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Trial record 4 of 15 for:    s2013

Immune Checkpoint Inhibitor Toxicity Risk Prediction in Solid Tumors

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04871542
Recruitment Status : Recruiting
First Posted : May 4, 2021
Last Update Posted : September 9, 2022
Sponsor:
Collaborator:
National Cancer Institute (NCI)
Information provided by (Responsible Party):
Southwest Oncology Group

Brief Summary:
This study examines how certain risk factors (such as age, gender, other medical conditions, and the type of immunotherapy used to treat the cancer) affect whether a patient with a malignant solid tumor will develop mild or serious side effects from the immunotherapy medications. Immunotherapy is the type of treatment that helps the body's immune system fight cancer. In the future, this information may help doctors make better decisions about cancer treatments.

Condition or disease Intervention/treatment
Malignant Solid Neoplasm Procedure: Biospecimen Collection Other: Questionnaire Administration

Detailed Description:

PRIMARY OBJECTIVE:

I. To both develop and independently validate a risk prediction model for Common Terminology Criteria for Adverse Events (CTCAE) grade 3 or higher non-hematological immune-related adverse events (irAEs) in the first year of immune checkpoint inhibitor (ICI)-based therapy for the treatment of solid tumors.

SECONDARY OBJECTIVES:

I. To prospectively assess the incidence of any grade of non-hematological irAEs and grade 4 hematological irAEs on ICI-based therapy.

II. To observe the trajectory of patient-reported quality of life and health preferences over 12 months.

III. To observe the trajectory of patient-reported adverse events over 12 months using serial assessment with select Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) measures.

IV. To measure the burden of chronic, grade 1 and 2 toxicities using methods such as toxicity over time (ToxT).

V. To track patterns of treatment of irAEs and patterns of toxicity resolution.

TRANSLATIONAL MEDICINE OBJECTIVES:

I. To evaluate the cytokine toxicity (CYTOX) score, a composite measure derived from 11 different cytokine levels, both prior to ICI-based therapy and after 1 cycle of ICI-based therapy as a predictive signature for the development of irAEs.

II. To establish a repository of archival tissue and blood/serum specimens for potential predictive and/or prognostic markers of irAE risk.

ADDITIONAL OBJECTIVE:

I. To assess the feasibility of using electronic (e)PRO in a multi-center clinical trial setting.

OUTLINE:

Patients undergo collection of a tissue sample at the start of their routine cancer treatment. Patients complete questionnaires at the start of cancer treatment, weeks 4, 12, 24, and 52. Patients will have the option of providing blood samples at several time points during the study.

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Study Type : Observational
Estimated Enrollment : 2062 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Immune Checkpoint Inhibitor Toxicity (I-CHECKIT): A Prospective Observational Study
Actual Study Start Date : August 16, 2021
Estimated Primary Completion Date : September 30, 2025
Estimated Study Completion Date : September 30, 2026

Group/Cohort Intervention/treatment
Observational (biospecimen collection, questionnaire)
Patients undergo collection of a tissue sample at the start of their routine cancer treatment. Patients complete questionnaires at the start of cancer treatment, weeks 4, 12, 24, and 52. Patients will have the option of providing blood samples at several time points during the study.
Procedure: Biospecimen Collection
Undergo collection of blood sample
Other Name: Biological Sample Collection

Other: Questionnaire Administration
Complete questionnaires




Primary Outcome Measures :
  1. Occurrence of severe or worse non-hematological immune-related adverse event (irAE) [ Time Frame: 52 weeks ]
    Adverse events will be recorded according to the physician rated Common Terminology Criteria for Adverse Events (CTCAE) scoring system.


Secondary Outcome Measures :
  1. Change in Patient-Reported Outcomes Measurement Information System (PROMIS)-29 [ Time Frame: Baseline to 52 weeks ]
    PROMIS-29 Includes 4 questions to evaluate each of 7 domains (physical function, anxiety, depression, fatigue, sleep disturbance, social functioning, and pain interference) using a 5- point Likert scale, as well as a single item to assess pain severity on a 0-10 scale. The PROMIS-29 assesses severity levels of symptoms and their effect on the patient's functioning, assessed over the preceding 7-day period.

  2. Change in PRO-CTCAE scores [ Time Frame: Baseline to 52 weeks ]
    Patients report severity, frequency, and/or interference of toxicities. For this protocol the following 11 items will be assessed: fatigue interference, neuropathy severity and interference, nausea frequency and severity, shortness of breath severity and interference, presence of rash, itching severity, and diarrhea severity and interference over the preceding 7 days.

  3. Change in PROMIS Cognitive Function- Short Form 4a version 2.0 scores [ Time Frame: Baseline to 52 weeks ]
    Assesses patient-perceived cognitive deficits over the past 7 days. Facets include mental acuity, concentration, verbal and nonverbal memory, verbal fluency, and perceived changes in these cognitive functions. The extent to which cognitive impairments interfere with daily functioning, whether other people observe cognitive impairments, and the impact of cognitive dysfunction on quality of life are also assessed. The PROMIS Short Form Cognitive Function 4a is a questionnaire composed of 4 items rated on a 5 level scale, ranging from Never to Very often (Several times a day), with raw scores ranging from 5 to 20, with higher scores representing better cognitive function. In combination with the PROMIS-29, the use of this questionnaire allows the calculation of the PROMIS-Preference score, which quantifies the value participants place on different health states.

  4. Change in toxicity over time (ToxT) [ Time Frame: Baseline to 52 weeks ]
    ToxT is a collection of statistical codes in Statistical Analysis Software that generate plots depicting summary statistics or individual patient data over discrete timepoints, combined with longitudinal statistical analyses (repeated measures modelling, and time-to-event and AUC analyses).

  5. Change in cytokine toxicity (CYTOX) score [ Time Frame: Baseline to 1 cycle after ICI-therapy ]
    The relationship between the CYTOX score and the occurrence of irAE will be evaluated using area under the curve (AUC). Separate evaluations will be conducted using both cytokine levels determined both prior to ICI-based therapy and after 1 cycle of ICI-based therapy.


Other Outcome Measures:
  1. Feasibility of the Patient Cloud electronic (e)PRO app [ Time Frame: Up to 52 weeks ]
    Will be assessed by comparing the extent of missing data at each assessment time between participants choosing the Patient Cloud ePRO application (app) versus the use of paper forms. The participant experience of using the Patient Cloud ePRO app will also be assessed using a one-time questionnaire at the end of the participant's participation in the study


Biospecimen Retention:   Samples With DNA
Tissue, blood, plasma, buffy coat


Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients planning to receive ICI-based therapy for a solid tumor malignancy.
Criteria

Inclusion Criteria:

  • Participants must be planning to receive ICI-based therapy for a solid tumor malignancy. This therapy must be given according to Food and Drug Administration (FDA) label or National Comprehensive Cancer Network (NCCN) guidelines at Category 1 or 2A and not in the context of a clinical trial
  • Participants who have received prior ICI-based therapy must have completed ICI based therapy at least 180 days prior to registration
  • Participants must not have discontinued any prior ICI-based therapy (if applicable) because of irAE
  • Participants must not have received chemotherapy, biologic, or targeted-therapy within 21 days prior to registration
  • Participants must have recovered from side effects of prior therapy to the following standards per treating physician's discretion:

    • =< Grade 1 for any non-hematologic side effects (excluding neuropathy and alopecia); lab-related parameters of liver and renal function will be considered at the discretion of the treating physician)
    • =< Grade 2 for neuropathy and/or alopecia
    • Grade 3 or less for any hematologic side effects
  • Participants must be planning to begin standard of care ICI-based therapy within 3 calendar days after registration
  • Participants must not be planning to receive ICI-based therapy in combination with chemotherapy or any other non-ICI therapy for treatment of their cancer
  • Participants must be at least 18 years of age
  • Participants must complete their history and physical examination within 28 days prior to registration
  • Participants who can complete the S2013 Feasibility Questionnaire in English or Spanish must participate at the scheduled assessments
  • Participants must be able to complete Patient-Reported Outcome (PRO) instruments in English, Spanish, or French and must be planning to complete PROs at all scheduled assessments
  • Participants must complete the pre-registration (baseline) PRO forms within 14 days prior to registration
  • Participants must be willing to participate in PRO data collection

    • Note: Prior to registration, participants must decide on their method (paper or electronic) of completing their follow-up questionnaires. Participants who elect electronic (ePRO) completion must have an iPhone, Android phone, or tablet with cellular or WiFi connectivity in order to download the Patient Cloud mobile applications onto the device (personal device or a site provisioned device for multi-users)
  • Participants must be offered the opportunity to participate in the optional specimen banking
  • Note: As a part of the OPEN registration process the treating institution's identity is provided in order to ensure that the current (within 365 days) date of institutional review board approval for this study has been entered in the system.

    • Participants must be informed of the investigational nature of this study and must sign and give informed consent in accordance with institutional and federal guidelines

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04871542


Locations
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United States, Iowa
Mary Greeley Medical Center Recruiting
Ames, Iowa, United States, 50010
Contact: Site Public Contact    515-956-4132      
Principal Investigator: Debra M. Prow         
McFarland Clinic PC - Ames Recruiting
Ames, Iowa, United States, 50010
Contact: Site Public Contact    515-239-4734    ksoder@mcfarlandclinic.com   
Principal Investigator: Debra M. Prow         
McFarland Clinic PC-Boone Recruiting
Boone, Iowa, United States, 50036
Contact: Site Public Contact    515-956-4132      
Principal Investigator: Debra M. Prow         
McFarland Clinic PC-Trinity Cancer Center Recruiting
Fort Dodge, Iowa, United States, 50501
Contact: Site Public Contact    515-956-4132      
Principal Investigator: Debra M. Prow         
McFarland Clinic PC-Jefferson Recruiting
Jefferson, Iowa, United States, 50129
Contact: Site Public Contact    515-956-4132      
Principal Investigator: Debra M. Prow         
McFarland Clinic PC-Marshalltown Recruiting
Marshalltown, Iowa, United States, 50158
Contact: Site Public Contact    515-956-4132      
Principal Investigator: Debra M. Prow         
Sponsors and Collaborators
Southwest Oncology Group
National Cancer Institute (NCI)
Investigators
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Principal Investigator: Krishna S Gunturu Southwest Oncology Group
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Responsible Party: Southwest Oncology Group
ClinicalTrials.gov Identifier: NCT04871542    
Other Study ID Numbers: S2013
NCI-2021-01262 ( Registry Identifier: CTRP (Clinical Trial Reporting Program) )
S2013 ( Other Identifier: SWOG )
SWOG-S2013 ( Other Identifier: DCP )
S2013 ( Other Identifier: CTEP )
UG1CA189974 ( U.S. NIH Grant/Contract )
First Posted: May 4, 2021    Key Record Dates
Last Update Posted: September 9, 2022
Last Verified: September 2022

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Product Manufactured in and Exported from the U.S.: No