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Neoadjuvant Chemotherapy for Locally Advanced Thymic Cancer

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01312324
First Posted: March 10, 2011
Last Update Posted: April 20, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Keunchil Park, Samsung Medical Center
  Purpose
We try to evaluate whether neoadjuvant docetaxel plus cisplatin can increase the complete resection rate in advanced thymic carcinoma.

Condition Intervention Phase
Locally Advanced Stage III or IV Thymic Cancer Drug: neoadjuvant docetaxel/cisplatin Phase 2

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Prospective, Phase II Trial of Induction Chemotherapy With Docetaxel/Cisplatin for Masaoka Stage III/IV Thymic Epithelial Tumors

Resource links provided by NLM:


Further study details as provided by Keunchil Park, Samsung Medical Center:

Primary Outcome Measures:
  • Complete resection rate [ Time Frame: 4-8 weeks later after completion of neoadjuvant chemotherapy ]

Secondary Outcome Measures:
  • the number of patients with adverse events [ Time Frame: from enrollment to 6 months after completion of chemotherapy ]

Enrollment: 27
Study Start Date: February 2007
Study Completion Date: March 2016
Primary Completion Date: July 2015 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: neoadjuvant chemotherapy
3 cycles of docetaxel/cisplatin before operation
Drug: neoadjuvant docetaxel/cisplatin
3 cycles of docetaxel plus cisplatin docetaxel 75mg/m2 D1 cisplatin 75mg/m2 D1 every 3 weeks

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • histologically confirmed thymic carcinoma
  • surgically inoperable Masaoka stage III or IV
  • ECOG 0-2
  • at least one measurable disease

Exclusion Criteria:

  • previous myocardiac infarct history within 1 year before the enrollment.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01312324


Locations
Korea, Republic of
Samsung Medical Center
Seoul, Korea, Republic of, 135-710
Sponsors and Collaborators
Samsung Medical Center
  More Information

Responsible Party: Keunchil Park, Principal investigator, Samsung Medical Center
ClinicalTrials.gov Identifier: NCT01312324     History of Changes
Other Study ID Numbers: 2007-01-040
First Submitted: March 6, 2011
First Posted: March 10, 2011
Last Update Posted: April 20, 2016
Last Verified: April 2016

Keywords provided by Keunchil Park, Samsung Medical Center:
neoadjuvant chemotherapy
thymic cancer

Additional relevant MeSH terms:
Thymus Neoplasms
Thoracic Neoplasms
Neoplasms by Site
Neoplasms
Lymphatic Diseases
Docetaxel
Cisplatin
Antineoplastic Agents
Tubulin Modulators
Antimitotic Agents
Mitosis Modulators
Molecular Mechanisms of Pharmacological Action