Evidence map›Paper›PMID 35653981›Full record

Trial reportESMO open2022

Quality of life with encorafenib plus cetuximab with or without binimetinib treatment in patients with BRAF V600E-mutant metastatic colorectal cancer: patient-reported outcomes from BEACON CRC.

S Kopetz, A Grothey, E Van Cutsem, R Yaeger, H Wasan, T Yoshino, J Desai, F Ciardiello, F Loupakis, Y S Hong and 7 more

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

Trial report in ESMO open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02928224 (A Multicenter, Randomized, Open-label, 3-Arm Phase 3 Study of Encorafenib + Cetuximab Plus or Minus Binimetinib vs. Irinotecan/Cetuximab or Infusional 5-Fluorouracil), which is not on this map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 9% 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.

NCT02928224 phase3completednot on this map

A Multicenter, Randomized, Open-label, 3-Arm Phase 3 Study of Encorafenib + Cetuximab Plus or Minus Binimetinib vs. Irinotecan/Cetuximab or Infusional 5-Fluorouracil (5-FU)/Folinic Acid (FA)/Irinotecan (FOLFIRI)/Cetuximab With a Safety Lead-in of Encorafenib + Binimetinib + Cetuximab in Patients With BRAF V600E-mutant Metastatic Colorectal Cancer

TypeinterventionalSponsorPfizerRan2016 to 2022Enrolled702ConditionsBRAF V600E-mutant Metastatic Colorectal CancerArmsEncorafenib, Binimetinib, Cetuximab, Irinotecan, Folinic Acid
3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Updates of CSCO guidelines for colorectal cancer version 2026.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Clinical research progress on BRAF V600E-mutant advanced colorectal cancer.Journal of cancer research and clinical oncology · 2023
    Review
  9. Review
  10. 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

17 authors at 16 institutions in 10 countries.

S KopetzUniversity of Texas MD Anderson Cancer Center, Houston, USA. Electronic address: skopetz@mdanderson.org.
A GrotheyWest Cancer Center and Research Institute, OneOncology, Germantown, USA.
E Van CutsemUniversity Hospitals Gasthuisberg Leuven and KU Leuven, Leuven, Belgium.
R YaegerMemorial Sloan-Kettering Cancer Center, New York, USA.
H WasanHammersmith Hospital, Department of Cancer Medicine, London, UK.
T YoshinoNational Cancer Center Hospital East, Kashiwa, Japan.
J DesaiRoyal Melbourne Hospital and Peter MacCallum Cancer Centre, Walter and Aliza Hall Institute, Parkville, Australia.
F CiardielloUniversity of Campania, Naples, Italy.
F LoupakisIstituto Oncologico del Veneto IRCCS, Padova, Italy.
Y S HongAsan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
N SteeghsNetherlands Cancer Institute, Amsterdam, The Netherlands.
T K GurenOslo University Hospital, Department of Oncology, Oslo, Norway.
H-T ArkenauSarah Cannon Research Institute, University College of London, London, UK.
P Garcia-AlfonsoGregorio Marañón Hospital, Madrid, Spain.
A BelaniPfizer Inc, New York, USA.
X ZhangPfizer Inc, New York, USA.
J TaberneroVall d'Hebron Hospital Campus, Vall d'Hebron Institute of Oncology (VHIO), IOB-Quiron, UVic-UCC, Barcelona, Spain.
Pfizer (United States) · USAsan Medical Center · KRHammersmith Hospital · GBHospital General Universitario Gregorio Marañón · ESIstituto Oncologico Veneto · ITMemorial Sloan Kettering Cancer Center · USNational Cancer Center Hospital East · JPOslo University Hospital · NOSarah Cannon Research Institute · GBThe Netherlands Cancer Institute · NLThe Royal Melbourne Hospital · AUThe University of Texas MD Anderson Cancer Center · USUniversitair Ziekenhuis Leuven · BEUniversity of Campania "Luigi Vanvitelli" · ITVall d'Hebron Institute of OncologyWest Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundIn the BEACON CRC study (NCT02928224), encorafenib plus cetuximab with binimetinib {9.3 versus 5.9 months; hazard ratio (HR) [95% confidence interval (CI)]: 0.60 [0.47-0.75]} or without binimetinib [9.3 versus 5.9 months; HR (95% CI): 0.61 (0.48-0.77)] significantly improved overall survival (OS) compared with the previous standard of care (control) in patients with BRAF V600E metastatic colorectal cancer (mCRC). Quality of life (QoL) was a secondary endpoint, assessed using validated instruments. PATIENTS AND

methodsBEACON CRC was a randomized, open-label, phase III study comparing encorafenib plus cetuximab with or without binimetinib and the investigator's choice of irinotecan plus cetuximab or FOLFIRI plus cetuximab (chemotherapy control) in patients with previously treated BRAF V600E mCRC. Patient-reported QoL assessments included the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC) and Functional Assessment of Cancer Therapy-Colorectal (FACT-C). The primary outcome for these tools was time to definitive 10% deterioration.

resultsEncorafenib plus cetuximab, both with and without binimetinib, was associated with longer median times to definitive 10% deterioration versus the control group in the EORTC Global Health Status scale [HR (95% CI): 0.65 (0.52-0.80) versus 0.61 (0.49-0.75), respectively] and the FACT-C functional well-being subscale [HR (95% CI): 0.62 (0.50-0.76) versus 0.58 (0.47-0.72), respectively]. Consistent results were observed across all subscales of the EORTC and FACT-C instruments. QoL was generally maintained during treatment for the global EORTC and FACT-C scales.

conclusionsIn addition to improving OS, encorafenib plus cetuximab with or without binimetinib delays QoL decline in previously treated patients with BRAF V600E-mutant mCRC.

Indexed as

Antineoplastic AgentsColorectal NeoplasmsProto-Oncogene Proteins B-rafAntineoplastic Combined Chemotherapy ProtocolsBenzimidazolesCarbamatesCetuximabHumansMutationPatient Reported Outcome MeasuresQuality of LifeSulfonamidesAntineoplastic AgentsBenzimidazolesbinimetinibBRAF protein, humanCarbamatesCetuximabencorafenibProto-Oncogene Proteins B-rafSulfonamidesBEACON CRCcetuximabcolorectal cancerencorafenibpatient-reported outcomesquality of life

Identifiers

PMID35653981
PMCPMC9271477
OpenAlexW4281666765

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.