Evidence map›Paper›PMID 40501414›Full record

Trial reportHaematologica2025

Chemotherapy-free combination of ibrutinib and obinutuzumab for untreated advanced follicular lymphoma: results of a phase II study from the German Lymphoma Alliance.

Christian Schmidt, Gabriel Scheubeck, Vindi Jurinovic, Martin Sökler, Roswitha Forstpointner, Christian Buske, Andreas Viardot, Ulrich Keller, Ullrich Graeven, Reinhard Marks and 7 more

Erratum issuedAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Haematologica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Haematologica · 2025
    Article
4 · The record

Corrections and comments

  • Erratum issued
    2025
5 · Who and what money

Authors and funding

17 authors.

Christian SchmidtDepartment of Medicine III, University Hospital, LMU Munich, Munich. Christian_Schmidt@med.uni-muenchen.de.
Gabriel ScheubeckDepartment of Medicine III, University Hospital, LMU Munich, Munich.
Vindi JurinovicDepartment of Medicine III, University Hospital, LMU Munich, Munich.
Martin SöklerDepartment of Medicine II, University Hospital Tuebingen, Tuebingen, Germany; Department of Oncology- and Hematology, Spital Thun, Thun.
Roswitha ForstpointnerDepartment of Medicine III, University Hospital, LMU Munich, Munich.
Christian BuskeDepartment of Medicine III, University Hospital Ulm, Ulm.
Andreas ViardotDepartment of Medicine III, University Hospital Ulm, Ulm.
Ulrich KellerDepartment of Internal Medicine III, Klinikum Rechts der Isar der TU München, Munich, Germany; Department of Hematology and Oncology, Charité University Hospital, Campus Benjamin Franklin, Berlin.
Ullrich GraevenDepartment of Hematology, Oncology, Gastroenterology, Kliniken Maria Hilf GmbH, Mönchengladbach.
Reinhard MarksDepartment of Medicine I, University Hospital Freiburg, Freiburg.
Mathias HänelDepartment of Medicine III, Klinikum Chemnitz GmbH, Chemitz.
Rüdiger LierschGEHO, Practice for Hematology and Medical Oncology, Münster.
Jan DürigDepartment of Hematology, University Hospital Essen, Essen.
Christiane PottDepartment of Medicine II, University Hospital Schleswig-Holstein, Kiel.
Eva HosterDepartment of Medicine III, University Hospital, LMU Munich, Munich, Germany; Institute for Medical Information Processing, Biometry, and Epidemiology, LMU Munich.
Michael UnterhaltDepartment of Medicine III, University Hospital, LMU Munich, Munich.
Wolfgang HiddemannDepartment of Medicine III, University Hospital, LMU Munich, Munich.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunochemotherapy induces long-term responses in patients with follicular lymphoma. However, the toxicity of chemotherapy remains a relevant challenge. The Bruton tyrosine kinase inhibitor ibrutinib has shown significant activity in patients with indolent B-cell lymphoma. Combining ibrutinib with obinutuzumab may, therefore, be an attractive chemotherapy-free option. We conducted a prospective, single-arm, multicenter phase II trial to evaluate the chemotherapy-free regimen of obinutuzumab plus ibrutinib in patients with previously untreated advanced-stage follicular lymphoma. Patients received six 21-day cycles of ibrutinib and obinutuzumab for induction and 12 additional 2-month cycles for maintenance. The primary endpoint was 1-year progression-free survival (PFS). The study was powered to detect an improvement of 10% over the 1-year PFS of 85%. Ninety-eight patients were enrolled in the trial. The median follow-up was 5.5 years. After induction, five patients (5%) had a complete response and 82 (85%) had a partial response. The 1-year PFS was 80%, missing the prospected improvement of a 1-year PFS of 85% (P=0.93). The median PFS was 4.5 years; median duration of response and overall survival were not reached. The most common adverse events of grade 3/4 were neutropenia, lung infection, hypertension, fatigue, rash and thrombocytopenia. The trial of a chemotherapy-free regimen of obinutuzumab and ibrutinib in follicular lymphoma patients failed to demonstrate a 10% improvement in the primary efficacy endpoint. However, the combination produced durable and deep responses and had an acceptable safety profile. Trial registration, EudraCT-Number: 2014-005164-15.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsLymphoma, FollicularAdenineAdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedFemaleHumansMaleMiddle AgedNeoplasm StagingPiperidinesPyrazolesTreatment OutcomeAdenineAntibodies, Monoclonal, HumanizedibrutinibobinutuzumabPiperidinesPyrazoles

Identifiers

PMID40501414
PMCPMC12666298

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.