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NCT03228537Active, not recruitingPhase 1

Atezolizumab, Pemetrexed Disodium, Cisplatin, and Surgery With or Without Radiation Therapy in Treating Patients With Stage I-III Pleural Malignant Mesothelioma

A Feasibility Trial of Neoadjuvant Cisplatin-Pemetrexed With Atezolizumab in Combination and in Maintenance for Resectable Malignant Pleural Mesothelioma

Source: ClinicalTrials.gov · Last updated 22 Oct 2026

Brief summary (registry, in English)

This phase I pilot trial studies how well atezolizumab, pemetrexed disodium, cisplatin, and surgery with or without radiation therapy works in treating patients with stage I-III pleural malignant mesothelioma. Immunotherapy with monoclonal antibodies, such as atezolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Pemetrexed disodium may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving atezolizumab, pemetrexed disodium, and cisplatin before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. Giving atezolizumab after surgery may kill any remaining tumor cells.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
28 (actual)
First submitted
24 Jul 2017
Start date
16 Jul 2018
Primary completion date
1 Oct 2022
Lead sponsor
National Cancer Institute (NCI)
NCT number
NCT03228537

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 28
  • From 16 Jul 2018 to the primary completion date, 1 Oct 2022
  • 174 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

  • STEP 1: NEOADJUVANT
  • Patient must have stage I-III malignant pleural mesothelioma that is deemed resectable and must be planning to undergo pleurectomy decortication (P/D) or extrapleural pneumonectomy (EPP)
  • Patient must have epithelioid or biphasic histology (sarcomatoid histology is excluded); histologic diagnosis and typing of mesothelioma requires at least a core needle biopsy or surgical biopsy of the pleura via thoracoscopy and small thoracotomy; cytology only will not be regarded as sufficient for the diagnosis
  • Patient must have computed tomography (CT) chest/abdomen/pelvis with contrast or fludeoxyglucose F-18 (FDG)-positron emission tomography (PET)/CT scan performed within 28 days prior to step 1 registration
  • Patients must have non-measurable or measurable disease documented by CT or magnetic resonance imaging (MRI); the CT from a combined PET/CT may be used to document only non-measurable disease unless it is of diagnostic quality; measurable disease must be assessed within 28 days prior to step 1 registration; non-measurable disease must be assessed within 42 days prior to step 1 registration; all disease must be assessed and documented on the RECIST 1.1 and modified RECIST baseline tumor assessment form
  • Patient must have undergone extended surgical staging including mediastinoscopy or endobronchial ultrasound; at minimum, samples must be obtained from the mediastinal stations 4R, 7 (subcarinal), and 4L; this surgical staging must be performed within 42 days prior to step 1 registration; patient must be T1-3 and N0-N2 (single station)
  • Patient must undergo video-assisted thoracoscopic surgery and diagnostic laparoscopy within 28 days prior to step 1 registration to rule out peritoneal disease spread
  • Patient must have consultation with a surgeon within 21 days prior to step 1 registration; the surgeon must confirm that the patient's disease is resectable by pleurectomy decortication (P/D) or extrapleural pneumonectomy (EPP) and that the patient is an appropriate candidate for the surgical procedures
  • Patient must not have had prior immunotherapy or chemotherapy for malignant pleural mesothelioma
  • Patient must have Zubrod performance status 0 or 1 documented within 28 days prior to step 1 registration
  • Patients requiring hearing aids or reporting hearing loss must have audiogram performed within 28 days prior to step 1 registration
  • Patient must have not had any major surgery or radiation within 28 days prior to step 1 registration; diagnostic thoracotomies and laparoscopies are not considered major surgeries
  • Patients must not have any anticancer therapy or investigational agent within 28 days prior to step 1 registration
  • Absolute neutrophil count (ANC) \>= 1,500/mcl (documented within 28 days prior to step 1 registration)
  • Hemoglobin \>= 9 g/dl (documented within 28 days prior to step 1 registration)
  • Platelets \>= 100,000/mcl (documented within 28 days prior to step 1 registration)
  • Creatinine =\< 1.5 x upper limit of normal (ULN) (documented within 28 days prior to step 1 registration)
  • Creatinine clearance \>= 45 ml/min (documented within 28 days prior to step 1 registration)
  • Total bilirubin =\< 1.5 x upper limit of normal (ULN) (within 28 days prior to step 1 registration)
  • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =\< 3 x ULN (within 28 days prior to step 1 registration)
  • No other prior malignancy is allowed except for the following: adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, adequately treated stage I or II cancer from which the patient is currently in complete remission, or any other cancer from which the patient has been disease free for three years
  • Patients must not be pregnant or nursing due to the potential teratogenic side effects of the protocol treatment; women of reproductive potential and men must have agreed to use an effective contraceptive method for the duration of study treatment and for 5 months (150 days) after the last dose of atezolizumab; a woman is considered to be of "reproductive potential" if she has had menses at any time in the preceding 12 consecutive months; in addition to routine contraceptive methods, "effective contraception" also includes heterosexual celibacy and surgery intended to prevent pregnancy (or with a side effect of pregnancy prevention) defined as a hysterectomy, bilateral oophorectomy or bilateral tubal ligation; however, if at any point a previously celibate patient chooses to become heterosexually active during the time period for use of contraceptive measures outlined in the protocol, he/she is responsible for beginning contraceptive measures
  • Patient must NOT have a history of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins
  • Patient must NOT have a known hypersensitivity or allergy to biopharmaceuticals produced in Chinese hamster ovary cells or any component of the atezolizumab formulation
  • Patients must not have severe infections within 28 days prior to step 1 registration, including but not limited to hospitalization for complications of infection, bacteremia, or severe pneumonia
  • Patients must not have active autoimmune disease that has required systemic treatment in past two years (i.e., with use of disease modifying agents, corticosteroids or immunosuppressive drugs); replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment; autoimmune diseases include, but are not limited to, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, vascular thrombosis associated with antiphospholipid syndrome, Wegener's granulomatosis, Sjogren's syndrome, Bell's palsy, Guillain-Barre syndrome, multiple sclerosis, autoimmune thyroid disease, vasculitis, or glomerulonephritis; this protocol includes an immunotherapy agent which can precipitate known autoimmune diseases
  • Patients must not have undergone prior allogeneic bone marrow transplantation or prior solid organ transplantation
  • Patient must not have active tuberculosis
  • Patient must not have history of idiopathic pulmonary fibrosis, pneumonitis (including drug induced), organizing pneumonia (i.e., bronchiolitis obliterans, cryptogenic organizing pneumonia, etc.), or evidence of active pneumonitis; this protocol includes an immunotherapy agent which can precipitate known pneumonitis
  • Patient must not have active (chronic or acute) hepatitis B virus (HBV) infection as evidenced by testing performed within 28 days prior to registration; patients with past or resolved HBV infection are eligible; active HBV is defined as having a positive hepatitis B surface antigen (HBsAg) test; past or resolved HBV is defined as having a negative HBsAG test and a positive total hepatitis B core antibody (HBcAb) test; patient must not have active hepatitis C virus (HCV) infection as evidenced by testing performed within 28 days prior to registration; active HCV is defined as having a positive HCV antibody test followed by a positive HCV RNA test
  • Patient must NOT have a known positive test for human immunodeficiency virus (HIV); patients do not need to be screened for HIV; patients with HIV are excluded due to a potential incompetent immune system and need for medications that could interfere with the treatment and immunotherapy
  • Patient must not have significant cardiovascular disease, such as New York Heart Association cardiac disease (class II or greater), myocardial infarction within 3 months prior to initiation of treatment, unstable arrhythmias, or unstable angina given the higher risks associated with surgical resection
  • Patient must not receive live, attenuated influenza vaccine within 4 weeks prior to registration or at any time during the study and until 5 months after the last dose of atezolizumab
  • Patient must be willing to have tissue specimens submitted for translational medicine studies
  • Patient must be offered the opportunity to participate in tissue and blood banking for future studies
  • Patient must be informed of the investigational nature of this study and must sign and give written informed consent in accordance with institutional and federal guidelines
  • As a part of the Oncology Patient Enrollment Network (OPEN) registration process, the treating institution's identity is provided in order to ensure that the current (within 365 days) date of institutional review board approval for this study has been entered in the system
  • STEP 2: SURGERY
  • Patient must have a CT of chest/abdomen with contrast or FDG-PET/CT scan within 28 days prior to step 2 registration; patients must not have evidence of progression per RECIST 1.1 or modified RECIST for pleural tumors
  • Patients planning to receive EPP must also be evaluated for appropriateness of radiation therapy (RT) by a radiation oncologist within 14 days prior to step 2 registration
  • Patients must have a Zubrod performance status of 0-1 documented within 28 days prior to step 2 registration
  • Patients must have postoperative predicted forced expiratory volume in 1 second (FEV1) \> 35% prior to surgery obtained within 28 days prior to step 2 registration; pulmonary function tests to ascertain these values must be obtained within 28 days prior to Step 2 registration
  • Patients must have postoperative predicted carbon monoxide diffusing capability (DLCO) \> 35% prior to surgery obtained within 28 days prior to step 2 registration; pulmonary function tests to ascertain these values must be obtained within 28 days prior to Step 2 registration
  • Patient must have received at least two cycles of triplet neoadjuvant therapy (all three drugs) during step 1
  • Patient must be registered to step 2 no less than 21 days and no more than 90 days after the end of their final cycle of neoadjuvant therapy
  • STEP 3: MAINTENANCE
  • Patient must have received either P/D or EPP and must have recovered from all effects of surgery with adequate wound healing; patients who received radiation therapy (RT) must be registered to step 3 within 90 days after discontinuing RT; patients who did not receive RT must be registered to step 3 within 90 days after surgery
  • Patient must have a CT of chest/abdomen/pelvis with contrast or FDG-PET/CT scan within 28 days prior to step 3 registration; patient must not have evidence of progression per RECIST 1.1 or modified RECIST for pleural tumors
  • Patient may have discontinued RT early due to toxicity or other reasons
  • Patients must have a Zubrod performance status of 0-1 documented within 28 days prior to step 3 registration
  • ANC \> 1,500/mcl (documented within 28 days prior to step 3 registration)
  • Hemoglobin \> 9 g/dl (documented within 28 days prior to step 3 registration)
  • Platelets \> 100,000/mcl (documented within 28 days prior to step 3 registration)
  • Creatinine \< 1.5 x ULN (documented within 28 days prior to step 3 registration)
  • Total bilirubin =\< 1.5 x upper limit of normal (ULN) (within 28 days prior to step 3 registration)
  • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =\< 3 x ULN (within 28 days prior to step 3 registration)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (174)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mary Greeley Medical Center
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AmesUnited StatesUnknown status
McFarland Clinic - Ames
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AmesUnited StatesUnknown status
Community Hospital of Anaconda
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AnacondaUnited StatesUnknown status
PCR Oncology
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Arroyo GrandeUnited StatesUnknown status
Rush-Copley Medical Center
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AuroraUnited StatesUnknown status
CommonSpirit Saint Joseph Hospital - Bardstown
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BardstownUnited StatesUnknown status
Overlake Medical Center
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BellevueUnited StatesUnknown status
Billings Clinic Cancer Center
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BillingsUnited StatesUnknown status
Illinois CancerCare-Bloomington
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BloomingtonUnited StatesUnknown status
Saint Alphonsus Cancer Care Center-Boise
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BoiseUnited StatesUnknown status
Parkland Health Center-Bonne Terre
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Bonne TerreUnited StatesUnknown status
McFarland Clinic - Boone
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BooneUnited StatesUnknown status
Bozeman Health Deaconess Hospital
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BozemanUnited StatesUnknown status
Henry Ford Cancer Institute-Downriver
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BrownstownUnited StatesUnknown status
Saint Joseph Regional Cancer Center
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BryanUnited StatesUnknown status
Saint Anne Hospital
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BurienUnited StatesUnknown status
Saint Alphonsus Cancer Care Center-Caldwell
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CaldwellUnited StatesUnknown status
Illinois CancerCare-Canton
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CantonUnited StatesUnknown status
Mercy Cancer Center - Cape Girardeau
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Cape GirardeauUnited StatesUnknown status
Saint Francis Medical Center
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Cape GirardeauUnited StatesUnknown status
Memorial Hospital of Carbondale
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CarbondaleUnited StatesUnknown status
SIH Cancer Institute
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CartervilleUnited StatesUnknown status
Illinois CancerCare-Carthage
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CarthageUnited StatesUnknown status
Centralia Oncology Clinic
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CentraliaUnited StatesUnknown status
Medical University of South Carolina
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CharlestonUnited StatesUnknown status
University of Virginia Cancer Center
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CharlottesvilleUnited StatesUnknown status
Memorial Hospital
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ChattanoogaUnited StatesUnknown status
TriHealth Cancer Institute-Anderson
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CincinnatiUnited StatesUnknown status
Bethesda North Hospital
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CincinnatiUnited StatesUnknown status
Good Samaritan Hospital - Cincinnati
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CincinnatiUnited StatesUnknown status
TriHealth Cancer Institute-Westside
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CincinnatiUnited StatesUnknown status
Henry Ford Macomb Hospital-Clinton Township
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Clinton TownshipUnited StatesUnknown status
Mercy Cancer Center-West Lakes
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CliveUnited StatesUnknown status
UI Health Care Mission Cancer and Blood - West Des Moines Clinic
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CliveUnited StatesUnknown status
Billings Clinic-Cody
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CodyUnited StatesUnknown status
Kootenai Health - Coeur d'Alene
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Coeur d'AleneUnited StatesUnknown status
Rocky Mountain Cancer Centers-Penrose
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Colorado SpringsUnited StatesUnknown status
Penrose-Saint Francis Healthcare
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Colorado SpringsUnited StatesUnknown status
UT MD Anderson - The Woodlands
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ConroeUnited StatesUnknown status
Commonwealth Cancer Center-Corbin
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CorbinUnited StatesUnknown status
Alegent Health Mercy Hospital
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Council BluffsUnited StatesUnknown status
Greater Regional Medical Center
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CrestonUnited StatesUnknown status
UT Southwestern/Simmons Cancer Center-Dallas
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DallasUnited StatesUnknown status
Carle at The Riverfront
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DanvilleUnited StatesUnknown status
Cancer Care Specialists of Illinois - Decatur
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DecaturUnited StatesUnknown status
Decatur Memorial Hospital
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DecaturUnited StatesUnknown status
AdventHealth Porter
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DenverUnited StatesUnknown status
UI Health Care Mission Cancer and Blood - Laurel Clinic
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Des MoinesUnited StatesUnknown status
Mercy Medical Center - Des Moines
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Des MoinesUnited StatesUnknown status
Henry Ford Hospital
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DetroitUnited StatesUnknown status
City of Hope Comprehensive Cancer Center
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DuarteUnited StatesUnknown status
CommonSpirit Cancer Center Mercy
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DurangoUnited StatesUnknown status
Mercy Medical Center
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DurangoUnited StatesUnknown status
Carle Physician Group-Effingham
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EffinghamUnited StatesUnknown status
Crossroads Cancer Center
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EffinghamUnited StatesUnknown status
Saint Elizabeth Hospital
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EnumclawUnited StatesUnknown status
Illinois CancerCare-Eureka
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EurekaUnited StatesUnknown status
Saint Francis Hospital
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Federal WayUnited StatesUnknown status
McFarland Clinic - Trinity Cancer Center
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Fort DodgeUnited StatesUnknown status
Western Illinois Cancer Treatment Center
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GalesburgUnited StatesUnknown status
Illinois CancerCare-Galesburg
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GalesburgUnited StatesUnknown status
Mountain Blue Cancer Care Center
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GoldenUnited StatesUnknown status
Nebraska Cancer Specialists/Oncology Hematology West PC
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Grand IslandUnited StatesUnknown status
Benefis Sletten Cancer Institute
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Great FallsUnited StatesUnknown status
Great Falls Clinic
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Great FallsUnited StatesUnknown status
Saint Peter's Community Hospital
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HelenaUnited StatesUnknown status
Comprehensive Cancer Centers of Nevada - Henderson
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HendersonUnited StatesUnknown status
Oncology Las Vegas - Henderson
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HendersonUnited StatesUnknown status
Pulmonary Medicine Center of Chattanooga-Hixson
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HixsonUnited StatesUnknown status
CHI Saint Vincent Cancer Center Hot Springs
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Hot SpringsUnited StatesUnknown status
UT MD Anderson Cancer Center
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HoustonUnited StatesUnknown status
UT MD Anderson - West Houston
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HoustonUnited StatesUnknown status
Lyndon Baines Johnson General Hospital
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HoustonUnited StatesUnknown status
Allegiance Health
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JacksonUnited StatesUnknown status
Baptist MD Anderson Cancer Center
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JacksonvilleUnited StatesUnknown status
McFarland Clinic - Jefferson
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JeffersonUnited StatesUnknown status
MU Health Care Goldschmidt Cancer Center
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Jefferson CityUnited StatesUnknown status
Logan Health Medical Center
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KalispellUnited StatesUnknown status
CHI Health Good Samaritan
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KearneyUnited StatesUnknown status
Fred and Pamela Buffett Cancer Center - Kearney
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KearneyUnited StatesUnknown status
Illinois CancerCare-Kewanee Clinic
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KewaneeUnited StatesUnknown status
Rocky Mountain Cancer Centers-Lakewood
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LakewoodUnited StatesUnknown status
Saint Clare Hospital
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LakewoodUnited StatesUnknown status
CommonSpirit Saint Anthony Hospital Cancer Center
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LakewoodUnited StatesUnknown status
Radiation Oncology Centers of Nevada Southeast
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Las VegasUnited StatesUnknown status
OptumCare Cancer Care at Charleston
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Las VegasUnited StatesUnknown status
OptumCare Cancer Care at MountainView
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Las VegasUnited StatesUnknown status
OptumCare Cancer Care at Fort Apache
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Las VegasUnited StatesUnknown status
Radiation Oncology Centers of Nevada Central
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Las VegasUnited StatesUnknown status
Comprehensive Cancer Centers of Nevada - Northwest
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Las VegasUnited StatesUnknown status
Comprehensive Cancer Centers of Nevada-Summerlin
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Las VegasUnited StatesUnknown status
Comprehensive Cancer Centers of Nevada - Central Valley
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Las VegasUnited StatesUnknown status
Alliance for Childhood Diseases/Cure 4 the Kids Foundation
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Las VegasUnited StatesUnknown status
Comprehensive Cancer Centers of Nevada
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Las VegasUnited StatesUnknown status
Lawrence Memorial Hospital
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LawrenceUnited StatesUnknown status
Cancer Centers of Southwest Oklahoma Research
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LawtonUnited StatesUnknown status
UT MD Anderson - League City
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League CityUnited StatesUnknown status
Saint Joseph Radiation Oncology Resource Center
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LexingtonUnited StatesUnknown status
CommonSpirit Saint Joseph Medical Center - East Lexington
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LexingtonUnited StatesUnknown status
Saint Elizabeth Regional Medical Center
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LincolnUnited StatesUnknown status
AdventHealth Littleton
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LittletonUnited StatesUnknown status
CommonSpirit Saint Joseph Hospital London
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LondonUnited StatesUnknown status
Longmont United Hospital
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LongmontUnited StatesUnknown status
Rocky Mountain Cancer Centers-Longmont
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LongmontUnited StatesUnknown status
Saints Mary and Elizabeth Hospital
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LouisvilleUnited StatesUnknown status
Jewish Hospital
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LouisvilleUnited StatesUnknown status
UofL Health Medical Center Northeast
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LouisvilleUnited StatesUnknown status
Illinois CancerCare-Macomb
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MacombUnited StatesUnknown status
McFarland Clinic - Marshalltown
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MarshalltownUnited StatesUnknown status
Carle Physician Group-Mattoon/Charleston
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MattoonUnited StatesUnknown status
Idaho Urologic Institute-Meridian
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MeridianUnited StatesUnknown status
Community Medical Center
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MissoulaUnited StatesUnknown status
Saint Alphonsus Cancer Care Center-Nampa
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NampaUnited StatesUnknown status
Ochsner Medical Center Jefferson
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New OrleansUnited StatesUnknown status
Cancer Care Center of O'Fallon
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O'FallonUnited StatesUnknown status
University of Oklahoma Health Sciences Center
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Oklahoma CityUnited StatesUnknown status
Alegent Health Bergan Mercy Medical Center
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OmahaUnited StatesUnknown status
Alegent Health Lakeside Hospital
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OmahaUnited StatesUnknown status
Alegent Health Immanuel Medical Center
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OmahaUnited StatesUnknown status
Hematology and Oncology Consultants PC
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OmahaUnited StatesUnknown status
Memorial GYN Plus
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OoltewahUnited StatesUnknown status
Illinois CancerCare-Ottawa Clinic
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OttawaUnited StatesUnknown status
Midlands Community Hospital
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PapillionUnited StatesUnknown status
AdventHealth Parker
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ParkerUnited StatesUnknown status
Rocky Mountain Cancer Centers-Parker
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ParkerUnited StatesUnknown status
OSF Saint Francis Radiation Oncology at Pekin
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PekinUnited StatesUnknown status
Illinois CancerCare-Pekin
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PekinUnited StatesUnknown status
Illinois CancerCare-Peoria
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PeoriaUnited StatesUnknown status
OSF Saint Francis Medical Center
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PeoriaUnited StatesUnknown status
OSF Saint Francis Radiation Oncology at Peoria Cancer Center
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PeoriaUnited StatesUnknown status
Methodist Medical Center of Illinois
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PeoriaUnited StatesUnknown status
Illinois CancerCare-Peru
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PeruUnited StatesUnknown status
Valley Radiation Oncology
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PeruUnited StatesUnknown status
Mayo Clinic Hospital in Arizona
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PhoenixUnited StatesUnknown status
UPMC Hillman Cancer Center
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PittsburghUnited StatesUnknown status
Kootenai Clinic Cancer Services - Post Falls
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Post FallsUnited StatesUnknown status
Harrison HealthPartners Hematology and Oncology-Poulsbo
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PoulsboUnited StatesUnknown status
Illinois CancerCare-Princeton
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PrincetonUnited StatesUnknown status
Rocky Mountain Cancer Centers - Pueblo
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PuebloUnited StatesUnknown status
Saint Mary Corwin Medical Center
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PuebloUnited StatesUnknown status
Radiation Oncology Associates
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RenoUnited StatesUnknown status
Saint Mary's Regional Medical Center
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RenoUnited StatesUnknown status
Renown Regional Medical Center
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RenoUnited StatesUnknown status
Valley Medical Center
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RentonUnited StatesUnknown status
UT Southwestern Clinical Center at Richardson/Plano
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RichardsonUnited StatesUnknown status
Mayo Clinic in Rochester
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RochesterUnited StatesUnknown status
University of California Davis Comprehensive Cancer Center
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SacramentoUnited StatesUnknown status
Sainte Genevieve County Memorial Hospital
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Sainte GenevieveUnited StatesUnknown status
Kootenai Clinic Cancer Services - Sandpoint
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SandpointUnited StatesUnknown status
Mayo Clinic in Arizona
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ScottsdaleUnited StatesUnknown status
University of Washington Medical Center - Montlake
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SeattleUnited StatesUnknown status
Fred Hutchinson Cancer Center
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SeattleUnited StatesUnknown status
Henry Ford Macomb Health Center - Shelby Township
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ShelbyUnited StatesUnknown status
Jewish Hospital Medical Center South
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ShepherdsvilleUnited StatesUnknown status
Welch Cancer Center
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SheridanUnited StatesUnknown status
Saint Joseph Medical Center Hematology and Oncology - Silverdale
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SilverdaleUnited StatesUnknown status
Springfield Clinic
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SpringfieldUnited StatesUnknown status
Southern Illinois University School of Medicine
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SpringfieldUnited StatesUnknown status
Springfield Memorial Hospital
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SpringfieldUnited StatesUnknown status
Missouri Baptist Medical Center
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St LouisUnited StatesUnknown status
UT MD Anderson - Sugar Land
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Sugar LandUnited StatesUnknown status
Missouri Baptist Sullivan Hospital
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SullivanUnited StatesUnknown status
Southwest Illinois Health Services LLP
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SwanseaUnited StatesUnknown status
Franciscan Research Center-Northwest Medical Plaza
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TacomaUnited StatesUnknown status
Northwest Medical Specialties PLLC
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TacomaUnited StatesUnknown status
Rocky Mountain Cancer Centers-Thornton
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ThorntonUnited StatesUnknown status
The Carle Foundation Hospital
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UrbanaUnited StatesUnknown status
Carle Cancer Center
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UrbanaUnited StatesUnknown status
Henry Ford West Bloomfield Hospital
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West BloomfieldUnited StatesUnknown status
Mercy Medical Center-West Lakes
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West Des MoinesUnited StatesUnknown status
Cancer Center of Kansas-Wichita Medical Arts Tower
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WichitaUnited StatesUnknown status
Ascension Via Christi Hospitals Wichita
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WichitaUnited StatesUnknown status
Cancer Center of Kansas - Wichita
Coordinator of this site? Confirm its status
WichitaUnited StatesUnknown status
Rush-Copley Healthcare Center
Coordinator of this site? Confirm its status
YorkvilleUnited StatesUnknown status

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