医学
伊立替康
内科学
养生
中性粒细胞减少症
肿瘤科
化疗
胃肠病学
发热性中性粒细胞减少症
无进展生存期
依托泊苷
化疗方案
外科
作者
C. Bardasi,Andrea Spallanzani,Stefania Benatti,Francesca Spada,Alice Laffi,Lorenzo Antonuzzo,Daniele Lavacchi,Riccardo Marconcini,Marco Ferrari,Margherita Rimini,Francesco Caputo,Chiara Santini,Krisida Cerma,Andrea Casadei-Gardini,Kalliopi Andrikou,Massimiliano Salati,Federica Bertolini,Annalisa Fontana,Massimo Dominici,Gabriele Luppi,Fabio Gelsomino
出处
期刊:Endocrine
[Springer Nature]
日期:2021-12-01
卷期号:74 (3): 707-713
标识
DOI:10.1007/s12020-021-02813-y
摘要
Neuroendocrine carcinomas (NECs) are a rare subgroup of neuroendocrine neoplasms that occasionally originate from gastro-entero-pancreatic (GEP) tract. Evidence of the effectiveness of chemotherapy is scarce. Platinum plus Etoposide regimens are currently the standard treatment in first-line, while little data are available on second-line treatments. The aim of this study is to evaluate the efficacy and safety of irinotecan (IRI)-based chemotherapy in a series of extrapulmonary NECs.Patients with NEC diagnosis treated at University Hospitals of Modena, Florence, Pisa, and European Institute of Oncology of Milan with an IRI-based regimen (FOLFIRI or XELIRI) after progression to a first-line platinum-based therapy were enrolled. Objective responses were assessed according to RECIST criteria. Progression-free survival (PFS) and overall survival (OS) were calculated.Thirty-four patients, 16 males, and 18 females, median age of 59 years (range 32-77), with metastatic NEC were included. Twenty-seven patients had Ki-67 ≥ 55% and four patients Ki-67 of <55% (for three patients data were not available). The median number of treatment cycles of the IRI-based regimen was 7.5 (range 1-16). Six partial responses (17.6%) and 9 stable diseases (26.5%) were observed, with a disease control rate of 44.1%. Median PFS and OS were 4.4 and 5.9 months, respectively. Neutropenia, anemia, and nausea were the only G3-G4 toxicities reported.Despite the relatively small sample size, IRI-based therapy demonstrated to be a valid option for patients with pretreated extrapulmonary NEC.
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