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OncoMatch/Clinical Trials/NCT04268121

Efficacy of Neoadjuvant Chemotherapy in Terms of DFS in Patients With Localized Digestive Neuroendocrine Carcinomas

Is NCT04268121 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Neoadjuvant treatment and Adjuvant treatment for neuroendocrine carcinoma.

Phase 2RecruitingGERCOR - Multidisciplinary Oncology Cooperative GroupNCT04268121Data as of May 2026

Treatment: Neoadjuvant treatment · Adjuvant treatmentNEONEC is a single-phase, phase II study evaluating the efficacy of the 12-month neoadjuvant chemotherapy in patients with locally differentiated digestive NEC. The recommended chemotherapy is based on the current reference combination of platinum (cisplatin or carboplatin) and etoposide (VP16). For anorectal locations, radiochemotherapy is proposed to avoid the morbidity of conventional surgery. The objective of the study is to improve relapse-free survival (RFS) in NEC patients treated with neoadjuvant chemotherapy followed by surgery or chemoradiotherapy. In parallel, we will perform a prospective cohort study with patients whose diagnosis is made during surgery, who have not received neoadjuvant treatment, and who are offered an adjuvant treatment of the same type (combination of platinum and platinum salts and etoposide).

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Extracted eligibility criteria

Cancer type

Neuroendocrine Tumor

Disease stage

Grade: poorly differentiated (WHO 2017)

Patients with localized CNE, without metastasis (computed tomography [CT], thoraco-abdominopelvic CT scan [TAP] according to RECIST 1.1; possible locoregional lymph node involvement defined according to the TNM classification)

Prior therapy

Cannot have received: platinum-etoposide chemotherapy

Other than platinum-etoposide chemotherapy administrated

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