Patient Characteristics, Treatment Patterns, and Healthcare Resource Utilization of Metastatic Melanoma Patients

NCT ID: NCT06369428

Last Updated: 2024-04-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1795 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-06-23

Study Completion Date

2023-04-13

Brief Summary

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This was a retrospective, non-interventional, registry study based on secondary electronic medical record (EMR) data collected in Helsinki and Uusimaa hospital district (HUS data lake), hospital district of Southwest Finland (VSSHP data lake) and Pirkanmaa hospital district (PSHP data lake) as a part of their routine clinical practice. Social Insurance Institution of Finland (SII; reimbursed drug purchases) was utilized in this study to complement the medication data. The metastatic melanoma patients were stratified by first-line treatment and by hospital district.

Detailed Description

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Conditions

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Metastatic Melanoma

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Distant Metastasis Cohort

Adult patients diagnosed with stage 4 (distant) metastatic melanoma between 2014 and 2021.

No interventions assigned to this group

Regional Metastasis Cohort

Adult patients diagnosed with stage 3 (regional) metastatic melanoma between 2014 and 2021.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Patients diagnosed with metastatic melanoma (C43) during 01 January 2014 and 31 December 2021.
* Adult (18 years or older) at the time of diagnosis of metastatic melanoma.
* Resident in the corresponding hospital district(s) at the time of diagnosis of metastatic melanoma.

Exclusion Criteria

* Metastasis recorded prior to 01 January 2014 (i.e. prevalent case).
* Record of any other cancer (The International Classification of Diseases, 10th Revision \[ICD-10\] diagnosis code starting with C, excluding C43, C77, C78, and C79) as last cancer diagnosis before metastasis.
* Participated in COBRA (vemurafenib, temozolomide, lomustine, vincristine) trial.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Novartis

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Novartis

Basel, , Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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CDRB436BFI02

Identifier Type: -

Identifier Source: org_study_id

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