should be aware that linsitinib (OSI 906) exposure may be altered by the
concomitant administration of these drugs

- While cytochrome P450 2C9 (CYP2C9) substrates are not specifically excluded,
investigators should be aware that levels of drugs metabolized by CYP2C9 may be
increased by the concomitant administration of linsitinib (OSI-906); caution should be
used when administering CYP2C9 substrates to patients who are on study drug

- Use of the potent CYP1A2 inhibitors ciprofloxacin and fluvoxamine are prohibited;
other less potent CYP1A2 inhibitors/inducers are not excluded

- Uncontrolled intercurrent illness including, but not limited to, ongoing or active
infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac
arrhythmia, or psychiatric illness/social situations that would limit compliance with
study requirements

- Prior treatment with another kinase inhibitor targeting insulin-like growth factor 1
receptor (IGF-1R) pathway, including monoclonal antibodies targeting IGF-1R

- Pregnant women are excluded from this study; breastfeeding should be discontinued if
the mother is treated with linsitinib (OSI-906)

- Fertile men and women of childbearing potential not employing an effective method of
birth control throughout the trial and for 3 months after last study drug
administration in both sexes; women of childbearing potential must have a negative
pregnancy test (serum or urine) within the 7 days prior to study drug administration

- NOTE: Women of childbearing potential include both pre-menopausal women and women
within the first 2 years of the onset of menopause

- NOTE: Effective methods of birth control includes: surgically sterile, barrier
device (condom, diaphragm), contraceptive coil, abstinence; oral contraceptive
pills (OCPs) alone are not considered an effective method

- Known human immunodeficiency virus (HIV)-positive patients on combination
antiretroviral therapy are ineligible

- Use of drugs that have a known risk of causing Torsades de Pointes (TdP) are
prohibited within 14 days prior to initiation of linsitinib (OSI-906)

- Patients with a history of solid organ transplant are ineligible



Age minimum: 18 Years
Age maximum: N/A
Gender: All

Health Condition(s) or Problem(s) studied

Gastrointestinal Stromal Tumor

Paraganglioma

Carney Complex

Chondrosarcoma

Intervention(s)

Drug: Linsitinib

Other: Laboratory Biomarker Analysis

Other: Pharmacological Study

Primary Outcome(s)

Number of Participants With Complete Response or Partial Response Using Response Evaluation Criteria in Solid Tumors Guideline Version 1.1 [Time Frame: At 6 months]

Secondary Outcome(s)

Correlations Between Glucose, Insulin, Tumor Tissue and Blood Biomarkers With FDG-PET Metabolic Response. [Time Frame: Up to 37 weeks]

Changes in Tumor Metabolism by FDG-PET Qualitatively and Semi-quantitatively With Standard Uptake Value (SUV) [Time Frame: Baseline and 8 weeks]

Number of Participants With Metabolic Response to Linsitinib Using FDG-PET. [Time Frame: Up to 37 weeks]

Overall Survival (OS) [Time Frame: Estimates at 9 months]

Patterns of Protein Expression in Serum and Tumor Tissues as Predictors of Response and PFS [Time Frame: Up to 37 weeks]

Progression Free Survival (PFS) [Time Frame: Time from date of enrollment to time of progression or death due to any cause, estimates at 9 months]

Response Duration [Time Frame: Up to 37 weeks]

Clinical Benefit Rate Defined as Stable Disease (SD) >= 9 Months, Partial Response (PR) or Complete Response (CR) [Time Frame: Up to 2 years]

Tolerability and Adverse Event Profile of Linsitinib [Time Frame: Up to 37 weeks]

Failure-free Survival [Time Frame: Up to 37 weeks]

Secondary ID(s)

SARC-022

CDR0000728619

SARC 022

8945

SARC022

NCI-2012-00708

Source(s) of Monetary Support

Please refer to primary and secondary sponsors

Results

• Results available: Yes
• Date Posted: 19/01/2017
• URL: https://clinicaltrials.gov/ct2/show/results/NCT01560260