Complete response to neoadjuvant pembrolizumab and capecitabine in microsatellite stable, Epstein-Barr virus-positive, locally advanced gastric adenocarcinoma: case report.

Epstein-Barr virus Gastric cancer case report immunotherapy neoadjuvant therapy pembrolizumab

Journal

AME case reports
ISSN: 2523-1995
Titre abrégé: AME Case Rep
Pays: China
ID NLM: 101730832

Informations de publication

Date de publication:
2021
Historique:
received: 04 02 2021
accepted: 14 05 2021
entrez: 27 7 2021
pubmed: 28 7 2021
medline: 28 7 2021
Statut: epublish

Résumé

Immunotherapy has been established as a standard in select molecular subgroups of treatment-refractory advanced gastric cancer. However, its role in resectable gastric cancer where perioperative systemic therapy is the standard remains unclear. We present a case of a man who was diagnosed with resectable gastric cancer that was microsatellite stable but programmed death-ligand 1 (PD-L1) and Epstein-Barr Virus (EBV)-positive. Given extenuating circumstances of the SARS-CoV-2 pandemic, preferences to limit exposure to the healthcare setting, and the unique tumor molecular features, neoadjuvant pembrolizumab and capecitabine was pursued after multidisciplinary discussion. He was able to achieve a complete response to this neoadjuvant regimen with no further signs of radiographic or pathologic disease on follow-up. We highlight a dramatic response to this novel approach that represents among the first cases to support a potentially viable neoadjuvant chemoimmunotherapy strategy to resectable gastric cancer. In select patients, perioperative immunotherapy-based therapy may constitute a promising strategy in resectable gastric cancer and warrants further investigation.

Identifiants

pubmed: 34312609
doi: 10.21037/acr-21-11
pii: acr-05-21-11
pmc: PMC8256116
doi:

Types de publication

Case Reports

Langues

eng

Pagination

30

Informations de copyright

2021 AME Case Reports. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/acr-21-11). The authors have no conflicts of interest to declare.

Références

N Engl J Med. 2015 Jun 25;372(26):2509-20
pubmed: 26028255
Lancet Oncol. 2019 Nov;20(11):1506-1517
pubmed: 31582355
Nat Med. 2018 Sep;24(9):1449-1458
pubmed: 30013197
Ann Oncol. 2016 Mar;27(3):494-501
pubmed: 26673353
N Engl J Med. 2006 Jul 6;355(1):11-20
pubmed: 16822992
CA Cancer J Clin. 2018 Nov;68(6):394-424
pubmed: 30207593
JAMA Oncol. 2020 Oct 1;6(10):1571-1580
pubmed: 32880601
Future Oncol. 2019 Mar;15(9):943-952
pubmed: 30777447
Curr Hematol Malig Rep. 2019 Aug;14(4):286-291
pubmed: 31187421
JAMA Oncol. 2018 May 10;4(5):e180013
pubmed: 29543932
Lancet. 2018 Jul 14;392(10142):123-133
pubmed: 29880231
BMJ Case Rep. 2020 Sep 22;13(9):
pubmed: 32963041
Lancet. 2019 May 11;393(10184):1948-1957
pubmed: 30982686

Auteurs

Ching Ying Lin (CY)

Department of Medicine, Cedars Sinai Medical Center, Los Angeles, CA, USA.

Pareen Mehta (P)

Department of Imaging, The Angeles Clinic and Research Institute, Los Angeles, CA, USA.

Kevin M Waters (KM)

Department of Pathology, Cedars Sinai Medical Center, Los Angeles, CA, USA.

Elena Chang (E)

Department of Pathology, Cedars Sinai Medical Center, Los Angeles, CA, USA.

Andrew Hendifar (A)

Department of Hematology/Oncology, Samuel Oschin Cancer Center, Los Angeles, CA, USA.

Arsen Osipov (A)

Department of Hematology/Oncology, Samuel Oschin Cancer Center, Los Angeles, CA, USA.

Miguel Burch (M)

Department of General Surgery, Cedars Sinai Medical Center, Los Angeles, CA, USA.

De-Chen Lin (DC)

Department of Medicine, Cedars Sinai Medical Center, Los Angeles, CA, USA.

Alexandra Gangi (A)

Department of Surgical Oncology, Samuel Oschin Cancer Center, Los Angeles, CA, USA.

May Cho (M)

Department of Medicine, UC Davis Comprehensive Cancer Center, Sacramento, CA, USA.

Jun Gong (J)

Department of Hematology/Oncology, Samuel Oschin Cancer Center, Los Angeles, CA, USA.

Classifications MeSH