Impressive response to dabrafenib, trametinib, and osimertinib in a metastatic EGFR-mutant/BRAF V600E lung adenocarcinoma patient

Abstract The survival outcomes of the FLAURA trial support osimertinib as the new standard of care for untreated patients harboring activating mutations in the epidermal growth factor receptor (EGFR). Despite the initial response, disease progression invariably occurs. Although uncommon, BRAF V600E...

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Main Authors: Maurício Fernando Silva Almeida Ribeiro, Franciele Hinterholz Knebel, Fabiana Bettoni, Rodrigo Saddi, Karina Perez Sacardo, Felipe Sales Nogueira Amorim Canedo, João Victor Machado Alessi, Andrea Kazumi Shimada, José Flávio Gomes Marin, Anamaria Aranha Camargo, Artur Katz
Format: Article
Language:English
Published: Nature Publishing Group 2021-02-01
Series:npj Precision Oncology
Online Access:https://doi.org/10.1038/s41698-021-00149-4
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spelling doaj-44561a7f82f943959883dc09c9964b772021-04-02T21:31:24ZengNature Publishing Groupnpj Precision Oncology2397-768X2021-02-01511710.1038/s41698-021-00149-4Impressive response to dabrafenib, trametinib, and osimertinib in a metastatic EGFR-mutant/BRAF V600E lung adenocarcinoma patientMaurício Fernando Silva Almeida Ribeiro0Franciele Hinterholz Knebel1Fabiana Bettoni2Rodrigo Saddi3Karina Perez Sacardo4Felipe Sales Nogueira Amorim Canedo5João Victor Machado Alessi6Andrea Kazumi Shimada7José Flávio Gomes Marin8Anamaria Aranha Camargo9Artur Katz10Oncology Center, Hospital Sírio-LibanêsMolecular Oncology Center, Hospital Sírio-LibanêsMolecular Oncology Center, Hospital Sírio-LibanêsOncology Center, Hospital Sírio-LibanêsOncology Center, Hospital Sírio-LibanêsOncology Center, Hospital Sírio-LibanêsOncology Center, Hospital Sírio-LibanêsOncology Center, Hospital Sírio-LibanêsNuclear Medicine Center, Hospital Sírio-LibanêsMolecular Oncology Center, Hospital Sírio-LibanêsOncology Center, Hospital Sírio-LibanêsAbstract The survival outcomes of the FLAURA trial support osimertinib as the new standard of care for untreated patients harboring activating mutations in the epidermal growth factor receptor (EGFR). Despite the initial response, disease progression invariably occurs. Although uncommon, BRAF V600E mutation arises as a unique mechanism of resistance, and thus far, no prospective studies are available to support concurrent EGFR/BRAF blockade. We report a case of impressive radiological and ctDNA response under dabrafenib, trametinib, and osimertinib in an advanced EGFR-mutant lung adenocarcinoma patient who developed BRAF V600E as one of the acquired resistance mechanisms to second-line osimertinib. Moreover, the patient experienced remarkable clinical improvement and good tolerance to combination therapy. The present case suggests the importance of prospective studies evaluating both efficacy and safety of the combination in later line settings and points towards the potential of ctDNA to monitor resistance mechanisms and treatment benefit in clinical practice.https://doi.org/10.1038/s41698-021-00149-4
collection DOAJ
language English
format Article
sources DOAJ
author Maurício Fernando Silva Almeida Ribeiro
Franciele Hinterholz Knebel
Fabiana Bettoni
Rodrigo Saddi
Karina Perez Sacardo
Felipe Sales Nogueira Amorim Canedo
João Victor Machado Alessi
Andrea Kazumi Shimada
José Flávio Gomes Marin
Anamaria Aranha Camargo
Artur Katz
spellingShingle Maurício Fernando Silva Almeida Ribeiro
Franciele Hinterholz Knebel
Fabiana Bettoni
Rodrigo Saddi
Karina Perez Sacardo
Felipe Sales Nogueira Amorim Canedo
João Victor Machado Alessi
Andrea Kazumi Shimada
José Flávio Gomes Marin
Anamaria Aranha Camargo
Artur Katz
Impressive response to dabrafenib, trametinib, and osimertinib in a metastatic EGFR-mutant/BRAF V600E lung adenocarcinoma patient
npj Precision Oncology
author_facet Maurício Fernando Silva Almeida Ribeiro
Franciele Hinterholz Knebel
Fabiana Bettoni
Rodrigo Saddi
Karina Perez Sacardo
Felipe Sales Nogueira Amorim Canedo
João Victor Machado Alessi
Andrea Kazumi Shimada
José Flávio Gomes Marin
Anamaria Aranha Camargo
Artur Katz
author_sort Maurício Fernando Silva Almeida Ribeiro
title Impressive response to dabrafenib, trametinib, and osimertinib in a metastatic EGFR-mutant/BRAF V600E lung adenocarcinoma patient
title_short Impressive response to dabrafenib, trametinib, and osimertinib in a metastatic EGFR-mutant/BRAF V600E lung adenocarcinoma patient
title_full Impressive response to dabrafenib, trametinib, and osimertinib in a metastatic EGFR-mutant/BRAF V600E lung adenocarcinoma patient
title_fullStr Impressive response to dabrafenib, trametinib, and osimertinib in a metastatic EGFR-mutant/BRAF V600E lung adenocarcinoma patient
title_full_unstemmed Impressive response to dabrafenib, trametinib, and osimertinib in a metastatic EGFR-mutant/BRAF V600E lung adenocarcinoma patient
title_sort impressive response to dabrafenib, trametinib, and osimertinib in a metastatic egfr-mutant/braf v600e lung adenocarcinoma patient
publisher Nature Publishing Group
series npj Precision Oncology
issn 2397-768X
publishDate 2021-02-01
description Abstract The survival outcomes of the FLAURA trial support osimertinib as the new standard of care for untreated patients harboring activating mutations in the epidermal growth factor receptor (EGFR). Despite the initial response, disease progression invariably occurs. Although uncommon, BRAF V600E mutation arises as a unique mechanism of resistance, and thus far, no prospective studies are available to support concurrent EGFR/BRAF blockade. We report a case of impressive radiological and ctDNA response under dabrafenib, trametinib, and osimertinib in an advanced EGFR-mutant lung adenocarcinoma patient who developed BRAF V600E as one of the acquired resistance mechanisms to second-line osimertinib. Moreover, the patient experienced remarkable clinical improvement and good tolerance to combination therapy. The present case suggests the importance of prospective studies evaluating both efficacy and safety of the combination in later line settings and points towards the potential of ctDNA to monitor resistance mechanisms and treatment benefit in clinical practice.
url https://doi.org/10.1038/s41698-021-00149-4
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