Pulmonary Neuroendocrine Tumors: Adjuvant and Systemic Treatments.


Journal

Current treatment options in oncology
ISSN: 1534-6277
Titre abrégé: Curr Treat Options Oncol
Pays: United States
ID NLM: 100900946

Informations de publication

Date de publication:
29 08 2020
Historique:
entrez: 31 8 2020
pubmed: 31 8 2020
medline: 1 12 2021
Statut: epublish

Résumé

Bronchial carcinoids are uncommon tumors accounting for 20 to 30% of all neuroendocrine tumors and about 1-2% of all cancers of pulmonary origin. Bronchial carcinoids are well-differentiated neuroendocrine tumors and have a favorable survival outcome when compared with other subtypes of lung cancers. Treatment of bronchial carcinoids is not simple owing to intricacy of symptom presentation and heterogeneity of disease biology. Successful treatment of patients requires a multimodality approach. Resection is curative in the majority of patients with localized tumors and adjuvant treatment is not routinely recommended. Multiple options for systemic therapy exist for patients with advanced disease. To date, very few randomized clinical trials have been done, partly owing to the relative rarity of this malignancy. Somatostatin analogs (SSAs) are reasonable first-line choice for patients with tumors expressing somatostatin receptors. Everolimus is an appropriate first-line choice for somatostatin receptor negative tumors and for any patients with progressive disease. PRRT can also be considered for progressive tumors expressing somatostatin receptors. Based on retrospective series, cytotoxic chemotherapy can be selected in patients with progressive tumors, primarily when cytoreduction is needed. Herein, we will discuss evidence supporting the role of adjuvant and systemic treatment therapies for those with bronchial carcinoid tumors by focusing on various studies.

Identifiants

pubmed: 32862320
doi: 10.1007/s11864-020-00786-0
pii: 10.1007/s11864-020-00786-0
doi:

Substances chimiques

Antineoplastic Agents 0
Immune Checkpoint Inhibitors 0
Organometallic Compounds 0
Protein Kinase Inhibitors 0
Radiopharmaceuticals 0
Receptors, Somatostatin 0
Somatostatin 51110-01-1
Capecitabine 6804DJ8Z9U
Etoposide 6PLQ3CP4P3
Everolimus 9HW64Q8G6G
lutetium Lu 177 dotatate AE221IM3BB
Cisplatin Q20Q21Q62J
Octreotide RWM8CCW8GP
Temozolomide YF1K15M17Y

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

86

Auteurs

Dipesh Uprety (D)

Division of Medical Oncology, Mayo Clinic, 200 First St SW, Rochester, MN, 55905, USA.

Thorvardur R Halfdanarson (TR)

Division of Medical Oncology, Mayo Clinic, 200 First St SW, Rochester, MN, 55905, USA.

Julian R Molina (JR)

Division of Medical Oncology, Mayo Clinic, 200 First St SW, Rochester, MN, 55905, USA.

Konstantinos Leventakos (K)

Division of Medical Oncology, Mayo Clinic, 200 First St SW, Rochester, MN, 55905, USA. Leventakos.Konstantinos@mayo.edu.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH