Cancer of unknown primary (CUP) is defned as a heterogeneous group of tumours that present with metastasis, and in which attempts to identify the original site have failed. They difer from other primary tumours in their biological features and how they spread, which means that they can be considered a separate entity. There are several hypotheses regarding their origin, but the most plausible explanation for their aggressiveness and chemoresistance seems to involve chromosomal instability. Depending on the type of study done, CUP can account for 2–9% of all cancer patients, mostly 60–75 years old. This article reviews the main clinical, pathological, and molecular studies conducted to analyse and determine the origin of CUP.The main strategies for patient management and treatment, by both clinicians and pathologists, are also addressed.
The authors are grateful for the editorial assistance of Dr. Fernando Sánchez-Barbero of HealthCo (Madrid, Spain) in the production of this manuscript. SEOM and SEAP are grateful for the fnancial support for this project in the form of unrestricted grants from Ferrer Diagnostic, OncoDNA and Foundation Medicine/Roche.
English
Cancer of unknown primary; Diagnosis; Immunohistochemistry; Biopsy; Prognosis; Chemotherapy; Molecular pathology; Histopathology
Springer
Reproducció del document publicat a https://doi.org/10.1007/s12094-018-1899-z
Clinical & Translational Oncology, 2018, vol. 20, núm. 11, p.1361-1372
cc-by (c) Losa et al., 2018
http://creativecommons.org/licenses/by/4.0/
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