Adjuvant Chemotherapy for High Risk Stage I Lung Adenocarcinoma
ECTOP-1004
Adjuvant Chemotherapy Versus Observation in Fully Resected Stage I Lung Adenocarcinoma With High Risk of Post-operative Recurrence
1 other identifier
interventional
300
1 country
1
Brief Summary
This is a clinical trial from Eastern Cooperative Thoracic Oncology Project (ECTOP), numbered as ECTOP-1004. Solid subtype, micropapillary subtype, vascular involvement, pleural involvement and low differentiation are high risk factors of post-operative recurrence for early-stage lung adenocarcinoma patients. The purpose of this clinical trial is to determine whether the widely used adjuvant chemotherapy strategy cisplatin/ pemetrexed is more effective than no further treatment for Stage pI lung adenocarcinoma patients with high post-operative recurrence risk - in terms of no dose related toxicities, premature treatment withdrawal or death.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_2
Started Jan 2018
Longer than P75 for phase_2
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 1, 2017
CompletedFirst Posted
Study publicly available on registry
December 21, 2017
CompletedStudy Start
First participant enrolled
January 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedJuly 20, 2023
July 1, 2023
6 years
November 1, 2017
July 18, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Recurrence free survival (RFS)
from date of randomization until the date of showing signs of relapse, including evidence of medical image or pathology.
up to 5 years
Secondary Outcomes (1)
Overall survival (OS)
up to 5 years
Other Outcomes (2)
Recurrence pattern
up to 5 years
Quality of life
up to 5 years
Study Arms (2)
Cisplatin plus pemetrexed
EXPERIMENTALDrug: cisplatin 75mg/m2 iv Drug: pemetrexed 500mg/m2 iv
Observation
NO INTERVENTIONObservation and follow up only
Interventions
Eligibility Criteria
You may qualify if:
- Stage pI lung adenocarcinoma confirmed through formalin-fixed paraffin-embedded tumor tissue, complete resection with mediastinal lymph node dissection
- Meet one of following conditions: a, Solid predominant adenocarcinomas; b, micropapillary predominant adenocarcinoma; c, low differentiation, unable to identify histological subtypes; d, pleural involvement; e, vascular involvement with solid subtype component or micropapillary component.
- Aged 18-70 years old.
- Eastern Cooperative Oncology Group score standard (ECOG) status 0-1.
- Medical condition permits adjuvant chemotherapy.
- Patients accept the clinical trial protocol and Informed Consent Form (ICF) signed.
You may not qualify if:
- Concurrent other malignancies
- Prior chemotherapy and/or radiation therapy for lung cancer
- Central type lung cancer
- Concurrent other unresected suspicious nodules or masses in lung
- Medical condition that will not permit treatment or follow up according to the protocol, or ECOG status \>1.
- Pregnant or nursing women.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Fudan Universitylead
Study Sites (1)
Fudan University Cancer Center
Shanghai, Shanghai Municipality, 200032, China
Related Publications (21)
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PMID: 8433390BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Haiquan Chen, MD
Fudan University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Chief,department of thoracic surgery, Fudan University Shanghai Cancer Center
Study Record Dates
First Submitted
November 1, 2017
First Posted
December 21, 2017
Study Start
January 1, 2018
Primary Completion
January 1, 2024
Study Completion
December 31, 2025
Last Updated
July 20, 2023
Record last verified: 2023-07