Study on Atezolizumab for Patients with Non-Small Cell Lung Cancer After Chemotherapy

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What is this study about?

This clinical trial is focused on studying the effects of a medication called atezolizumab in patients with Non-Small Cell Lung Cancer (NSCLC). Atezolizumab is an antibody that helps the immune system fight cancer cells. The study compares the use of atezolizumab with the best supportive care after patients have received chemotherapy based on another drug called cisplatin. The goal is to see if atezolizumab can help prevent the cancer from coming back after surgery.

Participants in the study will receive atezolizumab through an intravenous infusion, which means the medication is given directly into a vein. The study will also involve other chemotherapy medications such as vinorelbine, pemetrexed, docetaxel, and gemcitabine, which are small molecule drugs used to kill cancer cells. The study will last for a period of up to 48 weeks for those receiving atezolizumab, while the chemotherapy medications will be administered for a shorter duration.

The purpose of the study is to evaluate how effective atezolizumab is in keeping the cancer from returning, as well as to assess its safety. The study will monitor participants for any signs of cancer recurrence and overall survival rates. This research aims to provide valuable information on whether atezolizumab can be a beneficial treatment option for patients with NSCLC following surgery and chemotherapy.

1 joining the study

Upon joining the study, the patient will be informed about the trial’s purpose, which is to evaluate the effectiveness of the medication atezolizumab compared to standard care after chemotherapy in patients with non-small cell lung cancer.

The patient will be assessed to ensure they meet the eligibility criteria, including a performance status of 0 or 1 and a complete resection of the cancer within the specified timeframe.

2 initial treatment phase

The patient will receive a chemotherapy regimen based on cisplatin. This phase is crucial for preparing the body for the subsequent treatment with atezolizumab.

The chemotherapy drugs, including vinorelbine, cisplatin, docetaxel, and gemcitabine hydrochloride, will be administered through intravenous infusion. The specific dosage and frequency will be determined by the healthcare provider.

3 atezolizumab treatment phase

Following the chemotherapy, the patient will begin treatment with atezolizumab, which is administered as an intravenous infusion. The standard dosage is 1,200 mg.

This treatment aims to improve disease-free survival by preventing the recurrence of cancer. The duration and frequency of atezolizumab administration will be guided by the healthcare provider.

4 monitoring and follow-up

Throughout the trial, the patient’s health and response to treatment will be closely monitored. This includes regular assessments of disease status through imaging and clinical evaluations.

The primary goal is to track disease-free survival, which is the time from the start of the trial to any recurrence of cancer or death from any cause.

5 completion of the trial

The trial is expected to conclude by April 2026. At the end of the study, the patient’s overall survival and disease-free survival rates will be evaluated.

The results will contribute to understanding the effectiveness of atezolizumab in treating non-small cell lung cancer after chemotherapy.

Who Can Join the Study?

  • Must have a diagnosis of Non-Small Cell Lung Cancer (NSCLC).
  • Must have an ECOG performance status of 0 or 1, which means the patient is fully active or has some symptoms but can still carry out light work.
  • Must have a confirmed diagnosis of Stage IB to IIIA NSCLC, which refers to specific sizes and spread of the lung tumor.
  • Must have had complete removal of the lung cancer 4 to 12 weeks before joining the study and must have recovered well from the surgery.
  • If a procedure called mediastinoscopy was not done before surgery, a specific type of lymph node sampling must have been done during surgery. This involves checking certain lymph nodes in the chest area.
  • Must be eligible to receive a chemotherapy treatment that includes a drug called cisplatin.
  • Must have normal blood and organ function, meaning the body is working well enough to handle the treatment.
  • Both men and women can participate.
  • Participants must be adults, as the study includes age ranges for adults.

Who Cannot Join the Study?

  • Patients who have a different type of cancer other than Non-Small Cell Lung Cancer.
  • Patients who do not have the specific PD-L1 subpopulation marker. This marker is a protein that can be found on the surface of some cancer cells.
  • Patients who are not in the Stage II-IIIA of Non-Small Cell Lung Cancer. This refers to the size and spread of the cancer.
  • Patients who are not within the specified age range for the study.
  • Patients who are not able to provide informed consent or are part of a vulnerable population that cannot participate in the study.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Ospedale San Raffaele S.r.l. Milan Italy
Semmelweis University Budapest Hungary
Centre Hospitalier Universitaire De Nantes Nantes France
Hospital Del Mar Barcelona Spain
Instituto Portugues De Oncologia Do Porto Francisco Gentil E.P.E. Porto Portugal
Saarland University Hospital Homburg Germany
Katholisches Klinikum Koblenz Montabaur gGmbH Koblenz Germany
St. Antonius Ziekenhuis Nieuwegein The Netherlands
Centre Hospitalier De Saint-Quentin Saint Quentin France
Hospital Universitario De Canarias La Laguna Spain
Centro Di Riferimento Oncologico Di Aviano Aviano Italy
LungenClinic Grosshansdorf GmbH Grosshansdorf Germany
Gemeinschaftspraxis für Hämatologie und Onkologie Munster Germany
Aupknqikg Kzyyjcna Hgfkylv Gmjq Hamburg Germany
Hjpdaebt Vekl dlkatljo Barcelona Spain
Celomp Omgjlkfmus Dj Gmrhzjb A Coruna Galicia Spain
Shwmdgvwokvj Hievgbzcj Gjda Heilbronn Germany
Kiwwfeqm Cuslksmk grxyo Chemnitz Germany
Cquyrv Hpazcguepk E Uqmyckoolnikb De Ckxihno Eosmcf Coimbra Portugal
Hsyclaem Cbzelsj Spa Cquqfp Madrid Spain
Arpfolz Opjwmhmuvoh Urtmpiheihznm Cwueuomvlblf Dijsm Sapbun E Dmuvh Srgmczo Du Termbl Turin Italy
Keiaswde dcx Sdedg Kjwcn gmswn Cologne Germany
Arrbhdk Ofvxwnlxfynedwsdfguxbmarp Myuiiunh Dgwyr Cciopk Novara Italy
Tijgmqasfgcw Hlfjrrozly gghda Heidelberg Germany
Hwhvkkqb Di Li Syozj Cbqk I Serk Ptv Barcelona Spain
Coccnw Lnbd Bziind Lyon France
Ubkunekejt Mfmxnst Cltgaa Htkummrcdtnacnkbl Hamburg Germany
Huxtlage Upsqbwnvrsiib Macuxsr Df Vfiwupbroz Santander Spain
Ijiywgjd Cjbjeb Ditcbzaswlhirwnpg L'hospitalet De Llobregat Spain
Unlhxywetj Dxwjl Sqefv Do Bhwgxuq Brescia Italy
Sbuhhg Dd Sqyjs Dm Lai Imisz Bhkwwzz Palma Spain
Hyrlxpvy Cvlmzvg Uivcmiwrxwjcx Lpanuz Bsmdr Zaragoza Spain
Atyescv Ozmgutneuxf Uqcmdfsbusjch Pgijut Pisa Italy
Kvbdlqqwino Njdzsbfs Gnos Frankfurt Germany
Ixjnxeur Rlzoubeb Dn Cvblyp Dp Mzizlrozyka Montpellier France
Pcpmltoljyygi Oidqshmil Oldenburg In Holstein Germany
Cykzbu Hyheqfyxfdl Ighjlukwjextl Thuwrz / Lr Sfclhemrxttbf Toulon France
Cysbsqf Dc Olujymepq Sx Njiuohut Sdrvvb Craiova Romania
Hsp Syesbx Aopp Toulon France
Cjqvee Hbixujcwucs Ipeeoucvavzea Dy Mqav Dg Mpcghx Ew Dk Ptii Dah Stcgopl Mont-de-Marsan France
Cldkjh Hswutracqws Ef Uhfqqwrhasgdv Dc Lzxerfx Limoges France
Uqmzzruqyodbuqsbf Cuhflg Bjqytmybah Dd Rjgf Rome Italy
Ektutpggwazcm Krwufnim Bpnpzu gwnhl Bielefeld Germany
Hgydblkk Uaseayzlxqznn Lzmmg Alkdupl Lugo Spain
Hwvfliyr Gijmvkh Uyfcwkbddtlki Df Cwbsoseuv Castello De La Plana Spain
Hhdvfxh Sykzy Jtpxzi Marseille France
Mobriytq Kjtdge gavqk Munich Germany
Lwudaltpdgtj Hgvzb Ddfxeennx Gjaogkclemipiowclgboybulkyobe Gchw Hemer Germany
Tdogwtezpvpiastyx Tyruchitepvlz Torokbalint Hungary
Uztgw Dd Rjjxglkee Cyfrezlf Hgy Bunja Saint-Mande France
Apozdje Sqehtktmq Luhojp 2 Lvwocyjl Vtewx Cjijqr Chieti Italy
Wdnzrgjwwzens Clswpfw Pocyfgjuggda I Tbmgwrpdthuwdna Iwr Eajbthe I Jjgdmof Zywczsfyg Poznan Poland
Uahuadjuel Os Pdkq Pecs Hungary
Sddabfxnjtoc Kouzwcrh Bgyraumjzeaf gykbx Brunswick Germany
Sbvcmrqxx Mcgoqtq Zufcziquzw Groningen The Netherlands
Hthqvcyo Syxog Mflas Drenf Mlujxwhpqwmq Perugia Italy
Jrmkbu Bxunh Zowkdqetcj Sxqjqhbde S-Hertogenbosch The Netherlands
Jzemfmgsxndloztohund Vnrxaqhul Hzhyhfm Gwle Kvrbktreltkpoismsxxaq Szolnok Hungary
Mbmckslvvkus Kvlosjqcmwg Hwsuzhuateef gcglq Halle (Saale) Germany
Mupstjdxqvskp Vefhtpb Gfk Velbert Germany
Lkwlxaqnwmbqvmlk Iggaoowtdtn Immenhausen Germany
Mvzwnkoreen Coykoyr Lmcutigt Cgpyfc Pyhg i Gcmhoaup Otwock Poland

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
France France
Not recruiting
27.01.2016
Germany Germany
Not recruiting
27.01.2016
Hungary Hungary
Not recruiting
27.01.2016
Italy Italy
Not recruiting
27.01.2016
Poland Poland
Not recruiting
27.01.2016
Portugal Portugal
Not recruiting
27.01.2016
Romania Romania
Not recruiting
27.01.2016
Spain Spain
Not recruiting
27.01.2016
The Netherlands The Netherlands
Not recruiting
27.01.2016

Trial locations

Atezolizumab is a medication used in this clinical trial. It is an antibody that helps the immune system to detect and fight cancer cells. In this study, it is being tested for its effectiveness and safety in patients who have had surgery to remove non-small cell lung cancer. The goal is to see if it can help prevent the cancer from coming back after chemotherapy.

Non-Small Cell Lung Cancer – This is the most common type of lung cancer, accounting for about 85% of all cases. It typically grows and spreads more slowly than small cell lung cancer. The disease begins in the tissues of the lungs and can spread to other parts of the body. It is often categorized into subtypes, including adenocarcinoma, squamous cell carcinoma, and large cell carcinoma, based on the type of cells in which it starts. Symptoms may include a persistent cough, chest pain, and shortness of breath. As the disease progresses, it may lead to more severe respiratory issues and other systemic symptoms.

Trial ID:
2023-505981-26-00
Protocol code:
GO29527
Trial Phase:
Therapeutic confirmatory (Phase III)

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