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Perceptions on Expected Outcomes of Immunotherapy in Advanced Cancer Patients With Poor Performance Status

M.D. Anderson Cancer Center logo

M.D. Anderson Cancer Center

Status

Completed

Conditions

Non-small Cell Lung Cancer

Treatments

Behavioral: Questionnaires
Behavioral: Interview

Study type

Observational

Funder types

Other

Identifiers

NCT05634551
NCI-2022-09969 (Other Identifier)
2022-0348

Details and patient eligibility

About

To better understand your feelings and expectations about immunotherapy

Full description

Primary Objective:

  1. To compare expectations of survival benefit from immunotherapy between advanced cancer patients with poor performance status (PS) and their oncologists. We hypothesize that, compared to their oncologists, patients will have expectations for greater likelihood of survival beyond 2 years.

Secondary Objectives:

  1. To compare expectations of therapeutic benefit of immunotherapy between advanced cancer patients with poor PS and their oncologists. We hypothesize that, compared to their oncologists, patients will have expectations for greater likelihood of cure, quality of life improvement, and lower likelihood of adverse events.
  2. To qualitatively describe the priorities and preferences for information of advanced cancer patients with poor PS when considering immunotherapy treatment.
  3. To evaluate the associations between discrepant expectations with patients' sociodemographic and clinical characteristics.
  4. To compare patient and oncologist expectations with actual treatment outcomes and survival.

Enrollment

15 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients being considered for or within 2 months of starting immunotherapy for advanced cancer
  2. Patient ≥18 years of age
  3. ECOG ≥2
  4. Cognitively able to understand consent and complete questionnaire as determined by the interviewer at the time of study enrollment
  5. English speaking
  6. Willing to participate in the study and sign informed consent
  7. The study will include medical oncologists that treat advanced cancers

Exclusion criteria

  1. Treatment for curative intent
  2. Presence of Delirium (as determined by score >13 on MDAS 46, appendix A)

Trial design

15 participants in 2 patient groups

Questionnaires (All Participants)
Description:
If participants are found to be eligible and agree to take part in the study, information about you (such as age, gender, race, ethnicity, marital status, education, employment status, religious beliefs, and information about your cancer diagnosis and history, current therapy and goal of cancer therapy) will be collected.
Treatment:
Behavioral: Questionnaires
Interview (Some Participants)
Description:
Not every participant will be asked to have an interview. It is expected that about 20-30 participants will take part in the interview part of the study.
Treatment:
Behavioral: Interview

Trial contacts and locations

1

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Central trial contact

Sriram Yennu, MD

Data sourced from clinicaltrials.gov

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