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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03518814
Other study ID # RC-P0062
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 9, 2018
Est. completion date June 5, 2018

Study information

Verified date July 2018
Source Lille Catholic University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Few studies have been conducted on the quality of life of patients with stage IV melanoma. Particularly, there is no data regarding the quality of life of patients with a multimetastatic melanoma currently in remission.

Then, the main objective of this study is to evaluate the quality of life from a point of view medico-psycho-social in patients with multimetastatic melanoma in remission for more than 6 months.


Description:

The cutaneous melanoma, (9th rank of all cancers), was until recently neglected and poorly known by the general public. The metastatic stages have dramatic rates of survival: 25% at 1 year and 2% at 5 years with a median of about 6.2 months. However, in the last ten years, the treatment of metastatic forms has undergone a real revolution.

Its high metastatic potential for a very low initial tumor mass, gives evidence of a great aggressiveness. The cutaneous melanoma is resistant to the main therapeutics (chemotherapy and radiotherapy). Thanks to the emergence of immunotherapies and targeted therapies anti-RAF (Rapidly Accelerated Fibrosarcoma) and anti-MEK (Mitogen-activated Extracellular) the prognosis of patients with metastatic melanoma has considerably improved, increasing the number of "long-term survivors".

However, these treatments can cause many adverse effects that can impact patients' quality of life, despite a better tolerance compared to conventional chemotherapies. To our knowledge there are no data regarding the quality of life of patients with metastatic melanoma currently in remission.For this purpose, it is necessary to obtain solid data using validated questionnaires. Thus, we have chosen to evaluate quality of life using specific questionnaires to better understand patients' expectations, their difficulties, and then to improve the relationship between the patient and the physician.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date June 5, 2018
Est. primary completion date June 5, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult patients

- Presenting a stage IV melanoma of the American Joint Committee on Cancer (AJCC) classification (multimetastatic) in remission for more than 6 months:

- Complete remission (defined as the complete disappearance of target lesions according to the RECIST criteria, based on a thoraco-abdomino-pelvic CT scan and a brain Magnetic resonance imaging (MRI) or

- Complete metabolic remission (defined as the complete disappearance of target lesions in PET CT (positron emission tomography computed tomograph, that is to say, disappearance of the hypermetabolic character of the anatomic structures. There may remain target lesions in conventional CT but they are not hypermetabolic in PET CT)

- Patients able to answer the questionnaires

- Patients with enough understanding of the French language

Exclusion Criteria:

- Adjuvant treatment

- Patient under tutorship or curatorship

- Refusal to participate in the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Questionnaires
FACT-M (Functional Assessment of Cancer Therapy - Melanoma) questionnaire, MOS SF (medical outcome study short form) -36 questionnaire

Locations

Country Name City State
France CHRU Lille Lille Nord
France Lille Catholic Hospitals Lille Nord

Sponsors (2)

Lead Sponsor Collaborator
Lille Catholic University University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Quality of life assessed by the Functional Assessment of Cancer Therapy-Melanoma (FACT-M) questionnaire The FACT-M questionnaire is a specific quality of life scale for patients treated for melanoma. It includes 51 items grouped into nine multi-item scores: six subscale scores and three summary scores.
The six subscales consist of four subscales from the FACT-G:
physical well-being [PWB], score range: 0-28, higher values represent a worse outcome.
social well-being [SWB], score range: 0-28, higher values represent a better outcome.
emotional well-being [EWB], score range: 0-24, higher values represent a worse outcome.
functional well-being [FWB]), score range: 0-28, higher values represent a better outcome.
One Melanoma scale, score range: 0-64, higher values represent a worse outcome. One Melanoma surgery scale, score range: 0-32, higher values represent a worse outcome.
The three summary scores include:
the FACT-M Trial Outcome Index (TOI), score range: 0-120
the FACT-G total score, score range: 0-108
the FACT-M total score, score range: 0-172
day 0
Primary Health status surveyed by the Medical Outcome Study Short Form - 36 (MOS SF 36) questionnaire The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability.
The eight sections are:
vitality
physical functioning
bodily pain
general health perceptions
physical role functioning
emotional role functioning
social role functioning
mental health
day 0
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