Hypofractionated Proton Beam Radiation Therapy, Paclitaxel, and Carboplatin in Treating Patients With Stage II-III Non-Small Cell Lung Cancer

The Washington University

Status and phase: Completed; Phase 1

Conditions: Carcinoma, Non-Small-Cell Lung

Treatments: Drug: Carboplatin; Radiation: Proton beam radiation therapy (PBT); Drug: Paclitaxel

Study type: Interventional

Funder types: Other

Identifiers

NCT02172846

201404047

Details and patient eligibility

About

This phase I trial studies the side effects and best dose of hypofractionated proton beam radiation therapy when given together with paclitaxel and carboplatin in treating patients with stage II-III non-small cell lung cancer. Proton beam radiation therapy is a type of radiation therapy that uses streams of protons (tiny particles with a positive charge) to kill tumor cells. Giving proton beam radiation therapy at higher doses over fewer days (hypofractionation) may improve local control of the tumor. Giving hypofractionated proton beam radiation therapy with chemotherapy may be a better treatment for non-small cell lung cancer

Enrollment: 23 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Histologically or cytologically proven diagnosis of non-small cell lung cancer.

2. Clinical AJCC stage II-III (AJCC, 7th ed.) with plans to be treated with concurrent chemoradiotherapy.

   1. Recurrent non-small cell lung cancer is allowed, provided the intent of the current treatment is curative and there has been no prior radiation to the thorax.
   2. Prior chemotherapy, immunotherapy, or targeted therapy is permitted as long as patients have recovered from prior toxicities to grade ≤ 1

3. Appropriate stage for protocol entry based upon the following minimum diagnostic workup:

   1. History/physical examination within 30 days prior to registration;
   2. FDG-PET/CT scan for staging within 60 days prior to registration;
   3. MRI scan with contrast of the brain (preferred) or CT scan of the brain with contrast within 60 days prior to registration.

4. Zubrod Performance Status 0-2 within 30 days prior to registration.

5. Age ≥ 18 years.

6. CBC/differential obtained within 30 days prior to registration, with adequate bone marrow function defined as follows:

   1. Absolute neutrophil count (ANC) ≥ 1,500 cells/mm3;
   2. Platelets ≥ 100,000 cells/mm3;
   3. Hemoglobin ≥ 8.0 g/dl (Note: The use of transfusion or other intervention to achieve Hgb ≥ 8.0 g/dl is acceptable.);

7. AST and ALT ≤ 1.5 upper limit of normal within 30 days prior to registration.

8. Total bilirubin ≤ 1.5 upper limit of normal within 30 days prior to registration.

9. Serum creatinine < 1.5 mg/dL or calculated creatinine clearance ≥ 50 mL/min within 30 days prior to registration estimated by the Cockcroft-Gault formula:

   Creatinine Clearance (male) = [(140 - age) x (wt in kg)] [(Serum Creatinine mg/dl) x (72)]

   Creatinine Clearance (female) = 0.85 x Creatinine Clearance (male)

10. Peripheral neuropathy ≤ grade 1 at the time of registration.

11. Presence of measurable or evaluable disease.

12. Negative serum or urine pregnancy test within 2 weeks prior to registration for women of childbearing potential.

13. Women of childbearing potential and male participants must agree to use a medically effective means of birth control throughout their participation in the treatment phase of the study.

14. Able to understand and willing to sign an IRB-approved informed consent document.

Exclusion criteria

1. Severe, active comorbidity, defined as follows:

   1. Unstable angina, history of myocardial infarction and/or congestive heart failure requiring hospitalization within the last 6 months;
   2. Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration;
   3. Chronic Obstructive Pulmonary Disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy at the time of registration;
   4. Hepatic insufficiency resulting in clinical jaundice and/or coagulation defects; note, however, that laboratory tests for liver function and coagulation parameters are not required for entry into this protocol;
   5. Acquired Immune Deficiency Syndrome (AIDS) based upon current CDC definition; note, however, that HIV testing is not required for entry into this protocol. The need to exclude patients with AIDS from this protocol is necessary because the treatments involved in this protocol may be significantly immunosuppressive. Protocol-specific requirements may also exclude immuno-compromised patients.

2. Prior radiotherapy to the thorax.

3. Currently receiving any other investigational agents.

4. Pregnant or breastfeeding.

5. Presence of a cardiac pacemaker (due to the risk created by the proton magnet).

Inclusion of Women and Minorities

Both men and women and members of all races and ethnic groups are eligible for this trial.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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23 participants in 1 patient group

Treatment (PBT, paclitaxel, and carboplatin)

Experimental group

Description:

CHEMORADIATION THERAPY: * PBT daily 5 days a week over 3 weeks for a total of 15 fractions * Paclitaxel intravenously (IV) over 1 hour weekly for 3 weeks * Carboplatin intravenously (IV) over 30 minutes weekly for 3 weeks. CONSOLIDATION CHEMOTHERAPY (B=beginning 4-6 weeks after completion of radiation therapy, patients may receive): * Paclitaxel IV over 1 hour on day 1 * Carboplatin IV over 30 minutes on day 1 * At the discretion of the treating physician * Treatment repeats every 3 weeks for 2 courses in the absence of disease progression or unacceptable toxicity.

Treatment:

Drug: Paclitaxel

Radiation: Proton beam radiation therapy (PBT)

Drug: Carboplatin