NCT03380468

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

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
300

participants targeted

Target at P75+ for phase_2

Timeline
Completed

Started Jan 2018

Longer than P75 for phase_2

Geographic Reach
1 country

1 active site

Status
unknown

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

Completed
2 months until next milestone

First Posted

Study publicly available on registry

December 21, 2017

Completed
11 days until next milestone

Study Start

First participant enrolled

January 1, 2018

Completed
6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2024

Completed
2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
Last Updated

July 20, 2023

Status Verified

July 1, 2023

Enrollment Period

6 years

First QC Date

November 1, 2017

Last Update Submit

July 18, 2023

Conditions

Keywords

Lung adenocarcinomaadjuvant chemotherapy

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

EXPERIMENTAL

Drug: cisplatin 75mg/m2 iv Drug: pemetrexed 500mg/m2 iv

Drug: cisplatin plus pemetrexed

Observation

NO INTERVENTION

Observation and follow up only

Interventions

cisplatin 75mg/m2 iv; pemetrexed 500mg/m2 iv

Cisplatin plus pemetrexed

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Fudan University Cancer Center

Shanghai, Shanghai Municipality, 200032, China

RECRUITING

Related Publications (21)

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    PMID: 25364519BACKGROUND
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    PMID: 21587131BACKGROUND
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    PMID: 25704861BACKGROUND
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    PMID: 25675151BACKGROUND
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MeSH Terms

Conditions

Lung NeoplasmsAdenocarcinoma of Lung

Interventions

CisplatinPemetrexed

Condition Hierarchy (Ancestors)

Respiratory Tract NeoplasmsThoracic NeoplasmsNeoplasms by SiteNeoplasmsLung DiseasesRespiratory Tract DiseasesAdenocarcinomaCarcinomaNeoplasms, Glandular and EpithelialNeoplasms by Histologic Type

Intervention Hierarchy (Ancestors)

Chlorine CompoundsInorganic ChemicalsNitrogen CompoundsPlatinum CompoundsGuanineHypoxanthinesPurinonesPurinesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-RingHeterocyclic CompoundsGlutamatesAmino Acids, AcidicAmino AcidsAmino Acids, Peptides, and ProteinsAmino Acids, Dicarboxylic

Study Officials

  • Haiquan Chen, MD

    Fudan University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Haiquan Chen, MD

CONTACT

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

Locations