Radiotherapy or Autologous Stem-Cell Transplantation for Primary CNS Lymphoma in Patients Age 60 Years and Younger: Long-Term Results of the Randomized Phase II PRECIS Study

Author:

Houillier Caroline1ORCID,Dureau Sylvain2,Taillandier Luc3,Houot Roch4ORCID,Chinot Olivier5ORCID,Moluçon-Chabrot Cécile6,Schmitt Anna7,Gressin Rémy8,Choquet Sylvain9ORCID,Damaj Gandhi1011ORCID,Peyrade Frédéric12,Abraham Julie13,Delwail Vincent14,Gyan Emmanuel15,Sanhes Laurence16ORCID,Cornillon Jérôme1718,Garidi Reda19,Delmer Alain20ORCID,Al Jijakli Ahmad21,Morel Pierre2223ORCID,Waultier Agathe24,Paillassa Jérôme25,Chauchet Adrien26,Gastinne Thomas27,Laadhari Mouna28,Plissonnier Anne-Sophie29,Feuvret Loïc30ORCID,Cassoux Nathalie31,Touitou Valérie32ORCID,Ricard Damien33,Hoang-Xuan Khê1,Soussain Carole34ORCID,

Affiliation:

1. APHP, Sorbonne Université, IHU, ICM, Service de Neurologie-Mazarin, Groupe Hospitalier Pitié-Salpêtrière, Paris, France

2. Unité de Biométrie, Institut Curie, Saint-Cloud, France

3. Service de Neurologie, CHU de Nancy, France

4. Service d’Hématologie, CHU de Rennes, Inserm U1236 Université de Rennes 1, France

5. Aix-Marseille Université, CNRS, INP, AP-HM, Service de Neuro-Oncologie, CHU de la Timone, France

6. Service d’Hématologie, CHU de Clermont-Ferrand, France

7. Service d’Hématologie, Institut Bergonié, Bordeaux, France

8. Onco-Haematology Department, CHU de Grenoble, France

9. Service d’Hématologie Clinique, APHP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France

10. Service d’Hématologie, CHU d’Amiens, France

11. Current address: Hematology Institute, University Hospital Normandy, Caen, France

12. Service d’Hématologie, Centre Antoine Lacassagne, Nice, France

13. Service d’Hématologie et de Thérapie cellulaire, CHU de Limoges, France

14. Service d'Oncologie Hématologique et de Thérapie Cellulaire, CHU de Poitiers, INSERM, CIC 1402, Poitiers, Centre d'Investigation Clinique, Université de Poitiers, Poitiers, France

15. Service d’Hématologie et thérapie cellulaire, Centre d’Investigations Cliniques INSERM U1517, Centre hospitalier universitaire, Université de Tours, France

16. Service d’Hématologie, Centre Hospitalier de Perpignan, France

17. Service d’Hématologie, Institut de Cancérologie Lucien Neuwirth, Saint-Priest-en-Jarez, France

18. Current affiliation: Département d’Hématologie Clinique, CHU de ST-Etienne, France

19. Service d’Hématologie, Centre Hospitalier de Saint Quentin, France

20. Service d’Hématologie, CHU de Reims, France

21. Service d’Hématologie, Centre Hospitalier d’Argenteuil, France

22. Service d’Hématologie, Centre Hospitalier de Lens, France

23. Current affiliation: Service d’Hématologie, CHU d’Amiens, France

24. Service d’Hématologie, CHU de Nîmes, France

25. Service d’Hématologie, CHU d’Angers, France

26. Service d’Hématologie, CHU de Besançon, France

27. Service d’Hématologie, CHU de Nantes, France

28. Département d’Imagerie Médicale, Institut Curie, Site Saint-Cloud, France

29. DREH Pôle Promotion, Institut Curie, Saint-Cloud, France

30. Service de Radiothérapie, APHP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France

31. Service d’Ophtalmologie, Institut Curie, site de Paris, et Université Paris V Descartes et PSL (Paris Science et Lettre), Paris, France

32. Service d’Ophtalmologie, APHP, Groupe Hospitalier Pitié-Salpêtrière, Paris, France

33. Service de Neurologie, Hôpital d’Instruction des Armées Percy, Ecole du Val-de-Grâce, Service de Santé des Armées, Clamart, France

34. Service d’Hématologie, Institut Curie, site de Saint-Cloud et INSERM U932 Institut Curie, PSL Research University, Paris, France

Abstract

Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in JCO or elsewhere, for which the primary end point has already been reported. We previously reported the results of a randomized phase II study in patients with newly diagnosed primary CNS lymphoma (age 18-60 years). Patients were treated with high-dose methotrexate-based induction chemotherapy followed by whole-brain radiotherapy (WBRT) or high-dose chemotherapy (thiotepa-busulfan-cyclophosphamide) with autologous stem-cell transplantation (ASCT). The median follow-up was 33 months. In this report, we provide long-term data (median follow-up, 8 years) regarding the outcomes and toxicities. Fifty-three and 44 patients received induction chemotherapy followed by WBRT or ASCT, respectively. Their 8-year event-free survival from random assignment was 67% and 39% in the ASCT and WBRT arms, respectively ( P = .03), with a significantly lower risk of relapse after ASCT (hazard ratio, 0.13; P < .001). One third of patients who relapsed after WBRT were alive after salvage treatment. Five and four patients died of ASCT and WBRT-related toxicities, respectively. The 8-year overall survival was 69% and 65% in the ASCT and WBRT arms, respectively (not significant). Balance (52% v 10%, P ≤ 0.001) and neurocognition (64% v 13%, P < .001) significantly deteriorated after WBRT compared with ASCT during the follow-up. This study shows that 40 Gy WBRT should be avoided in first-line treatment because of its neurotoxicity and suboptimal efficacy in reducing relapses while ASCT appears to be highly efficient in preventing relapses.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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