Breathomics as Predictive Biomarker for Checkpoint Inhibitor Response

NCT ID: NCT04146064

Last Updated: 2023-06-05

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 425 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2020-02-24
• Study Completion Date: 2024-05-31

Brief Summary

Immunotherapy with agents stimulating the immune system to act against cancer are now a new standard of care in various cancers as lung cancer and melanoma, but also bladder cancer, kidney cancer and head & neck cancer. However, even though a subset of patients derives long-term benefit from these agents, depending of cancer type still at least half of patients do not respond to these new drugs. Our understanding of possible factors predicting whether a patient might actually benefit from immunotherapy is poor. Volatile organic compounds (VOCs) are gases exhaled with a person's breath, which are released into the lung from blood and bacteria and therefore can give information about infections as well as inflammation and possibly cancer cells in a person's body. Breath analysis of these VOCs with special devices called electronic noses (eNose) generate a specific electric signals patterns called breathprints. There is early evidence that specific breathprints can actually help to select patients who will be likely to benefit from immunotherapy.

This study is being undertaken in an effort to evaluate breathprint analysis as a potential predicting factor for benefit from immunotherapy, so that treatment selection can further be improved.

This study is designed to help us identify the role of breathprint analysis to better select patients for immunotherapy.

Detailed Description

Immune checkpoint blockade with anti-PD-1 and anti-PD-L1 antibodies has become a new standard of care in several cancer types as NSCLC and melanoma. However, in biomarker-unselected patient populations, overall response rate (ORR) depending on type of cancer and whether single or combination treatment is chosen remains still only 20%-60%. Though overall well tolerated approximately 5-10% of patients treated with PD1/PD-L1 targeting agents will experience grade 3 or 4 toxicities, including potentially life-threatening auto-immune toxicities such as colitis, hepatitis, and pneumonitis. Therefore, due to high costs of treatment and its possible complications, improved selection of patients is a crucial goal and an easily available non-invasive, point-of-care test for better patient selection is very much needed.

A promising approach in this regard is the analysis of volatile organic compounds (VOCs) in breath. Breath analysis for the detection of VOCs is increasingly investigated for its utility in diagnosis and management of cancer. Electronic noses (eNoses) are promising as cheap and clinically-practical devices that are designed to detect patterns of VOCs. Recently published prospective observational data showed very promising discriminant function for breathprint analysis for non-response to immunotherapy in NSCLC patients.

The principle goal of this study is to validate a prior study that found that breathomics-based classifiers predicted 12-week early progression vs non-progression in advanced NSCLC patients treated with nivolumab or pembrolizumab. Secondarily, we will expand assessment of breathomic-based classifiers to include other cohorts of advanced tumors treated with ICI, and also consider using response instead of non-progression as an endpoint. Exploratory goals include refinement of the breathomics classifier using alternative machine-learning techniques, and correlate with other biomarkers of immunotherapy outcomes.

Conditions

NSCLC; Melanoma; Kidney Cancer; Urothelial Carcinoma; Head and Neck Cancer

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Validation cohort: NSCLC

Patients with advanced/metastatic NSCLC planned for IO-treatment in one of the following categories

• Pembrolizumab monotherapy first-line
• Pembrolizumab or nivolumab monotherapy in second or later line

Breathprint analysis and patient-reported outcomes

Intervention Type: OTHER

Breathprint analysis: Patients will be providing breathprint samples into the eNose device at baseline and every 12 weeks thereafter as long as on immunotherapy treatment.

Questionnaires will be completed at the same timepoints.

Cohort 1: NSCLC

Patients with advanced/metastatic NSCLC planned for Pembrolizumab-chemotherapy combination therapy first-line

Breathprint analysis and patient-reported outcomes

Intervention Type: OTHER

Breathprint analysis: Patients will be providing breathprint samples into the eNose device at baseline and every 12 weeks thereafter as long as on immunotherapy treatment.

Questionnaires will be completed at the same timepoints.

Cohort 2: Melanoma

Patients with advanced/metastatic melanoma planned for IO-treatment in one of the following categories

• Nivolumab/ipilimumab combination treatment 1L
• Pembrolizumab or nivolumab monotherapy treatment 1L
• Ipilimumab monotherapy 2L

Breathprint analysis and patient-reported outcomes

Intervention Type: OTHER

Breathprint analysis: Patients will be providing breathprint samples into the eNose device at baseline and every 12 weeks thereafter as long as on immunotherapy treatment.

Questionnaires will be completed at the same timepoints.

Cohort 3: Mixed solid tumor cohort

Patients with advanced/metastatic solid tumors such as Head\&Neck tumors, kidney cancer and urothelial cancer planned for IO-treatment

Breathprint analysis and patient-reported outcomes

Intervention Type: OTHER

Breathprint analysis: Patients will be providing breathprint samples into the eNose device at baseline and every 12 weeks thereafter as long as on immunotherapy treatment.

Questionnaires will be completed at the same timepoints.

Cohort 4: NSCLC

Patients with advanced/metastatic NSCLC planned for treatment with Chemotherapy-only (either platinum-based combination treatment or docetaxel monotherapy)

Breathprint analysis and patient-reported outcomes

Intervention Type: OTHER

Breathprint analysis: Patients will be providing breathprint samples into the eNose device at baseline and every 12 weeks thereafter as long as on immunotherapy treatment.

Questionnaires will be completed at the same timepoints.

Interventions

Breathprint analysis and patient-reported outcomes

Breathprint analysis: Patients will be providing breathprint samples into the eNose device at baseline and every 12 weeks thereafter as long as on immunotherapy treatment.

Questionnaires will be completed at the same timepoints.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Patients 18 years of age or older
• Histologically confirmed advanced/metastatic non-small cell lung cancer, melanoma or solid tumor such as urothelial, kidney or head and neck cancer and planned treatment with

• NSCLC validation cohort: Pembrolizumab or Nivolumab
• NSCLC Cohort 1: Pembrolizumab-chemotherapy combination therapy 1L
• Melanoma Cohort 2: Nivolumab/ipilimumab combination treatment 1L, Pembrolizumab or nivolumab monotherapy treatment 1L , Ipilimumab
• Solid tumors Cohort 3: Any ICI-treatment, any line
• NSCLC Cohort 4: Chemotherapy-only (either platinum-based combination treatment or docetaxel monotherapy)
• At least one measurable lesion as defined by RECIST 1.1. A lesion at a previously irradiated site may only be counted as a target lesion if there is clear sign of progression since the irradiation.
• Able to provide informed consent.

Exclusion Criteria

• Patients who are unable to perform the breathing manoeuvres needed for eNose-analysis of exhaled air.
• Patients who are unable to independently consent to participation in the trial.
• Patients with severe, acute, or chronic medical conditions (including uncontrolled diabetes mellitus) or psychiatric conditions or laboratory abnormalities that in the opinion of the Investigator or their physician may cause undue harm or inconvenience to the patient, or that may interfere with the interpretation of study results.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Amsterdam

OTHER

Sponsor Role: collaborator

University Health Network, Toronto

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Geoffrey Liu, MD MSc

Role: PRINCIPAL_INVESTIGATOR

UHN

Locations

Princess Margaret Cancer Centre

Toronto, Ontario, Canada

Site Status: RECRUITING

Countries

Canada

Central Contacts

Sabine Schmid, MD

Role: CONTACT

sabine.schmid@uhn.ca

416-946-2000 ext. 5288

Facility Contacts

Sabine Schmid, MD

Role: primary

sabine.schmid@uhn.ca

Other Identifiers

19-5936

Identifier Type: OTHER

Identifier Source: secondary_id

IO-Breathomics

Identifier Type: -

Identifier Source: org_study_id