High-Dose Methotrexate as CNS Prophylaxis in High-Risk Aggressive B-Cell Lymphoma

Author:

Lewis Katharine L.123ORCID,Jakobsen Lasse H.4ORCID,Villa Diego5ORCID,Smedby Karin E.6ORCID,Savage Kerry J.5ORCID,Eyre Toby A.7ORCID,Cwynarski Kate8,Bishton Mark J.910ORCID,Fox Christopher P.910ORCID,Hawkes Eliza A.1112ORCID,Maurer Matthew J.13ORCID,El-Galaly Tarec C.4,Cheah Chan Y.12314ORCID,Bobillo Sabela,Caporn Paris L.,Van Zyl Joan,Klanova Magdalena,Trněny Marek,Puckrin Robert,Stewart Douglas A.,Tun Aung M.,Thanarajasingam Gita,Nair Ranjit,Nastoupil Loretta,Djebbari Faouzi,Joffe Erel,Eloranta Sandra,Harrysson Sara,Sehn Laurie H.,Maliske Seth M.,Poonsombudlert Kittika,Guo Xiao Y.,Hapgood Greg,Manos Kate,Khwaja Jahanzaib,Minson Adrian,Dickinson Michael,Øvlisen Andreas K.,Gregory Gareth P.,Gilbertson Michael,Streit Isaac T.,Scott Hamish W.,Ku Matthew,de Mel Sanjay,Ying Yong Kar,Xin Liu,Mokoonlall Mridula,Talaulikar Dipti,Hamad Nada,Srinivasan Sathia S.,McVilly Nicholas L.,Johnston Anna M.,Brunner Matthew J.,Pophali Priyanka A.,

Affiliation:

1. Linear Clinical Research, Nedlands, WA, Australia

2. Division of Haematology, Sir Charles Gairdner Hospital, Nedlands, WA, Australia

3. Division of Internal Medicine, Medical School, University of Western Australia, Perth, WA, Australia

4. Department of Haematology, Aalborg University Hospital, Aalborg, Denmark

5. BC Cancer Centre for Lymphoid Cancer, The University of British Columbia, Vancouver, BC, Canada

6. Department of Medicine Solna, Division of Clinical Epidemiology, Karolinska Institutet, Stockholm, Sweden

7. Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom

8. University College London Hospital NHS Foundation Trust, London, United Kingdom

9. Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom

10. University of Nottingham, Nottingham, United Kingdom

11. Olivia Newton-John Cancer Research & Wellness Centre at Austin Health, Heidelberg, VIC, Australia

12. Monash University School of Public Health and Preventive Medicine, Melbourne, VIC, Australia

13. Division of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN

14. Department of Haematology, PathWest, Nedlands, WA, Australia

Abstract

PURPOSE CNS progression or relapse is an uncommon but devastating complication of aggressive B-cell lymphoma. There is no consensus regarding the optimal approach to CNS prophylaxis. This study was designed to determine whether high-dose methotrexate (HD-MTX) is effective at preventing CNS progression in patients at high risk of this complication. PATIENTS AND METHODS Patients age 18-80 years with aggressive B-cell lymphoma and high risk of CNS progression, treated with curative-intent anti–CD20-based chemoimmunotherapy, were included in this international, retrospective, observational study. Cause-specific hazard ratios (HRs) and cumulative risks of CNS progression were calculated according to use of HD-MTX, with time to CNS progression calculated from diagnosis for all patients (all-pts) and from completion of frontline systemic lymphoma induction therapy, for patients in complete response at completion of chemoimmunotherapy (CR-pts). RESULTS Two thousand four hundred eighteen all-pts (HD-MTX; n = 425) and 1,616 CR-pts (HD-MTX; n = 356) were included. CNS International Prognostic Index was 4-6 in 83.4% all-pts. Patients treated with HD-MTX had a lower risk of CNS progression (adjusted HR, 0.59 [95% CI, 0.38 to 0.90]; P = .014), but significance was not retained when confined to CR-pts (adjusted HR, 0.74 [95% CI, 0.42 to 1.30]; P = .29), with 5-year adjusted risk difference of 1.6% (95% CI, –1.5 to 4.4; all-pts) and 1.4% (95% CI, –1.5 to 4.1; CR-pts). Subgroups were underpowered to draw definitive conclusions regarding the efficacy of HD-MTX in individual high-risk clinical scenarios; however, there was no clear reduction in CNS progression risk with HD-MTX in any high-risk subgroup. CONCLUSION In this large study, high-risk patients receiving HD-MTX had a 7.2% 2-year risk of CNS progression, consistent with the progression risk in previously reported high-risk cohorts. Use of HD-MTX was not associated with a clinically meaningful reduction in risk of CNS progression.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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