RFA to Prevent Metachronous Squamous Neoplasia Recurrence After Complete Endoscopic Submucosal Dissection

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-90
SponsorE-DA Hospital

About this trial

Esophageal cancer is a highly lethal disease, and its incidence is still increasing in the world. Recent advances in image-enhanced techniques such as Lugol chromoendoscopy and narrow band imaging, the number of patients with early esophageal squamous cell neoplasias (ESCNs) detected has markedly increased. Endoscopic submucosal dissection (ESD) enables en bloc resection of the neoplasia, and the resected specimen allows for a pathological assessment to evaluate the curability. However, the patients who received complete ESD for early ESCNs frequently developed metachronous recurrence. The cumulative metachronous recurrence rate at 5 years was 50%, and the mean annual incidence of newly diagnosed metachronous tumors was 10%. Among them, those with "speckled" lugol staining pattern over the esophageal background mucosa have the highest risk and should be seen as a precancerous lesion of ESCCs. This issue is gaining attention in the era of endoscopic treatment, but currently there was no appropriate strategy to prevent the tumor recurrence in these high-risk subjects.

Endoscopic radiofrequency ablation (RFA) is a rapidly evolving therapeutic modality, and recent studies have shown its efficacy and safety for eradicating for flat type early ESCNs. To search a best strategy for the prevention of ESCNs, the investigators thus propose a hypothesis that the preemptive RFA for esophageal "speckled" lugol background mucosa may prevent the metachronous neoplastic recurrence after complete endoscopic resection.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adults with early stage ESCNs (squamous high grade dysplasia, carcinoma in situ, or T1N0M0 SCC) who were treated by endoscopic submucosal dissection.

Lugol staining showed "speckled" (>10 small lugol-unstained lesions) pattern of background mucosa.

Disqualifiers

Having a history of incomplete endoscopic treatment, or complications during/after treatment (perforation, stricture).

Having history of systemic chemotherapy or radiation therapy for esophagus or post esophagectomy.

Life expectancy <2 yr.

Decompensated cirrhosis (Child score B, C).

Trial design

Design model

Parallel

Treatments tested in this trial

  • Radiofrequency ablation

    Procedure/Surgery

    HALO360 System (Covidien GI Solutions, Sunnyvale, California, USA), which has been approved by the US Food and Drug Administration (FDA) and is approved for use in Europe (CE mark) and Taiwan (Ministry of Health and Welfare). Because the HALO 360 balloon catheter has been phased out since 2019, a new Barrx™ 360 Express catheter was used thereafter.

  • Endoscopy

    Device

    The participants will receive meticulous endoscopic examination with Lugol chromoendoscopy and Narrow-band imaging

  • Lugol's Solution (1.5%)

    Drug

    Before the RFA intervention, the participants will received Lugol staining over the esophagus

Treatment groups

100 Participants
are divided into 2 treatment groups
Group A: RFA groupExperimental treatment 3 interventions
Group B: Control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Tumor recurrence

Metachronous tumor recurrence is defined as a tumor (high-grade dysplasia or squamous cell carcinoma) recurring at a new site after more than 6 months of complete remission status.

Time frame
From date of randomization until the date of first documented tumor recurrence, assessed up to 100 months

Secondary outcomes

1

Major adverse events

including perforation, dysphagia, stenosis, defined as the failure of a standard endoscope (9.8 mm in diameter) to pass through the stenosis, or others resulting in the patients intolerable and discontinued intervention.

Time frame
From date of intervention until the date of first documented adverse events, assessed up to 12months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

E-DA Hospital

Lead sponsor

National Taiwan University Hospital

Collaborator