Evidence map›Paper›PMID 34755244›Full record

Observational studyTargeted oncology2021

Retrospective Chart Review of Dabrafenib Plus Trametinib in Patients with Metastatic BRAF V600-Mutant Melanoma Treated in the Individual Patient Program (DESCRIBE Italy).

Massimo Aglietta, Vanna Chiarion-Sileni, Paolo Fava, Massimo Guidoboni, Roberta Depenni, Alessandro Minisini, Francesca Consoli, Paolo Ascierto, Gaetana Rinaldi, Maria Banzi and 10 more

Abstract readObservational Study
In one paragraph

Observational study in Targeted oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
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  5. 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

20 authors.

Massimo AgliettaDepartment of Oncology, University of Torino, Turin, Italy. massimo.aglietta@unito.it.
Vanna Chiarion-SileniDepartment of Clinical Oncology, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.ORCID http://orcid.org/0000-0001-9191-9124
Paolo FavaDermatologic Clinic, Department of Medical Sciences, University of Turin, Turin, Italy.ORCID http://orcid.org/0000-0002-8443-7458
Massimo GuidoboniImmunotherapy-Cell Therapy and Biobank, IRCCS-IRST, Meldola (FC), Italy.ORCID http://orcid.org/0000-0001-7703-790X
Roberta DepenniDepartment of Oncology and Hematology, University Hospital of Modena and Reggio Emilia, Modena, Italy.
Alessandro MinisiniDepartment of Oncology, Azienda Sanitaria Universitaria del Friuli Centrale, Udine, Italy.
Francesca ConsoliDepartment of Oncology, ASST Spedali Civili, Brescia, Italy.
Paolo AsciertoDepartment of Melanoma, Cancer Immunotherapy and Development Therapeutics, Istituto Nazionale Tumori IRCCS Fondazione Pascale, Naples, Italy.
Gaetana RinaldiUOC Oncologia Medica Aoup Paolo Giaccone, Palermo, Italy.
Maria BanziOncology Unit, Presidio Ospedaliero Arcispedale Santa Maria Nuova AUSL di Reggio Emilia-IRCCS, Reggio Emilia, Italy.
Riccardo MarconciniPresidio Ospedaliero S. Chiara-Az. Ospedaliero Universitaria Pisana, Pisa, Italy.
Rossana GueliMedical Oncology, ASST Sette Laghi, Circolo Hospital and Macchi Foundation, Varese, Italy.ORCID http://orcid.org/0000-0002-2674-6594
Virginia FerraresiSarcomas and Rare Tumors Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.ORCID http://orcid.org/0000-0001-6419-1668
Marco TucciDepartment of Biomedical Sciences and Clinical Oncology, University of Bari, "Aldo Moro", Bari, Italy.
Giuseppe ToniniDepartment of Medical Oncology, University Campus Bio-Medico, Rome, Italy.ORCID http://orcid.org/0000-0003-4442-8677
Giovanni Lo ReOncologia Medica e dei Tumori Immunocorrelati, CRO Aviano IRCCS, Aviano, Italy.
Michele GuidaRare Tumors and Melanoma Unit, IRCCS Istituto dei Tumori "Giovanni Paolo II", Bari, Italy.
Michele Del VecchioUnit of Melanoma Medical Oncology, Department of Medical Oncology and Hematology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.ORCID http://orcid.org/0000-0001-9060-2512
Ilaria Gioia MarconNovartis Farma S.p.A, Origgio, Italy.
Paola QueiroloOncology Division, Policlinico San Martino IRCCS, Genoa, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundReal-world data on extended follow-up of patients with BRAF V600-mutant metastatic melanoma are limited. We investigated dabrafenib plus trametinib (dab + tram) outside of a clinical trial setting (Individual Patient Program; DESCRIBE Italy).

objectiveTo describe the baseline features, treatment patterns, efficacy, and safety outcomes in patients with BRAF V600-mutant unresectable or metastatic melanoma who had received dab + tram as part of the Managed Access Program (MAP) in Italy. PATIENTS AND

methodsAn observational, retrospective chart review was conducted in Italian patients with BRAF V600-mutant unresectable stage III/IV melanoma receiving dab + tram as part of the MAP. Baseline features, treatment patterns, efficacy, and safety outcomes were evaluated.

resultsOverall, 499 patients were included in this analysis. BRAF V600E mutation was seen in 81.4% of patients. Overall response rate achieved in 243 of the 390 evaluable patients was 62.3% (95% CI 57.5-67.1). Median progression-free survival (PFS) was 9.3 months (95% CI 8.6-10.6). Subgroup analyses revealed that patients with normal lactate dehydrogenase (LDH) and ≤ three metastatic sites without brain metastases at baseline had better outcomes. With normal LDH at baseline, median PFS for patients with one or two metastatic sites other than cerebral was 18 months. No new safety signals were observed. Treatment was permanently discontinued because of treatment-emergent adverse events (TEAEs) in 9.2% of patients, and pyrexia (27.3%) was the most common TEAE, with a lower incidence than that in the phase 3 studies of dab + tram.

conclusionTreatment of BRAF V600E-mutant metastatic melanoma with dab + tram in the real-world setting was effective and safe, including the unselected population with several patients having a high tumor burden - concordant with the results of the pivotal phase 3 studies of dab + tram.

Indexed as

MelanomaNeoplasms, Second PrimarySkin NeoplasmsAntineoplastic Combined Chemotherapy ProtocolsCutaneous Malignant MelanomaHumansImidazolesMutationOximesProto-Oncogene Proteins B-rafPyridonesPyrimidinonesRetrospective StudiesBRAF protein, humandabrafenibImidazolesOximesProto-Oncogene Proteins B-rafPyridonesPyrimidinonestrametinib

Identifiers

PMID34755244
PMCPMC8613139

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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.