Reduced Corticosteroid Exposure Is Safe and Does Not Reduce Disease Control among Hodgkin Lymphoma Patients Treated with Escalated BEACOPP (eBEACOPP)

Author:

Hude Dragičević Ida1ORCID,Bašić-Kinda Sandra1,Markotić Helena2,Morić-Perić Martina3,Dujmović Dino1,Radman Ivo1,Dreta Barbara1,Dotlić Snježana45,Ilić Ivana45,Galunić Bilić Lea6ORCID,Dobrenić Margareta7,Kralik Marko8,Aurer Igor15

Affiliation:

1. Department of Internal Medicine, Division of Hematology, University Hospital Center Zagreb, Kišpatićeva 12, 10000 Zagreb, Croatia

2. Department of Internal Medicine, University Hospital Mostar, Ulica Kralja Tvrtka bb, 88000 Mostar, Bosnia and Herzegovina

3. Department of Internal Medicine, General Hospital Zadar, Bože Peričića 5, 23000 Zadar, Croatia

4. Department of Pathology and Cytology, University Hospital Center Zagreb, Kišpatićeva 12, 10000 Zagreb, Croatia

5. School of Medicine, University of Zagreb, Šalata 2b, 10000 Zagreb, Croatia

6. Department of Oncology and Radiotherapy, University Hospital Center Zagreb, Kišpatićeva 12, 10000 Zagreb, Croatia

7. Department of Nuclear Medicine and Radiation Protection, University Hospital Center Zagreb, Kišpatićeva 12, 10000 Zagreb, Croatia

8. Department of Radiology, University Hospital Center Zagreb, Kišpatićeva 12, 10000 Zagreb, Croatia

Abstract

Background and Objectives: eBEACOPP is the most effective chemotherapy regimen for younger patients with early unfavorable (EU) and advanced-stage (AS) Hodgkin lymphoma (HL), albeit with significant toxicities. The 14-day/cycle prednisone course contributes to side effects, including osteoarticular events like avascular bone necrosis (AVN). Our center has been using eBEACOPP since 2009 for AS and 2014 for EU patients. In 2016, we reduced prednisone treatment to 7–10 days to lessen AVN risk. We analyzed the effects of this approach. Materials and Methods: We retrospectively collected data on patients who received at least two cycles of eBEACOPP for first-line HL treatment. Results: A total of 162 patients (33 EU, 129 AS) were included. Their median age was 31 (range 19–59 years), and 88 were males. A total of 94 patients received full corticosteroid courses, and 68 received reduced corticosteroid courses. The overall response rate (ORR) was 98%. Different corticosteroid dosings had no significant effect on ORR, febrile neutropenia episodes, or hospital admissions. After a median follow-up (mFU) of 58 months, the 5yPFS for the entire cohort was 98% vs. 95% for the standard course vs. the short corticosteroids course, respectively (p = 0.37), while the 5yOS was 98% vs. 99% for the standard course vs. short corticosteroids course, respectively (p = 0.87). In AS patients intended to be treated with six eBEACOPP cycles, 5yPFS and 5yOS were 100% vs. 97% and 100% vs. 99% for standard vs. short corticosteroid courses, respectively (p = 0.56 and p = 0.17). In EU patients, 5yPFS was 97% (standard) vs. 95% (short) (p = 0.98) and 5yOS 100% vs. 93.3% (p = 0.87). Osteoarticular events were numerically lower in patients receiving the shorter prednisone course, both in the whole cohort and in the subgroup of patients treated with six cycles of eBEACOPP, but this difference failed to reach statistical significance. Conclusions: eBEACOPP provides excellent and durable first-line disease control. Shortening the corticosteroid course does not compromise efficacy, potentially reducing toxicity. However, longer follow-ups and larger studies are needed for confirmation.

Publisher

MDPI AG

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