Safety and Efficacy of TTFields (150 kHz) Concomitant With Pemetrexed and Cisplatin or Carboplatin in Malignant Pleural Mesothelioma (STELLAR)
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ClinicalTrials.gov Identifier: NCT02397928 |
Recruitment Status :
Completed
First Posted : March 25, 2015
Last Update Posted : September 25, 2018
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Condition or disease | Intervention/treatment | Phase |
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Malignant Pleural Mesothelioma | Device: NovoTTF-100L device Drug: Pemetrexed Drug: Cisplatin or Carboplatin | Phase 2 |

Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 82 participants |
Allocation: | N/A |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | A Phase II Trial of Pemetrexed and Cisplatin or Carboplatin in Combination With TTFields (150 kHz) as First-line Treatment in Malignant Pleural Mesothelioma |
Actual Study Start Date : | February 2015 |
Actual Primary Completion Date : | April 2018 |
Actual Study Completion Date : | April 2018 |

Arm | Intervention/treatment |
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Experimental: TTFields concomitant to pemetrexed plus cisplatin/carboplatin
Patients will be treated continuously with TTFields, in addition to pemetrexed plus cisplatin/carboplatin
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Device: NovoTTF-100L device
Patients will be treated continuously with the NovoTTF-100L device. NovoTTF-100L treatment will consist of wearing four electrically insulated electrode arrays on the thorax. The treatment enables the patient to maintain regular daily routine.
Other Name: TTFields Drug: Pemetrexed Pemetrexed 500 mg/m2 will be administered by intravenous infusion over 10 minutes or according to institutional administration timing on day 1 of a 21-day cycle. Drug: Cisplatin or Carboplatin Cisplatin 75 mg/m2 or carboplatin AUC 5 will be administered by infusion after adequate hydration according to institutional practices beginning approximately 30 minutes after the end on the pemetrexed infusion on day 1 of a 21-day cycle. |
- Overall Survival [ Time Frame: 1 year ]
- Progression Free Survival [ Time Frame: 1 year ]
- Response Rate [ Time Frame: 1 year ]
- Toxicity- incidence of adverse events [ Time Frame: 1 year ]

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Pathological or histological evidence of mesothelioma
- ≥ 18 years of age
- Not candidate for curative treatment (surgery or radiotherapy)
- At least 4 weeks since major surgery
- At least one measurable or evaluable lesion according to modified RECIST Criteria
- ECOG Performance Status of 0-1
- Life expectancy of at least 3 months
- Participants of childbearing age must use effective contraception as indicated by the investigator
- All subjects must sign written informed consent.
- Able to operate the NovoTTF-100L System independently or with the help of a caregiver
Exclusion Criteria:
- Patient candidate for surgery or radiotherapy with curative intent
- Previous chemotherapy or radiation
- Prior malignancy requiring anti-tumor treatment (apart from in-situ cervical cancer, in situ breast cancer, non-melanomatous skin cancers, or any malignancy for which treatment was received and there is no evidence of disease for at least 5 years) or concurrent malignancy
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Significant co-morbidities within 4 weeks prior to enrollment, resulting in the following laboratory findings:
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Significant liver function impairment:
- AST or ALT > 3 times the upper limit of normal
- Total bilirubin ≥ 1.5 times upper limit of normal
- Significant renal impairment (serum creatinine > 1.7 mg/dL)
- Coagulopathy (as evidenced by PT or APTT >1.5 times control in subjects not undergoing anticoagulation)
- Thrombocytopenia (platelet count < 100 x 10^3/μL)
- Neutropenia (absolute neutrophil count < 1.5 x 10^3/μL)
- Anemia (Hb < 10 g/dL)
- Severe acute infection
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Significant comorbidity which is expected to affect patient's prognosis or ability to receive the combined therapy:
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History of significant cardiovascular disease unless the disease is well controlled.
Significant cardiac disease includes second/third degree heart block; significant ischemic heart disease; poorly controlled hypertension; congestive heart failure of the New York Heart Association (NYHA) Class II or worse (slight limitation of physical activity; comfortable at rest, but ordinary activity results in fatigue, palpitation or dyspnea)
- History of arrhythmia that is symptomatic or requires treatment. Patients with atrial fibrillation or flutter controlled by medication are not excluded from participation in the trial
- Active infection or any serious underlying medical condition that would impair the ability of the patient to receive protocol therapy
- History of any psychiatric condition that might impair the patient's ability to understand or comply with the requirements of the study or to provide consent
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- Untreated brain metastases. Asymptomatic, pretreated brain metastases not requiring steroids are allowed
- Implanted pacemaker, defibrillator or other electrical medical devices
- Known allergies to medical adhesives or hydrogel
- Pregnant or breast feeding (all patients of childbearing potential must use effective contraception method during the entire period of the study based on the recommendation of the investigator or a gynecologist)

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02397928
Belgium | |
Antwerp University Hospital, Thoracic Oncology | |
Antwerp, Belgium | |
France | |
Goustave Roussy - Cancer Campus Grand Paris | |
Villejuif, France | |
Germany | |
Universitätsklinikum Halle (Saale) | |
Halle, Germany | |
Italy | |
A.S.O. "SS Antonio e Biagio e Cesare Arrigo" | |
Alessandria, Italy | |
Cliniche Humanitas Gavazzeni | |
Bergamo, Italy | |
Ospedale Villa Scassi | |
Genoa, Italy | |
Ospedaliera di Perugia | |
Perugia, Italy | |
Ospedaliero Universitaria Pisana | |
Pisa, Italy | |
Netherlands | |
Erasmus Mc | |
Rotterdam, Netherlands | |
Poland | |
Medical University Gdansk | |
Gdansk, Poland | |
Katedra i Klinika Onkologii Uniwersytetu Medycznegi im. Karola Marcinkowskiego w Poznaniu | |
Poznań, Poland | |
Klinika Nowotworów Pluca I Klatki Piersiowej | |
Warsaw, Poland | |
Spain | |
Vall d' Hebron Institute of Oncology (VHIO) Hospital Vall d'Hebron | |
Barcelona, Spain |
Principal Investigator: | Giovanni Luca Ceresoli, MD | Cliniche Humanitas Gavazzeni |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | NovoCure Ltd. |
ClinicalTrials.gov Identifier: | NCT02397928 |
Other Study ID Numbers: |
EF-23 |
First Posted: | March 25, 2015 Key Record Dates |
Last Update Posted: | September 25, 2018 |
Last Verified: | September 2018 |
Malignant Pleural Mesothelioma Treatment Minimal toxicity TTFields Tumor Treating Fields |
Novocure Pemetrexed Carboplatin Cisplatin |
Mesothelioma Mesothelioma, Malignant Adenoma Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms Neoplasms, Mesothelial Lung Neoplasms Respiratory Tract Neoplasms Thoracic Neoplasms Neoplasms by Site |
Pleural Neoplasms Lung Diseases Respiratory Tract Diseases Carboplatin Pemetrexed Antineoplastic Agents Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Folic Acid Antagonists Nucleic Acid Synthesis Inhibitors |