Stereotactic Radiosurgery in Treating Patients Undergoing Chemotherapy and Radiation Therapy For Stage III Non-Small Cell Lung Cancer

NCT ID: NCT00945451

Last Updated: 2019-09-16

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 35 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-04-24
• Study Completion Date: 2016-11-17

Brief Summary

RATIONALE: Drugs used in chemotherapy, such as docetaxel and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Stereotactic radiosurgery can send x-rays directly to the tumor and cause less damage to normal tissue. Giving stereotactic radiosurgery after docetaxel and cisplatin may kill more tumor cells.

PURPOSE: This phase I/II trial is studying the side effects and the best dose of stereotactic radiosurgery when given after docetaxel, cisplatin, and radiation therapy and to see how well it works in treating patients with stage III non-small cell lung cancer.

Detailed Description

OBJECTIVES:

Primary

• Evaluate the maximum tolerated dose of stereotactic radiosurgery in patients with locally advanced non-small cell lung cancer undergoing concurrent chemoradiotherapy. (Phase I)
• Assess the response rate (complete and partial response) in these patients by RECIST criteria. (Phase II)

Secondary

• Determine the tolerability. (Phase I)
• Assess the quality of life of these patients by QLQ-C30 v3. (Phase I)
• Assess the overall and disease-free survival of these patients. (Phase II)
• Assess progression-free survival of these patients. (Phase II)

OUTLINE: This is a multicenter, phase I dose escalation study of stereotactic radiosurgery followed by a phase II study.

Patients receive docetaxel IV and cisplatin IV on days 1, 22, 43, 50, 57, and 64 in the absence of disease progression or unacceptable toxicity. Beginning on day 43, patients undergo concurrent radiotherapy to the mediastinum 5 days a week. Beginning 2-3 weeks after chemoradiotherapy, patients undergo stereotactic radiosurgery on days 1, 3, and 5.

Quality of life is assessed by the QLQ-C30 v3 questionnaire at baseline, after radiosurgery, and at 6 and 12 months after completion of study treatment.

After completion of study treatment, patients are followed up monthly for 6 months, every 3 months for 1 year, and then every 6 months for 3 years.

Conditions

Lung Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

CyberKnife irradiation

Group Type: EXPERIMENTAL

CK

Intervention Type: DEVICE

Cyberknife Irradiation

Interventions

CK

Cyberknife Irradiation

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed non-small cell lung cancer

• Locally advanced disease
• No metastatic disease
• Unable to undergo surgery after concurrent chemoradiotherapy
• Must have 1-3 tumor target masses < 5 cm in greatest diameter and separated by ≥ 2 cm after concurrent chemoradiotherapy

PATIENT CHARACTERISTICS:

• WHO performance status 0-2
• Platelet count > 100,000/mm³
• Hemoglobin > 9 g/dL
• Neutrophil > 1.0 x 10^9/L
• FEV_1 > 30% of vital capacity
• Vital capacity > 25% of predicted value
• DLCO > 25% of predicted value
• LVEF ≥ 35%
• PT > 80
• aPTT > 35 sec
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception during and for 6 months after completion of study treatment
• Not under guardianship
• No dyspnea related to NYHA class III-IV heart failure
• No indirect signs of pulmonary arterial hypertension (pulmonary arterial systolic BP > 45 mm Hg)
• No pulmonary acceleration time < 100 ms
• No contraindication to fiducial insertion
• No geographical, social, or psychological conditions that would interfere with medical follow-up

PRIOR CONCURRENT THERAPY:

• Docetaxel and platinum-based drugs with concurrent irradiation allowed
• No prior surgery or surgery after the first phase of treatment with concurrent chemoradiotherapy
• No prior irradiation to lung
• No concurrent participation in another study trial

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 120 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Centre Antoine Lacassagne

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Pierre-Yves Bondiau, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Centre Antoine Lacassagne

Locations

Centre Antoine Lacassagne

Nice, , France

Countries

France

Other Identifiers

CALACASS-CYBERTAXCIS

Identifier Type: -

Identifier Source: secondary_id

INCA-RECF0941

Identifier Type: -

Identifier Source: secondary_id

2008-A01104-51

Identifier Type: -

Identifier Source: secondary_id

CDR0000639362

Identifier Type: -

Identifier Source: org_study_id