A plain language summary of results from the ADAURA study: osimertinib after surgery for patients who have early-stage EGFR-mutated non-small cell lung cancer.

CNS metastases Chemotherapy EGFR gene mutation Lay summary Non-small cell lung cancer Osimertinib Plain language summary Surgery

Journal

Future oncology (London, England)
ISSN: 1744-8301
Titre abrégé: Future Oncol
Pays: England
ID NLM: 101256629

Informations de publication

Date de publication:
01 Dec 2021
Historique:
pubmed: 2 11 2021
medline: 27 11 2021
entrez: 1 11 2021
Statut: ppublish

Résumé

Here, we summarize the initial results from the ADAURA clinical study looking at treatment with osimertinib in patients with a specific type of non-small cell lung cancer (also called NSCLC). Osimertinib (TAGRISSO®) is a medication used to treat a type of NSCLC with a change (mutation) in the EGFR gene, known as EGFR-mutated NSCLC. EGFR stands for 'epidermal growth factor receptor'. It is a protein present on the surface of both healthy and cancer cells that can regulate how cells grow and divide. Sometimes, certain mutations in EGFR can result in the EGFR protein malfunctioning, which can lead to the formation of cancer, like EGFR-mutated NSCLC. Based on previous clinical studies, osimertinib is already approved for use in patients with EGFR-mutated NSCLC that has spread beyond the lung (metastatic disease). This medication works to stop, prevent, or slow the growth of EGFR-mutated NSCLC tumors, by specifically blocking the activity of EGFR. In the ADAURA clinical study, participants had resectable EGFR-mutated NSCLC, which means they had tumors that can be removed by surgery. Participants took either osimertinib or a placebo (a dummy drug with no active ingredient) after having their tumors removed by surgery. Post-surgery chemotherapy was allowed, but not compulsory (this was decided by the participant and their doctor). To date, the study has shown that osimertinib could be beneficial for patients with resectable EGFR-mutated NSCLC. Participants who took osimertinib have stayed cancer-free for longer than those who took the placebo, regardless of whether or not they received chemotherapy after surgery. Osimertinib treatment also reduced the risk of tumors spreading to the brain and spinal cord, otherwise known as the central nervous system (also called CNS). The side effects experienced by the participants taking osimertinib have been consistent with what we already know. Based on the results from ADAURA, osimertinib has been approved for the treatment of resectable EGFR-mutated NSCLC after tumor removal. The ADAURA study is still ongoing and more results are expected to be released in the future. ClinicalTrials.gov NCT number: NCT02511106.

Identifiants

pubmed: 34723634
doi: 10.2217/fon-2021-0752
doi:

Substances chimiques

Acrylamides 0
Aniline Compounds 0
osimertinib 3C06JJ0Z2O
EGFR protein, human EC 2.7.10.1
ErbB Receptors EC 2.7.10.1

Banques de données

ClinicalTrials.gov
['NCT02511106']

Types de publication

Journal Article Comment

Langues

eng

Sous-ensembles de citation

IM

Pagination

4827-4835

Commentaires et corrections

Type : CommentOn

Auteurs

Yi-Long Wu (YL)

Guangdong Lung Cancer Institute, Guangdong Provincial People's Hospital and Guangdong Academy of Medical Sciences, Guangzhou, China.

Masahiro Tsuboi (M)

Department of Thoracic Surgery and Oncology, National Cancer Center Hospital East, Kashiwa, Japan.

Thomas John (T)

Department of Medical Oncology, Austin Health, Melbourne, Australia.

Christian Grohe (C)

Department of Respiratory Diseases, Evangelische Lungenklinik, Berlin, Germany; 5Department of Medical Oncology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Margarita Majem (M)

Department of Medical Oncology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Jonathan W Goldman (JW)

David Geffen School of Medicine at University of California Los Angeles, CA, USA.

Konstantin Laktionov (K)

Center of Innovative Technologies and Oncology, N.N. Blokhin Russian Cancer Center, Russian Academy of Medical Sciences, Moscow, Russia.

Sang-We Kim (SW)

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.

Terufumi Kato (T)

Department of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Japan.

Huu-Vinh Vu (HV)

Department of Thoracic Surgery, Choray Hospital, Ho Chi Minh City, Vietnam.

Shun Lu (S)

Lung Cancer Center, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, China.

Kye-Young Lee (KY)

Precision Medicine, Lung Cancer Center, Konkuk University Medical Center, Seoul, South Korea.

Charuwan Akewanlop (C)

Division of Medical Oncology, Faculty of Medicine, Siriraj Hospital, Bangkok, Thailand.

Chong-Jen Yu (CJ)

Department of Internal Medicine, National Taiwan University Hospital Hsinchu Branch and National Taiwan University College of Medicine, Taipei, Taiwan.

Filippo de Marinis (F)

Thoracic Oncology Division, European Institute of Oncology (IEO), IRCCS, Milan, Italy.

Laura Bonanno (L)

Medical Oncology 2, Istituto Oncologico Veneto IOV IRCCS, Padova, Italy.

Manuel Domine (M)

Instituto de Investigacion Sanitaria-Fundacion de la Jimenez Diaz, Madrid, Spain.

Frances A Shepherd (FA)

Department of Medical Oncology and Hematology, University Health Network, Princess Margaret Hospital and the University of Toronto, Toronto, Ontario, Canada.

Lingmin Zeng (L)

Late Oncology Statistics, AstraZeneca, Gaithersburg, MD, USA.

Rachel Hodge (R)

Late Oncology Statistics, AstraZeneca, Cambridge, UK.

Ajlan Atasoy (A)

Late Oncology Research & Development, AstraZeneca, Cambridge, UK.

Yuri Rukazenkov (Y)

Late Oncology Research & Development, AstraZeneca, Cambridge, UK.

Roy S Herbst (RS)

Medical Oncology, Yale School of Medicine and Yale Cancer Center, New Haven, CT, USA.

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Classifications MeSH