JoLT-Ca Sublobar Resection (SR) Versus Stereotactic Ablative Radiotherapy (SAbR) for Lung Cancer



Status:Recruiting
Conditions:Lung Cancer, Lung Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - 99
Updated:12/16/2018
Start Date:July 2015
End Date:December 2024
Contact:Robert Timmerman, MD
Phone:214-645-8525

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JoLT-Ca A Randomized Phase III Study of Sublobar Resection (SR) Versus Stereotactic Ablative Radiotherapy (SAbR) in High Risk Patients With Stage I Non-Small Cell Lung Cancer (NSCLC), The STABLE-MATES Trial

To Determine if SAbR improves survival over SR in High Risk Operable Stage I NSCLC

Stereotactic Ablative Radiotherapy has been shown in single institution phase II and matched
cohort studies to be effective at controlling primary early lung cancer. Recent pooled
analysis of both the STARS and ROSEL randomized trials comparing SABR versus lobectomy have
shown a significantly improved 3-year survival with SABR, giving further impetus for
successful completion of a randomized trial .

Pre-randomized trial- Patients will be screened and pre-randomized to either SR or SAbR.
Informed consent will be obtained after patients are made aware of the randomized assignment.
Despite pre-randomization prior to consent, patients maintain their right to accept or
decline any/all study activities. Only consenting patients will be allowed to participate in
study activities, including observation after either randomized treatments or observation
after standard of care treatment, while those declining consent will be managed by their
physician(s) off study.Patients will be accrued and followed for a minimum of 2-years after
treatment.

Inclusion Criteria:

- Age > 18 years.

- ECOG performance status (PS) 0, 1, or 2.

- Radiographic findings consistent with non-small cell lung cancer, including lesions
with ground glass opacities with a solid component of 50% or greater. Those with
ground glass opacities and <50% solid component will be excluded.

- Biopsy confirmed non-small cell lung cancer.

- Tumor ≤ 4 cm maximum diameter, including clinical stage IA and selected IB by PET/CT
scan of the chest and upper abdomen performed within 60 days prior to registration.

- All clinically suspicious mediastinal N1, N2, or N3 lymph nodes (> 1 cm short-axis
dimension on CT scan and/or positive on PET scan) confirmed negative for involvement
with NSCLC by one of the following methods: mediastinoscopy, anterior mediastinotomy
EUS/EBUS guided needle aspiration, CT-guided, video-assisted thoracoscopic or open
lymph node biopsy.

- Tumor verified by a thoracic surgeon to be in a location that will permit sublobar
resection.

- Tumor located peripherally within the lung. NOTE: Peripheral is defined as not
touching any surface within 2 cm of the proximal bronchial tree in all directions. See
below. Patients with non-peripheral (central) tumors are NOT eligible.

- No evidence of distant metastases.

- Availability of pulmonary function tests (PFTs - spirometry, DLCO, +/- arterial blood
gases) within 90 days prior to registration. Patients with tracheotomy, etc, who are
physically unable to perform PFTs (and therefore cannot be tested for the Major
criteria in 3.1.10 below) are potentially still eligible if a study credentialed
thoracic surgeon documents that the patient's health characteristics would otherwise
have been acceptable for eligibility as a high risk but nonetheless operable patient
(in particular be eligible for sublobar resection).

- Patient at high-risk for surgery by meeting a minimum of one major criteria or two
minor criteria

- No prior intra-thoracic radiation therapy. NOTE: Previous radiotherapy as part of
treatment for head and neck, breast, or other non-thoracic cancer is permitted so long
as possible radiation fields would not overlap. Previous chemotherapy or surgical
resection specifically for the lung cancer being treated on this protocol is NOT
permitted. No prior lung resection on the ipsilateral side.

- Non-pregnant and non-lactating. Women of child-bearing potential must have a negative
urine or serum pregnancy test within 60 days prior to registration. Peri-menopausal
women must be amenorrheic > 12 months prior to registration to be considered not of
childbearing potential.

- No prior invasive malignancy, unless disease-free for ≥ 3 years prior to registration
(exceptions: non-melanoma skin cancer, in-situ cancers).

- Ability to understand and the willingness to sign a written informed consent.

Exclusion Criteria:

- evidence of distant metastases

- prior intra-thoracic radiation therapy. NOTE: Previous radiotherapy as part of
treatment for head and neck, breast, or other non-thoracic cancer is permitted so long
as possible radiation fields would not overlap. Previous chemotherapy or surgical
resection specifically for the lung cancer being treated on this protocol is NOT
permitted. No prior lung resection on the ipsilateral side.

- pregnant and lactating women

- prior invasive malignancy, unless disease-free for ≥ 3 years prior to registration
(exceptions: non-melanoma skin cancer, in-situ cancers).
We found this trial at
37
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Chapel Hill, North Carolina 27599
(919) 962-2211
Phone: 919-966-3381
Univ of North Carolina Carolina’s vibrant people and programs attest to the University’s long-standing place...
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9500 Euclid Avenue
Cleveland, Ohio 44106
216.444.2200
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101 Jessup Hall
Iowa City, Iowa 52242
(319) 335-3500
University of Iowa With just over 30,000 students, the University of Iowa is one of...
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Annapolis, Maryland 21401
Phone: 443-481-1000
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Aurora, Colorado 80045
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22 S Greene St
Baltimore, Maryland 21201
(410) 328-8667
Phone: 410-740-9300
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Boston, Massachusetts 02118
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1215 Lee St
Charlottesville, Virginia 22903
(434) 924-0211
University of Virginia Health System UVA Health System includes a 604-bed hospital, level I trauma...
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2600 Clifton Ave
Cincinnati, Ohio 45267
(513) 556-6000
University of Cincinnati The University of Cincinnati offers students a balance of educational excellence and...
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11100 Euclid Avenue
Cleveland, Ohio 44106
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Colorado Springs, Colorado 80907
Phone: 719-776-2842
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410 W 10th Ave
Columbus, Ohio 43210
(614) 293-8652
Phone: 614-293-8415
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1801 Inwood Rd
Dallas, Texas 75390
(214) 645-3300
Principal Investigator: Robert Timmerman, MD
Phone: 214-645-8525
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Detroit, Michigan 48202
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Falls Church, Virginia 22042
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41 Victoria Parade
Fitzroy, Victoria 3065
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3901 Rainbow Blvd
Kansas City, Kansas 66160
(913) 588-5000
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La Jolla, California 92093
Phone: 858-822-6100
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Lexington, Kentucky 40536
Phone: 859-323-6880
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Louisville, Kentucky 40202
Phone: 502-588-6000
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Memphis, Tennessee 38163
Phone: 901-448-2918
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Milwaukee, Wisconsin 53295
Phone: 414-384-2000
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8701 W Watertown Plank Rd
Milwaukee, Wisconsin
(414) 955-8296
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1945 New Jersey 33
Neptune, New Jersey 07753
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1514 Jefferson Hwy.
New Orleans, Louisiana 70121
504-842-3000
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550 1st Ave
New York, New York 10016
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1020 Walnut St
Philadelphia, Pennsylvania 19107
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5050 Northeast Hoyt Street
Portland, Oregon 97213
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Providence, Rhode Island 02903
Phone: 401-444-8311
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200 First Street SW
Rochester, Minnesota 55905
507-284-2511
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Salt Lake City, Utah 84157
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4700 Waters Ave
Savannah, Georgia 31404
(912) 350-8000
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Memorial Health University Medical Center Memorial University Medical Center (MUMC) is a nonprofit, 622-bed tertiary...
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Seattle, Washington 98104
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State College, Pennsylvania 16803
Phone: 814-238-8418
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766 Irving Avenue
Syracuse, New York 13210
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Winston-Salem, North Carolina 27157
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