Multiple Myeloma Clinical Trial
Incidence of Hyperpigmentation in Black Patients With Multiple Myeloma Treated With Immunomodulatory Drugs
Summary
The purpose of this study is to measure the incidence of hyperpigmentation in Black participants with multiple myeloma (MM) treated with immunomodulatory drugs (IMiDs) compared with Black participants with MM not treated with IMiDs. The study will use de-identified data from electronic medical records in the Flatiron Health database.
Eligibility Criteria
Inclusion Criteria:
Participants ≥18 years of age at index date
Participants with new diagnosis of MM as defined by:
ICD-9-CM: 203.0x and/or ICD-10-CM: C90.0x or C90 during the study period
At least two documented clinical visits for MM on different days and occurring on or after January 1, 2011
Participants who received at least one systemic MM therapy on or after initial MM diagnosis
Participants who did not receive clinical study drug at any time during the observation period
Participants with race information
Exclusion Criteria:
Exclusion Criteria
Patients with less than 6 months of medical data during the prior or follow-up period
Patients in more than one race category (mix race), missing race, unknown race, and "other" race
Patients diagnosed with the following hematological cancers on or prior to the index date:
myelodysplastic syndromes (ICD-9: 238.74, 238.75; ICD-10: D46.xx)
mantle cell lymphoma (ICD-9: 200.4x, ICD-10: C83.1x)
follicular lymphoma (ICD-9: 202.0x, ICD-10: C82.xx)
marginal zone lymphoma (ICD-9: 200.3x, ICD-10: C83.4x)
Patients with evidence of skin hyperpigmentation (ICD-9: 709.00, 709.09; ICD-10: L81.0, L81.1, L81.4, L81.8) on or prior to the index date
709.00 Dyschromia, unspecified
709.09 Other dyschromia
L81.0 Post inflammatory hyperpigmentation
L81.1 Chloasma/melasma
L81.4 Other melanin hyperpigmentation
L81.8 Other specified disorders of pigmentation
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There is 1 Location for this study
New York New York, 10013, United States
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