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Adjuvant Radiotherapy for Esophageal Squamous Cell Carcinoma With Positive Circumstantial Resection Margin

Adjuvant Radiotherapy for T3N0M0 Esophageal Squamous Cell Carcinoma With Positive Circumstantial Resection Margin(a Randomized Controlled Trial)

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03273647
Enrollment
60
Registered
2017-09-06
Start date
2017-12-01
Completion date
2024-12-01
Last updated
2017-10-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophageal Squamous Cell Carcinoma, Positive Circumferential Resection Margin

Brief summary

The purpose of this study is to determine the efficacy of adjuvant radiotherapy for esophageal squamous cell carcinoma with positive circumstantial resection margin.

Detailed description

Although preoperative chemoradiation therapy followed by surgery is the most common approach for patients with resectable esophageal cancer, the considerable number of esophageal cancer patients received operation as the first treatment modality. Accordingly, postoperative treatments have been playing an important role because of the poor survival rates of the patients who have been treated with resection alone. The existing data shows that the 5-yeal survival rate of stage T2-3N0M0(UICC 7th edition) of thoracic esophageal squamous cell carcinoma(TESCC) after surgery is about 50% ,and locoregional lymph nodes metastases is responsible for the main cause of failure while distal metastases account for relatively less ratio. Therefore, the subclinical residual tumor is affirmative even if the early disease has been undergone curable excision and local adjuvant treatment may be essential. In rectal cancer, the involvement of the circumferential resection margin (CRM) is one of the key factors for local recurrence and poor prognosis,based on reports in which CRM with \< 1mm was found to be prognostically significant, whereas the clinical and prognostic significance of the CRM involvement in EC has been investigated only in a few series showing conflicting results, as some studies suggest a significant influence of CRM. There is lack of clear evidence for prophylactic radiation therapy in positive Circumferential Resection Margin(CRM) patients of TESCC now. In view of this, the randomized controlled trial will determine the clinical efficacy and toxicity of adjuvant radiotherapy in positive Circumferential Resection Margin(CRM) for thoracic esophageal squamous cell carcinoma.

Interventions

RADIATIONradiation

A total dose of 40Gy will be delivered in 20 fractions at 2.0Gy/fraction, 5 fractions per week in 4 weeks. The CTV encompassed the bilateral supraclavicular region, all mediastinal lymph nodes, the anastomosis site, and the left gastric and Celiac nodes.

Sponsors

Fudan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

Patients with esophageal cancer who received R0 operations in Fudan University Shanghai Cancer Center and postoperative pathology: squamous cell cancer,positive Circumferential Resection Margin(CRM)+ * KPS≥70 before radiotherapy; * Did not receive neoadjuvant or adjuvant treatment; * No clear recurrent or metastatic lesions before radiotherapy; * Intensity modulated radiation therapy(IMRT) is accepted; * Regular follow-up.

Exclusion criteria

* Exploratory thoracotomy or palliative surgery; * No clear recurrent or metastatic sites; * Recurrence or metastasis is not certain; * death of no definite cause. * Irregular follow-up;

Design outcomes

Primary

MeasureTime frameDescription
Disease-free survival timeup to 3 yearsincluding survival time from randomization to locoregional recurrence and to distal metastasis

Secondary

MeasureTime frameDescription
overall survival timeup to 3 yearssurvival time from randomization to death

Contacts

Primary ContactJiaqing Xiang, MD
j.q.xiang@hotmail.com+86 13901992249
Backup ContactYiliang Zhang, MD
ilya616@126.com+86 18017317284

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026