Combination Chemotherapy and Radiation Therapy in Treating Patients With Stage III Non-Small Cell Lung Cancer That Cannot Be Removed by Surgery

Lung Cancer Clinical Trial

Official title:

Phase II Trial Irinotecan and Cisplatin Induction Chemotherapy Followed by Radiotherapy Concurrently With Etoposide/Cisplatin in Locally Advanced, Unresectable Stage III Non-Small Cell Lung Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT00616785
• Other study ID #: CDR0000584442
• Secondary ID: YONSEI-4-2007-01
• Status: Recruiting
• Phase: Phase 2
• First received: February 14, 2008
• Last updated: February 6, 2009
• Start date: June 2007

Study information

• Verified date: September 2008
• Source: National Cancer Institute (NCI)
• Contact: n/a
• Is FDA regulated: No
• Health authority: Unspecified
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Drugs used in chemotherapy, such as irinotecan, cisplatin, and etoposide work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to damage tumor cells. Giving combination chemotherapy together with radiation therapy may kill more tumor cells.

PURPOSE: This phase II trial is studying how well giving combination chemotherapy together with radiation therapy works in treating patients with stage III non-small cell lung cancer that cannot be removed by surgery.

Description:

OBJECTIVES:

Primary

• To evaluate the efficacy of induction chemotherapy comprising irinotecan hydrochloride and cisplatin in patients with locally advanced, unresectable stage III non-small cell lung cancer.

• To evaluate the feasibility of radiotherapy administered concurrently with etoposide and cisplatin chemotherapy after induction chemotherapy in these patients.

Secondary

• To evaluate the toxicity of induction chemotherapy comprising irinotecan hydrochloride and cisplatin in these patients.

• To assess whether this induction chemotherapy regimen will improve patient survival when compared with outcomes from the predecessor study, SWOG-9019.

OUTLINE: Patients receive dose-dense induction chemotherapy comprising irinotecan hydrochloride IV and cisplatin IV on days 1 and 8. Treatment repeats every 21 days for up to 2 courses.

After completion of induction chemotherapy, patients undergo radiotherapy five days a week for approximately 7 weeks. Patients receive concurrent chemotherapy comprising cisplatin IV on days 1, 8, 29, and 36 and etoposide IV on days 1-5 and 29-33.

After completion of study therapy, patients are followed at 6 weeks.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 41
• Est. primary completion date: November 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 75 Years

Eligibility

DISEASE CHARACTERISTICS:

• Histologically or cytologically confirmed non-small cell lung cancer (NSCLC)

• Stage IIIA (N2) or IIIB disease

• Pathologic documentation of N2-3 mediastinal lymph nodes is encouraged but not required if nodal size is = 1.5 cm in largest diameter

• No stage IIIB disease with malignant pleural effusion or superior sulcus tumor

• At least one measurable lesion as defined by Response Evaluation Criteria in Solid Tumors

• Unresectable disease

• No known brain metastasis

PATIENT CHARACTERISTICS:

• ECOG performance status 0-2

• Life expectancy > 3 months

• ANC = 1,500/mm³

• Hemoglobin = 9.0 g/dL (can be corrected by transfusion)

• Platelet count = 100,000/mm³

• Creatinine < 1.5 mg/dL

• Total bilirubin < 2 times upper limit of normal (ULN)

• Transaminases < 3 times ULN

• Patient compliance and geographic proximity that allow adequate follow up

• No serious, uncontrolled systemic intercurrent illness (e.g., infections or poorly controlled diabetes)

• No history of significant neurological or mental disorder, including seizures or dementia

• No other malignancy within the past 5 years except carcinoma in situ of the cervix or nonmelanoma skin cancer

• No active cardiac disease not controlled by therapy

• No myocardial infarction within the past 12 months

PRIOR CONCURRENT THERAPY:

• No prior chemotherapy or radiotherapy for NSCLC

• No other concurrent systemic chemotherapy, investigational drug, or radiotherapy

Study Design

Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Carcinoma, Non-Small-Cell Lung
• Lung Cancer
• Lung Neoplasms

Intervention

Drug:
• cisplatin

• etoposide

• irinotecan hydrochloride

Radiation:
• radiation therapy

Locations

Country	Name	City	State
Korea, Republic of	Yonsei Cancer Center at Yonsei University Medical Center	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of local/regional control			No
Primary	Rate of systemic disease control			No
Primary	Feasibility of radiotherapy administered concurrently with etoposide and cisplatin chemotherapy			Yes
Secondary	Toxicity of irinotecan hydrochloride and cisplatin induction chemotherapy as assessed by NCI CTCAE v3.0			Yes
Secondary	Progression-free survival			No
Secondary	Overall survival			No