Purpose: 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. Methods: 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. Results: 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. Conclusions: Despite the relatively small sample size, IRI-based therapy demonstrated to be a valid option for patients with pretreated extrapulmonary NEC.

Irinotecan-based chemotherapy in extrapulmonary neuroendocrine carcinomas: survival and safety data from a multicentric Italian experience / Bardasi, C.; Spallanzani, A.; Benatti, S.; Spada, F.; Laffi, A.; Antonuzzo, L.; Lavacchi, D.; Marconcini, R.; Ferrari, M.; Rimini, M.; Caputo, F.; Santini, C.; Cerma, K.; Casadei-Gardini, A.; Andrikou, K.; Salati, M.; Bertolini, F.; Fontana, A.; Dominici, M.; Luppi, G.; Gelsomino, F.. - In: ENDOCRINE. - ISSN 1559-0100. - 74:3(2021), pp. 707-713. [10.1007/s12020-021-02813-y]

Irinotecan-based chemotherapy in extrapulmonary neuroendocrine carcinomas: survival and safety data from a multicentric Italian experience

Dominici M.;
2021

Abstract

Purpose: 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. Methods: 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. Results: 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. Conclusions: Despite the relatively small sample size, IRI-based therapy demonstrated to be a valid option for patients with pretreated extrapulmonary NEC.
2021
74
3
707
713
Irinotecan-based chemotherapy in extrapulmonary neuroendocrine carcinomas: survival and safety data from a multicentric Italian experience / Bardasi, C.; Spallanzani, A.; Benatti, S.; Spada, F.; Laffi, A.; Antonuzzo, L.; Lavacchi, D.; Marconcini, R.; Ferrari, M.; Rimini, M.; Caputo, F.; Santini, C.; Cerma, K.; Casadei-Gardini, A.; Andrikou, K.; Salati, M.; Bertolini, F.; Fontana, A.; Dominici, M.; Luppi, G.; Gelsomino, F.. - In: ENDOCRINE. - ISSN 1559-0100. - 74:3(2021), pp. 707-713. [10.1007/s12020-021-02813-y]
Bardasi, C.; Spallanzani, A.; Benatti, S.; Spada, F.; Laffi, A.; Antonuzzo, L.; Lavacchi, D.; Marconcini, R.; Ferrari, M.; Rimini, M.; Caputo, F.; Santini, C.; Cerma, K.; Casadei-Gardini, A.; Andrikou, K.; Salati, M.; Bertolini, F.; Fontana, A.; Dominici, M.; Luppi, G.; Gelsomino, F.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1251819
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