Proton Radiation Therapy With Cisplatin and Etoposide Followed by Surgery in Stage III Non-Small Cell Lung Cancer

Mass General Brigham

Status and phase: Terminated; Phase 1

Conditions: Non-Small Cell Lung Cancer

Treatments: Radiation: Proton Beam Radiation; Drug: Cisplatin; Drug: Etoposide

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT01565772

11-253

Details and patient eligibility

About

This research study is looking at an alternative way of delivering radiation therapy with protons. Protons are tiny particles with a positive charge that can be controlled to travel a certain distance and stop inside the body. In theory, this allows better control of where the radiation dose is delivered as compared to photons. Information from other research studies suggests that proton radiation may help to reduce unwanted side effects from radiation and allow an increase in radiation dose that increase the odds of tumor killing.

The purpose of this study is to determine the safest dose of proton radiation therapy to give in combination with standard chemotherapy in participants with Non-Small Cell Lung Cancer (NSCLC).

Full description

Proton radiation will be delivered daily Monday through Friday for 5 weeks. Study therapy will be give as an outpatient at the Francis H. Burr Proton Center at Massachusetts General Hospital.

During the weeks that subjects receive radiation, they will also receive 2 cycles of chemotherapy. Each cycle will last 28 days.

Cisplatin will be give as an IV infusion over 30-60 minutes or 1-2 hours on Days 1 and 8 of Cycles 1 and 2.

Etoposide will be given as an IV infusion over 60 minutes on Days 1, 2, 3, 4, 5 of Cycles 1 and 2.

After radiation and 2 cycles of chemotherapy are completed, subjects may have surgery to remove their tumor.

Following surgery, subjects may receive another 2 cycles of chemotherapy (Cycles 3 and 4). Each cycles lasts 21 days. Cisplatin is given on Day 1. Etoposide is given on Days 1, 2, and 3.

Enrollment: 4 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Histologically confirmed non-small cell lung cancer with a clinical stage of IIIA
• Candidate for chemoradiation and surgical resection
• Measurable disease
• Life expectancy > 6 months
• Normal organ and marrow function

Exclusion criteria

• Pregnant or breast-feeding
• Prior therapy for lung cancer with chemotherapy
• Prior chest radiation
• Compromised pulmonary function
• Severe neurovascular disease
• History of high cardiac risk including unstable angina
• History of allergic reactions attributed to compounds of similar chemical or biologic composition to cisplatin or etoposide
• Uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive hear failure, unstable angina pectoris, clinically significant or serious cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
• History of a different malignancy unless disease-free for at least 3 years and at low risk for recurrence. Individuals with the following cancers are eligible if diagnosed and treated within the past 3 years: cervical cancer in situ, non muscle-invasive bladder cancer, basal cell or squamous cell carcinoma of the skin
• Subjects with HIV

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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4 participants in 1 patient group

Radiation, Chemotherapy and Surgery

Experimental group

Description:

Proton beam radiation, plus chemotherapy with cisplatin and etoposide, followed by surgery.

Treatment:

Drug: Etoposide

Drug: Cisplatin

Radiation: Proton Beam Radiation