Abstract
Carcinoids are malignant neuroendocrine tumors consisting of a spectrum of neoplasms from low-grade typical carcinoid to high-grade small cell carcinoma. We report a case of atypical thymic carcinoid that responded to neoadjuvant therapy with octreotide and sunitinib, an oral multikinase inhibitor. After 3 weeks of treatment, tumor size significantly decreased to allow for a safe surgical resection with clear margins. We believe that further study of sunitinib and octreotide with the neoadjuvant intent of preparing tumors for resection is warranted as a strategy to improve curative management of neuroendocrine tumors.
MeSH terms
-
Adult
-
Antineoplastic Agents, Hormonal / therapeutic use*
-
Biopsy, Needle
-
Carcinoid Tumor / diagnosis
-
Carcinoid Tumor / diagnostic imaging
-
Carcinoid Tumor / drug therapy*
-
Carcinoid Tumor / pathology
-
Follow-Up Studies
-
Humans
-
Indoles / therapeutic use*
-
Ki-67 Antigen / metabolism
-
Lymphatic Diseases / pathology
-
Male
-
Necrosis / pathology
-
Neoplasm Staging
-
Octreotide / therapeutic use*
-
Pneumonectomy
-
Positron-Emission Tomography
-
Proto-Oncogene Proteins c-kit / metabolism
-
Pyrroles / therapeutic use*
-
Radiography, Thoracic
-
Sunitinib
-
Synaptophysin / metabolism
-
Thymus Neoplasms / diagnosis
-
Thymus Neoplasms / diagnostic imaging
-
Thymus Neoplasms / drug therapy*
-
Thymus Neoplasms / pathology
-
Time Factors
-
Tomography, X-Ray Computed
-
Treatment Outcome
Substances
-
Antineoplastic Agents, Hormonal
-
Indoles
-
Ki-67 Antigen
-
Pyrroles
-
Synaptophysin
-
Proto-Oncogene Proteins c-kit
-
Octreotide
-
Sunitinib