Purpose

This study will develop an algorithm of identifying patients with stage IV NSCLC and Melanoma who could benefit from cancer treatment they receive.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Cancer patients with stage IV NSCLC or stage IV malignant melanoma - Patient must have at least one measurable lesion and the relevant images in order to enable assessment of response - ECOG PS - 0/1-2 - Normal hematologic, renal and liver function: 1. Absolute neutrophil count higher than 1500/mm3 2. Platelets count higher than 100,000/mm3 3. haemoglobin higher than 9 g/dL 4. Creatinine concentration ≤1.4 mg/dL, or creatinine clearance higher than 40 mL/min 5. Total bilirubin lower than 1.5 mg/dL, ALT and AST levels ≤ 3 times above the upper normal limit.

Exclusion Criteria

  • Concurrent and/or other active malignancy that has required systemic treatment within 2 years of first dose of study drug - Generalized impairment or mental incompetence that would render the patient unable to understand his/her participation in the study.

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Newly diagnosed NSCLC stage IV Patients with newly diagnosed stage IV NSCLC treated with Immunotherapy or Immunotherapy + Chemotherapy.
  • Other: Plasma sample collection
    Collect at least two plasma samples
NSCLC stage IV 2nd line and further of immunotherapy Patients with NSCLC stage IV treated with Immunotherapy at 2nd line or consecutive lines.
  • Other: Plasma sample collection
    Collect at least two plasma samples
Malignant melanoma stage IV Patients with stage IV malignant melanoma treated with Immunotherapy with or without targeted therapy.
  • Other: Plasma sample collection
    Collect at least two plasma samples
Malignant melanoma stage IIIb-d Patients with stage IIIb-d malignant melanoma treated with Immunotherapy as adjuvant therapy.
  • Other: Plasma sample collection
    Collect at least two plasma samples
SCLC stage IV Patients with stage IV SCLC treated with Immunotherapy or Immunotherapy + Chemotherapy.
  • Other: Plasma sample collection
    Collect at least two plasma samples

Recruiting Locations

Birmingham VAHCS
Birmingham, Alabama 35233
Contact:
Davika Das, MD
devika.das@va.gov

Mayo Clinic
Jacksonville, Florida 32224
Contact:
Yanyan Lou, MD
Lou.Yanyan@mayo.edu

University of Miami
Miami, Florida 33136
Contact:
Jose Lutzky, MD
jose.lutzky@med.miami.edu

Florida Cancer Specialist and Research Institute
Orlando, Florida 32827
Contact:
Ernesto Bustinza, MD
ebustinza@flcancer.com

Protean Biodiagnosics
Orlando, Florida 32827
Contact:
Anthony Magliocco, MD

Northwest Community Healthcare
Rolling Meadows, Illinois 60008
Contact:
So Hyeon Park
marina.messinger@gmail.com

Helen Nassif Community Cancer Center
Cedar Rapids, Iowa 52403
Contact:
So Hyeon Park
wfusselman@ocofiowa.com

Rutgers Cancer Institute
New Brunswick, New Jersey 08903
Contact:
Adam Berger, MD
ab2047@cinj.rutgers.edu

Roswell Park
Buffalo, New York 14263
Contact:
Igor Puzanov, MD
Igor.Puzanov@RoswellPark.org

West Clinic
Germantown, Tennessee 38138
Contact:
Noam VanderWalde, MD
nvanderwalde@westclinic.com

Michael E. Debakey VA Medical Center
Houston, Texas 77030
Contact:
Anita Sabichi, MD
Anita.Sabichi@va.gov

151-Christus Health St. Michael
Texarkana, Texas 75503
Contact:
Sunil Patel, MD
sapd@pm.me

More Details

NCT ID
NCT04056247
Status
Recruiting
Sponsor
OncoHost Ltd.

Study Contact

Shani Raveh Shoval, Ph.D.
97248537554
shani@oncohost.com

Detailed Description

The goal of this research study is to develop an algorithm that predicts the patient's treatment outcome.This algorithm will serve as a tool for physicians when making treatment decisions, specifically for stage IV NSCLC and malignant melanoma patients receiving anti-cancer treatments. The investigators also aim to identify the metabolic pathways that could lead to better therapeutic options. The patients will be given their treatment according to the institute's standard of care. The patients will provide two blood samples and clinical data will be collected from their medical records. In the first part of the trial, the data obtained from the blood samples and the medical records of the patients will be used to develop the prediction algorithm, and in the second part of the trial, the algorithm will be validated by comparing the objective response rate of the patients to the theoretical response prediction of the algorithm.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.