Complete and durable response of pulmonary large-cell neuroendocrine carcinoma to pembrolizumab.


Journal

Cancer reports (Hoboken, N.J.)
ISSN: 2573-8348
Titre abrégé: Cancer Rep (Hoboken)
Pays: United States
ID NLM: 101747728

Informations de publication

Date de publication:
08 2022
Historique:
revised: 21 09 2021
received: 28 07 2021
accepted: 25 10 2021
pubmed: 25 11 2021
medline: 9 8 2022
entrez: 24 11 2021
Statut: ppublish

Résumé

Pulmonary large cell neuroendocrine carcinoma (LCNEC) is a rare and aggressive tumor with a poor prognosis and standard therapy has not yet been established. A 65-year-old male with a cough for 2 months presented to our hospital. He was clinically diagnosed with non small cell lung cancer cT3N1M0 stage IIIA and underwent right pneumonectomy. The final diagnosis was pulmonary LCNEC pT3N1M0 stage IIIA. Multiple subcutaneous masses were detected 4 months after surgery, and biopsy revealed postoperative recurrence and metastasis. Chemotherapy with carboplatin plus etoposide was initiated. Subcutaneous masses increased and multiple new brain metastases developed after two cycles. Additional tests revealed that epidermal growth factor receptor and anaplastic lymphoma kinase were negative, and the programmed death ligand 1 (PD-L1) expression rate in tumor cells was 40% (22C3 clones). The primary cells infiltrating the tumor were CD3-positive T cells and CD138-positive plasma cells. Second-line treatment with pembrolizumab was started. The shrinkage of subcutaneous masses was observed after one cycle, and the tumor had completely disappeared after six cycles. Treatment was continued for approximately 2 years. This response has been maintained for 4 years and is still ongoing. Pembrolizumab may be used as a treatment option for pulmonary LCNEC.

Sections du résumé

BACKGROUND
Pulmonary large cell neuroendocrine carcinoma (LCNEC) is a rare and aggressive tumor with a poor prognosis and standard therapy has not yet been established.
CASE
A 65-year-old male with a cough for 2 months presented to our hospital. He was clinically diagnosed with non small cell lung cancer cT3N1M0 stage IIIA and underwent right pneumonectomy. The final diagnosis was pulmonary LCNEC pT3N1M0 stage IIIA. Multiple subcutaneous masses were detected 4 months after surgery, and biopsy revealed postoperative recurrence and metastasis. Chemotherapy with carboplatin plus etoposide was initiated. Subcutaneous masses increased and multiple new brain metastases developed after two cycles. Additional tests revealed that epidermal growth factor receptor and anaplastic lymphoma kinase were negative, and the programmed death ligand 1 (PD-L1) expression rate in tumor cells was 40% (22C3 clones). The primary cells infiltrating the tumor were CD3-positive T cells and CD138-positive plasma cells. Second-line treatment with pembrolizumab was started. The shrinkage of subcutaneous masses was observed after one cycle, and the tumor had completely disappeared after six cycles. Treatment was continued for approximately 2 years. This response has been maintained for 4 years and is still ongoing.
CONCLUSION
Pembrolizumab may be used as a treatment option for pulmonary LCNEC.

Identifiants

pubmed: 34817132
doi: 10.1002/cnr2.1589
pmc: PMC9351647
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Carboplatin BG3F62OND5
pembrolizumab DPT0O3T46P

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1589

Informations de copyright

© 2021 The Authors. Cancer Reports published by Wiley Periodicals LLC.

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Auteurs

Naoki Kadota (N)

Department of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.

Nobuo Hatakeyama (N)

Department of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.

Hiroyuki Hino (H)

Department of Thoracic Surgery, National Hospital Organization Kochi Hospital, Kochi, Japan.

Michihiro Kunishige (M)

Department of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.

Yoshihiro Kondo (Y)

Department of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.

Yoshio Okano (Y)

Department of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.

Hisanori Machida (H)

Department of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.

Keishi Naruse (K)

Department of Pathology, National Hospital Organization Kochi Hospital, Kochi, Japan.

Tsutomu Shinohara (T)

Department of Community Medicine for Respirology, Graduate School of Biomedical Sciences, Tokushima University, Tokushima, Japan.

Shoji Sakiyama (S)

Department of Thoracic Surgery, National Hospital Organization Kochi Hospital, Kochi, Japan.

Fumitaka Ogushi (F)

Department of Respiratory Medicine, National Hospital Organization Kochi Hospital, Kochi, Japan.

Eiji Takeuchi (E)

Department of Clinical Investigation, National Hospital Organization Kochi Hospital, Kochi, Japan.

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Classifications MeSH