Evidence map›Paper›PMID 42007452›Full record

ArticleHemaSphere2026

Dynamics of complete responses (CRs) in patients with relapsed or refractory follicular lymphoma (R/R FL) treated with odronextamab in the ELM-2 study.

Stefano Luminari, Ana Jiménez-Ubieto, Geoffrey Chong, David Tucker, Srikanth Ambati, Chinjune Lin, Hesham Mohamed, Jurriaan Brouwer-Visser, Chetachi Akunna Otele, Giovanni Antico and 1 more

Registry-linked trialAbstract read
In one paragraph

Article in HemaSphere, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03888105 (An Open-Label Study to Assess the Anti-Tumor Activity and Safety of REGN1979, an Anti-CD20 x Anti-CD3 Bispecific Antibody, in Patients With Relapsed or Refractory B-cell Non-Hodgkin Lymphoma), which is not on this 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.

NCT03888105 phase2active not recruitingnot on this map

An Open-Label Study to Assess the Anti-Tumor Activity and Safety of REGN1979, an Anti-CD20 x Anti-CD3 Bispecific Antibody, in Patients With Relapsed or Refractory B-cell Non-Hodgkin Lymphoma

TypeinterventionalSponsorRegeneron PharmaceuticalsRan2019 to 2028Enrolled515ConditionsB-cell Non-Hodgkin Lymphoma (B-NHL)ArmsOdronextamab
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.

Stefano LuminariHematology Unit, Azienda Unità Sanitaria Locale - IRCCS of Reggio Emilia Reggio Emilia Italy.ORCID https://orcid.org/0000-0001-8446-2285
Ana Jiménez-UbietoHematology Department Hospital Universitario 12 de Octubre Madrid Spain.
Geoffrey ChongDepartment of Medical Oncology and Clinical Haematology Olivia Newton-John Cancer Wellness & Research Centre, Austin Hospital Heidelberg Victoria Australia.
David TuckerHaematology Department Royal Cornwall Hospital Truro United Kingdom.
Srikanth AmbatiRegeneron Pharmaceuticals, Inc. Tarrytown New York United States.
Chinjune LinRegeneron Pharmaceuticals, Inc. Tarrytown New York United States.
Hesham MohamedRegeneron Pharmaceuticals, Inc. Tarrytown New York United States.
Jurriaan Brouwer-VisserRegeneron Pharmaceuticals, Inc. Tarrytown New York United States.
Chetachi Akunna OteleRegeneron Pharmaceuticals, Inc. Tarrytown New York United States.
Giovanni AnticoRegeneron Pharmaceuticals, Inc. Tarrytown New York United States.
Jose C VillasboasHematology Mayo Clinic Rochester Minnesota United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complete response (CR) is an important treatment goal in follicular lymphoma (FL). In relapsed or refractory (R/R) FL, CR rates decline, and disease progression accelerates with each treatment line, with particularly poor outcomes in patients with high-risk features. Odronextamab, a CD20 × CD3 bispecific antibody, demonstrated deep, durable responses and generally manageable safety in R/R FL in the Phase 2 ELM-2 study (NCT03888105); we present an exploratory analysis in patients who attained a CR. Patients received intravenous odronextamab with step-up dosing in Cycle 1, 80 mg weekly in Cycles 2-4, then 160 mg once every 2 weeks until disease progression or other protocol-defined reason for discontinuation. Patients with CR lasting ≥9 months switched to dosing once every 4 weeks. Overall, 73.4% (94/128) of patients attained CR, 93.6% (88/94) by first response assessment (~Week 12). Median time to CR was 2.7 months (range 2.3-7.9). Median duration of CR was 25.1 months (95% confidence interval [CI] 20.5-not evaluable [NE]) overall and 23.7 months (18.2-NE) in patients with high-risk features. Overall, 79.5% (35/44) of patients who switched to Q4W dosing maintained CR at last assessment. Patients with low/undetectable CD20 expression by immunohistochemistry (<10% CD20

Identifiers

PMID42007452
PMCPMC13086623

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Registered trials

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 OpenQuestion graph.