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Endoscopic Calcium Electroporation in Gastric Tumors (GASTRIC-CaEP)

9 juin 2026 mis à jour par: Mª Henar Núñez Rodriguez, MD PhD, Hospital del Rio Hortega

Evaluation of Endoscopic Calcium Electroporation in Gastric Tumors: A Minimally Invasive Treatment Strategy

Brief Summary Background

Gastric cancer (GC) remains a major global public health challenge, ranking as the fifth most common malignancy worldwide and the third leading cause of cancer-related mortality. In 2018, approximately 1 million new cases and 783,000 deaths were reported globally. The median age at diagnosis is around 60 years, with relatively few cases occurring in younger patients.

Despite advances in systemic therapies, up to 60% of patients are diagnosed with advanced-stage disease, and approximately 20% present with significant comorbidities that limit available treatment options. This highlights the need for effective, safe, and well-tolerated therapeutic alternatives, particularly for frail patients and those with advanced disease.

In this context, calcium electroporation (CaEP) has emerged as a novel therapeutic approach with the potential to address an important unmet clinical need. CaEP is a local, minimally invasive treatment that may provide effective control of debilitating symptoms such as tumor-related gastrointestinal bleeding, while improving patients' functional status and quality of life. Importantly, these benefits may be achieved without the additional morbidity and mortality associated with more invasive therapeutic interventions. The implementation of CaEP could represent a significant advance in the management of gastric cancer, particularly in patients with limited treatment options.

Primary Objective

To evaluate the efficacy and safety of calcium electroporation (CaEP) in controlling gastrointestinal bleeding secondary to gastric cancer in patients undergoing palliative treatment, either in combination with systemic therapy or in clinical situations where control of tumor-related bleeding is required.

Study Design

This is a multicenter, non-randomized, non-pharmacological interventional study with longitudinal follow-up.

The intervention consists of two scheduled sessions of endoscopic calcium electroporation (CaEP). The second procedure will be performed 4 weeks after the first treatment unless contraindicated for clinical reasons.

Primary Outcome Measure

Clinical control of gastrointestinal bleeding secondary to gastric neoplasia.

Study Population

Patients with histologically confirmed gastric cancer who present with gastrointestinal bleeding symptoms or secondary anemia will be prospectively enrolled.

Eligible participants will include patients who are candidates for palliative treatment, either as monotherapy or in combination with systemic medical treatment and/or radiotherapy. Patients experiencing tumor-related bleeding during neoadjuvant treatment prior to surgery may also be included.

Estimated Enrollment

A total sample size of 25 evaluable patients is required. Assuming a 10% loss to follow-up, the planned enrollment is 28 patients.

Aperçu de l'étude

Description détaillée

Study Design This is a prospective, multicenter, non-randomized, non-pharmacological interventional study with longitudinal follow-up designed to evaluate the efficacy and safety of endoscopic calcium electroporation (CaEP) for the management of tumor-related gastrointestinal bleeding in patients with gastric cancer.

Participants will undergo two scheduled sessions of endoscopic calcium electroporation. The second treatment session will be performed 4 weeks after the initial procedure unless a clinical or technical contraindication arises.

Patient recruitment and follow-up are planned from JUNE 2026 through May 2028. Data analysis and dissemination of results will take place between June 2028 and December 2028.

Study Population Adult patients (≥18 years) with histologically confirmed gastric cancer presenting with iron-deficiency anemia and/or gastrointestinal bleeding attributable to the primary tumor will be prospectively enrolled after providing written informed consent.

The study will be conducted in the Gastroenterology Departments of participating hospitals.

Sample Size Based on previously published data suggesting a 90% improvement in quality of life and reduction in transfusion requirements following calcium electroporation, a clinically meaningful improvement of 20% was assumed. Using a two-sided alpha error of 0.05 and a statistical power of 80%, the required sample size was calculated as 25 evaluable patients. Allowing for an anticipated 10% loss to follow-up, the target enrollment is 28 participants.

Intervention Procedures Baseline Assessment

Before treatment, participants will undergo:

  • Clinical evaluation and medical history review.
  • Symptom assessment, including pain evaluation using a visual analogue scale (VAS).
  • Quality-of-life assessment using the EORTC QLQ-C30 questionnaire.
  • Nutritional assessment, including anthropometric measurements and laboratory testing.
  • Complete blood analysis, including hemoglobin, hematocrit, albumin, prealbumin, iron studies, vitamin levels, electrolytes, and metabolic profile.
  • Endoscopic tumor assessment with photographic documentation and tumor size estimation.

Tumor biopsies, non-tumoral gastric mucosal biopsies (when technically feasible), and peripheral blood samples will be collected before the first treatment and again prior to the second treatment at week 4.

Calcium Electroporation Procedure The procedure will be performed on an outpatient basis under deep sedation with standard monitoring and supplemental oxygen.

Following endoscopic evaluation of the lesion, intratumoral calcium gluconate (220 mM; 9 mg/mL) will be injected using a 23-gauge needle. The administered volume will be calculated according to the European Standard Operating Procedures of Electrochemotherapy (ESOPE) guidelines and adjusted to tumor size.

Electroporation will then be performed using the EndoVE® device connected to the distal end of the endoscope and the ePORE® pulse generator. Electrical pulses will be delivered to cover the entire tumor surface whenever technically feasible. Procedural parameters, including treated tumor percentage, number of pulses, impedance, and applied voltage, will be recorded.

After treatment, patients will remain under observation for 60-120 minutes for monitoring of immediate adverse events, including pain, bleeding, nausea, or perforation.

Follow-up A telephone safety assessment will be conducted 1 week after each treatment session.

The second CaEP treatment will be performed 4 weeks after the first procedure and will include repeat clinical assessment, laboratory evaluation, and biological sample collection.

Subsequently, patients will undergo monthly follow-up visits (in-person or by telephone, according to clinical status) to record bleeding episodes, transfusion requirements, hospital admissions, and clinical outcomes.

From month 3 onward, follow-up assessments will occur every 12 weeks (weeks 12, 24, 36, and 48) and will include:

  • Clinical evaluation.
  • Laboratory testing.
  • Symptom assessment.
  • EORTC QLQ-C30 quality-of-life questionnaire.
  • Upper gastrointestinal endoscopy.
  • Computed tomography (CT) imaging. Additional CaEP treatments may be offered in cases of recurrent tumor-related bleeding or anemia after exclusion of alternative causes. Retreatment may be considered in patients experiencing a decrease in hemoglobin of ≥2 g/dL from previous assessments or clinical evidence of recurrent gastrointestinal bleeding.

Type d'étude

Interventionnel

Inscription (Estimé)

28

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

  • Nom: Mª Henar Núñez Rodriguez, MD PhD
  • Numéro de téléphone: 84433 34 983 420 400
  • E-mail: henarnrod@yahoo.es

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

Inclusion Criteria:

Participants must meet all of the following criteria:

  • Age ≥18 years.
  • Histologically confirmed gastric malignancy.
  • Presence of anemia and/or gastrointestinal bleeding secondary to gastric cancer.
  • Ability and willingness to provide written informed consent.

In addition, participants must meet at least one of the following conditions:

  • Patients considered unsuitable for surgical and/or oncological treatment with curative or palliative intent due to advanced age, frailty, or significant comorbidities (Charlson Comorbidity Index ≥3 and/or ECOG Performance Status ≥2), following multidisciplinary team assessment.
  • Patients with metastatic disease receiving palliative systemic therapy in whom CaEP is indicated for symptomatic control of tumor-related gastrointestinal bleeding.
  • Patients receiving neoadjuvant therapy who develop tumor-related gastrointestinal bleeding requiring bleeding control to avoid interruption of systemic treatment prior to surgery.
  • Patients who decline surgical and/or oncological treatment when CaEP is considered appropriate for symptomatic control of gastrointestinal bleeding.

Exclusion Criteria:

Participants meeting any of the following criteria will be excluded:

  • Pregnancy or breastfeeding.
  • Presence of an endoluminal prosthesis within the intended treatment area.
  • Implanted electrical devices (e.g., pacemakers, implantable cardioverter-defibrillators) when temporary deactivation is not feasible or procedural safety cannot be guaranteed.
  • Uncorrectable coagulation disorders.
  • Medical contraindication to deep sedation or therapeutic upper gastrointestinal endoscopy.
  • Estimated life expectancy of less than 1 month.
  • Refusal or inability to provide informed consent

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Soins de soutien
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: endoscopic calcium electroporation
Participants will undergo two scheduled sessions of endoscopic calcium electroporation. The second treatment session will be performed 4 weeks after the initial procedure unless a clinical or technical contraindication arises.

Calcium Electroporation Procedure

The procedure will be performed on an outpatient basis under deep sedation with standard monitoring and supplemental oxygen.

Following endoscopic evaluation of the lesion, intratumoral calcium gluconate (220 mM; 9 mg/mL) will be injected using a 23-gauge needle. The administered volume will be calculated according to the European Standard Operating Procedures of Electrochemotherapy (ESOPE) guidelines and adjusted to tumor size.

Electroporation will then be performed using the EndoVE® device connected to the distal end of the endoscope and the ePORE® pulse generator. Electrical pulses will be delivered to cover the entire tumor surface whenever technically feasible. Procedural parameters, including treated tumor percentage, number of pulses, impedance, and applied voltage, will be recorded.

Calcium Electroporation Procedure

The procedure will be performed on an outpatient basis under deep sedation with standard monitoring and supplemental oxygen.

Following endoscopic evaluation of the lesion, intratumoral calcium gluconate (220 mM; 9 mg/mL) will be injected using a 23-gauge needle. The administered volume will be calculated according to the European Standard Operating Procedures of Electrochemotherapy (ESOPE) guidelines and adjusted to tumor size.

Electroporation will then be performed using the EndoVE® device connected to the distal end of the endoscope and the ePORE® pulse generator. Electrical pulses will be delivered to cover the entire tumor surface whenever technically feasible. Procedural parameters, including treated tumor percentage, number of pulses, impedance, and applied voltage, will be recorded.

Autres noms:
  • Endoscopic electrochemotherapy

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Proportion of participants achieving clinical hemostasis
Délai: From the first CaEP treatment through 24 months of follow-up, including monthly assessments after the two scheduled procedures and quarterly assessments from Month 3 onward.
Number of participants with episodes of hematemesis, melena, or hematochezia recorded during follow-up, as assessed by clinical evaluation and medical record review.
From the first CaEP treatment through 24 months of follow-up, including monthly assessments after the two scheduled procedures and quarterly assessments from Month 3 onward.

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Differential protein expression in tumor tissue and peripheral blood following calcium electroporation (CaEP).
Délai: Baseline (prior to the first CaEP treatment) and Week 4 (prior to the second CaEP treatment).
To identify differentially expressed proteins in tumor biopsy specimens and peripheral blood samples and to evaluate changes in protein expression profiles following treatment with calcium electroporation.
Baseline (prior to the first CaEP treatment) and Week 4 (prior to the second CaEP treatment).
Need for Rescue Hemostatic Intervention
Délai: From the first CaEP treatment through 24 months of follow-up, including monthly assessments after the two scheduled procedures and quarterly assessments from Month 3 onward.
Percentage of participants requiring additional endoscopic, radiological, or surgical hemostatic treatment for recurrent gastric tumor-related bleeding during follow-up.
From the first CaEP treatment through 24 months of follow-up, including monthly assessments after the two scheduled procedures and quarterly assessments from Month 3 onward.
Change From Baseline in Maximum Tumor Diameter Measured by Computed Tomography
Délai: From the first CaEP treatment through 24 months of follow-up, including monthly assessments after the two scheduled procedures and quarterly assessments from Month 3 onward.
Change in maximum tumor diameter (mm) from baseline to follow-up, measured on contrast-enhanced computed tomography scans according to RECIST 1.1 criteria.
From the first CaEP treatment through 24 months of follow-up, including monthly assessments after the two scheduled procedures and quarterly assessments from Month 3 onward.
Change From Baseline in Endoscopic Tumor Size
Délai: From the first CaEP treatment through 24 months of follow-up, including monthly assessments after the two scheduled procedures and quarterly assessments from Month 3 onward.
Change in the maximum endoscopic tumor diameter (mm) from baseline to follow-up, measured during upper gastrointestinal endoscopy using endoscopic size estimation and photographic documentation.
From the first CaEP treatment through 24 months of follow-up, including monthly assessments after the two scheduled procedures and quarterly assessments from Month 3 onward.

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Mª Henar Núñez Rodríguez, Digestive Department, Hospital Rio Hortega, Valladolid, Sapin

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Publications générales

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 juin 2026

Achèvement primaire (Estimé)

1 juin 2029

Achèvement de l'étude (Estimé)

1 décembre 2031

Dates d'inscription aux études

Première soumission

3 juin 2026

Première soumission répondant aux critères de contrôle qualité

9 juin 2026

Première publication (Réel)

15 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

15 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

9 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

OUI

Description du régime IPD

Demographic characteristics (e.g., age and sex). Baseline clinical characteristics, including ECOG Performance Status, Charlson Comorbidity Index, and disease stage.

Laboratory parameters, including hematological, biochemical, and nutritional markers collected according to the study protocol.

Symptom and quality-of-life assessments, including EORTC QLQ-C30 and Visual Analog Scale (VAS) scores.

Tumor characteristics and endoscopic findings. Treatment-related data, including calcium electroporation (CaEP) procedural parameters, calcium dose administered, number of treatment sessions, and technical treatment characteristics.

Clinical outcomes, including control of tumor-related gastrointestinal bleeding, transfusion requirements, hospital admissions, adverse events, progression, and survival outcomes.

De-identified molecular, proteomic, and biomarker data generated from tumor tissue, non-tumoral gastric mucosa, and peripheral blood samples.

Délai de partage IPD

Data will be available beginning 6-12 months after publication of the primary study results and will remain available for at least 5 years.

Critères d'accès au partage IPD

Access to de-identified individual participant data will be granted to qualified researchers upon submission of a methodologically sound research proposal. Requests will be reviewed by the study investigators and must comply with applicable ethical, legal, and data protection requirements. Data sharing agreements may be required before access is granted.

Type d'informations de prise en charge du partage d'IPD

  • PROTOCOLE D'ÉTUDE
  • SÈVE
  • CIF

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

produit fabriqué et exporté des États-Unis.

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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