Evidence map›Paper›PMID 35537101›Full record

ArticleBlood advances2022

SAKK 35/15: a phase 1 trial of obinutuzumab in combination with venetoclax in patients with previously untreated follicular lymphoma.

Anastasios Stathis, Ulrich Mey, Sämi Schär, Felicitas Hitz, Christiane Pott, Nicolas Mach, Fatime Krasniqi, Urban Novak, Christian Schmidt, Karin Hohloch and 15 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Blood advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02877550 (A Phase I Trial of Obinutuzumab in Combination With Venetoclax in Previously Untreated Follicular Lymphoma Patients), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 23% of its field
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.

NCT02877550 phase1completednot on this map

A Phase I Trial of Obinutuzumab in Combination With Venetoclax in Previously Untreated Follicular Lymphoma Patients

TypeinterventionalSponsorSwiss Cancer InstituteRan2017 to 2022Enrolled25ConditionsFollicular LymphomaArmsObinutuzumab, Venetoclax
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
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

25 authors at 9 institutions in 3 countries.

Anastasios StathisMedical Oncology, Oncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland.
Ulrich MeyOncology and Hematology, Kantonsspital Graubuenden, Chur, Switzerland.
Sämi SchärSAKK Coordinating Center, Bern, Switzerland.
Felicitas HitzOncology/Hematology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Christiane PottMedizinischen Klinik II Hämatologie und Internistische Onkologie, Universitätsklinikum Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Nicolas MachService d'Oncologie, Département d'Oncologie, Hôpitaux Universitaires de Genève, Geneva, Switzerland.ORCID 0000-0001-8944-1088
Fatime KrasniqiMedical Oncology, University Hospital of Basel, Basel, Switzerland.
Urban NovakDepartment of Medical Oncology, Inselspital/Bern University Hospital, Bern, Switzerland.
Christian SchmidtDepartment of Medicine III, University of Munich, Munich, Germany.
Karin HohlochOncology and Hematology, Kantonsspital Graubuenden, Chur, Switzerland.ORCID 0000-0003-1412-3274
Dirk Lars KienleOncology and Hematology, Kantonsspital Graubuenden, Chur, Switzerland.
Dagmar HessOncology/Hematology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Alden A MocciaMedical Oncology, Oncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland.
Michael UnterhaltDepartment of Medicine III, University of Munich, Munich, Germany.
Katrin EckhardtSAKK Coordinating Center, Bern, Switzerland.
Stefanie HayozSAKK Coordinating Center, Bern, Switzerland.ORCID 0000-0002-2265-6559
Gabriela ForestieriLaboratory of Experimental Hematology, Institute of Oncology Research, Bellinzona, Switzerland.
Davide RossiLaboratory of Experimental Hematology, Institute of Oncology Research, Bellinzona, Switzerland.
Stefan DirnhoferInstitute of Medical Genetics and Pathology, University Hospital Basel, University of Basel, Basel, Switzerland.
Luca CerianiNuclear Medicine and PET-CT Center, Imaging Institute of Southern Switzerland, EOC, Bellinzona, Switzerland.ORCID 0000-0002-6371-097X
Giulio SartoriLymphoma Genomics, Institute of Oncology Research, Faculty of Biomedical Sciences, USI, Bellinzona, Switzerland.ORCID 0000-0001-6704-9755
Francesco BertoniMedical Oncology, Oncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland.ORCID 0000-0001-5637-8983
Christian BuskeInstitute of Experimental Cancer Research, CCC Ulm, University Hospital Ulm, Ulm, Germany; and.
Emanuele ZuccaMedical Oncology, Oncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland.
Wolfgang HiddemannDepartment of Medicine III, University of Munich, Munich, Germany.
Institute of Oncology Research · CHKantonsspital Graubünden · CHLudwig-Maximilians-Universität München · DEKantonsspital St. Gallen · CHUniversity Hospital of Bern · CHUniversity Hospital of Basel · CHUniversity Hospital Schleswig-Holstein · DEUniversity Hospital Ulm · DEUniversity of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This phase 1 study evaluated safety, tolerability, and preliminary efficacy of obinutuzumab in combination with venetoclax in patients with previously untreated grade 1-3a follicular lymphoma in need of systemic therapy. Two DLs of venetoclax were evaluated with an expansion cohort at the recommended phase 2 dose. Twenty-five patients were enrolled. The recommended phase 2 dose was venetoclax 800 mg OD continuously for 6 cycles starting on day 2 of cycle 1, with obinutuzumab 1000 mg on days 1, 8, and 15 of cycle 1 and on day 1 of cycles 2 to 6, followed by obinutuzumab maintenance every 2 months for 2 years. Only 1 patient had a DLT consisting of grade 4 thrombocytopenia after the first obinutuzumab infusion. Neutropenia was the most common adverse event of grade ≥3 at least possibly attributed to study treatment. Twenty-four patients were evaluable for response after cycle 6 by computed tomography (CT) and 19 by positron emission tomography/CT (PET/CT): overall and complete response rates were 87.5% (95% CI, 67.6% to 97.3%) and 25% (95% CI, 9.8% to 46.7%) in the CT-evaluated patients and 84.2% (95% CI, 60.4% to 96.6%) and 68.4% (95% CI, 43.4% to 87.4%), respectively, in the PET/CT-evaluated patients. One-year progression-free survival was 77.8% (95% CI, 54.6% to 90.1%) and 79% (95% CI, 47.9% to 92.7%) for CT and PET/CT-evaluable patients, respectively, whereas progression-free survival at 30 months was 73.2% (95% CI, 49.8%, 87.0%) as assessed by CT and 79.0% (95% CI, 47.9%, 92.7%) by PET/CT. Despite the activity observed, our results do not support further development of the combination in this patient population. This trial was registered at www.clinicaltrials.gov as #NCT02877550.

Indexed as

Lymphoma, FollicularAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsBridged Bicyclo Compounds, HeterocyclicHumansPositron Emission Tomography Computed TomographySulfonamidesTreatment OutcomeAntibodies, Monoclonal, HumanizedBridged Bicyclo Compounds, HeterocyclicobinutuzumabSulfonamidesvenetoclax

Identifiers

PMID35537101
PMCPMC9278307
OpenAlexW4229444744

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.