A phase 1/2 study of thiotepa-based immunochemotherapy in relapsed/refractory primary CNS lymphoma: the TIER trial

Author:

Fox Christopher P.12ORCID,Ali Ayesha S.3,McIlroy Graham3ORCID,Thust Steffi4ORCID,Martinez-Calle Nicolás1ORCID,Jackson Aimee E.3,Hopkins Louise M.3,Thomas Catherine M.3,Kassam Shireen5,Wright Josh6,Chaganti Sridhar7,Smith Jeffery8,Chau Ian9,Culligan Dominic10,Linton Kim M.11ORCID,Collins Graham P.12,Ferreri Andrés J. M.13ORCID,Lewis David14,Davies Andrew J.15,Johnson Rod16,Auer Dorothee P.217ORCID,Cwynarski Kate18

Affiliation:

1. Department of Clinical Haematology, Nottingham University Hospitals National Health Service (NHS) Trust, Nottingham, United Kingdom;

2. Faculty of Medicine and Health Sciences, University of Nottingham, Nottingham, United Kingdom;

3. Cancer Research UK (CRUK) Clinical Trials Unit, University of Birmingham, Birmingham, United Kingdom;

4. National Hospital for Neurology and Neurosurgery, University College London Hospitals NHS Foundation Trust, London, United Kingdom;

5. Department of Haemato-oncology, King’s College Hospital NHS Foundation Trust, London, United Kingdom;

6. Department of Haematology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, United Kingdom;

7. Centre for Clinical Haematology, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom;

8. Department of Clinical Haematology, Liverpool University Hospitals NHS Foundation Trust, Liverpool, United Kingdom;

9. Haemato-Oncology Unit, Royal Marsden NHS Foundation Trust, Sutton, United Kingdom;

10. Department of Haematology, Aberdeen Royal Infirmary, Aberdeen, United Kingdom;

11. Haematology and Transplant Unit, The Christie NHS Foundation Trust, Manchester, United Kingdom;

12. Department of Clinical Haematology, Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom;

13. Lymphoma Unit, Department of Onco-Haematology, IRCCS San Raffaele Scientific Institute, Milan, Italy;

14. Department of Haematology, University Hospitals Plymouth NHS Trust, Plymouth, United Kingdom;

15. Southampton CRUK/National Institute for Health Research (NIHR) Experimental Cancer Medicines, University of Southampton, Southampton, United Kingdom;

16. Department of Clinical Haematology, The Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom;

17. NIHR Nottingham Biomedical Research Centre, University of Nottingham, United Kingdom; and

18. Department of Haematology, University College London Hospitals NHS Foundation Trust, London, United Kingdom

Abstract

Abstract Relapsed or refractory primary central nervous system lymphoma (rrPCNSL) confers a poor prognosis with no accepted standard of care. Very few prospective studies have been conducted in this patient group. This study was a multicenter phase 1/2 study that investigated thiotepa in combination with ifosfamide, etoposide, and rituximab (TIER) for the treatment of PCNSL relapsed or refractory to high-dose methotrexate-based chemotherapy. A 3 + 3 design investigated the recommended phase 2 dose of thiotepa for a single-stage phase 2 cohort by assessing the activity of 2 cycles of TIER against rrPCNSL. The primary outcome was overall response rate. The dose-finding study demonstrated that 50 mg/m2 of thiotepa could be safely delivered within the TIER regimen. No dose-limiting toxicities were encountered in phase 1, and TIER was well-tolerated by the 27 patients treated in phase 2. The most common grade 3 to 4 toxicities were neutropenia (56% of patients) and thrombocytopenia (39%). An overall response was confirmed in 14 patients (52%), which met the prespecified threshold for clinically relevant activity. The median progression-free survival was 3 months (95% confidence interval [CI], 2 to 6 months) and overall survival 5 months (95% CI, 3 to 9 months). Exploratory analyses suggest a greater benefit for thiotepa-naïve patients. Six patients successfully completed autologous stem cell transplantation (ASCT) consolidation, with 4 experiencing durable remissions after a median follow-up of 50 months. The TIER regimen can be delivered safely and is active against rrPCNSL. When it is followed by ASCT, it can provide durable remission and long-term survival. However, for the majority of patients, prognosis remains poor, and novel treatment strategies are urgently needed. This trial was registered at https://www.clinicaltrialsregister.eu/ctr-search/search as EudraCT 2014-000227-24 and ISRCTN 12857473.

Publisher

American Society of Hematology

Subject

Hematology

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