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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

Full criteria on ClinicalTrials.gov

Sites (34)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Universitätsspital Basel
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BaselSwitzerlandUnknown status
University Hospital Inselspital
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BernSwitzerlandUnknown status
Inselspital
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BernSwitzerlandUnknown status
Kantonsspital Graubunden
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ChurSwitzerlandUnknown status
Kantonsspital Olten - Solothurner Spitäler
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OltenSwitzerlandUnknown status
Cantonal Hospital of St. Gallen
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Sankt GallenSwitzerlandUnknown status
Spital STS AG
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ThunSwitzerlandUnknown status
Kantonsspital Winterthur
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WinterthurSwitzerlandUnknown status
Hirslanden Klinik
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ZurichSwitzerlandUnknown status
Aalborg University Hospital
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AalborgDenmarkActive, not recruiting
Rigshospitalet
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Copenhagen OeDenmarkActive, not recruiting
Odense University Hospital
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Odense CDenmarkActive, not recruiting
Nacionalinis Vezio Institutas
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VilniusLithuaniaActive, not recruiting
Noordwest Ziekenhuisgroep Stichting
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AlkmaarNetherlandsActive, not recruiting
Netherlands Cancer Institute
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AmsterdamNetherlandsActive, not recruiting
Rijnstate Ziekenhuis Stichting
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ArnhemNetherlandsActive, not recruiting
Amphia Hospital
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BredaNetherlandsActive, not recruiting
Erasmus Universitair Medisch Centrum Rotterdam (Erasmus MC)
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RotterdamNetherlandsActive, not recruiting
St Antonius Ziekenhuis
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UtrechtNetherlandsActive, not recruiting
Isala Klinieken Stichting
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ZwolleNetherlandsActive, not recruiting
Helse Moere Og Romsdal HF
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AalesundNorwayActive, not recruiting
Helse Bergen HF
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BergenNorwayActive, not recruiting
Sorlandet Sykehus HF
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Kristiansand SNorwayActive, not recruiting
Nord-Trondelag Hospital Trust
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LevangerNorwayActive, not recruiting
Akershus University Hospital
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LorenskogNorwayActive, not recruiting
Oslo University Hospital HF
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OsloNorwayActive, not recruiting
Universitetssykehuset Nord-Norge HF
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TromsoeNorwayActive, not recruiting
St. Olavs hospital HF
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TrondheimNorwayActive, not recruiting
Region Gaevleborg
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GavleSwedenActive, not recruiting
Sahlgrenska University Hospital-Vaestra Goetalandsregionen
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GoteborgSwedenActive, not recruiting
Region Oestergoetland
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LinkopingSwedenActive, not recruiting
Lund University Hospital
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LundSwedenActive, not recruiting
Region Oerebro Laen
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OrebroSwedenActive, not recruiting
Karolinska University Hospital
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StockholmSwedenActive, not recruiting

This page is information, not medical advice. Discuss any trial with your doctor.