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

被引:0
作者
Hude Dragicevic, Ida [1 ]
Basic-Kinda, Sandra [1 ]
Markotic, Helena [2 ]
Moric-Peric, Martina [3 ]
Dujmovic, Dino [1 ]
Radman, Ivo [1 ]
Dreta, Barbara [1 ]
Dotlic, Snjezana [4 ,5 ]
Ilic, Ivana [4 ,5 ]
Galunic Bilic, Lea [6 ]
Dobrenic, Margareta [7 ]
Kralik, Marko [8 ]
Aurer, Igor [1 ,5 ]
机构
[1] Univ Hosp Ctr Zagreb, Dept Internal Med, Div Hematol, Kispaticeva 12, Zagreb 10000, Croatia
[2] Univ Hosp Mostar, Dept Internal Med, Ulica Kralja Tvrtka Bb, Mostar 88000, Bosnia & Herceg
[3] Gen Hosp Zadar, Dept Internal Med, Boze Pericica 5, Zadar 23000, Croatia
[4] Univ Hosp Ctr Zagreb, Dept Pathol & Cytol, Kispaticeva 12, Zagreb 10000, Croatia
[5] Univ Zagreb, Sch Med, Salata 2b, Zagreb 10000, Croatia
[6] Univ Hosp Ctr Zagreb, Dept Oncol & Radiotherapy, Kispaticeva 12, Zagreb 10000, Croatia
[7] Univ Hosp Ctr Zagreb, Dept Nucl Med & Radiat Protect, Kispaticeva 12, Zagreb 10000, Croatia
[8] Univ Hosp Ctr Zagreb, Dept Radiol, Kispaticeva 12, Zagreb 10000, Croatia
来源
MEDICINA-LITHUANIA | 2024年 / 60卷 / 03期
关键词
Hodgkin lymphoma; eBEACOPP; corticosteroids; toxicity; avascular hip necrosis; TRIAL COMPARING ABVD; OPEN-LABEL; STAGE-III; HIGH-RISK; INDUCED OSTEOPOROSIS; BRENTUXIMAB VEDOTIN; 8; CYCLES; PET-CT; CHEMOTHERAPY; RADIOTHERAPY;
D O I
10.3390/medicina60030430
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页数:12
相关论文
共 49 条
[1]   Long-term cause-specific mortality of patients treated for Hodgkin's disease [J].
Aleman, BMP ;
van den Belt-Dusebout, AW ;
Klokman, WJ ;
van't Veer, MB ;
Bartelink, H ;
van Leeuwen, FE .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (18) :3431-3439
[2]   Long-term overall survival and toxicities of ABVD vs BEACOPP in advanced Hodgkin lymphoma: A pooled analysis of four randomized trials [J].
Andre, Marc P. E. ;
Carde, Patrice ;
Viviani, Simonetta ;
Bellei, Monica ;
Fortpied, Catherine ;
Hutchings, Martin ;
Gianni, Alessandro M. ;
Brice, Pauline ;
Casasnovas, Olivier ;
Gobbi, Paolo G. ;
Zinzani, Pier Luigi ;
Dupuis, Jehan ;
Iannitto, Emilio ;
Rambaldi, Alessandro ;
Briere, Josette ;
Clement-Filliatre, Laurianne ;
Heczko, Marian ;
Valagussa, Pinuccia ;
Douxfils, Jonathan ;
Depaus, Julien ;
Federico, Massimo ;
Mounier, Nicolas .
CANCER MEDICINE, 2020, 9 (18) :6565-6575
[3]   PET-CT for staging and early response: results from the Response-Adapted Therapy in Advanced Hodgkin Lymphoma study [J].
Barrington, Sally F. ;
Kirkwood, Amy A. ;
Franceschetto, Antonella ;
Fulham, Michael J. ;
Roberts, Thomas H. ;
Almquist, Helen ;
Brun, Eva ;
Hjorthaug, Karin ;
Viney, Zaid N. ;
Pike, Lucy C. ;
Federico, Massimo ;
Luminari, Stefano ;
Radford, John ;
Trotman, Judith ;
Fossa, Alexander ;
Berkahn, Leanne ;
Molin, Daniel ;
D'Amore, Francesco ;
Sinclair, Donald A. ;
Smith, Paul ;
O'Doherty, Michael J. ;
Stevens, Lindsey ;
Johnson, Peter W. .
BLOOD, 2016, 127 (12) :1531-1538
[4]   High incidence of aseptic hip necrosis in Hodgkin lymphoma patients treated with escalated BEACOPP receiving methylprednisolone [J].
Basic-Kinda, Sandra ;
Karlak, Ivan ;
Durakovic, Nadira ;
Lubina, Zvonimir, I ;
Radman, Ivo Livaja ;
Dotlic, Snjezana ;
Peric, Zinaida ;
Hude, Ida ;
Aurer, Igor .
INTERNAL MEDICINE JOURNAL, 2018, 48 (05) :523-+
[5]   Gonadal Function and Fertility in Survivors After Hodgkin Lymphoma Treatment Within the German Hodgkin Study Group HD13 to HD15 Trials [J].
Behringer, Karolin ;
Mueller, Horst ;
Goergen, Helen ;
Thielen, Indra ;
Eibl, Angelika Diana ;
Stumpf, Volker ;
Wessels, Carsten ;
Tz, Martin Wiehlpu ;
Rosenbrock, Johannes ;
Halbsguth, Teresa ;
Reiners, Katrin S. ;
Schober, Thomas ;
Renno, Jorg H. ;
von Wolff, Michael ;
van der Ven, Katrin ;
Kuehr, Marietta ;
Fuchs, Michael ;
Diehl, Volker ;
Engert, Andreas ;
Borchmann, Peter .
JOURNAL OF CLINICAL ONCOLOGY, 2013, 31 (02) :231-239
[6]  
Borchmann P., 2023, Hematol. Oncol, V41, P881, DOI DOI 10.1002/HON.3196LBA5
[7]  
Borchmann P, 2021, LANCET ONCOL, V22, P223, DOI 10.1016/S1470-2045(20)30601-X
[8]   PET-guided treatment in patients with advanced-stage Hodgkin's lymphoma (HD18): final results of an open-label, international, randomised phase 3 trial by the German Hodgkin Study Group [J].
Borchmann, Peter ;
Goergen, Helen ;
Kobe, Carsten ;
Lohri, Andreas ;
Greil, Richard ;
Eichenauer, Dennis A. ;
Zijlstra, Josee M. ;
Markova, Jana ;
Meissner, Julia ;
Feuring-Buske, Michaela ;
Huttmann, Andreas ;
Dierlamm, Judith ;
Soekler, Martin ;
Beck, Hans-Joachim ;
Willenbacher, Wolfgang ;
Ludwig, Wolf-Dieter ;
Pabst, Thomas ;
Topp, Max S. ;
Hitz, Felicitas ;
Bentz, Martin ;
Keller, Ulrich Bernd ;
Kuhnhardt, Dagmar ;
Ostermann, Helmut ;
Schmitz, Norbert ;
Hertenstein, Bernd ;
Aulitzky, Walter ;
Maschmeyer, Georg ;
Vieler, Tom ;
Eich, Hans ;
Baues, Christian ;
Stein, Harald ;
Fuchs, Michael ;
Kuhnert, Georg ;
Diehl, Volker ;
Dietlein, Markus ;
Engert, Andreas .
LANCET, 2017, 390 (10114) :2790-2802
[9]   Eight Cycles of Escalated-Dose BEACOPP Compared With Four Cycles of Escalated-Dose BEACOPP Followed by Four Cycles of Baseline-Dose BEACOPP With or Without Radiotherapy in Patients With Advanced-Stage Hodgkin's Lymphoma: Final Analysis of the HD12 Trial of the German Hodgkin Study Group [J].
Borchmann, Peter ;
Haverkamp, Heinz ;
Diehl, Volker ;
Cerny, Thomas ;
Markova, Jana ;
Ho, Anthony D. ;
Eich, Hans-Theodor ;
Mueller-Hermelink, Hans Konrad ;
Kanz, Lothar ;
Greil, Richard ;
Rank, Andreas ;
Paulus, Ursula ;
Smardova, Lenka ;
Huber, Christoph ;
Doerken, Bernd ;
Nerl, Christoph ;
Krause, Stefan W. ;
Mueller, Rolf-Peter ;
Fuchs, Michael ;
Engert, Andreas .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (32) :4234-4242
[10]   Symptomatic osteonecrosis as a treatment complication in Hodgkin lymphoma: an analysis of the German Hodgkin Study Group (GHSG) [J].
Borchmann, Sven ;
Mueller, Horst ;
Haverkamp, Heinz ;
Baues, Christian ;
Markova, Jana ;
Huettmann, Andreas ;
Glunz, Axel ;
Fuchs, Michael ;
Borchmann, Peter ;
Engert, Andreas .
LEUKEMIA, 2019, 33 (02) :439-446