Study of trastuzumab deruxtecan with pembrolizumab versus platinum chemotherapy with pembrolizumab for patients with untreated HER2-positive non-small cell lung cancer

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What is this study about?

This study focuses on treating people with Non-small Cell Lung Cancer that has spread to other parts of the body or cannot be removed by surgery. Specifically, it involves patients whose cancer cells show high levels of a protein called HER2. The study will test a combination of two medications: trastuzumab deruxtecan (also known as DS-8201a) with pembrolizumab, comparing it to standard treatment that combines platinum-based chemotherapy (either cisplatin or carboplatin) with pembrolizumab.

The purpose of this research is to determine if the combination of trastuzumab deruxtecan with pembrolizumab works better than the standard treatment in controlling the disease. The medications will be given through an intravenous infusion, which means they are delivered directly into a vein. Trastuzumab deruxtecan is a type of medication that specifically targets cancer cells with high HER2 levels, while pembrolizumab helps the body’s immune system fight cancer cells.

During the study, participants will be randomly assigned to receive either the new combination treatment or the standard treatment. Their cancer will be monitored regularly using imaging scans to check how well the treatment is working. The doctors will continue to check the participants’ health and watch for any side effects throughout the study period.

1 Initial screening and qualification

Your eligibility for the study will be evaluated if you are an adult (18 years or older) with advanced lung cancer that cannot be removed by surgery.

A tissue sample from your tumor will be required to test for specific markers called HER2 and PD-L1.

Your medical history will be reviewed to confirm you have not received previous treatment for advanced lung cancer.

2 Treatment assignment

You will be randomly assigned to one of two treatment groups:

Group 1: You will receive a combination of trastuzumab deruxtecan and pembrolizumab through intravenous infusion.

Group 2: You will receive platinum-based chemotherapy (either cisplatin or carboplatin) with pemetrexed and pembrolizumab through intravenous infusion.

3 Treatment period

Regular treatment sessions will be scheduled for the administration of medications through intravenous infusion.

Your cancer will be monitored through imaging scans to evaluate how the treatment is working.

The treatment will continue until either your disease progresses or you are unable to continue with the treatment.

4 Follow-up period

After completing or stopping treatment, your health status will continue to be monitored.

Regular check-ups will be scheduled to track your progress and overall survival.

The study is planned to continue until June 2032.

Who Can Join the Study?

  • Must be at least 18 years old at the time of signing the consent form
  • Must be diagnosed with non-squamous non-small cell lung cancer that is either:
    – Advanced and cannot be surgically removed, or
    – Has spread to other parts of the body (metastatic)
  • Must have cancer that tests positive for HER2 (a protein that promotes cancer growth) and has specific PD-L1 (an immune system marker) levels
  • Must not have received any previous systemic treatment (treatment that affects the whole body) for advanced or metastatic lung cancer
  • If received previous cancer treatment (such as adjuvant or neoadjuvant therapy), it must have been completed at least 6 months before starting this trial
  • Must have suitable tumor tissue sample available for laboratory testing that has not been previously treated with radiation
  • Must be willing and able to sign and date the required consent forms before any trial procedures begin
  • Must not have any known gene changes (mutations) in the HER2 gene that could be treated with other available therapies
  • For mixed type tumors, the main type must be adenocarcinoma (a type of non-squamous lung cancer)

Who Cannot Join the Study?

  • Prior treatment with anti-HER2 therapy (therapy targeting a specific protein related to cancer growth)
  • Active brain metastases (cancer that has spread to the brain) or other active cancers requiring treatment
  • History of severe allergic reactions to monoclonal antibodies (a type of targeted therapy)
  • Serious heart conditions including heart failure, uncontrolled high blood pressure, or recent heart attack
  • Active autoimmune disease requiring systemic treatment (conditions where the immune system attacks healthy cells)
  • Current use of immunosuppressive medications (drugs that reduce immune system activity)
  • Active infection requiring treatment, including hepatitis B, hepatitis C, or HIV
  • Pregnant or breastfeeding women
  • Major surgery within 4 weeks before starting the study treatment
  • Participation in another clinical trial within 4 weeks before starting this study
  • Any condition that, in the opinion of the study doctor, would interfere with the safe conduct of the study

Where you can join this trial?

Verified and Recommended Sites

Site Name City Country Status
Samodzielny Publiczny Szpital Kliniczny Nr 4 W Lublinie Lublin Poland

Verified Sites

Other Sites

Site Name City Country Status
Hopital Tenon Paris France
Metaxa Cancer Center Hospital Of Piraeus Piraeus Greece
Centro Ricerche Cliniche Di Verona S.r.l. Verona Italy
Centre hospitalier universitaire de Liege Liege Belgium
Hospital General Universitario Gregorio Maranon Madrid Spain
Hospital Universitario 12 De Octubre Madrid Spain
Hospital Del Mar Barcelona Spain
Hospital Universitari Dexeus Grupo Quironsalud Barcelona Spain
Fundacion Instituto Valenciano De Oncologia Valencia Spain
Grand Hopital De Charleroi Charleroi Belgium
Delta Health Care S.R.L. Bucharest Romania
Humanitas Istituto Clinico Catanese S.p.A. Misterbianco Italy
Centre De Cancerologue Du Grand Montpellier Montpellier France
Klinikum Esslingen GmbH Esslingen Am Neckar Germany
Complejo Hospitalario Universitario Insular Materno Infantil Las Palmas De Gran Canaria Spain
Azienda Socio Sanitaria Territoriale Dei Sette Laghi Varese Italy
Spitalul Municipal Ploiesti Ploiesti Romania
Henry Dunant Hospital Center Athens Greece
Spital Clinic Militar De Urgenta Dr. Constantin Papilian Cluj Napoca Cluj Napoca Romania
General University Hospital Of Larissa Larissa Greece
Centrul De Oncologie SF Nectarie S.R.L. Craiova Romania
Spitalul Clinic Colentina Bucuresti Bucharest Romania
General Hospital Of Thessaloniki Papageorgiou Thessaloniki Greece
Institutul Regional De Oncologie Iasi Iasi Romania
Ospedale San Raffaele S.r.l. Milan Italy
Azienda Ospedaliero-Universitaria San Luigi Gonzaga Orbassano Italy
Istituto Di Candiolo Fondazione Del Piemonte Per Loncologia IRCCS Candiolo Italy
Hospital Clinic De Barcelona Barcelona Spain
Hospital Da Luz S.A. Lisbon Portugal
Hopital Ambroise Pare Boulogne-Billancourt France
IRCCS Ospedale Policlinico San Martino Genoa Italy
Universidade De Santiago De Compostela Santiago De Compostela Spain
Hospital Universitario Virgen De Valme Sevilla Spain
Pratia S.A. Skorzewo Poland
General University Hospital Of Patras Patras Greece
Hospital Universitario Lucus Augusti Lugo Spain
Hospital General Universitario De Castellon Castello De La Plana Spain
Justus-Liebig-Universitaet Giessen Giessen Germany
Institute Of Oncology Prof. Dr. Ion Chiricuta Cluj-Napoca Cluj Napoca Romania
Centre Hospitalier Universitaire De Nantes Nantes France
St. Luke’s Hospital S.A. Thessaloniki Greece
Centro Hospitalar Universitario De Santo Antonio E.P.E. Porto Portugal
Radiology Therapeutic Center S.R.L. Otopeni Romania
Spitalul De Oncologie Monza S.R.L. Bucharest Romania
CHU Helora La Louviere Belgium
Centre Hospitalier Lyon Sud Pierre Benite France
Area De Salud De Burgos Y Soria Burgos Spain
Azienda Sanitaria Territoriale Di Pesaro E Urbino Pesaro Italy
Provita Centrum Medyczne Sp. z o.o. Tomaszow Mazowiecki Poland
L’Hopital Prive Du Confluent Nantes France
Hospital CUF Porto S.A. Porto Portugal
Hospital Universitario Virgen De La Victoria Malaga Spain
Metropolitan Hospital Athens Greece
University General Hospital Attikon General Hospital Of West Attica H Agia Varvara Chaidari Greece
Inst Medecine Epidemiologie Appliquee Paris France
Cdvvqa Lgqt Bljfdk Lyon France
Uhwqicrfqhzlgdwdrcgbc Eznqe Aes Essen Germany
Ikgpvz Iubnbzqz Flkjpehvhxiti Ohavgvojipn Rome Italy
Ixznnfxy Cqftwc Depoiykbxfpclpdsg L'hospitalet De Llobregat Spain
Akfopof Olslfmpbeom S Gormymld Aecowufshv Rome Italy
Lrray Gcafxhq Hakktpbp Oz Aupkxy Athens Greece
Amshuos Uqb Tnvqhdx nzvq oeqai Leghorn Italy
Abkcyoyhaa Pndajinb Hiygowem Df Mnqhxnvpw Marseille France
Aabwki Mfsclvs Cixzsu Swdg Thessaloniki Greece
Apkpudk Uniux Snkdunihe Lzzsmm De Buhghnp Bologna Italy
Uwnbzzhizu Og Acuyzlo Edegem Belgium
Cdhmzc Hooflfqrujl Rjjqflxd Drxmrsrytmzcbm Angers France
Fssazeflh Pbgb Lv Isdjgbyqtzdnn Bybevaijd Dtu Hkkugafz Uxqsmjlvrtwab Lz Pnm Madrid Spain
Hlcbilsi Vkcl dqtvqnca Barcelona Spain
Heranmsl Uueekfvoynmuk ds A Chozjp A Coruna Galicia Spain
Wurvxacejx Sdkrfkm Inc Sumhmlz Pgk W Pglxuejbd Przemysl Poland

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

Trial status

Country Status Recruitment Start
Belgium Belgium
Recruiting
24.11.2025
France France
Recruiting
24.11.2025
Germany Germany
Not yet recruiting
24.11.2025
Greece Greece
Recruiting
24.11.2025
Italy Italy
Recruiting
24.11.2025
Poland Poland
Not recruiting
24.11.2025
Portugal Portugal
Recruiting
24.11.2025
Romania Romania
Not yet recruiting
24.11.2025
Spain Spain
Recruiting
24.11.2025

Trial locations

Trastuzumab Deruxtecan is a targeted therapy medication used to treat certain types of cancer. It combines an antibody that targets HER2-positive cancer cells with a chemotherapy drug. This medication is designed to deliver the chemotherapy directly to cancer cells while potentially limiting damage to healthy cells.

Pembrolizumab is an immunotherapy medication that helps your immune system fight cancer cells. It works by blocking a protein called PD-L1, which can help your immune system recognize and attack cancer cells more effectively.

Platinum-based Chemotherapy refers to traditional cancer treatment medications that contain platinum. These medications work by damaging the DNA of cancer cells, which prevents them from dividing and growing. This type of chemotherapy is commonly used to treat various types of cancer, including lung cancer.

Non-small Cell Lung Cancer – A type of lung cancer that begins in the large lung cells, including squamous cells, adenocarcinomas, and large-cell carcinomas. It typically grows and spreads more slowly than small cell lung cancer. The disease develops when lung cells begin to grow abnormally and form tumors. In non-squamous variants, the cancer originates specifically in glandular cells. When HER2-overexpressing, the cancer cells have too many HER2 proteins on their surface, which can make the cancer grow more aggressively. The disease can progress to become unresectable (unable to be removed by surgery) or metastatic (spread to other parts of the body).

Trial ID:
2024-515658-26-00
Protocol code:
DS8201-793
NCT ID:
NCT06899126
Trial Phase:
Therapeutic confirmatory (Phase III)

Other Trials to Consider

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  • Pumitamig Versus Pembrolizumab in Patients With Previously Untreated Advanced Non-Small Cell Lung Cancer and PD-L1 ≥ 50%

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