Timing of high-dose methotrexate CNS prophylaxis in DLBCL: a multicenter international analysis of 1384 patients

Author:

Wilson Matthew R.1ORCID,Eyre Toby A.2ORCID,Kirkwood Amy A.3,Wong Doo Nicole4ORCID,Soussain Carole5,Choquet Sylvain6,Martinez-Calle Nicolás7ORCID,Preston Gavin8,Ahearne Matthew9ORCID,Schorb Elisabeth10,Moles-Moreau Marie-Pierre11,Ku Matthew12ORCID,Rusconi Chiara13,Khwaja Jahanzaib14ORCID,Narkhede Mayur15,Lewis Katharine L.16ORCID,Calimeri Teresa17,Durot Eric18ORCID,Renaud Loïc19ORCID,Øvlisen Andreas Kiesbye20,McIlroy Graham21,Ebsworth Timothy J.22,Elliot Johnathan23,Santarsieri Anna24ORCID,Ricard Laure25ORCID,Shah Nimish26,Liu Qin27,Zayac Adam S.28ORCID,Vassallo Francesco29,Lebras Laure30,Roulin Louise31,Lombion Naelle32,Manos Kate33,Fernandez Ruben34,Hamad Nada35ORCID,Lopez-Garcia Alberto36ORCID,O'Mahony Deirdre37,Gounder Praveen4,Forgeard Nathalie6,Lees Charlotte2ORCID,Agbetiafa Kossi5,Strüßmann Tim10,Htut Thura Win8ORCID,Clavert Aline11,Scott Hamish12,Guidetti Anna13,Barlow Brett R.15,Tchernonog Emmanuelle38,Smith Jeffery39,Miall Fiona9,Fox Christopher P.7ORCID,Cheah Chan Y.16ORCID,El Galaly Tarec Christoffer20ORCID,Ferreri Andrés J. M.17ORCID,Cwynarski Kate14,McKay Pamela1ORCID

Affiliation:

1. Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom;

2. Oxford University Hospitals NHS Trust, Churchill Cancer Center, Oxford, United Kingdom;

3. Cancer Research UK and UCL Cancer Trials Centre, UCL Cancer Institute, London, United Kingdom;

4. Concord Clinical School, Concord Hospital University of Sydney, Sydney, NSW, Australia;

5. Institut Curie Hôpital René Huguenin, Saint-Cloud, France;

6. La Pitie Salpetriere Hospital, Assistance Publique–Hôpitaux de Paris (AP-HP)–Sorbonne Universite, Paris, France;

7. Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom;

8. Aberdeen Royal Infirmary, Aberdeen, United Kingdom;

9. University Hospitals of Leicester NHS Trust, Leicester, United Kingdom;

10. Department of Medicine, University Medical Center Freiburg, Freiburg, Germany;

11. Service des Maladies du Sang, CHU Angers, Angers, France;

12. St Vincent's Private Hospital Melbourne, Melbourne, VIC, Australia;

13. Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy;

14. University College London Hospitals NHS Foundation Trust, London, United Kingdom;

15. University of Alabama at Birmingham, Birmingham, AL;

16. Linear Clinical Research and Sir Charles Gairdner Hospital, Perth, WA, Australia;

17. IRCCS San Raffaele Scientific Institute, Milan, Italy;

18. Hôpital Robert Debré CHU de Reims, Reims, France;

19. Hôpital Saint-Louis, AP-HP, Paris, France;

20. Aalborg University Hospital, Aalborg, Denmark;

21. University Hospitals Birmingham, Birmingham, United Kingdom;

22. University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom;

23. The Christie NHS Foundation Trust, Manchester, United Kingdom;

24. Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom;

25. Hospital Saint-Antoine AP-HP, Paris, France;

26. Norfolk and Norwich University Hospitals NHS Foundation Trust, Norwich, United Kingdom;

27. Princess Margaret Cancer Centre, Toronto, ON, Canada;

28. Brown University and Lifespan Cancer Institute, Providence, RI;

29. Città della Salute e della Scienza di Torino, Torino, Italy;

30. Centre Léon Bérard, Lyon, France;

31. University Hospital Henri-Mondor AP-HP, Paris, France;

32. Hopital Mignot Centre Hospitalier de Versailles, Versailles, France;

33. Austin Hospital, Melbourne, VIC, Australia;

34. Hospital de Cabueñes, Gijon, Spain;

35. St Vincent's Hospital Sydney, Sydney, Australia;

36. Fundacion Jimenez Diaz University Hospital, Health Research Institute Instituto de Investigaciòn Sanitaria–Fundacion Jimenex Diaz (IIS-FJD), Madrid, Spain;

37. Bon Secours Cork Cancer Centre, Cork, Ireland;

38. CHU de Montpellier, Montpellier, France; and

39. Liverpool University Hospitals Foundation Trust, Liverpool, United Kingdom

Abstract

Abstract Prophylactic high-dose methotrexate (HD-MTX) is often used for diffuse large B-cell lymphoma (DLBCL) patients at high risk of central nervous system (CNS) relapse, despite limited evidence demonstrating efficacy or the optimal delivery method. We conducted a retrospective, international analysis of 1384 patients receiving HD-MTX CNS prophylaxis either intercalated (i-HD-MTX) (n = 749) or at the end (n = 635) of R-CHOP/R-CHOP-like therapy (EOT). There were 78 CNS relapses (3-year rate 5.7%), with no difference between i-HD-MTX and EOT: 5.7% vs 5.8%, P = .98; 3-year difference: 0.04% (−2.0% to 3.1%). Conclusions were unchanged on adjusting for baseline prognostic factors or on 6-month landmark analysis (n = 1253). In patients with a high CNS international prognostic index (n = 600), the 3-year CNS relapse rate was 9.1%, with no difference between i-HD-MTX and EOT. On multivariable analysis, increasing age and renal/adrenal involvement were the only independent risk factors for CNS relapse. Concurrent intrathecal prophylaxis was not associated with a reduction in CNS relapse. R-CHOP delays of ≥7 days were significantly increased with i-HD-MTX vs EOT, with 308 of 1573 (19.6%) i-HD-MTX treatments resulting in a delay to subsequent R-CHOP (median 8 days). Increased risk of delay occurred in older patients when delivery was later than day 10 in the R-CHOP cycle. In summary, we found no evidence that EOT delivery increases CNS relapse risk vs i-HD-MTX. Findings in high-risk subgroups were unchanged. Rates of CNS relapse in this HD-MTX-treated cohort were similar to comparable cohorts receiving infrequent CNS prophylaxis. If HD-MTX is still considered for certain high-risk patients, delivery could be deferred until R-CHOP completion.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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