Δευτέρα 6 Απριλίου 2015

FOLFOX FOR HIGH GRADE NEUROENDOCRINE CARCINOMA

 2015 Mar 13. pii: ERC-15-0075. [Epub ahead of print]

Post-first line FOLFOX chemotherapy in Grade 3 neuroendocrine carcinoma.

Abstract

There is no standard for second line chemotherapy in poorly differentiated grade 3 neuroendocrine carcinoma (G3-NEC) patients. We analyzed the antitumor efficacy of 5-fluroruracil and Oxaliplatin (FOLFOX) chemotherapy in this population. A single center retrospective analysis of G3-NEC consecutive patients treated with FOLFOX chemotherapy after failure of cisplatinum-based regimen between December 2003 and June 2012 was performed. Progression-free survival, overall survival, response rate and safety were assessed according to RECIST 1.1 and NCI.CTC v4 criteria. Twenty consecutive patients were included (7 males, 13 females; median age 55; range 23-87 years) with a performance status of 0 to 1 in 75% of them. Primary location was gastro-enteropancreatic in 12, thoracic in 4, other in 2 and unknown in 2 patients. There were 12 (65%) large cell, 7 (30%) small cell grade 3 neuroendocrine carcinoma tumors and 1 (5%) unknown. All patients had distant metastases. Twelve (60%) patients received FOLFOX as second line and 8 (40%) as third line or more and median number of administered cycles was 6 (range 3-14). The median follow-up was 19 months. Median progression-free survival was 4.5 months. Among the 17 evaluable patients, 5 partial responses (29%), 6 stable diseases (35%) and 6 progressive diseases (35%) were observed. Median overall survival was 9.9 months. Main Grade 3-4 toxicities were neutropenia (35%), thrombopenia (20%), nausea/vomiting (10%), anemia (10%) and elevated liver transaminases (10%). Our results suggest that FOLFOX regimen could be considered as a second-line option in poorly differentiated grade 3 neuroendocrine carcinoma patients after cisplatinum-based first line treatment but warrant further confirmation in future larger prospective studies.

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