Evidence map›Paper›PMID 34156166›Full record

Trial reportCancer reports (Hoboken, N.J.)2022

Observational, prospective, phase 4 study in patients with first-line recurrent and/or metastatic squamous cell carcinoma of the head and neck treated with cetuximab and platinum-based therapy: DIRECT.

Joël Guigay, Emmanuel Chamorey, Gautier Lefebvre, Maciej Rotarski, Jean-Philippe Wagner, Emmanuel Blot, Marc Alfonsi, Audrey Seronde, Jeltje Schulten, Frédéric Peyrade and 1 more

Open access · goldAbstract readClinical Trial, Phase IVMulticenter StudyObservational Study
In one paragraph

Trial report in Cancer reports (Hoboken, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the 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 22% 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.

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

6 citing papers in PubMed, 7 citations in OpenAlex.

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

11 authors at 8 institutions in 3 countries.

Joël GuigayComprehensive Cancer Center Antoine Lacassagne, FHU OncoAge, Université Côte d'Azur, Nice, France.
Emmanuel ChamoreyComprehensive Cancer Center Antoine Lacassagne, FHU OncoAge, Université Côte d'Azur, Nice, France.
Gautier LefebvreCentre Oscar Lambret, Lille, France.
Maciej RotarskiCentre d'Oncologie et de Radiothérapie de Haute Énergie du Pays Basque, Bayonne, France.
Jean-Philippe WagnerInstitut Andrée Dutreix, Dunkerque, France.
Emmanuel BlotElsan Hôpital Privé Océane, Vannes, France.
Marc AlfonsiClinique Sainte Catherine, Avignon, France.
Audrey SerondeDepartment of Medical Affairs, Merck Biopharma, Lyon, France.
Jeltje SchultenMerck KGaA, Darmstadt, Germany.
Frédéric PeyradeComprehensive Cancer Center Antoine Lacassagne, FHU OncoAge, Université Côte d'Azur, Nice, France.
Christophe Le TourneauDepartment of Drug Development and Innovation (D3i), Institut Curie, Saint-Cloud, France.
Centre Antoine Lacassagne · FRCentre de Haute Energie · FRCentre hospitalier Bretagne Atlantique · FRCentre Oscar Lambret · FRInstitut Curie · FRInstitut Sainte Catherine · FRMerck (France) · FRMerck (Germany) · DE

Funding

Merck KGaAMerck Santé SAS, Lyon, France, an affiliate of Merck KGaA, Darmstadt, Germany
6 · The paper itself

Abstract

backgroundCetuximab plus platinum-based therapy (PBT) followed by cetuximab maintenance until progression (EXTREME) is a guideline-recommended first-line treatment option in recurrent/metastatic squamous cell carcinoma of the head and neck (R/M SCCHN). DIRECT (Dose Intensity RElative to CeTuximab) was the first phase 4 observational study evaluating EXTREME administration in the real-world setting.

aimsThe primary aim of this study was to assess the relative dose intensity of cetuximab in patients with R/M SCCHN treated with first-line cetuximab according to the EXTREME regimen. METHODS AND

resultsPatients were ≥18 years old and eligible to receive cetuximab/PBT. Primary endpoint was cetuximab relative dose intensity (RDI). Of prospectively enrolled patients (n = 157), 119 received ≥1 cycle of EXTREME. Practices differing from the EXTREME trial were 5-fluorouracil omission (14%), maintenance cetuximab given every other week (54%), prior cetuximab, disease-free interval <6 months. 64% of patients reached cetuximab RDI ≥80%; mean cetuximab RDI was 88%. 46% of patients received maintenance cetuximab (mean RDI, 91%). Median progression-free survival and overall survival were 4.5 and 9.4 months. No new/unexpected safety findings were observed.

conclusionsThe DIRECT study showed that first-line cetuximab plus PBT was a feasible, beneficial first-line treatment regimen in patients with R/M SCCHN in the real-world setting.

Indexed as

AdultAgedAntineoplastic Combined Chemotherapy ProtocolsCarboplatinCetuximabCisplatinFemaleFranceHumansLongitudinal StudiesMaleMiddle AgedNeoplasm Recurrence, LocalNeoplasm StagingProspective StudiesSquamous Cell Carcinoma of Head and NeckCarboplatinCetuximabCisplatin5-fluorouracilcarboplatincetuximabcisplatinhead and neck neoplasmspalliative care

Identifiers

PMID34156166
PMCPMC8842698
OpenAlexW3176730595

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.