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Communicating With Patients on Cancer Resistance to Treatment: the Development of a Communication Tool. (HECTOR)

I

Institut Curie

Status

Completed

Conditions

Metastatic Uveal Melanoma
Luminal B Breast Cancer
Pediatric Cancer
Triple Negative Breast Cancer

Treatments

Other: DELPHI Consensus Method
Other: Focus Group
Behavioral: Questionnaires
Behavioral: Semi-structured individual interviews

Study type

Interventional

Funder types

Other

Identifiers

NCT04118062
IC 2018-09

Details and patient eligibility

About

Resistance to treatment is one of the major themes in cancer research. Despite this, the definition and clinical implications of resistance to treatment remain under-explored, and patient-physician communication in this context still constitutes a challenge. When resistance to cancer treatments occurs, physicians not only have to explain to the patient the phenomenon of resistance, often based on complex results (biological results, genomic tests, imaging, etc.), but also need to offer alternative therapies, whilst fostering shared medical decision-making. These different tasks are particularly challenging for clinicians, especially since there are large individual differences at patient level. Indeed, each patient has his or her own unique information needs, capacity for understanding, and level of desire to participate in treatment decisions.

Full description

Although a challenge, better communicating around resistance to treatment carries many potential benefits. Indeed, in similar contexts of announcement of bad news and choice of care, Parker and collaborators (1) have highlighted the positive impact of individualized care, respecting the needs, quality of care, and quality of life of patients. Given the clinical stake, and the lack of scientific knowledge devoted to communication in the context of resistance to treatment, it appears necessary to better understand its modalities. In this perspective, research has proven the value of tools for supporting communication, including the issue of question booklets for patients. These tools provide patients with a list of questions submitted to them before the medical consultation, and which they can ask during the consultation, and throughout the treatment. This tool fosters communication by helping the patient obtain a level of information that is adapted to his or her needs and experience, and thus, to be better prepared for care. Despite significant interest for these booklets in the field of oncology, none has yet been developed in the specific context of resistance to treatment.

Enrollment

128 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients:

    1. To be 18 years of age or older ;
    2. To have metastatic uveal melanoma (MUM) or triple negative or luminal B breast cancer ;
    3. To have received the information that the disease is resistant to treatment ;
    4. To have read the information and signed the informed consent.
  • Parents of a sick child:

    1. To be a parent (parental authority holder) of a child with cancer ;
    2. To have received the information that the child disease is resistant to treatment ;
    3. To have read the information and signed the informed consent.
  • Expert patients:

    1. To be 18 years of age or older ;
    2. To have had cancer (regardless the cancer site) ;
    3. To participated to an expert patient training (fine knowledge of the illness, experience with the disease) ;
    4. To have read the information and signed the informed consent.
  • Professionals:

    1. To be an oncologist (medical oncologist, surgeon, radiotherapist, supportive care specialist) and/or to be a researcher in oncology (doctor, biologist, geneticist ...) ;
    2. To have patients with a triple-negative or luminal B breast cancer or metastatic uveal melanoma which is resistant to anti-tumor treatments and/or to take part to a research on resistance to cancer treatment;
    3. To have read the information and signed the informed consent.

Exclusion criteria

  • Patients & parents of a sick child:

    1. To have difficulties in understanding the French language.
    2. Have or have had cancer (criteria only for parents);
    3. Pregnant woman, likely to be pregnant or breastfeeding (criteria only for patients).
    4. Persons deprived of their liberty or under guardianship;
    5. Impossibility of study requirements respect for geographical, social or psychological reasons.
  • Expert patients:

    1. To have difficulties in understanding the French language ;
    2. Currently being undergoing anti-tumor treatment.
  • Professionals:

    1. To have difficulties in understanding the French language ;
    2. Not to be confronted in professional practice with resistance to anti-tumor treatments.

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

128 participants in 6 patient groups

Metastatic Uveal Melanoma
Other group
Description:
Questionnaires and semi-structured individual interviews with patients with Metastatic Uveal Melanoma
Treatment:
Behavioral: Semi-structured individual interviews
Behavioral: Questionnaires
Triple Negative Breast Cancer
Other group
Description:
Questionnaires and semi-structured individual interviews with patients with Triple Negative Breast Cancer
Treatment:
Behavioral: Semi-structured individual interviews
Behavioral: Questionnaires
Luminal B Breast Cancer
Other group
Description:
Questionnaires and semi-structured individual interviews with patients with Luminal B Breast Cancer
Treatment:
Behavioral: Semi-structured individual interviews
Behavioral: Questionnaires
Pediatric Cancer
Other group
Description:
Questionnaires and semi-structured individual interviews with parents of children with cancer.
Treatment:
Behavioral: Semi-structured individual interviews
Behavioral: Questionnaires
Expert Patients
Other group
Description:
Focus groups (or group interviews) and DELPHI consensus method with expert patients
Treatment:
Other: Focus Group
Other: DELPHI Consensus Method
Researchers and Clinicians
Other group
Description:
Focus groups (or group interviews) and DELPHI consensus method with Researchers and Clinicians
Treatment:
Other: Focus Group
Other: DELPHI Consensus Method

Trial contacts and locations

1

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Central trial contact

Johanna TERRASSON, PHD; Anne-Claire COYNE, PhD

Data sourced from clinicaltrials.gov

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