Neoadjuvant Chemotherapy Compared With Surgery for Esophageal Carcinoma

Sponsor
Henan Cancer Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT05569668
Collaborator
(none)
826
1
19
43.6

Study Details

Study Description

Brief Summary

Most ESCC received NAC in China without supportive evidence from local RCTs. The negative conclusion about NAC originated from Western countries in the 1990s. Whether two-field extensive mediastinal lymphadenectomy and paclitaxel/platinum-based chemotherapy results in better survival should be determined. As the highest ESCC incidence area worldwid, we tried to analyze this top with big data by using a single-center case-control retrospective PMS study. Paclitaxel- and platinum-based NAC combined with two-field of the extensive mediastinal lymphadenectomy might provide better survival benefits than primary esophagectomy for stage II/III SCC.

Condition or Disease Intervention/Treatment Phase
  • Drug: Paclitaxel- and platinum-based chemotherapy

Detailed Description

Treatment Neoadjuvant Chemotherapy Standard NAC comprised 2 cycles. Platinum plus paclitaxel or docetaxel was repeated once every 3 weeks. Cis-platinum was administered at a total dose of 75 mg/m2 by continuous infusion on d1 or equal divided on Days 2-4 or Days 1-3. Paclitaxel, 175 mg/m2, d1, or paclitaxel, 87.5 mg/m2, d1, d8. If the docetaxel was adopted, it was given as 75 mg/m2 on Day 1.

Surgical Procedure At approximately 6-8 weeks after NAC, open (McKeown, left thoracic incision left cervical anastomosis) or MIE via thoracoscopy and/or laparoscopy was performed in the patients. Bilateral laryngeal recurrent nerve lymph node dissection was requested for every patient.

Comparisons between the NAC and primary surgery groups were performed using the chi-square test, Mann-Whitney U test and Fisher's exact test for categorical parameters after PMS. Kaplan-Meier curves and a Cox proportional hazards regression model were adopted to perform OS analysis.

Study Design

Study Type:
Observational
Actual Enrollment :
826 participants
Observational Model:
Case-Control
Time Perspective:
Retrospective
Official Title:
Neoadjuvant Chemotherapy Compared With Surgery for Esophageal Carcinoma: A Missing Evidence and A Retrospective Case-control Study
Actual Study Start Date :
Jan 1, 2021
Actual Primary Completion Date :
Aug 1, 2022
Actual Study Completion Date :
Aug 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Neoadjuvant chemotherapy group

Standard NAC comprised 2 cycles. Platinum plus paclitaxel or docetaxel was repeated once every 3 weeks. Cis-platinum was administered at a total dose of 75 mg/m2 by continuous infusion on d1 or equal divided on Days 2-4 or Days 1-3. Paclitaxel, 175 mg/m2, d1, or paclitaxel, 87.5 mg/m2, d1, d8. If the docetaxel was adopted, it was given as 75 mg/m2 on Day 1. Then surgery----esophagectomy and two-field extensive mediastinal lymphadenectomy. After surgery, there might be a adjuvant chemotherayp for pathologically positive lymph nodes patients.

Primary surgery group

The patients would receive primary surgery----esophagectomy and two-field extensive mediastinal lymphadenectomy. After surgery, there might be a adjuvant chemotherayp for pathologically positive lymph nodes patients. .

Drug: Paclitaxel- and platinum-based chemotherapy
Neoadjuvant Chemotherapy

Outcome Measures

Primary Outcome Measures

  1. OS(overall survival) [From date of patient admission to the inpatient thoracic surgery department until the date of first documented death from any cause, assessed up to 100 months]

    OS was defined as the first date of patient admission to the inpatient thoracic surgery department to the date of death from any cause.

Secondary Outcome Measures

  1. DFS(disease-free survival) [From date of patient admission to the inpatient thoracic surgery department until the date of first documented progression, assessed up to 100 months]

    DFS was defined as the first day of patients admission to the inpatient department to the date of tumor recurrence confirmed by the follow-up tests.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Clinical diagnosis of Esophageal Squamous Cell Carcinoma(ESCC) at Henan Cancer Hospital between January 1, 2015, and December 31, 2018 and the data was prospectively collected in the hubble of the LinkDoc data company

  • Surgery performed in the thoracic surgery department

  • No previous cancer treatment

Exclusion Criteria:
  • Patients with secondary cancer were excluded

Contacts and Locations

Locations

Site City State Country Postal Code
1 Henan Cancer Hospital (The Affiliated Cancer Hospital of Zhengzhou University) Zhengzhou Henan China 450003

Sponsors and Collaborators

  • Henan Cancer Hospital

Investigators

  • Principal Investigator: Yan Zheng, PhD, MD, Henan Cancer Hospital/The affiliated Cancer Hospital of ZhengZhou university

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Henan Cancer Hospital
ClinicalTrials.gov Identifier:
NCT05569668
Other Study ID Numbers:
  • HCH2101
First Posted:
Oct 6, 2022
Last Update Posted:
Oct 6, 2022
Last Verified:
Oct 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 6, 2022