NCT03540420Active, not recruitingPhase 2
Atezolizumab After Concurrent Chemo-radiotherapy Versus Chemo-radiotherapy Alone in Limited Disease Small-cell Lung Cancer
A Randomized Phase II Study Comparing Atezolizumab After Concurrent Chemo-radiotherapy With Chemo-radiotherapy Alone in Limited Disease Small-cell Lung Cancer
Source: ClinicalTrials.gov · Last updated 13 Apr 2026
Brief summary (registry, in English)
Some patients with limited disease small-cell lung cancer (LD SCLC) are cured after chemo-radiotherapy, but the majority relapse and die from their cancer. Better therapy is needed. Immunotherapy represents the largest advance in cancer therapy in recent years and has demonstrated promising activity in SCLC. In this study we will investigate whether atezolizumab prolongs survival in LD SCLC patients who have undergone chemo-radiotherapy.
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 212 (actual)
- First submitted
- 16 May 2018
- Start date
- 31 Jul 2018
- Primary completion date
- 1 Apr 2024
- Lead sponsor
- Norwegian University of Science and Technology
- Diseases
- Lung cancer
- NCT number
- NCT03540420
- EU CT number
- 2024-515755-37-00
- EudraCT number
- 2017-004572-62
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 212
- From 31 Jul 2018 to the primary completion date, 1 Apr 2024
- 34 sites in 6 countries
- 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.
Prior treatment
- previous systemic therapy for SCLC or immune checkpoint blockade therapy
- serious concomitant systemic disorders (for example active infection, unstable cardiovascular disease) which in the opinion of the investigator would compromise the patient's ability to complete the study, or would interfere with the evaluation of the efficacy and safety of the study treatment
- previous allogeneic or organ transplant
- live vaccine administered in the last 30 days
Other illness
- lung disease requiring systemic steroids in doses of \>10 mg prednisolone (or equivalent dose of other steroid)
- active or history of autoimmune disease or immune deficiency, including, but not limited to myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, antiphospholipid antibody syndrome, Wegener granulomatosis, Sjögren syndrome, Guillain-Barré syndrome, or multiple sclerosis
- history of idiopathic pulmonary fibrosis, organizing pneumonia (e.g., bronchiolitis obliterans), drug-induced pneumonitis, or idiopathic pneumonitis, or evidence of active pneumonitis on screening chest computed tomography (CT) scan
- active infection requiring IV antibiotics
- active viral hepatitis or HIV-positive
- conditions - medical, social, psychological - which could prevent adequate information and follow-up
- clinically active cancer other than SCLC with the exception of malignancies with a negligible risk of metastases or death (e.g. 5-years OS rate of \>90%), such as adequately treated carcinoma in situ of the cervix, non-melanoma skin carcinoma, localized prostate cancer, ductal carcinoma in situ, or stage I uterine cancer. Hormonal therapy for non-metastatic prostate or breast cancer is allowed.
Other
- pregnant or lactating women
Who the study is looking for
- Histologically or cytologically confirmed small-cell lung cancer
- Previous radiotherapy to the thorax is allowed as long as the patient can receive TRT of 45 Gy.
- Stage I-III according to TNM v8 ineligible for surgery provided all lesions can be included in a tolerable radiotherapy field ("limited disease")
- ECOG performance status 0-2
- Measureable disease according to the RECIST 1.1
- Adequate organ function defined as: (a) Serum alanine transaminase (ALT) ≤ 2.5 x upper limit of normal (ULN); (b) Total serum bilirubin ≤ 1.5 x ULN; (c)Absolute neutrophil count (ANC) ≥ 1.5 x 10 superscr 9/L; (d) Platelets ≥ 100 x 10 superscr 9/L ; (e) Creatinine \< 100 µmol/L and calculated creatinine-clearance \> 50 ml/min. If calculated creatinine-clearance is \< 50 ml/min, an EDTA clearance should be performed
- No malignant cells in pericardial or pleural fluid (at least 1 sample should be obtained if pleural fluid is present) If there is so little fluid that it cannot easily be collected, the patient is considered eligible.
- Pulmonary function: FEV1 \> 1 l or \> 30 % of predicted value and DLCO \> 30 % of predicted value
- Female patients of childbearing potential (Postmenarcheal, not postmenopausal (\>12 continuous months of amenorrhea with no identified cause other than menopause), and no surgical sterilization) should use highly effective contraception and take active measures to avoid pregnancy while undergoing atezolizumab treatment and for at least 5 months after the last dose. Birth control methods considered to be highly effective are listed in Appendix D of the protocol
- Written informed consent
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (34)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Universitätsspital Basel Coordinator of this site? Confirm its status | Basel | Switzerland | Unknown status |
| University Hospital Inselspital Coordinator of this site? Confirm its status | Bern | Switzerland | Unknown status |
| Inselspital Coordinator of this site? Confirm its status | Bern | Switzerland | Unknown status |
| Kantonsspital Graubunden Coordinator of this site? Confirm its status | Chur | Switzerland | Unknown status |
| Kantonsspital Olten - Solothurner Spitäler Coordinator of this site? Confirm its status | Olten | Switzerland | Unknown status |
| Cantonal Hospital of St. Gallen Coordinator of this site? Confirm its status | Sankt Gallen | Switzerland | Unknown status |
| Spital STS AG Coordinator of this site? Confirm its status | Thun | Switzerland | Unknown status |
| Kantonsspital Winterthur Coordinator of this site? Confirm its status | Winterthur | Switzerland | Unknown status |
| Hirslanden Klinik Coordinator of this site? Confirm its status | Zurich | Switzerland | Unknown status |
| Aalborg University Hospital Coordinator of this site? Confirm its status | Aalborg | Denmark | Active, not recruiting |
| Rigshospitalet Coordinator of this site? Confirm its status | Copenhagen Oe | Denmark | Active, not recruiting |
| Odense University Hospital Coordinator of this site? Confirm its status | Odense C | Denmark | Active, not recruiting |
| Nacionalinis Vezio Institutas Coordinator of this site? Confirm its status | Vilnius | Lithuania | Active, not recruiting |
| Noordwest Ziekenhuisgroep Stichting Coordinator of this site? Confirm its status | Alkmaar | Netherlands | Active, not recruiting |
| Netherlands Cancer Institute Coordinator of this site? Confirm its status | Amsterdam | Netherlands | Active, not recruiting |
| Rijnstate Ziekenhuis Stichting Coordinator of this site? Confirm its status | Arnhem | Netherlands | Active, not recruiting |
| Amphia Hospital Coordinator of this site? Confirm its status | Breda | Netherlands | Active, not recruiting |
| Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC) Coordinator of this site? Confirm its status | Rotterdam | Netherlands | Active, not recruiting |
| St Antonius Ziekenhuis Coordinator of this site? Confirm its status | Utrecht | Netherlands | Active, not recruiting |
| Isala Klinieken Stichting Coordinator of this site? Confirm its status | Zwolle | Netherlands | Active, not recruiting |
| Helse Moere Og Romsdal HF Coordinator of this site? Confirm its status | Aalesund | Norway | Active, not recruiting |
| Helse Bergen HF Coordinator of this site? Confirm its status | Bergen | Norway | Active, not recruiting |
| Sorlandet Sykehus HF Coordinator of this site? Confirm its status | Kristiansand S | Norway | Active, not recruiting |
| Nord-Trondelag Hospital Trust Coordinator of this site? Confirm its status | Levanger | Norway | Active, not recruiting |
| Akershus University Hospital Coordinator of this site? Confirm its status | Lorenskog | Norway | Active, not recruiting |
| Oslo University Hospital HF Coordinator of this site? Confirm its status | Oslo | Norway | Active, not recruiting |
| Universitetssykehuset Nord-Norge HF Coordinator of this site? Confirm its status | Tromsoe | Norway | Active, not recruiting |
| St. Olavs hospital HF Coordinator of this site? Confirm its status | Trondheim | Norway | Active, not recruiting |
| Region Gaevleborg Coordinator of this site? Confirm its status | Gavle | Sweden | Active, not recruiting |
| Sahlgrenska University Hospital-Vaestra Goetalandsregionen Coordinator of this site? Confirm its status | Goteborg | Sweden | Active, not recruiting |
| Region Oestergoetland Coordinator of this site? Confirm its status | Linkoping | Sweden | Active, not recruiting |
| Lund University Hospital Coordinator of this site? Confirm its status | Lund | Sweden | Active, not recruiting |
| Region Oerebro Laen Coordinator of this site? Confirm its status | Orebro | Sweden | Active, not recruiting |
| Karolinska University Hospital Coordinator of this site? Confirm its status | Stockholm | Sweden | Active, not recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.