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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00614484
Other study ID # OSR #49168
Secondary ID
Status Terminated
Phase Phase 1/Phase 2
First received December 26, 2007
Last updated April 28, 2014
Start date August 1999
Est. completion date June 2011

Study information

Verified date April 2014
Source Loma Linda University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the effectiveness of proton beam radiotherapy combined with chemotherapy for treatment of locally advanced non-small cell lung cancer.


Recruitment information / eligibility

Status Terminated
Enrollment 28
Est. completion date June 2011
Est. primary completion date June 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Clinical stage 2, 3A or 3B (unresectable)

- Histologic evidence of non-small cell carcinoma

- Age > 18 years

- Karnofsky performance status 70 or greater

- No prior radiation to the chest

- No previous chemotherapy

Exclusion Criteria:

- Clinical stage 1 or 4

- Previous malignancies except for non-melanoma skin cancer unless disease free for > 3 years

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Radiation:
Proton Radiation Therapy
A five week coarse of proton radiotherapy begins on day 28 and is given once daily for the first two weeks and twice daily for the final 3 weeks. The total dose given with proton beam is 76 Gy. Weekly chemotherapy with carboplatin and taxol is given during proton therapy.
Drug:
Taxol
200 mg/m2, IV, for 2 cycles followed by 50 mg/m2 weekly for 5 weeks during radiotherapy.
Carboplatin
AUC 6, IV, for two cycles followed by AUC 2 weekly for 5 weeks during radiotherapy.

Locations

Country Name City State
United States Loma Linda University Medical Center Loma Linda California

Sponsors (1)

Lead Sponsor Collaborator
Loma Linda University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall Survival. Median survival time following treatment. Monthly for duration of participant lifespan. Average lifespan 1-2 years Yes
Secondary Treatment Related Toxicities. grade 3 or higher esophageal toxicity
Toxicity is categorized either early or late phase.
Early phase- toxicity occurring during or within 30 days s/p treatment Late phase- toxicity occurring thereafter
Monthly for duration of participant lifespan. Average lifespan 1-2 years Yes
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