• There is an opportunity to improve patient awareness of BsAbsa and CAR T-cell therapies1

When asked about approved immunotherapies

  • Up to 42% of patients had never heard of BsAbs1,a
  • Up to 33% had never heard of CAR T-cell therapies1
  • Patient awareness was highest in the US and lowest in the EU and Japan1,b

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Patient Characteristics and Socioeconomic Factors on therapy awareness

aIncludes B-cell maturation antigen-directed or G protein–coupled receptor class C group 5 member D-directed BsAbs.1 bAt the time of the survey (March–June 2024), CAR T-cell therapies were not available in the UK and BsAbs were not available in Japan.1 cIncludes France, Germany, Italy, Spain, and UK.1
BsAb, bispecific antibody; CAR, chimeric antigen receptor; CAR-T, chimeric antigen receptor T-cell therapies.

Click here for the impact of

Patient Characteristics and Socioeconomic Factors on therapy awareness

Patients Who Recalled Physicians Offering BsAbs or CAR T-Cell Therapies1,2,a

Click here to see how patient and treatment factors impact being offered BsAb or CAR T-cell therapy

Asian or Pacific Islander, Black or African American, Hispanic or Latino, Native American or other indigenous community, or other.

  • Few patients recalled physicians offering BsAbs or CAR T-cell therapies1,a
Although the Unite for MM Survey did not capture treatment eligibility, a small proportion of patients recalled HCPs offering BsAbs or CAR T-cell therapy.1 This suggests that for some patients, treatment awareness may be driven by their own knowledge/research.
  • Data revealed disparities in awareness of the therapies between White and patients of other ethnicities/races in the US1,b
  • Awareness of the therapies was lower in underserved (ethnicities/races other than White) populations in the US1
  • In the US, patients of ethnicities/races other than White were less likely to report being treated by a doctor specializing in MM1

Asian or Pacific Islander, Black or African American, Hispanic or Latino, Native American or other indigenous community, or other.

Learn how BsAbs and CAR T-cell therapies work in multiple myeloma
aAt the time of the survey (March-June 2024), CAR T-cell therapies were not available in the UK and BsAbs were not available in Japan.1 Note that patients who reported they had never heard of these therapies were not asked if their physician had discussed or offered these therapies. bThe only country for which racial data were available was the US.1
HCP, health care professional; MM, multiple myeloma.
Learn how BsAbs and CAR T-cell therapies work in multiple myeloma

Efficacy was the most important consideration for patients who chose BsAbs or CAR T-cell therapies1

  • Of patients who were offered BsAbs, 57% (n=51) chose to receive treatment1,2
  • Convenience and physician recommendation were also among top reasons patients chose BsAbs1

  • Of patients who were offered CAR T-cell therapies, 76% (n=103) received treatment1,2
  • Learning that CAR T-cell therapies worked well for others was one of the top reasons for choosing the therapies, suggesting demand for CAR T-cell therapies may be influenced by other patients’ experiences1

aSurvey respondents could select up to 5 responses from a choice of 15.3 bSurvey respondents could select up to 5 responses from a choice of 13.3

The top reason patients declined BsAbs or CAR T-cell therapy was due to feeling overwhelmed1

Reasons for patients declining treatment as reported by HCPs were generally similar between the 2 therapies, yet1:

tIn the survey sample, 11 patients each declined BsAbs or CAR T-cell therapies. Due to this small number of patients, patient data on their reasons for declining therapies were not included. HCPs were asked to choose the top 5 reasons their patients declined each type of therapy from a selection of 15.1,4
AE, adverse event.

Steering Committee Recommendations on Positive Steps for the MM Community to Consider
CALL TO ACTION

Improve Patient Familiarity with Approved Immunotherapies

Partner with patient advocacy groups to increase awareness of BsAbs and CAR T-cell therapies, particularly among patients in underserved populations

Who Can Take Action?

HCPs, patients, patient advocacy groups, industry

Rationale

The limited awareness among patients with RRMM (up to 42% of patients had never heard of BsAbs, and up to 33% had never heard of CAR T-cell therapies) indicates a need for broad patient education.1 Awareness was lowest in the EU and Japan, and among patients of ethnicities/races other than Whitea in the US, suggesting educational efforts may be particularly needed for these groups.1 Patient advocacy groups and other organizations can be important sources of patient information and improve awareness through educational outreach, helping to ensure patients are fully informed when making treatment decisions.5 In addition, survey results suggest that including platforms for patient-to-patient communication may be particularly impactful.1

aAsian or Pacific Islander, Black or African American, Hispanic or Latino, Native American or other indigenous community, or other.

Support creation and distribution of information to make patients and care partners more comfortable receiving these types of immunotherapies

Who Can Take Action?

Clinical experts, HCPs, patient advocacy groups

Rationale

For both BsAbs and CAR T-cell therapies, feeling overwhelmed was the top reason patients declined treatment.1 Providing practical advice through multiple methods of communication (verbal, written, and video content, patient mentors, etc) may help reduce complexity for patients.

References