Evaluating the Uptake and Utility of Clinical Pathways for Newly Diagnosed Patients With Multiple Myeloma

Last updated: May 2, 2024
Sponsor: All4Cure
Overall Status: Active - Recruiting

Phase

N/A

Condition

Multiple Myeloma

Bone Diseases

Leukemia

Treatment

All4Cure Platform

Multiple Myeloma Pathway

Documentation Pathway

Clinical Study ID

NCT06149910
All4Cure03
  • Ages > 18
  • All Genders

Study Summary

All4Cure is partnering with community oncology practices participating in the Quality Cancer Care Alliance (QCCA) and Exigent Research to develop a clinical pathway that standardizes the evaluation, treatment and ongoing management of patients with newly diagnosed multiple myeloma who wish to achieve and maintain MRD negativity.

This is a longitudinal retrospective study that will collect data from three separate cohorts of patients with newly diagnosed multiple myeloma (NDMM). The cohorts classify patients based on whether care is delivered under an intention to adhere to an MRD-targeted clinical pathway, and if so, whether the implementation of that clinical pathway occurs through participation in the All4Cure platform vs. through written documentation. The three cohorts are labeled: Platform, Documentation, and Off-Pathway.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Diagnosis of multiple myeloma
  • Diagnosis must occur on or after the formal launch of the MRD-targeted clinicalpathway in the Exigent network
  • Diagnosis must be indicated by the presence of any of the following diagnosticcodes for multiple myeloma: [C90.00]
  • Diagnosis must be confirmed on human review of the medical record
  • Age ≥ 18 years at qualifying diagnosis.
  • Patient has continued to receive care at a QCCA/Exigent Research practice for at least 90 days after the index date. Patients in the Documentation Cohort must meet the following additional inclusion criteria.

• Evidence in the record of a threshold level of adherence to the clinical pathway, orimplied intention to adhere to the clinical pathway. In addition to the inclusion criteria for the documentation cohort, patients in thePlatform Cohort must meet the following additional inclusion criteria.

  • A record of registration by the patient for participation in the All4Cure platform,including signed HIPAA release forms that allow All4Cure to access their medicalrecords.
  • A record of registration by the patient's primary treating physician for participationin the All4Cure platform.

Exclusion

Exclusion Criteria:

  • Patients with a concurrent other malignancy (except basal cell carcinoma, squamouscell carcinoma of the skin, or in situ malignancies of breast or cervix), or those whohave received treatment of another malignancy within three years prior to diagnosis ofmultiple myeloma (except for treatment of basal cell carcinoma, squamous cellcarcinoma of the skin, or in situ malignancies of breast or cervix), are excluded fromeligibility.
  • Patients with multiple myeloma subtypes Immunoglobulin D (IgD) or Immunoglobulin E (IgE) are excluded due to the very low rate of these subtypes.
  • Patients who transfer their care to another facility outside the QCCA/Exigent Researchnetwork within the first 90 days after NDMM diagnosis are excluded.

Study Design

Total Participants: 450
Treatment Group(s): 3
Primary Treatment: All4Cure Platform
Phase:
Study Start date:
April 18, 2024
Estimated Completion Date:
December 01, 2026

Study Description

The study will employ two implementations of an MRD-targeted pathway one that disseminates pathway guidance through written documentation, and another that leverages the All4Cure platform to support pathway adherence through direct engagement of other experts, and through integration of elements of the MRD-targeted pathway into the structured components of the platform. The study also includes a comparator cohort of patients not being treated according to the clinical pathway. Analysis under the primary objective will evaluate outcomes between patients being treated following written pathway documentation and patients being treated off pathway. The primary endpoints are the proportion of patients with achievement of VGPR or better (≥VGPR), and the proportion of patients with a CR or better (≥CR), within 12 months. Secondary endpoints include MRD negativity, pathway adherence, time to next treatment (TTNT), progression-free survival (PFS), overall survival (OS), and obstacles to getting daratumumab treatment. Sustained MRD negativity is an exploratory endpoint.

Data will be collected retrospectively, through stratified random sampling by race within cohort, with patients accrued over a 12-month period. All patients will be followed over time after accrual, with minimum available follow-up of 12 months. Accordingly, the estimated period from first accrual to last follow-up will be approximately 24 months.

Connect with a study center

  • All4Cure

    Seattle, Washington 98126
    United States

    Active - Recruiting

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