Purpose

Participants will complete questionnaires before surgery, between 2 to 4 weeks after surgery, and 6 months after surgery.

Conditions

Eligibility

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

Inclusion Criteria

  • Age ≥18 years - Clinical Stage I with suspected NSCLC, classified preoperatively based on the AJCC TNM staging manual, 9th edition o Note: Tissue diagnosis of NSCLC is not required before enrollment. A pathologic diagnosis of NSCLC may be confirmed preoperatively with biopsy, intraoperatively with frozen section, or postoperatively on final pathology

Exclusion Criteria

  • Actively receiving lung cancer treatment or a history of lung cancer in the previous 5 years - History of chemotherapy or radiation therapy for a previous lung cancer - Synchronous secondary cancer in the lung or elsewhere in the body at the time of surgery - Carcinoid tumors - History of other malignancies within the past 3 years, with the exception of non-melanoma skin cancer, superficial bladder cancer, and carcinoma in situ of the cervix - Actively receiving treatment for other malignancies - Cases of lobectomy in conjunction with segmentectomy from another lobe and ≥2 segmentectomies from different lobes either en bloc or separate will be excluded from the primary analysis. - Multi-segmental resection from the same lobe is not a criterion for exclusion.

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Participants with Lung Cancer Participants undergoing planned pulmonary segmentectomy for primary lung cancer
  • Other: Patient-Reported Outcomes Measurement Information System
    Participants-reported outcomes will be collected using the Patient-Reported Outcomes Measurement Information System (PROMIS). PROMIS is a web-based platform developed by the National Institutes of Health. Scoring is standardized on a scale from 0 to 100, with a population mean of 50 and standard deviation of 10 units. High scores mean more of the concept being measured. This study will use PROMIS surveys assessing three domains: physical function (PROMIS bank version 2.0), pain interference (PROMIS bank version 1.1), and dyspnea severity (PROMIS bank version 1.0)
    Other names:
    • PROMIS

Recruiting Locations

University of Arizona (Data Collection Only)
Tucson, Arizona 85704
Contact:
Praveen Sridhar, MD
520-694-2873
psridhar@arizona.edu

University of California San Diego (Data collection)
San Diego, California 92103
Contact:
Joshua Boys, MD
858-657-7777

Rush University Medical Center (Data collection only)
Chicago, Illinois 606012
Contact:
Christopher Seder, MD
312-738-3732

Endeavor Health
Evanston, Illinois 60201
Contact:
Seth Krantz, MD
847-570-2868

University of Michigan (Data Collection Only)
Ann Arbor, Michigan 48109
Contact:
Jules Lin, MD
734-936-8857

Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities)
Basking Ridge, New Jersey 07920
Contact:
David Jones, MD
212-639-6428

Memorial Sloan Kettering Monmouth (Limited Protocol Activities)
Middletown, New Jersey 07748
Contact:
David Jones, MD
212-639-6428

Memorial Sloan Kettering Bergen (Limited Protocol Activities)
Montvale, New Jersey 07645
Contact:
David Jones, MD
212-639-6428

Memorial Sloan Kettering Suffolk - Commack (Limited Protocol Activities)
Commack, New York 11725
Contact:
David Jones, MD
212-639-6428

Memorial Sloan Kettering Westchester (Limited Protocol Activities)
Harrison, New York 10604
Contact:
David Jones, MD
212-639-6428

Memorial Sloan Kettering Cancer Center (All Protocol Activities)
New York, New York 10065
Contact:
David Jones, MD
212-639-6428

Memorial Sloan Kettering Nassau (Limited Protocol Activities)
Uniondale, New York 11553
Contact:
David Jones, MD
212-639-6428

Thomas Jefferson University Hospital (Data Collection Only)
Philadelphia, Pennsylvania 19107
Contact:
Nathaniel Evans III, MD
nathaniel.evans@jefferson.edu

ALLEGHENY HEALTH NETWORK (Data Collection Only)
Pittsburgh, Pennsylvania 15212
Contact:
Benny Weksler, MD
412-359-6137

Baylor University Medical Center (Data Collection Only)
Dallas, Texas 75246
Contact:
Shanda Blackmon, MD, MPH
713-198-6376
sshanda.blackmon@bcm.edu

MD Anderson Cancer Center (Data Collection Only)
Houston, Texas 77030
Contact:
David Rice, MD
800-392-1611

More Details

Status
Recruiting
Sponsor
Memorial Sloan Kettering Cancer Center

Study Contact

David Jones, MD
212-639-6428
jonesd2@mskcc.org

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.