Evidence map›Paper›PMID 42317052›Full record

Trial reportFuture oncology (London, England)2026

IGNITE: a phase III study of tirabrutinib versus rituximab and temozolomide combination therapy in relapsed/refractory primary central nervous system lymphoma.

Lakshmi Nayak, Christian Grommes, Charles Psoinos, Frederic J Reu, Akira Takazawa, Mayur Uttarwar, Binfeng Xia, Luis A Carvajal, Soojin Kim, Matthew L Sherman and 1 more

Abstract readClinical Trial, Phase IIIRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in Future oncology (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Lakshmi NayakNeuro-oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Christian GrommesNeurology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Charles PsoinosClinical Development, Deciphera Pharmaceuticals LLC, Waltham, MA, USA.
Frederic J ReuClinical Development, Deciphera Pharmaceuticals LLC, Waltham, MA, USA.
Akira TakazawaClinical Development, ONO Pharmaceutical Co, Ltd, Osaka, Japan.
Mayur UttarwarClinical Development, Deciphera Pharmaceuticals LLC, Waltham, MA, USA.
Binfeng XiaClinical Development, Deciphera Pharmaceuticals LLC, Waltham, MA, USA.
Luis A CarvajalClinical Development, Deciphera Pharmaceuticals LLC, Waltham, MA, USA.
Soojin KimClinical Development, Deciphera Pharmaceuticals LLC, Waltham, MA, USA.
Matthew L ShermanClinical Development, Deciphera Pharmaceuticals LLC, Waltham, MA, USA.
Tracy T BatchelorNeurology, Brigham and Women's Hospital, Boston, MA, USA.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Primary central nervous system lymphoma (PCNSL) is a rare, highly aggressive form of non-Hodgkin lymphoma. Although initial responses to the guideline-recommended first-line high-dose methotrexate induction treatment are high, some patients have refractory disease and most experience relapse. Approved therapies for relapsed or refractory (R/R) PCNSL are limited in the US, and there are none in Europe, creating an urgent unmet need for effective treatments. Tirabrutinib is a highly potent and selective second-generation Bruton tyrosine kinase inhibitor approved in Japan, Taiwan, and South Korea for patients with R/R PCNSL. Here, we describe the rationale and design of IGNITE (ONO-4059-17), an ongoing, phase III, multiregional, open-label, randomized study of tirabrutinib vs rituximab and temozolomide combination therapy in R/R PCNSL. The primary endpoint is progression-free survival based on blinded independent review committee (BIRC) per International PCNSL Collaborative Group (IPCG) criteria. Key secondary endpoints are overall response rate based on BIRC per IPCG criteria and overall survival. Safety will be assessed by the incidence and severity of treatment-emergent adverse events.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCentral Nervous System NeoplasmsLymphoma, Non-HodgkinNeoplasm Recurrence, LocalAdultAgedDrug Resistance, NeoplasmFemaleHumansMaleMiddle AgedRituximabTemozolomideRituximabTemozolomideclinical trialprimary central nervous system lymphomaprotocolrelapsed/refractoryTirabrutinib

Identifiers

PMID42317052
PMCPMC13374761

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.