Tumor-Treating Fields Therapy in Preventing Brain Tumors in Participants With Extensive-Stage Small Cell Lung Cancer

A Multi-Institutional Pilot Study of Prophylactic Cranial Tumor-Treating Fields for Patients With Extensive-stage Small Cell Lung Cancer

This trial studies how well tumor-treating fields therapy works in preventing brain tumors in participants with small cell lung cancer that has spread to other places in the body. Tumor-treating fields therapy involves the use of the NovoTTF-200A which delivers alternating electrical fields, or tumor treating fields, through ceramic discs placed on the head. This electric force may slow and/or reverse tumor growth by disrupting the way cancer cells grow.

Study Overview

• Status: Terminated
• Conditions: Extensive Stage Small Cell Lung Carcinoma
• Intervention / Treatment: Other: Quality-of-Life Assessment; Procedure: Tumor Treating Fields (TTF) Therapy; Device: NovoTTF-200A Device

Detailed Description

PRIMARY OBJECTIVES:

I. To measure the feasibility and compliance of NovoTTF-200A as prophylactic cranial tumor treatment fields (TTF) therapy, determined by percent (%) of patients continuing TTF therapy until intracranial tumor progression, discontinuation due to dose limiting toxicity (DLT), or 6 months.

SECONDARY OBJECTIVES:

I. To evaluate time to intracranial failure after NovoTTF-200A. II. To evaluate overall survival after NovoTTF-200A. III. To evaluate the rates of intracranial failure at 2, 4, 6, 8, 10, 12 months after NovoTTF-200A.

IV. To evaluate intracranial failure free survival after NovoTTF-200A. V. To evaluate the rate of decline in Hopkins Verbal Language Test-Revised (HVLT-R) free recall, delayed recall and delayed recognition, Controlled Oral Word Association Test (COWAT) and Trail Making Test (TMT) Parts A and B at 2, 4, 6, 8, 10, 12 months after NovoTTF-200A.

VI. To evaluate time to neurocognitive failure after NovoTTF-200A. VII. To evaluate neurocognitive failure-free survival after NovoTTF-200A. VIII. To evaluate quality of life using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC Quality of life Questionnaire C30) with BN20 addendum after NovoTTF-200A.

IX. To assess adverse events, severity, and frequency associated with NovoTTF-200A using the Common Terminology Criteria for Adverse Events (CTCAE) version 4.0.

OUTLINE:

Participants undergo tumor-treating fields therapy using the NovoTTF-200A device over 18 hours per day for a minimum of 4 weeks and up to 1 year in the absence of disease progression, unacceptable toxicity, or intracranial failure.

After completion of study treatment, participants are followed up at 8 weeks.

• Study Type: Interventional
• Enrollment (Actual): 2
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Tennessee
    • Nashville, Tennessee, United States, 37232
      • Vanderbilt-Ingram Cancer Center

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 22 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Life expectancy of > 3 months
• Histologically proven extensive stage small cell lung carcinoma (ES-SCLC) (any T any N and any M stage) within 6 months prior to start of study treatment with the NovoTTF-200A, with a partial or complete response to at least four cycles of first-line chemotherapy
• Karnofsky performance status (KPS) > 70
• Neutrophil count > 1.5 x 10^9/L
• Platelet count > 100 x 10^9/L
• Bilirubin < 1.5 x upper limit of normal (ULN)
• Aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) < 2.5 x ULN or < 5 x ULN if patient has documented liver metastases
• Serum creatinine < 1.5 x ULN

Exclusion Criteria:

• Evidence of brain metastases on magnetic resonance imaging (MRI) of brain with and without contrast
• History of other prior malignancy within the past 5 years except for superficial skin cancers

• No severe comorbidities:

  • History of significant cardiovascular disease unless the disease is well controlled. Significant cardiac disease includes second/third degree heart block; significant ischemic heart disease; poorly controlled hypertension; congestive heart failure of the New York Heart Association (NYHA) Class II or worse (slight limitation of physical activity; comfortable at rest, but ordinary activity results in fatigue, palpitation or dyspnea)
  • History of arrhythmia that is symptomatic or requires treatment. Patients with atrial fibrillation or flutter controlled by medication are not excluded from participation in the trial
  • History of cerebrovascular accident (CVA) within 6 months prior to start of study treatment
  • Active infection or serious underlying medical condition that would impair the ability of the patient to receive protocol therapy
  • History of any psychiatric condition that might impair patient's ability to understand or comply with the requirements of the study or to provide consent
• Active implantable electronic medical devices in the brain; a skull defect, a shunt, or bullet fragments
• Known allergies to medical adhesives or hydrogel
• Unable to operate the NovoTTF-200A device independently or with the help of a caregiver
• If a female, currently pregnant, breastfeeding, or unwilling to avoid pregnancy while on study treatment
• Concurrent brain directed therapy (beyond NovoTTF-200A as per protocol)
• Prior clinical trial participation with brain directed therapy
• Concurrent treatment clinical trials

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Prevention (TTF therapy, NovoTTF-200A device)	Other: Quality-of-Life Assessment; Ancillary studies; Procedure: Tumor Treating Fields (TTF) Therapy; Undergo TTF therapy; Device: NovoTTF-200A Device; Undergo TTF therapy

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Percentage of Patients Continuing Therapy Until Intracranial Tumor	Count of patients developed intracranial tumor divided by total number of patients.	Up to 6 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Time to Intracranial Failure	Time to intracranial failure with death as a competing risk will be estimated using cumulative incidence function (CIF) and reported with a one-sided 95% confidence interval.	Up to 3 years
Overall Survival	Estimated using the Kaplan-Meier method.	Up to 3 years
Rate of Intracranial Failure	Estimated using the cumulative incidence function	Up to 12 months
Rate of Decline in Cognitive Function	Measured by Hopkins Verbal Language Test	Up to 12 months
Time to Neurocognitive Failure	Measured by Hopkins Verbal Language Test	Up to 3 years
Neurocognitive Failure-free Survival	Measured by Hopkins Verbal Language Test	Up to 3 years
Evaluate Quality of Life Using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30	Measured by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (scale 1-4)	Up to 3 years
Incidence of Adverse Events	Graded according to Common Terminology Criteria for Adverse Events (CTCAE) version 4.0	Up to 12 months

Collaborators and Investigators

• Sponsor: Vanderbilt-Ingram Cancer Center
• Collaborators: NovoCure Ltd.
• Investigators: Principal Investigator: Albert Attia, MD, Vanderbilt-Ingram Cancer Center

Study record dates

Study Major Dates

• Study Start (Actual): September 5, 2018
• Primary Completion (Actual): June 2, 2020
• Study Completion (Actual): July 13, 2020

Study Registration Dates

• First Submitted: July 11, 2018
• First Submitted That Met QC Criteria: July 30, 2018
• First Posted (Actual): July 31, 2018

Study Record Updates

• Last Update Posted (Actual): August 4, 2020
• Last Update Submitted That Met QC Criteria: July 17, 2020
• Last Verified: July 1, 2020

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Respiratory Tract Diseases; Neoplasms; Lung Diseases; Neoplasms by Site; Respiratory Tract Neoplasms; Thoracic Neoplasms; Carcinoma, Bronchogenic; Bronchial Neoplasms; Lung Neoplasms; Small Cell Lung Carcinoma
• Other Study ID Numbers: VICC THO 1747; NCI-2018-01428 (Registry Identifier: NCI, Clinical Trials Reporting Program)

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: Yes