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Psychosocial Experiences in Relapsed/Refractory DLBCL: CAR-T vs. Other Therapies


A Cross-Sectional Study of Psychosocial Experiences in Patients with Relapsed/Refractory Diffuse Large B Cell (DLBCL) Who Received CAR-T Compared to Other Therapies

Authors: C. Bates¹, S. Kalloger¹, A. Watson¹, L. Warwick¹
¹Lymphoma Coalition, Mississauga, Canada

Topic: Patient Advocacy Data


Short Title

Psychosocial experiences in patients receiving CAR-T compared to other therapies


Background

Chimeric antigen receptor T-cell (CAR-T) therapy continues to expand as a treatment option for patients with relapsed/refractory diffuse large B cell lymphoma (DLBCL). This study provides insight into the psychosocial experiences of patients with relapsed and refractory DLBCL treated with CAR-T compared to other therapies.


Methods

  • Survey Population:
    • Total respondents: 8,637
    • Patients: 7,113
    • Caregivers: 1,524
    • Countries: 84
    • Survey: 2022 Lymphoma Coalition Global Patient Survey (GPS)
  • Subgroup Analysis:
    • Diagnosed with DLBCL: 996
    • Classified as relapsed/refractory disease: 204
    • Received CAR-T treatment: 28
    • Received non-CAR-T regimens: 176
  • Focus:
    Survey questions related to psychological experiences (depression, anxiety, fear, communication) were analyzed for both patient groups.
    • Differences in proportions tested using Fisher’s Exact Test.

Flow of Participants

  • Total Respondents (N=8637)
    → Diagnosed with DLBCL (N=996)
    → Excluded (N=7641)
  • Classified as Relapsed/Refractory (N=204)
    → Excluded (N=792)
  • Treated with CAR-T (N=28)
  • Treated with Other Therapies (N=176)

Results

  • Depression:
    Similar incidence between CAR-T (28%) and non-CAR-T (32%).
  • Anxiety:
    Similar between groups (CAR-T: 46%, Others: 44%).
  • Fear of Progression:
    Higher in those who received non-CAR-T therapies.
  • Support and Education:
    Patients receiving CAR-T more frequently received psychosocial support and education for depression, anxiety, and fear from healthcare teams and caregivers.
  • Communication:
    Communication between doctors and patients was over twice as prevalent in CAR-T (31%) compared to non-CAR-T (15%).

Table 1. Psychosocial Support and Experiences

Psychosocial MeasureCAR-TOther TherapiesP-value
Received written/oral information for depression3/5 (60%)0/21 (0.0%)0.004
Received medications to help with depression5/5 (100%)11/21 (52.4%)0.05
Received education/support group for depression3/5 (60%)4/21 (19.1%)0.1
Doctor was able to help (with anxiety)6/7 (85.7%)29/40 (72.5%)0.7
Received written/oral information for anxiety3/6 (50%)3/28 (10.7%)0.05
Received empathetic understanding from nurse3/6 (50%)2/28 (7.1%)0.03
Pursued exercise (for fear)4/6 (66.7%)11/42 (26.2%)0.1
Doctor was able to help with fear of relapse12/16 (75.0%)37/49 (75.5%)1.0
Communication / Doctor follow-up6/19 (31.6%)14/94 (14.9%)0.1

Conclusions

  • Patients who received CAR-T reported greater access to psychosocial support compared to those who received other non-CAR-T regimens.
  • The disparity may be partly due to CAR-T being a newer therapy, often delivered through clinical trials, requiring more intensive follow-up than standard care.
  • The inequity in psychosocial support for novel therapeutics highlights the need for improved interventions to support patients with relapsed and refractory DLBCL.
  • Future research should include larger sample sizes to strengthen these findings.

Summary

This cross-sectional study compared the psychosocial experiences of patients with relapsed/refractory diffuse large B cell lymphoma (DLBCL) who received CAR-T therapy versus other treatments.

  • Study Population:
    • 8,637 survey respondents from 84 countries
    • 204 patients with relapsed/refractory DLBCL
    • 28 treated with CAR-T, 176 with other therapies
  • Key Findings:
    • Depression & Anxiety: Similar rates between CAR-T and non-CAR-T groups.
    • Fear of Progression: Higher in non-CAR-T patients.
    • Support & Education: CAR-T patients received more frequent psychosocial support and education from healthcare teams and caregivers.
    • Communication: More than twice as common between doctors and CAR-T patients compared to non-CAR-T patients (31% vs. 15%).
  • Conclusion:
    CAR-T patients had greater access to psychosocial support, likely due to the intensive monitoring and follow-up associated with newer therapies and clinical trials. The study highlights inequities in support for non-CAR-T patients and calls for improved interventions and larger future studies.