MedPath

A Study of Amivantamab and mFOLFOX6 or FOLFIRI Versus Cetuximab and mFOLFOX6 or FOLFIRI as First-line Treatment in Participants With KRAS/NRAS and BRAF Wild-type Unresectable or Metastatic Left-sided Colorectal Cancer

Registration Number
NCT06662786
Lead Sponsor
Janssen Research & Development, LLC
Brief Summary

The purpose of this study is to compare how long the participants are disease-free (progression-free survival) when treated with amivantamab and chemotherapy with 5-fluorouracil, leucovorin calcium (folinic acid) or levoleucovorin, oxaliplatin (mFOLFOX6) or 5-fluorouracil, leucovorin calcium (folinic acid) or levoleucovorin, and irinotecan hydrochloride (FOLFIRI) versus cetuximab and mFOLFOX6 or FOLFIRI in adult participants with Kirsten rat sarcoma viral oncogene homolog (KRAS)/ Neuroblastoma RAS viral oncogene homolog (NRAS) and v-Raf murine sarcoma viral oncogene homolog B1 (BRAF) wild type (WT) unresectable or metastatic left-sided colorectal cancer.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
1000
Inclusion Criteria
  • Have histologically or cytologically confirmed adenocarcinoma of the left-sided colorectal cancer. Participants must have unresectable or metastatic disease
  • Be diagnosed to have Kirsten rat sarcoma viral oncogene (KRAS), neuroblastoma RAS viral oncogene homolog (NRAS), and v-raf murine sarcoma viral oncogene homolog B (BRAF) wild-type (WT) tumor as determined by local testing
  • Must agree to the submission of fresh tumor tissue
  • Have measurable disease according to RECIST v1.1
  • Have an eastern cooperative oncology group (ECOG) performance status (PS) of 0 or 1
Exclusion Criteria
  • Has medical history of (noninfectious) interstitial lung disease (ILD) /pneumonitis/pulmonary fibrosis or has current ILD/pneumonitis/pulmonary fibrosis, or where suspected ILD/pneumonitis/pulmonary fibrosis cannot be ruled out by imaging at screening
  • Has known allergies, hypersensitivity, or intolerance to excipients of any of the following: (a) amivantamab or cetuximab, (b) any component of mFOLFOX6 and, (c) any component of FOLFIRI
  • Has a prior or concurrent second malignancy other than the disease under study or one whose natural history or treatment is unlikely to interfere with any study endpoints of safety or the efficacy of the study treatment(s)
  • Participant with known mismatch repair deficiency (dMMR)/ high microsatellite instability (MSI-H) status and human epidermal growth factor receptor 2 (HER2)-positive/amplified tumor
  • Has prior exposure to any agents that target epidermal growth factor receptor (EGFR) or mesenchymal epithelial transition (MET)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Arm B: Cetuximab in Combination With ChemotherapyLeucovorin calcium/LevoleucovorinParticipants will receive cetuximab in combination with chemotherapy (mFOLFOX6 or FOLFIRI) for 28-days treatment cycles and will continue to receive the treatment until radiographic disease progression or other discontinuation criteria are met.
Arm A: Amivantamab in Combination With ChemotherapyAmivantamabParticipants will receive amivantamab in combination with chemotherapy (mFOLFOX6 \[chemotherapy consisting of 5-fluorouracil, leucovorin calcium (folinic acid) or levoleucovorin, and oxaliplatin\] or FOLFIRI \[chemotherapy consisting of 5-fluorouracil, leucovorin calcium (folinic acid) or levoleucovorin, and irinotecan hydrochloride\]) for 28-days treatment cycles and will continue to receive the treatment until radiographic disease progression or other discontinuation criteria are met.
Arm A: Amivantamab in Combination With Chemotherapy5-fluorouracilParticipants will receive amivantamab in combination with chemotherapy (mFOLFOX6 \[chemotherapy consisting of 5-fluorouracil, leucovorin calcium (folinic acid) or levoleucovorin, and oxaliplatin\] or FOLFIRI \[chemotherapy consisting of 5-fluorouracil, leucovorin calcium (folinic acid) or levoleucovorin, and irinotecan hydrochloride\]) for 28-days treatment cycles and will continue to receive the treatment until radiographic disease progression or other discontinuation criteria are met.
Arm A: Amivantamab in Combination With ChemotherapyLeucovorin calcium/LevoleucovorinParticipants will receive amivantamab in combination with chemotherapy (mFOLFOX6 \[chemotherapy consisting of 5-fluorouracil, leucovorin calcium (folinic acid) or levoleucovorin, and oxaliplatin\] or FOLFIRI \[chemotherapy consisting of 5-fluorouracil, leucovorin calcium (folinic acid) or levoleucovorin, and irinotecan hydrochloride\]) for 28-days treatment cycles and will continue to receive the treatment until radiographic disease progression or other discontinuation criteria are met.
Arm A: Amivantamab in Combination With ChemotherapyOxaliplatinParticipants will receive amivantamab in combination with chemotherapy (mFOLFOX6 \[chemotherapy consisting of 5-fluorouracil, leucovorin calcium (folinic acid) or levoleucovorin, and oxaliplatin\] or FOLFIRI \[chemotherapy consisting of 5-fluorouracil, leucovorin calcium (folinic acid) or levoleucovorin, and irinotecan hydrochloride\]) for 28-days treatment cycles and will continue to receive the treatment until radiographic disease progression or other discontinuation criteria are met.
Arm A: Amivantamab in Combination With ChemotherapyIrinotecan HydrochlorideParticipants will receive amivantamab in combination with chemotherapy (mFOLFOX6 \[chemotherapy consisting of 5-fluorouracil, leucovorin calcium (folinic acid) or levoleucovorin, and oxaliplatin\] or FOLFIRI \[chemotherapy consisting of 5-fluorouracil, leucovorin calcium (folinic acid) or levoleucovorin, and irinotecan hydrochloride\]) for 28-days treatment cycles and will continue to receive the treatment until radiographic disease progression or other discontinuation criteria are met.
Arm B: Cetuximab in Combination With ChemotherapyCetuximabParticipants will receive cetuximab in combination with chemotherapy (mFOLFOX6 or FOLFIRI) for 28-days treatment cycles and will continue to receive the treatment until radiographic disease progression or other discontinuation criteria are met.
Arm B: Cetuximab in Combination With Chemotherapy5-fluorouracilParticipants will receive cetuximab in combination with chemotherapy (mFOLFOX6 or FOLFIRI) for 28-days treatment cycles and will continue to receive the treatment until radiographic disease progression or other discontinuation criteria are met.
Arm B: Cetuximab in Combination With ChemotherapyOxaliplatinParticipants will receive cetuximab in combination with chemotherapy (mFOLFOX6 or FOLFIRI) for 28-days treatment cycles and will continue to receive the treatment until radiographic disease progression or other discontinuation criteria are met.
Arm B: Cetuximab in Combination With ChemotherapyIrinotecan HydrochlorideParticipants will receive cetuximab in combination with chemotherapy (mFOLFOX6 or FOLFIRI) for 28-days treatment cycles and will continue to receive the treatment until radiographic disease progression or other discontinuation criteria are met.
Primary Outcome Measures
NameTimeMethod
Progression-Free Survival (PFS) as Assessed by Blinded Independent Central Review (BICR)Up to 4 years and 2 months

PFS is defined as the time from randomization until the date of objective disease progression or death (due to any cause), whichever comes first, as assessed by BICR using response evaluation criteria in solid tumors (RECIST) version (v) 1.1. Participants who have not progressed or have not died at the time of analysis will be censored at their last evaluable RECIST v1.1 assessment date.

Secondary Outcome Measures
NameTimeMethod
Progression Free Survival (PFS) as Assessed by InvestigatorUp to 7 Years 3 Months

PFS is defined as the time from randomization until the date of objective disease progression or death (due to any cause), whichever comes first, as assessed by the investigator.

Objective Response Rate (ORR) as Assessed by InvestigatorUp to 7 Years 3 Months

ORR is defined as the percentage of randomized participants achieving complete CR or PR, as assessed by the investigator.

Overall Survival (OS)Up to 7 Years 3 Months

OS is defined as the time from the date of randomization to the date of participant's death due to any cause. Any participant not known to have died at the time of analysis will be censored based on the last recorded date on which the participant was known to be alive.

Objective Response Rate (ORR) as Assessed by BICRUp to 7 Years 3 Months

ORR is defined as the percentage of randomized participants achieving complete response (CR) or partial response (PR), as determined by BICR using RECIST v1.1 criteria.

Duration of Response (DOR) as Assessed by BICRUp to 7 Years 3 Months

DOR is defined as time from the date of first documented response (CR or PR) until the date of documented progression or death, whichever comes first, for participants who have PR or CR, as assessed by BICR using RECIST v1.1 criteria.

Duration of Response (DOR) as Assessed InvestigatorUp to 7 Years 3 Months

DOR is defined as time from the date of first documented response (CR or PR) until the date of documented progression or death, whichever comes first, for participants who have PR or CR, as assessed by the investigator.

Progression-free Survival After Subsequent Therapy (PFS2)Up to 7 Years 3 Months

PFS2 is defined as the time from randomization until the date of second objective disease progression, after initiation of subsequent anticancer therapy, based on investigator assessment (after that used for PFS) or death, whichever comes first.

Disease Control Rate (DCR) as Assessed by BICRUp to 7 Years 3 Months

DCR is defined as the percentage of randomized participants achieving CR, PR, or stable disease (with minimum duration of 7 weeks) as assessed by BICR using RECIST v1.1 criteria.

Disease Control Rate (DCR) as Assessed by InvestigatorUp to 7 Years 3 Months

DCR is defined as the percentage of randomized participants achieving CR, PR, or stable disease (with minimum duration of 7 weeks) as assessed by the investigator.

Time to Treatment FailureUp to 7 Years 3 Months

Time to treatment failure is defined as time from randomization to discontinuation of therapy for any reason including death, progression, toxicity, or initiation of new anticancer therapy.

Curative Resection (R0) RateUp to 7 Years 3 Months

Curative resection (R0) rate is defined as the percentage of participants (or participants with limited disease at baseline) who underwent curative surgery.

Number of Participants with Adverse Events (AEs) by SeverityUp to 7 Years 3 Months

An AE can be any unfavorable and unintended sign (including an abnormal finding), symptom, or disease temporally associated with the use of a medicinal (investigational or non-investigational) product, whether or not related to that medicinal (investigational or non-investigational) product. AE severity will be graded according to the national cancer institute common terminology criteria for adverse events (NCI-CTCAE) v5.0. by using the standard grades as follows: Grade 1: Mild; asymptomatic or mild symptoms; Grade 2: Moderate; minimal, local or noninvasive intervention indicated; Grade 3: Severe or medically significant but not immediately life threatening; hospitalization or prolongation of hospitalization indicated; Grade 4: Life-threatening consequences; and Grade 5: Death related to AE.

Number of Participants with Abnormalities in Laboratory ValuesUp to 7 Years 3 Months

Participants with abnormalities in laboratory values (such as serum chemistry, hematology) will be reported.

Change From Baseline in European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30) ScoreFrom Baseline up to 7 Years 3 Months

The EORTC QLQ-C30, is a self-administered, 30-item questionnaire measuring the health-related quality of life (HRQoL) of participants with cancer. EORTC QLQ-C30 includes 5 functional scales, 3 symptom scales, a global health status / quality of life scale, and 6 single items. Responses to items 1-28 are rated on a 4-point Likert response scale ranging from 1 "Not at all" to 4 "Very much." Two global health status items are rated on a 7-point numeric rating scale from 1 "Very Poor" to 7 "Excellent." Higher scores indicate greater functioning, better global health status, and more severe symptoms.

Time to Worsening in Symptoms and Functioning as Measured by EORTC QLQ-C30Up to 7 Years 3 Months

The EORTC QLQ-C30, is a self-administered, 30-item questionnaire measuring the HRQoL of participants with cancer. EORTC QLQ-C30 includes 5 functional scales, 3 symptom scales, a global health status / quality of life scale, and 6 single items. Responses to items 1-28 are rated on a 4-point Likert response scale ranging from 1 "Not at all" to 4 "Very much." Two global health status items are rated on a 7-point numeric rating scale from 1 "Very Poor" to 7 "Excellent." Higher scores indicate greater functioning, better global health status, and more severe symptom.

Change from Baseline in European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Colorectal Cancer Module 29 (EORTC-QLQ-C30) ScoreFrom Baseline up to 7 Years 3 Months

The EORTC QLQ-CR29, is a self-administered, 29-item questionnaire measuring the HRQoL of participants with colorectal cancer. The QLQ CR29 includes items that evaluate symptoms (gastrointestinal, urinary, pain, and others) and functional areas (sexual, body image, weight, and anxiety) that are associated with colorectal cancer and its treatments. Responses are rated on a 4-point Likert response scale ranging from 1 "Not at all" to 4 "Very much". All scores are linearly converted into a scale from 0 to 100. Higher scores indicate greater functioning and more severe symptoms.

Time to Worsening in Symptoms and Functioning as Measured by EORTC QLQ-CR29Up to 7 Years 3 Months

The EORTC QLQ-CR29, is a self-administered, 29-item questionnaire measuring the HRQoL of participants with colorectal cancer. The QLQ CR29 includes items that evaluate symptoms (gastrointestinal, urinary, pain, and others) and functional areas (sexual, body image, weight, and anxiety) that are associated with colorectal cancer and its treatments. Responses are rated on a 4-point Likert response scale ranging from 1 "Not at all" to 4 "Very much". All scores are linearly converted into a scale from 0 to 100. Higher scores indicate greater functioning and more severe symptoms.

Overall Side Effect Burden as Measured by European Organisation for Research and Treatment of Cancer (EORTC) Item 168 Scale ScoreUp to 7 Years 3 Months

The EORTC item 168 is a single item used to measure the overall impact of treatment side effects. Responses are rated on a 4-point Likert response scale ranging from 1 "not at all" to 4 "very much." Higher scores indicate severe side effects.

Trial Locations

Locations (178)

Fundacao Doutor Amaral Carvalho

🇧🇷

Jau, Brazil

Sun Yat Sen University Cancer Center

🇨🇳

Guangzhou, China

Universitatsklinikum Ulm

🇩🇪

Ulm, Germany

Semmelweis Egyetem

🇭🇺

Budapest, Hungary

Azienda Ospedaliero Universitaria Pisana

🇮🇹

Pisa, Italy

Istituto Clinico Humanitas

🇮🇹

Rozzano, Italy

Chiba Cancer Center

🇯🇵

Chiba, Japan

Hospital Canselor Tuanku Muhriz UKM

🇲🇾

Cheras, Malaysia

Hospital Pulau Pinang

🇲🇾

Georgetown, Malaysia

Hospital Raja Permaisuri Bainun

🇲🇾

Ipoh, Malaysia

Hospital Kuala Lumpur

🇲🇾

Kuala Lumpur, Malaysia

University Malaya Medical Centre

🇲🇾

Kuala Lumpur, Malaysia

Hospital Umum Sarawak

🇲🇾

Kuching, Malaysia

Hosp Univ Vall D Hebron

🇪🇸

Barcelona, Spain

Hosp. Gral. Univ. Gregorio Maranon

🇪🇸

Madrid, Spain

Hosp. Univ. Ramon Y Cajal

🇪🇸

Madrid, Spain

Hosp. Univ. 12 de Octubre

🇪🇸

Madrid, Spain

Clinica Univ. de Navarra

🇪🇸

Pamplona, Spain

Hosp. Virgen Del Rocio

🇪🇸

Sevilla, Spain

Hosp. Clinico Univ. de Valencia

🇪🇸

Valencia, Spain

Sahlgrenska University Hospital

🇸🇪

Goteborg, Sweden

Skanes universitetssjukhus

🇸🇪

Lund, Sweden

Sodersjukhuset

🇸🇪

Stockholm, Sweden

Adana City Hospital

🇹🇷

Adana, Turkey

Institut Jules Bordet

🇧🇪

Anderlecht, Belgium

Universitair Ziekenhuis Antwerpen

🇧🇪

Edegem, Belgium

AZ Maria Middelares

🇧🇪

Gent, Belgium

Huizhou Central People's Hospital

🇨🇳

Huizhou, China

St. Bernard's Medical Center

🇺🇸

Jonesboro, Arkansas, United States

CBCC Global Research

🇺🇸

Bakersfield, California, United States

Cancer and Blood Specialty Clinic

🇺🇸

Los Alamitos, California, United States

USC Norris Comprehensive Cancer Center

🇺🇸

Los Angeles, California, United States

Providence Medical Foundation

🇺🇸

Santa Rosa, California, United States

Torrance Memorial Physicians Network

🇺🇸

Torrance, California, United States

Yale University School Of Medicine

🇺🇸

New Haven, Connecticut, United States

Georgetown Univ Medical Center Lombardi Cancer Center

🇺🇸

Washington, District of Columbia, United States

Grady Memorial Hospital

🇺🇸

Atlanta, Georgia, United States

Winship Cancer Institute Emory University

🇺🇸

Atlanta, Georgia, United States

Fort Wayne Medical Oncology & Hematology

🇺🇸

Fort Wayne, Indiana, United States

MedStar Franklin Square Medical Center

🇺🇸

Baltimore, Maryland, United States

Hattiesburg Clinic

🇺🇸

Hattiesburg, Mississippi, United States

Washington University School Of Medicine

🇺🇸

Saint Louis, Missouri, United States

Nebraska Cancer Specialists Midwest Cancer Center

🇺🇸

Omaha, Nebraska, United States

Comprehensive Cancer Centers of Nevada

🇺🇸

Las Vegas, Nevada, United States

Astera Cancer Care

🇺🇸

East Brunswick, New Jersey, United States

B P Poddar Hospital and Medical research Limited

🇮🇳

Kolkata, India

Hosp. de La Santa Creu I Sant Pau

🇪🇸

Barcelona, Spain

Hopital de Jolimont

🇧🇪

Haine Saint Paul La Louviere, Belgium

Cleveland Clinic Cancer Center Mansfield

🇺🇸

Mansfield, Ohio, United States

Rutgers Cancer Institute

🇺🇸

New Brunswick, New Jersey, United States

University of New Mexico Cancer Center

🇺🇸

Albuquerque, New Mexico, United States

Mount Sinai

🇺🇸

New York, New York, United States

Herbert Irving Comprehensive Cancer Center Columbia University Medical Center

🇺🇸

New York, New York, United States

New York Cancer and Blood Specialists

🇺🇸

Shirley, New York, United States

University of North Carolina at Chapel Hill

🇺🇸

Chapel Hill, North Carolina, United States

Cleveland Clinic Cancer Center Fairview Hospital Moll Pavilion

🇺🇸

Cleveland, Ohio, United States

Taussig Cancer Insititute Cleveland Clinic

🇺🇸

Cleveland, Ohio, United States

Cleveland Clinic Cancer Center Independence Family Health Center

🇺🇸

Independence, Ohio, United States

Cleveland Clinic Cancer Center Hillcrest Hospital

🇺🇸

Mayfield Heights, Ohio, United States

Cleveland Clinic Cancer Centers Sandusky

🇺🇸

Sandusky, Ohio, United States

Cleveland Clinic Cancer Center Strongsville

🇺🇸

Strongsville, Ohio, United States

Cleveland Clinic Cancer Center South Pointe Hospital

🇺🇸

Warrensville Heights, Ohio, United States

Wooster Milltown Specialty and Surgery Center

🇺🇸

Wooster, Ohio, United States

Fox Chase Cancer Center

🇺🇸

Philadelphia, Pennsylvania, United States

MD Anderson Cancer Center

🇺🇸

Houston, Texas, United States

Baylor Scott and White Health

🇺🇸

Temple, Texas, United States

Swedish Cancer Institute

🇺🇸

Seattle, Washington, United States

Az Groeninge

🇧🇪

Kortrijk, Belgium

Universitair Ziekenhuis Leuven

🇧🇪

Leuven, Belgium

Fundacao Pio XII

🇧🇷

Barretos, Brazil

Fundacao Universidade de Caxias do Sul

🇧🇷

Caxias do Sul, Brazil

Hospital Santa Izabel Santa Casa de Misericordia da Bahia

🇧🇷

Salvador, Brazil

Clinica de Hematologia e Oncologia Viver Ltda

🇧🇷

Santa Maria, Brazil

Fundacao Faculdade Regional De Medicina S Jose Rio Preto Hospital De Base

🇧🇷

Sao Jose do Rio Preto, Brazil

Fundacao Antonio Prudente A C Camargo Cancer Center

🇧🇷

Sao Paulo, Brazil

Associacao Feminina de Educacao e Combate ao Cancer Hospital Santa Rita de Cassia

🇧🇷

Vitoria, Brazil

Arthur J E Child Comprehensive Cancer Centre

🇨🇦

Calgary, Alberta, Canada

Ottawa Hospital

🇨🇦

Ottawa, Ontario, Canada

Princess Margaret Cancer Centre

🇨🇦

Toronto, Ontario, Canada

Peking University First Hospital

🇨🇳

Beijing, China

Beijing Friendship Hospital Capital Medical University

🇨🇳

Beijing, China

Beijing Cancer Hospital

🇨🇳

Beijing, China

Peking University Third Hospital

🇨🇳

Beijing, China

The First Bethune Hospital of Jilin University

🇨🇳

Changchun, China

Klinikum der Universitaet Muenchen

🇩🇪

Munich, Germany

The Sixth Affiliated Hospital Sun Yat sen University

🇨🇳

Guangzhou, China

Guangdong Provincial People's Hospital

🇨🇳

Guangzhou, China

The First Affiliated Hospital Zhejiang University College of Medicine

🇨🇳

Hangzhou, China

The Second Affiliated Hospital of Zhejiang University College of Medicine

🇨🇳

Hangzhou, China

Zhejiang Cancer Hospital

🇨🇳

Hangzhou, China

The First Affiliated Hospital of NanChang University

🇨🇳

Nanchang, China

Fudan University Shanghai Cancer Center

🇨🇳

Shanghai, China

Peking University Shenzhen Hospital

🇨🇳

Shenzhen, China

West China Hospital of Sichuan University

🇨🇳

Sichuan, China

First Hospital of Shanxi Medical University

🇨🇳

Taiyuan, China

Tianjin Medical University Cancer Institute and Hospital

🇨🇳

Tianjin, China

Hubei Cancer Hospital

🇨🇳

Wuhan, China

Institut Sainte Catherine

🇫🇷

Avignon Cedex 9, France

Hopital Claude Huriez

🇫🇷

Lille, France

Hopital Prive Jean Mermoz

🇫🇷

Lyon, France

Institut du Cancer de Montpellier

🇫🇷

Montpellier, France

CHU Nantes

🇫🇷

Nantes Cedex 1, France

Hopital Saint Antoine

🇫🇷

Paris, France

Hopital Haut Leveque

🇫🇷

Pessac, France

CHU De Poitiers

🇫🇷

Poitiers Cedex, France

Gustave Roussy

🇫🇷

Villejuif, France

Charite Universitatsmedizin Berlin Campus Virchow Klinikum

🇩🇪

Berlin, Germany

Universitaetsklinikum Carl Gustav Carus TU Dresden

🇩🇪

Dresden, Germany

Essen University Hospital

🇩🇪

Essen, Germany

Krankenhaus NorthWest

🇩🇪

Frankfurt am Main, Germany

Praxis fur interdisziplinare Onkologie & Hamatologie GbR

🇩🇪

Freiburg, Germany

Asklepios Klinik Altona

🇩🇪

Hamburg, Germany

Markhot Ferenc Oktatokorhaz es Rendelointezet

🇭🇺

Eger, Hungary

Pecsi Tudomanyegyetem

🇭🇺

Pecs, Hungary

Rajiv Gandhi Cancer Institute and Research Centre

🇮🇳

Delhi, India

Tata Memorial Hospital

🇮🇳

Mumbai, India

Deenanath Mangeshkar Hospital and Research Centre

🇮🇳

Pune, India

Yitzhak Shamir Medical Center

🇮🇱

Beer Yaakov, Israel

Rambam Medical Center

🇮🇱

Haifa, Israel

Hadassah University Hospita Ein Kerem

🇮🇱

Jerusalem, Israel

Rabin Medical Center

🇮🇱

Petah Tikva, Israel

Sheba Medical Center

🇮🇱

Ramat Gan, Israel

Tel Aviv Sourasky Medical Center

🇮🇱

Tel Aviv Yafo, Israel

Assuta MC

🇮🇱

Tel Aviv Yafo, Israel

Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori

🇮🇹

Meldola, Italy

Istituto Dei Tumori Di Milano

🇮🇹

Milano, Italy

Istituto Oncologico Veneto - IRCCS

🇮🇹

Padova, Italy

National Cancer Center Hospital

🇯🇵

Chuo Ku, Japan

National Cancer Center Hospital East

🇯🇵

Kashiwa, Japan

Aichi Cancer Center

🇯🇵

Nagoya Shi, Japan

Osaka International Cancer Institute

🇯🇵

Osaka City, Japan

National Hospital Organization Osaka National Hospital

🇯🇵

Osaka-Shi, Japan

Shizuoka Cancer Center

🇯🇵

Shizuoka, Japan

Osaka University Hospital

🇯🇵

Suita, Japan

The Cancer Institute Hospital of JFCR

🇯🇵

Tokyo, Japan

Kyungpook National University Chilgok Hospital

🇰🇷

Daegu, Korea, Republic of

Seoul National University Hospital

🇰🇷

Seoul, Korea, Republic of

Severance Hospital Yonsei University Health System

🇰🇷

Seoul, Korea, Republic of

Asan Medical Center

🇰🇷

Seoul, Korea, Republic of

Samsung Medical Center

🇰🇷

Seoul, Korea, Republic of

The Catholic University of Korea Seoul St Marys Hospital

🇰🇷

Seoul, Korea, Republic of

National Cancer Institute

🇲🇾

Putrajaya, Malaysia

Meander Medisch Centrum

🇳🇱

Amersfoort, Netherlands

Radboud University Medical Center

🇳🇱

Nijmegen, Netherlands

Erasmus MC

🇳🇱

Rotterdam, Netherlands

Elisabeth-TweeSteden Ziekenhuis

🇳🇱

Tilburg, Netherlands

Wojewodzki Szpital Specjalistyczny

🇵🇱

Biala Podlaska, Poland

Bialostockie Centrum Onkologii im Marii Sklodowskiej Curie w Bialymstoku

🇵🇱

Bialystok, Poland

Szpital Specjalistyczny w Brzozowie Podkarpacki Osrodek Onkologiczny im Ks B Markiewicza

🇵🇱

Brzozow, Poland

Uniwersyteckie Centrum Kliniczne

🇵🇱

Gdansk, Poland

Narodowy Instytut Onkologii im Marii Sklodowskiej Curie Panstwowy Instytut BadawczyOddz w Gliwicach

🇵🇱

Gliwice, Poland

Instytut Centrum Zdrowia Matki Polki

🇵🇱

Lodz, Poland

SPZOZ Ministerstwa Spraw Wewnetrznych z Warminsko Mazurskim Centrum Onkologii w Olsztynie

🇵🇱

Olsztyn, Poland

SPZOZ Opolskie Centrum Onkologii im. Prof. Tadeusza Koszarowskiego

🇵🇱

Opole, Poland

Centrum Onkologii - Instytut im. Marii Sklodowskiej-Curie

🇵🇱

Warszawa, Poland

Pan American Center for Oncology Trials LLC

🇵🇷

Barrio Monacillos, Puerto Rico

Karolinska Universitetssjukhuset

🇸🇪

Stockholm, Sweden

Uppsala University

🇸🇪

Uppsala, Sweden

Kaohsiung Medical University Chung Ho Memorial Hospital

🇨🇳

Kaohsiung, Taiwan

Kaohsiung Chang Gung Memorial Hospital

🇨🇳

Kaohsiung, Taiwan

National Cheng Kung University Hospital

🇨🇳

Tainan, Taiwan

National Taiwan University Hospital

🇨🇳

Taipei, Taiwan

Linkou Chang Gung Memorial Hospital

🇨🇳

Taoyuan, Taiwan

Gulhane Egitim ve Arastirma Hastanesi

🇹🇷

Ankara, Turkey

Dr Abdurrahman Yurtaslan Oncology Training and Research Hospital

🇹🇷

Ankara, Turkey

Gazi University Hospital

🇹🇷

Ankara, Turkey

Bakirkoy Training and Research Hospital

🇹🇷

Istanbul, Turkey

Marmara University Pendik Training Hospital

🇹🇷

İstanbul, Turkey

Necmettin Erbakan University Meram Medical Faculty

🇹🇷

Konya, Turkey

Sakarya University Training and Research Hospital

🇹🇷

Sakarya, Turkey

Addenbrooke's Hospital

🇬🇧

Cambridge, United Kingdom

Western General Hospital

🇬🇧

Edinburgh, United Kingdom

Castle Hill Hospital

🇬🇧

Hull, United Kingdom

St James University Hospital

🇬🇧

Leeds, United Kingdom

St Bartholomew's Hospital

🇬🇧

London, United Kingdom

University College Hospital

🇬🇧

London, United Kingdom

Mount Vernon Cancer Centre

🇬🇧

Northwood, United Kingdom

Royal Marsden Hospital (Sutton)

🇬🇧

Sutton, United Kingdom

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