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NCT Number: NCT07192991

Neuroendocrine Carcinomas: Patient Journey And Treatment Outcomes In Latin America

This observational, retrospective study aims to understand the treatment patterns and outcomes of patients with pulmonary and extra-pulmonary neuroendocrine carcinomas (NEC) in Latin America (Brazil, Mexico, Argentina, and Peru). The research will collect data from medical records to analyze factors like patient demographics, diagnosis methods, tumor characteristics, treatment approaches, and disease progression. The study is non-interventional, meaning patient care will follow standard clinical practice, with data gathered via an electronic system.

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Key information

Conditions

Neuroendocrine Carcinomas Adenocarcinoma Carcinoma Carcinoma, Neuroendocrine Lung Neuroendocrine Carcinoma Neoplasms Neoplasms by Histologic Type Neoplasms, Germ Cell and Embryonal Neoplasms, Glandular and Epithelial Neoplasms, Nerve Tissue Neuroectodermal Tumors Neuroendocrine Tumors

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

About this study

Currently, there is a hypothesis that there is not enough evidence to fully understand the patient journey and accurately determine the clinical outcomes of neuroendocrine carcinomas (NEC) in Latin America. A better understanding of this landscape, including its unique regional aspects, could lead to improved patient care.

To address this gap, this observational, retrospective, non-interventional study aims to describe treatment patterns and outcomes for patients with both pulmonary and extra-pulmonary NEC in Latin America. Eligible patients diagnosed with either form of NEC will be included, and data will be collected from medical records at selected sites across Brazil, Mexico, Argentina, and Peru.

Data to be retrieved include but are not limited to age at diagnosis, gender, ECOG at diagnosis, stage (TNM), resources used for primary diagnosis (imaging, upfront surgery etc.), primary site, tumor size and grade, setting of initial treatment (reference center vs community hospital), type of initial surgical approach, data of anti-cancer treatments (including (neo)adjuvant and advanced settings) and relapse and/or progression/death. Data regarding anti-cancer treatments (including (neo)adjuvant and advanced settings), as well as radiotherapy use will also be recorded.

As this project is non-interventional, patients will still receive treatment and clinical assessments for extra-pulmonary and pulmonary NEC as determined by their attending physician, according to the standard of care and routine clinical practice at each site. No visits are demanded by the study, but for those required for the consent process whenever determined by the local ethics committee. Patient source data will be taken from the patient's medical records and reported by means of an electronic data capture (EDC) system.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ≥18 years old
  • Diagnosed between August 2014 and August 2024 with one of the following:
  • Extrapulmonary Neuroendocrine Carcinoma (EP-NEC)
  • Large-cell neuroendocrine carcinoma (LCNEC) or mixed
  • Small Cell Lung Cancer (SCLC) or mixed
  • Adequate and accessible medical records for data collection
  • Tumor block collected from 2014 onwards

Exclusion criteria

  • Patients with active, concurrent malignancies at the time of NEC diagnosis, except for non-invasive cancers like basal cell carcinoma or squamous cell carcinoma of the skin, or in situ cervical cancer.
  • Patients or their legal representatives unwilling or unable to provide informed consent (if needed per ethics committee).

Treatment and study plan

observational study

Other

This is an observational study; patients will not be exposed to clinical interventions different from those belonging to the standard of care.

Primary outcomes

  1. Patterns of Initial Cancer Treatment: number of participants treated within vs. outside high-volume sites and associated treatment characteristics

    Time frame: Throughout the study period, an average of 24 months

    Treatment patterns will be analyzed descriptively using tables and graphs to illustrate the distribution of patients receiving initial cancer treatment within versus outside high-volume treatment centers. Key characteristics of the initial treatment will be assessed.

  2. Event-free survival (EFS)

    Time frame: Throughout the study period, an average of 24 months

    defined as time from diagnosis until relapse, death, or definitive failure of treatment strategy that implicates failure of curative-intent treatment [for patients treated with curative intent]. Participants who are lost to follow up or reach the study end will be censored at their last date of contact.

  3. Time to treatment failure (TTF)

    Time frame: Throughout the study period, an average of 24 months

    in first and second-line: defined as time from first dose of treatments until date of discontinuation of treatment for any reason, including progression of disease, treatment toxicity, and death. Participants who are lost to follow up or reach the study end will be censored at their last date of contact

  4. Progression-free survival (PFS)

    Time frame: Throughout the study period, an average of 24 months

    defined as time from treatment initiation until progression or death [for patients treated with palliative intent]. Participants who are lost to follow up or reach the study end will be censored at their last date of contact.

  5. Overall survival

    Time frame: Throughout the study period, an average of 24 months

    [according to disease stage/setting], defined as time from initial diagnosis until date of death from any cause. Participants who are lost to follow up or reach the study end will be censored at their last date of contact.

  6. Frequency of DLL-3 immunohistochemistry expression

    Time frame: After the end of recruitment, an average of 1 year

    Rate of patients with DLL3 expression in extra-pulmonary and pulmonary NEC by IHC [stratified by tumor primary site]

Study contacts

Contact information is provided by the study sponsor or research team.

Laura Voelcker

CONTACT

[email protected]

+55 51 3384 5334

Project Manager

CONTACT

[email protected]

+55 51 3384 5334

Sponsors and collaborators

Lead sponsor

Latin American Cooperative Oncology Group

Other

Collaborators

  • Boehringer Ingelheim
  • Grupo Argentino de Investigación Clínica en Oncología
  • Grupo de Estudios Clínicos Oncológicos Peruano

Registry information

Acronym: NECTARINE

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Sep 25, 2025
Registry last updated
Sep 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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