Survival Prolongation by Rationale Innovative Genomics

• Register: ClinicalTrials.gov
• Last refreshed on: 23 October 2023
• Main ID: NCT03386929
• Date of registration: 14/12/2017
• Prospective Registration: No
• Primary sponsor: Worldwide Innovative Network Association
• Public title: Survival Prolongation by Rationale Innovative Genomics SPRING
• Scientific title: A Proof of Concept Study to Explore Safety and Efficacy of Tri-therapy Approach in Advanced/Metastatic NSCLC and Retrospectively Assess the Ability of Integrated Genomics and Transcriptomics to Match Patients to the Combination
• Date of first enrolment: November 29, 2017
• Target sample size: 15
• Recruitment status: Terminated
• URL: https://clinicaltrials.gov/ct2/show/NCT03386929
• Study type: Interventional
• Study design: Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Treatment. Masking: None (Open Label).
• Phase: Phase 1/Phase 2

Countries of recruitment

France, Israel, Luxembourg, Spain, United States

Contacts

• Name: RAZELLE KURZROCK, MD
• Affiliation: Medical College of Wisconsin, Milwaukee, WI, USA

Key inclusion & exclusion criteria

ELIGIBILITY CRITERIA

- Age: Men and women aged >18 years,

- Signed written informed consent,

- Any histologic type of locally advanced or metastatic NSCLC,

- Life expectancy of = 12 weeks,

- Measurable or evaluable (cytologically or radiologically detectable disease such as
ascites, peritoneal deposits, or lesions which do not fulfill RECIST 1.1 criteria for
measurable disease) lesions according to RECIST 1.1 criteria for phase 1 portion. For
phase 2, all patients must have RECIST 1.1 measurable disease,

- Physiologic function:

- Hematologic: Absolute neutrophil count (ANC) = 1.5 × 109/L, platelet count = 100
× 109/L, and hemoglobin = 9 g/dL (may have been transfused),

- Hepatic: Total bilirubin level = 1.5 × the upper limit of normal (ULN) range and
aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels = 2.5
× ULN,

- Renal: Estimated creatinine clearance = 30 mL/min according to the
Cockcroft-Gault formula (or local institutional standard method).

- Pregnancy and contraception:

- Pregnancy test: Negative serum or urine pregnancy test at screening for women of
childbearing potential.

- Contraception: Highly effective contraception for both male and female subjects
throughout the study and for at least 90 days after last treatment administration
if the risk of conception exists.

- Ability to comply with protocol requirements,

- Willingness to consent and ability to undergo a trucut biopsy to obtain a fresh
metastasis or primary tumor biopsy, and to undergo bronchoscopy to obtain a biopsy
from normal bronchial mucosa,

- No serious or medically uncontrolled concomitant conditions that are likely to make
the patient unfit for SPRING combination therapy, as per investigator assessment,

- ECOG performance status of 0 to 1.

EXCLUSION CRITERIA

- Patients with documented oncogenic aberrations at enrollment: EGFR, ALK, ROS1 when
available, MET exon 14 skipping when available. For squamous undifferentiated cell
carcinoma, documentation of these aberrations is not mandatory. Note: For Phase 1
portion, all patients with adenocarcinoma histology must have documentation of results
for druggable oncogenic aberrations (EGFR mutations, ALK rearrangements, and ROS1 when
available) prior to enrollment on the study.

- For Phase 1 portion, >2 lines of prior therapy in the metastatic setting.

- For the dose escalation phase of the study or until the MTD for the combination
regimen has been determined, patients with moderate hepatic impairment defined as AST,
ALT, alkaline phosphatase (ALP) >5 times ULN, which would be grade 3 or higher.
However, patients with liver metastases with AST/ALT = 5 x ULN can be included in the
study.

- For Phase 2 portion, any prior therapy in the metastatic setting.

Clinical criteria for phase 1 and phase 2 studies:

- Patients with treated brain metastases are eligible as are patients with new, active
untreated brain metastasis.

- Participants with a history of myocardial infarction within the last 2 years or with
significant cardiac arrhythmias uncontrolled by medication or pacemaker,

- Participants with any history of interstitial lung disease,

- Prior clinically significant toxicities from anticancer agents or radiotherapy which
have not regressed to Grade = 1 severity (NCI-CTCAE version 4.03) apart from
peripheral neuropathy and alopecia,

- History of any second malignancy in the last two years; patients with prior history of
in-situ cancer or basal or squamous cell skin cancer are eligible. Patients with a
history of other malignancies are eligible if they have been continuously disease-free
for at least two years,

- Autoimmune condition requiring medical intervention,

- Uncontrolled concomitant illness, active infection requiring i.v. antibiotics,

- Patients who have had a thromboembolic event within six months are excluded, as are
patients on anticoagulants, except for low dose aspirin (<100 mg/day) and low doses of
anticoagulants meant to keep line access open;

- Patients with Grade 3 or 4 (serious) gastrointestinal bleeding within the last six
months are excluded.

- Prior > G3 hemoptysis, major blood vessel involvement (specifically including aorta,
superior and inferior vena cave, main pulmonary arteries and veins, subclavian
arteries and veins and other large blood vessels that in the investigator's opinion
places the patients at high risk for major bleeding), and/or central cavitations,

- Known or suspected drug hypersensitivity to any drug used in the combination,

- Difficulty swallowing, malabsorption or other chronic gastrointestinal disease, or
conditions that may hamper compliance and/or absorption of the oral drugs,

- Any condition (e.g., known or suspected poor compliance, psychological instability,
geographical location, etc.) that, in the judgment of the investigator may affect the
patient's ability to sign the informed consent and undergo study procedures,

- Taking another experimental drug within 28 days prior to day 1 of the protocol
medications in this study,

- Pregnant or breast-feeding women,

- Both male and female patients of reproductive potential must agree to use highly
effective contraception, during the study and for 3 months following the last dose of
study drug,

- Patients currently taking strong CYP3A4 inducers and inhibitors,

- Patients currently taking proton pump inhibitors due to their impact on the
disposition of palbociclib during the phase 1.

- Patients taking other anticancer agents with the exception of denosumab or equivalent
medication for bone metastases.

- A time period of at least three weeks (including radiotherapy) or five drug
half-lives, whichever is shorter must have elapsed from last non-investigational
therapy before first day of treatment on this study,

- A time period of at least 10 days must have elapsed from last palliative radiotherapy
before the first day of treatment on this study,

- Specific exclusion criteria for administration of avelumab, in combination:

- IMMUNOSUPRESSANTS: Current use of immunosuppressive medication, EXCEPT for the
following: a. intranasal, inhaled, topical steroids, or local steroid injection
(e.g., intra-articular injection); b. Systemic corticosteroids at physiologic


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

Health Condition(s) or Problem(s) studied

Non-small Cell Lung Cancer Metastatic

Non-small Cell Lung Cancer Stage IIIB

Intervention(s)

Drug: Palbociclib

Drug: Avelumab

Drug: Axitinib

Primary Outcome(s)

Response Rate (RR) [Time Frame: Baseline up to approximately 24 months]

Overall Survival (OS) [Time Frame: Baseline up to approximately 24 months]

Incidence of the tested 3-Drug Combination Therapy-Emergent Adverse Events and Serious Adverse Events [Time Frame: From informed consent signature through 90 days after administration of the treatment (last dose)]

Duration of the Response [Time Frame: Baseline up to approximately 24 months]

Progression-Free Survival (PFS) [Time Frame: Baseline up to approximately 24 months]

SIMS Algorithm to Predict Clinical Outcome [Time Frame: 4 years]

Secondary Outcome(s)

Genomic and Transcriptomic Profile [Time Frame: 4 years]

Incidence of Treatment-related and or Biopsy-related Serious Adverse Events [Time Frame: 4 years]

Secondary ID(s)

2017-001455-32

WIN001

Source(s) of Monetary Support

Please refer to primary and secondary sponsors

Secondary Sponsor(s)

Pfizer

ARC Foundation for Cancer Research