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Abstracts PO58

Comparison of Intensive and Less Intensive Chemotherapy on Cognitive Impairment in Survivors of Hodgkin Lymphoma

Tomas Kozak1,2, Dan Fayette3, Iveta Fajnerova3, Veronika Jurickova3, Heidi Mocikova1,2 and Jiri Horacek3

Introduction/Background/Significance: Cognitive impairment related to cancer or chemotherapy (CRCI) is frequently reported in Hodgkin lymphoma (HL) patients, but the influence of treatment intensity remains unclear. This prospective study aimed to evaluate whether more intensive chemotherapy regimens, particularly BEACOPPesc, lead to greater cognitive decline than less intensive protocols such as ABVD.1,2

Materials and Methods/Case Presentation/Objective: We conducted a longitudinal study of 44 HL patients (mean age: 36.94 ± 11.88 years; 54.5% male), divided into two groups based on treatment intensity
  • Group 1 (n = 23): early/intermediate-stage HL treated with 4× ABVD + 30 Gy IF RT or 2× BEACOPPesc + 2× ABVD + 30 Gy IF RT
  • Group 2 (n = 21): advanced-stage HL treated with 6× BEACOPPesc3,4

Neuropsychological assessments and affective/quality-of-life measures were conducted at three time points: pre-treatment, post-treatment (~6 months), and 12-month follow-up. Cognitive domains included memory, attention, processing speed, and executive function.

Results/Description/Main Outcome Measures: Results:

Significant within-group improvements were seen in working memory, speed of processing, and verbal memory over time (e.g., verbal memory z-score change from −0.37 to +0.03; p ≤ 0.001). However, no statistically significant differences in cognitive performance were found between the two treatment groups at any time point (p > 0.05 for all comparisons).
  • Anxiety scores (BAI) were highest before treatment in the advanced-stage group (mean = 8.52), but significantly decreased by follow-up (p < 0.01).
  • No associations were found between cognitive outcomes and age, sex, or education level.

Conclusions: Our findings indicate that neither disease stage nor chemotherapy intensity affects cognitive performance in HL patients. Intensive regimens like 6× BEACOPPesc did not pose greater cognitive risk than milder treatments. These results offer reassurance to clinicians and patients that effective, aggressive therapies need not be avoided for fear of exacerbating CRCI. However, further studies with larger cohorts are warranted to confirm these findings.

References

1. Trachtenberg, E.; Mashiach, T.; Hayun, B. R.; Tadmor, T.; Fisher, T.; Aharon-Peretz, J.; Dann, E.J. Cognitive impairment in Hodgkin lymphoma

survivors. Br J Haematol. 2018, 182(5), 670-678.

2. Fayette, D.; Juríčková, V.; Kozák, T.; Mociková, H.; Gaherová, L.; Fajnerová, I.; Horáček, J. Cognitive impairment associated with Hodgkin's

lymphoma and chemotherapy. Neurosci. Lett. 2023, 797:137082.

3. Ansell, S.M.; Hodgkin lymphoma: 2018 update on diagnosis, risk-stratification, and management. Am J Hematol 2018, 93, 704–715.

4. Engert, A. ABVD or BEACOPP for Advanced Hodgkin Lymphoma. J Clin Oncol 2016, 34, 1167-1169