Evidence map›Paper›PMID 39422604›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2024

Phase Ib Study of the Immunocytokine Simlukafusp Alfa (FAP-IL2v) in Combination with Cetuximab in Patients with Head and Neck Squamous Cell Carcinoma.

Aaron R Hansen, Carlos A Gomez-Roca, Debbie G J Robbrecht, Loic Verlingue, Antoine Italiano, Julie E Bauman, Neeltje Steeghs, Hans Prenen, Jérôme Fayette, James Spicer and 14 more

Registry-linked trialAbstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02627274 (An Open-Label, Multicenter, Dose-Escalation, Phase Ia/Ib Study to Evaluate Safety, Pharmacokinetics, and Therapeutic Activity of RO6874281, an Immunocytokine Consisting of Interleukin 2 Variant), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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.

NCT02627274 phase1completednot on this map

An Open-Label, Multicenter, Dose-Escalation, Phase Ia/Ib Study to Evaluate Safety, Pharmacokinetics, and Therapeutic Activity of RO6874281, an Immunocytokine Consisting of Interleukin 2 Variant (IL-2v) Targeting Fibroblast Activation Protein-α (FAP), as a Single Agent (Part A) or in Combination With Trastuzumab or Cetuximab (Part B or C)

TypeinterventionalSponsorHoffmann-La RocheRan2015 to 2022Enrolled134ConditionsSolid Tumor, Breast Cancer, Cancer of Head and NeckArmsRO6874281, Trastuzumab, Cetuximab
3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Review
  2. T-Cell Immunity and Lung Cancer.Respirology (Carlton, Vic.) · 2026
    Review
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  7. Article
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

24 authors.

Aaron R HansenDivision of Medical Oncology, Princess Margaret Cancer Center, Toronto, Canada.ORCID 0000-0002-2363-8707
Carlos A Gomez-RocaMedical Oncology and Clinical Research Department, Institut Universitaire du Cancer, Toulouse, France.ORCID 0000-0002-8043-2529
Debbie G J RobbrechtMedical Oncology Department, Erasmus MC - University Medical Center, Rotterdam, the Netherlands.ORCID 0000-0003-2490-9991
Loic VerlingueDrug Development Department, Institut Gustave Roussy, Villejuif, France.ORCID 0000-0002-5694-4022
Antoine ItalianoEarly Phase Trials Unit, Institute Bergonié, and Faculty of Medicine, University of Bordeaux, Bordeaux, France.ORCID 0000-0002-8540-5351
Julie E BaumanDepartment of Medicine, University of Arizona College of Medicine, Tucson, Arizona.ORCID 0000-0002-1398-6636
Neeltje SteeghsDepartment of Medical Oncology, Netherlands Cancer Institute, Amsterdam, the Netherlands.ORCID 0000-0003-2989-2279
Hans PrenenOncology Department, Antwerp University Hospital, Edegem, Belgium.ORCID 0000-0001-8802-7352
Jérôme FayetteOncology, Centre Léon Bérard, Lyon, France.ORCID 0000-0002-8126-7019
James SpicerKing's College London, Guy's Hospital, London, United Kingdom.ORCID 0000-0003-3732-8491
Jiaxin NiuBanner MD Anderson Cancer Center, Gilbert, Arizona.ORCID 0000-0001-9018-287X
Christin HabigtRoche Pharma Research and Early Development, Early Clinical Development Oncology, Roche Innovation Center Munich, Munich, Germany.ORCID 0009-0008-5806-7650
Meike SchneiderRoche Pharma Research and Early Development, Early Clinical Development Oncology, Roche Innovation Center Basel, Basel, Switzerland.ORCID 0009-0006-4378-7343
Stefan EversRoche Pharma Research and Early Development, Early Clinical Development Oncology, Roche Innovation Center Basel, Basel, Switzerland.ORCID 0009-0001-3060-9429
Nassim SleimanRoche Pharma Research and Early Development, Early Clinical Development Oncology, Roche Innovation Center Basel, Basel, Switzerland.ORCID 0009-0004-5705-0786
David DejardinRoche Pharma Research and Early Development, Early Clinical Development Oncology, Roche Innovation Center Basel, Basel, Switzerland.ORCID 0000-0001-8960-5345
Caroline ArdeshirF. Hoffmann-La Roche Ltd., Welwyn Garden City, United Kingdom.ORCID 0009-0004-9845-8307
Daniela SchmidRoche Pharma Research and Early Development, Early Clinical Development Oncology, Roche Innovation Center Munich, Munich, Germany.ORCID 0000-0002-8674-593X
Christophe BoetschRoche Pharma Research and Early Development, Early Clinical Development Oncology, Roche Innovation Center Basel, Basel, Switzerland.ORCID 0009-0005-8467-0339
Jehad CharoRoche Pharma Research and Early Development, Early Clinical Development Oncology, Roche Innovation Center Zurich, Schlieren, Switzerland.ORCID 0000-0002-5409-9160
Anton KraxnerRoche Pharma Research and Early Development, Early Clinical Development Oncology, Roche Innovation Center Basel, Basel, Switzerland.ORCID 0009-0003-5831-8054
Volker TeichgräberRoche Pharma Research and Early Development, Early Clinical Development Oncology, Roche Innovation Center Basel, Basel, Switzerland.ORCID 0009-0008-0526-6584
Nino KeshelavaRoche Pharma Research and Early Development, Early Clinical Development Oncology, Roche Innovation Center Zurich, Schlieren, Switzerland.ORCID 0009-0001-0978-3393
Marcelo R BonomiMedical Oncology Department, The Ohio State University Comprehensive Cancer Center, James, Virginia.ORCID 0000-0002-9399-3608

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis phase Ib trial evaluated fibroblast activation protein-α-targeted IL2 variant (FAP-IL2v), a novel immunocytokine engineered to minimize CD25-mediated toxicities, in combination with cetuximab, in patients with recurrent, unresectable, or metastatic head and neck squamous cell carcinoma (HNSCC). PATIENTS AND

methodsPatients received FAP-IL2v either on a continuous weekly (QW) schedule or QW for 4 weeks and then every 2 weeks (Q2W). Cetuximab was dosed at QW or Q2W schedules. The primary objectives were to evaluate the safety and tolerability, maximum tolerated dose, pharmacokinetics, and clinical activity for the combination of FAP-IL2v with cetuximab. Exploratory objectives included pharmacodynamic analyses.

resultsA total of 58 patients were enrolled, 19 patients into the dose-escalation part, and 39 patients into the expansion part. The maximum tolerated dose of FAP-IL2v was defined as 10 mg (QW/Q2W) in combination with cetuximab (500 mg/m2, Q2W), which was further tested in the expansion part. The most common FAP-IL2v-related adverse events with a grade 3 or 4 severity were hypophosphatemia (19%), lymphopenia (16%), and infusion-related reaction (14%). The pharmacokinetics of FAP-IL2v in combination with cetuximab was similar to that after administration as monotherapy. Consistent with the proposed mode of action, FAP-IL2v preferentially expanded intratumoral NK and CD8 T cells. Four patients achieved a partial response, and the objective response rate was 7% (95% confidence interval, 3.2-14.7).

conclusionsThe safety profile of FAP-IL2v in combination with cetuximab was acceptable, and pharmacodynamic markers support the proposed mode of action of this combination, but the overall low antitumor activity does not warrant further clinical exploration in HNSCC. [Part C of Study BP29842 (NCT02627274).].

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCetuximabMaximum Tolerated DoseSquamous Cell Carcinoma of Head and NeckAdultAgedAged, 80 and overEndopeptidasesFemaleFibroblast Activation Protein AlphaHead and Neck NeoplasmsHumansInterleukin-2MaleMembrane ProteinsMiddle AgedCetuximabEndopeptidasesFibroblast Activation Protein AlphaInterleukin-2Membrane ProteinsRecombinant Fusion Proteins

Identifiers

PMID39422604
PMCPMC11647204

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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.