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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03425643
Other study ID # 3475-671
Secondary ID MK-3475-67118397
Status Active, not recruiting
Phase Phase 3
First received
Last updated
Start date April 24, 2018
Est. completion date June 29, 2026

Study information

Verified date November 2023
Source Merck Sharp & Dohme LLC
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This trial will evaluate the safety and efficacy of pembrolizumab (MK-3475) in combination with platinum doublet neoadjuvant chemotherapy (NAC) before surgery [neoadjuvant phase], followed by pembrolizumab alone after surgery [adjuvant phase] in participants with resectable stage II, IIIA, and resectable IIIB (T3-4N2) non-small cell lung cancer (NSCLC). The primary hypotheses of this study are that neoadjuvant pembrolizumab (vs. placebo) in combination with NAC, followed by surgery and adjuvant pembrolizumab (vs. placebo) will improve: 1) event free survival (EFS) by biopsy assessed by local pathologist or by investigator-assessed imaging using Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1); and 2) overall survival (OS).


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 797
Est. completion date June 29, 2026
Est. primary completion date July 10, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Have previously untreated and pathologically confirmed resectable Stage II, IIIA, or IIIB (N2) NSCLC. - If male, must agree to use contraception or practice abstinence as well as refrain from donating sperm during the treatment period and for the time needed to eliminate each study intervention after the last dose of study intervention. - If female, may participate if not pregnant or breastfeeding, and at least one of the following conditions apply: 1) not a woman of childbearing potential (WOCBP); or 2) a WOCBP who agrees to follow contraceptive guidance during the treatment period and for the time needed to eliminate each study intervention after the last dose of study intervention and agrees not to donate eggs (ova, oocytes) to others or freeze/store for her own use for the purpose of reproduction during this period. - Have available formalin-fixed paraffin embedded (FFPE) tumor tissue sample blocks for submission. If blocks are not available, have unstained slides for submission for central programmed death-ligand 1 (PD-L1) testing. - Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1 within 10 days of randomization. - Have adequate organ function. Exclusion Criteria: - Has one of the following tumor locations/types:1) NSCLC involving the superior sulcus; 2) Large cell neuro-endocrine cancer (LCNEC); or 3) Sarcomatoid tumor. - Has a history of (non-infectious) pneumonitis /interstitial lung disease that required steroids or has current pneumonitis/interstitial lung disease that requires steroids. - Has an active infection requiring systemic therapy. - Has had an allogenic tissue/sold organ transplant. - Has a known severe hypersensitivity (= Grade 3) to pembrolizumab, its active substance and/or any of its excipients. - Has a known severe hypersensitivity (= Grade 3) to any of the study chemotherapy agents and/or to any of their excipients. - Has an active autoimmune disease that has required systemic treatment in past 2 years. - Has a known history of human immunodeficiency virus (HIV) infection. - Has a known history of Hepatitis B or Hepatitis C. - Has a known history of active tuberculosis. - Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the participant's participation for the full duration of the trial, or is not in the best interest of the participant to participate. - Has known psychiatric or substance abuse disorders that would interfere with cooperating with the requirements of the trial. - Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent or with an agent directed to another co-inhibitory T-cell receptor. - Has received prior systemic anti-cancer therapy including investigational agents for the current malignancy prior to randomization/allocation. - Has received prior radiotherapy within 2 weeks of start of trial treatment. - Has received a live vaccine within 30 days prior to the first dose of trial drug. - Is currently participating in or has participated in a trial of an investigational agent or has used an investigational device within 4 weeks prior to the first dose of trial treatment. - Has a diagnosis of immunodeficiency or is receiving either systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior the first dose of trial drug. - Has a known additional malignancy that is progressing or requires active treatment within the past 5 years.

Study Design


Intervention

Biological:
Pembrolizumab
200 mg by IV infusion every 3 weeks (Q3W), given on cycle day 1.
Drug:
Placebo
Normal saline by IV infusion Q3W, given on cycle day 1.
Cisplatin
75 mg/m^2 by IV infusion Q3W, given on cycle day 1.
Gemcitabine
1000 mg/m^2 by IV infusion Q3W, given on cycle days 1 and 8. Given only to participants with squamous NSCLC.
Pemetrexed
500 mg/m^2 by IV infusion Q3W, given on cycle day 1. Given only to participants with nonsquamous NSCLC.

Locations

Country Name City State
Argentina Centro de Oncologia e Investigacion Buenos Aires COIBA ( Site 0136) Berazategui Buenos Aires
Argentina Fundacion Favaloro ( Site 0128) Ciudad de Buenos Aires Caba
Argentina Hospital Privado Universitario de Córdoba ( Site 0139) Cordoba
Argentina Sanatorio Allende ( Site 0129) Cordoba
Argentina Hospital Privado de Comunidad. ( Site 0130) Mar del Plata Buenos Aires
Argentina Hospital Universitario Austral ( Site 0127) Pilar Buenos Aires
Argentina Hospital Provincial del Centenario ( Site 0131) Rosario Santa Fe
Argentina Sanatorio Britanico ( Site 0125) Rosario Santa Fe
Argentina Sanatorio Parque ( Site 0135) Rosario Santa Fe
Argentina CER San Juan Centro Polivalente de Asistencia e Investigacion Clinica ( Site 0133) San Juan
Australia Orange Health Services ( Site 0624) Orange New South Wales
Australia Westmead Hospital ( Site 0621) Westmead New South Wales
Belgium UZ Gent ( Site 0224) Gent Oost-Vlaanderen
Belgium UZ Leuven ( Site 0221) Leuven Vlaams-Brabant
Belgium Centre Hospitalier Universitaire de Liège - Domaine Universitaire du Sart Tilman ( Site 0223) Liège Liege
Belgium AZ Sint-Maarten ( Site 0226) Mechelen Antwerpen
Belgium AZ Delta ( Site 0222) Roeselare West-Vlaanderen
Belgium AZ Nikolaas ( Site 0225) Sint-Niklaas Oost-Vlaanderen
Brazil Fundacao Pio XII - Hospital de Cancer de Barretos ( Site 0144) Barretos Sao Paulo
Brazil Sirio-Libanes Brasilia - Centro de Oncologia - Asa Sul ( Site 0159) Brasilia Distrito Federal
Brazil YNOVA Pesquisa Clinica ( Site 0823) Florianopolis Santa Catarina
Brazil Centro Regional Integrado de Oncologia ( Site 0160) Fortaleza Ceara
Brazil Instituto do Cancer do Ceara ( Site 0152) Fortaleza Ceara
Brazil Hospital de Caridade de Ijui ( Site 0153) Ijui Rio Grande Do Sul
Brazil Liga Norte Riograndense Contra o Cancer ( Site 0150) Natal Rio Grande Do Norte
Brazil Hospital Nossa Senhora da Conceicao ( Site 0145) Porto Alegre Rio Grande Do Sul
Brazil Uniao Brasileira de Educacao e Assistencia Hospital Sao Lucas da Pucrs ( Site 0146) Porto Alegre Rio Grande Do Sul
Brazil Instituto Nacional do Cancer Jose Alencar Gomes da Silva INCA ( Site 0149) Rio de Janeiro
Brazil Hospital Alemao Oswaldo Cruz ( Site 0158) Sao Paulo
Brazil Hospital Paulistano - Amil Clinical Research ( Site 0822) Sao Paulo
Canada CIUSSS du Saguenay-Lac-St-Jean ( Site 0101) Chicoutimi Quebec
Canada Centre Hospitalier de l Universite de Montreal - CHUM ( Site 0110) Montreal Quebec
Canada CIUSSS Ouest de l Ile - St-Mary s Hospital ( Site 0104) Montreal Quebec
Canada McGill University Health Centre ( Site 0111) Montreal Quebec
Canada Princess Margaret Cancer Centre ( Site 0109) Toronto Ontario
China Beijing Cancer Hospital ( Site 0810) Beijing Beijing
China Beijing Cancer Hospital ( Site 0811) Beijing Beijing
China Cancer Hospital Chinese Academy of Medical Sciences ( Site 0801) Beijing Beijing
China Peking Union Medical College Hospital ( Site 0809) Beijing Beijing
China Peking University Third Hospital ( Site 0812) Beijing Beijing
China Hunan Cancer Hospital ( Site 0815) Changsha Hunan
China Sun Yat-Sen University Cancer Center ( Site 0816) Guangzhou Guangdong
China The First Affiliated Hospital of Zhejiang University ( Site 0804) Hangzhou Zhejiang
China Zhejiang Cancer Hospital.... ( Site 0814) Hangzhou Zhejiang
China Hwa Mei Hospital University of Chinese Academy of Sciences ( Site 0802) Ningbo Zhejiang
China Fudan University Shanghai Cancer Center ( Site 0813) Shanghai Shanghai
China Shanghai Pulmonary Hospital-Thoracic Surgery department ( Site 0817) Shanghai Shanghai
China Zhongshan Hospital of Fudan University ( Site 0808) Shanghai Shanghai
China Tianjin Medical University General Hospital ( Site 0806) Tianjin Anhui
China Tang Du Hospital ( Site 0803) XI An Shanxi
Estonia SA Pohja-Eesti Regionaalhaigla ( Site 1100) Tallinn Harjumaa
France Hôpital Avicenne - Service d oncologie medicale ( Site 0249) Bobigny Seine-Saint-Denis
France Centre Hospitalier Metropole Savoie Site de Chambery ( Site 0245) Chambery Savoie
France Clinique Francois Chenieux ( Site 0246) Limoges Haute-Vienne
France Institut Curie ( Site 0250) Paris
France Hospices Civils de Lyon Centre Hospitalier Lyon Sud ( Site 0241) Pierre-Benite Rhone-Alpes
France Centre Hospitalier Annecy Genevois ( Site 0242) Pringy Savoie
France CHU de Rouen ( Site 0252) Rouen Seine-Maritime
France Nouvel Hopital Civil ( Site 0255) Strasbourg Bas-Rhin
France Hopital Foch ( Site 0243) Suresnes Ain
France H.I.A. Sainte-Anne ( Site 0251) Toulon Var
France CHU de Toulouse - Hopital Larrey ( Site 0258) Toulouse Haute-Garonne
Germany Zentralklinik Bad Berka GmbH ( Site 0264) Bad Berka Thuringen
Germany Evangelische Lungenklinik Berlin ( Site 0274) Berlin
Germany HELIOS Klinikum Emil von Behring ( Site 0280) Berlin
Germany Universitaetsklinikum Carl Gustav Carus ( Site 0273) Dresden Sachsen
Germany Florence Nightingale Krankenhaus ( Site 0874) Duesseldorf Nordrhein-Westfalen
Germany Klinikum Esslingen GmbH ( Site 0875) Esslingen Baden-Wurttemberg
Germany SRH Waldklinikum Gera GmbH ( Site 0272) Gera Thuringen
Germany LungenClinic Grosshansdorf GmbH ( Site 0267) Grosshansdorf Schleswig-Holstein
Germany Asklepios Klinikum Hamburg ( Site 0271) Hamburg
Germany Lungenklinik Hemer ( Site 0269) Hemer Nordrhein-Westfalen
Germany LKI Lungenfachklinik Immenhausen ( Site 0268) Immenhausen Hessen
Germany Universitaetsklinikum Schleswig Holstein ( Site 0871) Kiel Schleswig-Holstein
Germany Katholisches Klinikum Koblenz Haus Marienhof ( Site 0873) Koblenz Rheinland-Pfalz
Germany Universitaetsklinikum Leipzig AOeR ( Site 0277) Leipzig Sachsen
Germany Mathias Spital Rheine ( Site 0261) Rheine Nordrhein-Westfalen
Ireland St James Hospital ( Site 0451) Dublin
Ireland Mid Western Cancer Centre ( Site 0450) Limerick
Ireland Cork University Hospital ( Site 0452) Wilton Cork
Italy Azienda Ospedaliera Spedali Civili di Brescia ( Site 0307) Brescia
Italy IRST-Istituto Scientifico Romagnolo per lo Studio e la cura dei Tumori ( Site 0300) Meldola Forli-Cesena
Italy ASST Grande Ospedale Metropolitano Niguarda-Oncologia Falck ( Site 0315) Milan Milano
Italy IRCCS Ospedale San Raffaele di Milano ( Site 0303) Milano
Italy Istituto Nazionale Tumori ( Site 0309) Milano Abruzzo
Italy Azienda Ospedaliera San Gerardo ( Site 0308) Monza Monza E Brianza
Italy Azienda Ospedaliera dei Colli V. Monaldi ( Site 0301) Napoli Campania
Italy AOU San Luigi Gonzaga di Orbassano ( Site 0313) Orbassano Torino
Italy Azienda Ospedaliera San Camillo Forlanini ( Site 0311) Roma
Italy Istituto Clinico Humanitas Research Hospital ( Site 0314) Rozzano Lombardia
Japan Hyogo Cancer Center ( Site 0764) Akashi Hyogo
Japan Fukushima Medical University Hospital ( Site 0772) Fukushima
Japan Hiroshima University Hospital ( Site 0762) Hiroshima
Japan National Cancer Center Hospital East ( Site 0761) Kashiwa Chiba
Japan St. Marianna University School of Medicine Hospital ( Site 0769) Kawasaki Kanagawa
Japan HP of the Univ. of Occupational and Environmental Health, Japan ( Site 0770) Kitakyushu Fukuoka
Japan Aichi Cancer Center Hospital ( Site 0765) Nagoya Aichi
Japan Juntendo University Hospital ( Site 0768) Tokyo
Japan National Cancer Center Hospital ( Site 0767) Tokyo
Japan Tokyo Medical University Hospital ( Site 0771) Tokyo
Japan Kanagawa Cancer Center ( Site 0763) Yokohama Kanagawa
Japan Oita University Hospital ( Site 0766) Yufu Oita
Korea, Republic of National Cancer Center ( Site 0702) Gyeonggi-do Kyonggi-do
Korea, Republic of The Catholic University of Korea St. Vincent s Hospital ( Site 0705) Gyeonggi-do Kyonggi-do
Korea, Republic of Asan Medical Center ( Site 0701) Seoul
Korea, Republic of Samsung Medical Center ( Site 0704) Seoul
Korea, Republic of SMG-SNU Boramae Medical Center ( Site 0707) Seoul
Latvia Pauls Stradins Clinical University Hospital ( Site 0911) Riga
Latvia Riga East Clinical University Hospital ( Site 0912) Riga
Lithuania LSMUL Kauno Klinikos ( Site 0932) Kaunas
Lithuania Nacionalinis Vezio Institutas ( Site 0931) Vilnius
Malaysia University Malaya Medical Centre ( Site 0781) Kuala Lumpur
Malaysia Sarawak General Hospital ( Site 0782) Kuching Sarawak
Poland Centrum Onkologii im. Prof. Franciszka Lukaszczyka ( Site 0488) Bydgoszcz Kujawsko-pomorskie
Poland Centrum Pulmonologii i Torakochirurgii w Bystrej ( Site 0484) Bystra Dolnoslaskie
Poland Wojewodzki Szpital Specjalistyczny im. M. Kopernika w Lodzi ( Site 0493) Lodz Lodzkie
Poland Wielkopolskie Centrum Pulmonologii i Torakochirurgii ( Site 0487) Poznan Wielkopolskie
Poland Szpital Specjalistyczny w Prabutach Sp. z o.o. ( Site 0483) Prabuty Pomorskie
Poland Dolnoslaskie Centrum Onkologii. ( Site 0491) Wroclaw Dolnoslaskie
Romania Spitalul Sf. Constantin ( Site 0512) Brasov
Romania Centrul Medical Medicover Victoria ( Site 0514) Bucharest Bucuresti
Romania Euroclinic Hospital Bucharest ( Site 0510) Bucuresti
Romania S.C.Focus Lab Plus S.R.L ( Site 0513) Bucuresti
Romania Institutul Oncologic Prof.Dr. Ion Chiricuta Cluj-Napoca ( Site 0501) Cluj Napoca Cluj
Romania Institutul Oncologic Prof.Dr. Ion Chiricuta Cluj-Napoca ( Site 0515) Cluj-Napoca Cluj
Romania SC Radiotherapy Center Cluj SRL ( Site 0509) Comuna Floresti Cluj
Romania Spitalul clinic Judetean de urgenta Constanta ( Site 0508) Constanta
Romania S.C. Centrul de Oncologie Sf. Nectarie SRL ( Site 0504) Craiova Dolj
Romania S C Pelican Impex SRL ( Site 0506) Oradea Bihor
Romania S.C.R.T.C.Radiology Therapeutic Center SRL ( Site 0511) Otopeni Ilfov
Romania Spitalul Judetean de Urgenta .Sf. Ioan cel Nou. ( Site 0503) Suceava
Romania S C Oncocenter Oncologie Medicala S R L ( Site 0505) Timisoara Timis
Russian Federation Chelyabinsk Regional Clinical Oncological Dispensary ( Site 0530) Chelyabinsk Chelyabinskaya Oblast
Russian Federation Republican Clinical Oncology Dispensary of Tatarstan MoH ( Site 0529) Kazan Tatarstan, Respublika
Russian Federation Medical Rehabilitation Center ( Site 0534) Moscow Moskva
Russian Federation N.N. Blokhin NMRCO ( Site 0521) Moscow Moskva
Russian Federation National Medical Research Radiology Centre ( Site 0535) Moscow Moskva
Russian Federation Municipal Clinical Oncology Center ( Site 0523) Saint Petersburg Sankt-Peterburg
Russian Federation SBHI Leningrad Regional Clinical Hospital ( Site 0524) Saint Petersburg Sankt-Peterburg
Russian Federation Scientific Research Oncology Institute n.a. N.N.Petrov ( Site 0533) Saint Petersburg Sankt-Peterburg
Russian Federation Tomsk Scientific Research Institute of Oncology ( Site 0526) Tomsk Tomskaya Oblast
South Africa The Oncology Centre ( Site 0571) Durban Kwazulu-Natal
South Africa Cape Town Oncology Trials Pty Ltd ( Site 0572) Kraaifontein Western Cape
South Africa Wits Clinical Research ( Site 0570) Parktown-Johannesburg Gauteng
South Africa Wilgers Oncology Centre ( Site 0573) Pretoria Gauteng
Spain Hospital Germans Trias i Pujol. ICO de Badalona ( Site 0381) Badalona Barcelona
Spain Hospital de la Santa Creu i Sant Pau ( Site 0385) Barcelona
Spain Hospital Universitari Vall d Hebron ( Site 0389) Barcelona
Spain Hospital Universitario de Girona Doctor Josep Trueta ( Site 0386) Girona La Coruna
Spain Instituto Catalan de Oncologia - ICO ( Site 0388) L Hospitalet De Llobregat Barcelona
Spain Hospital Universitario Insular de Gran Canaria ( Site 0383) Las Palmas de Gran Canaria Las Palmas
Spain Hospital General Universitario Gregorio Maranon ( Site 0382) Madrid
Spain Hospital Virgen del Rocio ( Site 0387) Sevilla
Taiwan Kaohsiung Chang Gung Memorial Hospital ( Site 0725) Kaohsiung
Taiwan China Medical University Hospital ( Site 0724) Taichung
Taiwan National Taiwan University Hospital ( Site 0721) Taipei
Taiwan Taipei Veterans General Hospital ( Site 0722) Taipei
Taiwan Tri-Service General Hospital ( Site 0726) Taipei
Taiwan Chang Gung Medical Foundation.Linkou Branch ( Site 0723) Taoyuan
Ukraine Cherkassy Regional Oncological Center ( Site 0613) Cherkasy Cherkaska Oblast
Ukraine City Clinical Hosp.4 of DCC ( Site 0607) Dnipro Dnipropetrovska Oblast
Ukraine MI Precarpathian Clinical Oncology Center ( Site 0603) Ivano-Frankivsk Ivano-Frankivska Oblast
Ukraine MI KhRC Kherson Regional Oncology Dispensary ( Site 0614) Kherson Khersonska Oblast
Ukraine PP PPC Acinus Medical and Diagnostic Centre ( Site 0609) Kropyvnytsky Kirovohradska Oblast
Ukraine Kyiv City Clinical Oncological Center ( Site 0601) Kyiv Kyivska Oblast
Ukraine National Cancer Institute of the MoH of Ukraine ( Site 0605) Kyiv Kyivska Oblast
Ukraine MI Odessa Regional Oncological Centre ( Site 0608) Odesa Odeska Oblast
Ukraine Zaporizhzhya Regional Clinical Oncology Center ( Site 0606) Zaporizhzhya Zaporizka Oblast
United Kingdom Heartlands Hospital in Birmingham ( Site 0455) Birmingham
United Kingdom Leicester Royal Infirmary ( Site 0447) Leicester Leicestershire
United Kingdom Royal Marsden NHS Foundation Trust ( Site 0458) London London, City Of
United Kingdom Freeman Hospital ( Site 0444) Newcastle upon Tyne
United Kingdom Nottingham City Hospital Campus ( Site 0441) Nottingham Nottinghamshire
United Kingdom Plymouth Hospitals NHS Trust ( Site 0443) Plymouth
United Kingdom Royal Marsden Hospital ( Site 0457) Sutton London, City Of
United Kingdom The Clatterbridge Cancer Centre NHS Foundation Trust ( Site 0456) Wirral Liverpool
United States St. Peter's Hospital Cancer Care Center ( Site 0039) Albany New York
United States Pacific Cancer Medical Center, Inc. ( Site 0004) Anaheim California
United States Ashland-Bellefonte Cancer Center ( Site 0021) Ashland Kentucky
United States Harry & Jeanette Weinberg Cancer Institute ( Site 0081) Baltimore Maryland
United States Memorial Sloan Kettering Cancer Center Basking Ridge ( Site 0074) Basking Ridge New Jersey
United States St. Vincent Healthcare Frontier Cancer Center ( Site 0005) Billings Montana
United States Boston Medical Center ( Site 0057) Boston Massachusetts
United States Montefiore Einstein Center ( Site 0016) Bronx New York
United States Providence Saint Joseph Medical Center ( Site 0061) Burbank California
United States Emily Couric Clinical Cancer Center ( Site 0013) Charlottesville Virginia
United States Memorial Sloan-Kettering Cancer Center at Commack ( Site 0076) Commack New York
United States Henry Ford Health System ( Site 0031) Detroit Michigan
United States Northwest Oncology and Hematology ( Site 0001) Elk Grove Village Illinois
United States Providence Regional Cancer Partnership ( Site 0065) Everett Washington
United States Inova Schar Cancer Institute ( Site 0032) Fairfax Virginia
United States Virginia Cancer Specialists, PC ( Site 0080) Fairfax Virginia
United States PPG-Oncology ( Site 0043) Fort Wayne Indiana
United States Banner MD Anderson Cancer Center ( Site 0028) Gilbert Arizona
United States Western Regional Medical Center, Inc. ( Site 0050) Goodyear Arizona
United States Saint Francis Cancer Center ( Site 0096) Greenville South Carolina
United States UPMC Pinnacle Health System - East Location ( Site 0063) Harrisburg Pennsylvania
United States Memorial Sloan Kettering Cancer Center Westchester ( Site 0079) Harrison New York
United States Hartford Hospital ( Site 0069) Hartford Connecticut
United States Ingalls Memorial Hospital ( Site 0044) Harvey Illinois
United States University of Iowa Hospital and Clinics ( Site 0010) Iowa City Iowa
United States Mayo Clinic Jacksonville ( Site 0022) Jacksonville Florida
United States Herbert Herman Cancer Center, Sparrow Hospital ( Site 0034) Lansing Michigan
United States Miami Cancer Institute-Baptist Hospital ( Site 0068) Miami Florida
United States Memorial Sloan Kettering Cancer Center- Monmouth ( Site 0077) Middletown New Jersey
United States Pacific Cancer Care ( Site 0035) Monterey California
United States MSKCC-Bergen ( Site 0075) Montvale New Jersey
United States Memorial Sloan Kettering Cancer Center ( Site 0060) New York New York
United States Helen F. Graham Cancer Center & Research Institute ( Site 0015) Newark Delaware
United States Southeastern Regional Medical Center ( Site 0051) Newnan Georgia
United States University of Nebraska Medical Center ( Site 0047) Omaha Nebraska
United States Cancer Treatment Centers of America-Eastern Regional Medical Center ( Site 0053) Philadelphia Pennsylvania
United States University of Arizona Cancer Center - Dignity Health ( Site 0062) Phoenix Arizona
United States Allegheny General Hospital ( Site 0009) Pittsburgh Pennsylvania
United States UPMC Hillman Cancer Centers ( Site 0041) Pittsburgh Pennsylvania
United States VA Pittsburgh Healthcare System ( Site 0052) Pittsburgh Pennsylvania
United States OHSU Center for Health & Healing ( Site 1006) Portland Oregon
United States Mayo Clinic ( Site 0026) Rochester Minnesota
United States John Wayne Cancer Institute ( Site 0049) Santa Monica California
United States St Joseph Heritage Healthcare ( Site 0040) Santa Rosa California
United States Stanford University, Stanford Cancer Center ( Site 0046) Stanford California
United States Stony Brook University Medical Center - Cancer Center ( Site 0019) Stony Brook New York
United States University of Arizona Cancer Center ( Site 0012) Tucson Arizona
United States Southwestern Regional Medical Center, Inc. ( Site 0054) Tulsa Oklahoma
United States Memorial Sloan Kettering Cancer Center - Nassau ( Site 0078) Uniondale New York
United States White Plains Hospital Center for Cancer Care ( Site 0007) White Plains New York
United States UMass Memorial Medical Center ( Site 0030) Worcester Massachusetts

Sponsors (1)

Lead Sponsor Collaborator
Merck Sharp & Dohme LLC

Countries where clinical trial is conducted

United States,  Argentina,  Australia,  Belgium,  Brazil,  Canada,  China,  Estonia,  France,  Germany,  Ireland,  Italy,  Japan,  Korea, Republic of,  Latvia,  Lithuania,  Malaysia,  Poland,  Romania,  Russian Federation,  South Africa,  Spain,  Taiwan,  Ukraine,  United Kingdom, 

References & Publications (1)

Wakelee H, Liberman M, Kato T, Tsuboi M, Lee SH, Gao S, Chen KN, Dooms C, Majem M, Eigendorff E, Martinengo GL, Bylicki O, Rodriguez-Abreu D, Chaft JE, Novello S, Yang J, Keller SM, Samkari A, Spicer JD; KEYNOTE-671 Investigators. Perioperative Pembrolizu — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Event Free Survival (EFS) EFS is defined as the time from randomization until radiographic disease progression, local progression precluding surgery, inability to resect the tumor, local or distant recurrence, or death due to any cause. EFS determined either by biopsy assessed by local pathologist or by investigator-assessed imaging using RECIST 1.1. Up to approximately 5 years
Primary Overall Survival (OS) OS is defined as the time from randomization until death from any cause. Up to approximately 5 years
Secondary Major Pathological Response (mPR) Rate mPR rate is defined as the percentage of participants having =10% viable tumor cells in the resected primary tumor and all resected lymph nodes following completion of neoadjuvant therapy. Up to approximately 7 weeks following completion of neoadjuvant treatment (up to Study Week 20)
Secondary Pathological Complete Response (pCR) Rate pCR rate is defined as the percentage of participants having an absence of residual invasive cancer in resected lung specimens and lymph nodes following completion of neoadjuvant therapy. Up to approximately 7 weeks following completion of neoadjuvant treatment (up to Study Week 20)
Secondary Global Health Status/Quality of Life (GHS/QoL) Score using the European Organization for Research and Treatment (EORTC) QoL Questionnaire (QLQ-C30) Change from baseline in GHS/QoL score using the EORTC QLQ-C30 will be determined. The EORTC QLQ-C30 is the most widely used cancer-specific, health-related QoL instrument comprised of 30 individual items arranged as both multi-item scales and individual items. Specifically, these items are divided into 5 functional scales (15 items total), 3 symptom scales (7 items total), 6 individual items, and a GHS/QoL scale composed of 2 items: GHS and QoL. The GHS/QoL score measured here refers to only the composite score calculated for the GHS/QoL scale. Both items on the GHS/QoL scale are scored from 1 (very poor GHS/QoL) to 7 (excellent GHS/QoL) and scores for both items are averaged and a linear transformation applied to standardize the overall GHS/QoL score from 0 to 100, with higher overall scores indicating higher GHS/QoL. Baseline (cycle 1 in neoadjuvant phase) and end of follow-up (up to approximately 5 years)
Secondary Adverse Events (AEs) The number of participants experiencing an AE will be assessed. An AE is defined as any unfavorable and unintended sign, symptom, or disease (new or worsening) temporally associated with the use of study therapy, regardless of whether or not a causal relationship with the study therapy can be determined. Up to approximately 71 weeks
Secondary Perioperative Complications The number of participants experiencing perioperative complications will be assessed. Perioperative complications are a discrete set of both intraoperative and postoperative complications, potentially contributing to increased length of inpatient care and/or delay of adjuvant therapy. Up to approximately 51 weeks following surgery
Secondary Treatment Discontinuations Due to AEs The number of participants discontinuing study therapy due to an AE will be assessed. Up to approximately 57 weeks
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