MedPath

A Study of Amivantamab and FOLFIRI Versus Cetuximab/Bevacizumab and FOLFIRI in Participants With KRAS/NRAS and BRAF Wild-type Colorectal Cancer Who Have Previously Received Chemotherapy

Registration Number
NCT06750094
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) and and the length of time until a participant dies (overall survival), when treated with amivantamab and chemotherapy with 5-fluorouracil, leucovorin calcium (folinic acid) or levoleucovorin, and irinotecan hydrochloride (FOLFIRI) versus either cetuximab or bevacizumab and FOLFIRI given to participants with Kirsten rat sarcoma viral oncogene/ neuroblastoma RAS viral oncogene homolog (KRAS/ NRAS) and v-raf murine sarcoma viral oncogene homolog B (BRAF) wild-type recurrent, unresectable or metastatic colorectal cancer who have previously received chemotherapy.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
700
Inclusion Criteria
  • Have histologically or cytologically confirmed adenocarcinoma of the colon or rectum. Participants must have recurrent, unresectable or metastatic disease
  • Be diagnosed to have KRAS, NRAS, and BRAF wild-type (WT) tumor as determined by local testing
  • Must agree to the submission of fresh or archival tumor tissue post-progression from the most recent therapy, if clinically feasible
  • Have measurable disease according to RECIST v1.1
  • Have an eastern cooperative oncology group (ECOG) performance status (PS) of 0 or 1
  • Participant must have received 1 line of systemic therapy (fluoropyrimidine-based and oxaliplatin-based) for metastatic colorectal cancer (mCRC), with documented radiographic disease progression on or after this line of therapy
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: amivantamab, cetuximab or bevacizumab or 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 who has not received immunotherapy treatments
  • Participant with known human epidermal growth factor receptor 2 (HER2)- positive/amplified tumor
  • Has prior exposure to irinotecan, 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 A: Amivantamab + FOLFIRIAmivantamabParticipants will receive amivantamab along with FOLFIRI (consisting of 5-fluorouracil, leucovorin calcium \[folinic acid\] or levoleucovorin, and irinotecan) as a chemotherapy regimen 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 + FOLFIRI5-fluorouracilParticipants will receive amivantamab along with FOLFIRI (consisting of 5-fluorouracil, leucovorin calcium \[folinic acid\] or levoleucovorin, and irinotecan) as a chemotherapy regimen 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 + FOLFIRIIrinotecanParticipants will receive amivantamab along with FOLFIRI (consisting of 5-fluorouracil, leucovorin calcium \[folinic acid\] or levoleucovorin, and irinotecan) as a chemotherapy regimen 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 or Bevacizumab + FOLFIRICetuximabParticipants will receive either cetuximab or bevacizumab along with FOLFIRI as a chemotherapy regimen 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 or Bevacizumab + FOLFIRIBevacizumabParticipants will receive either cetuximab or bevacizumab along with FOLFIRI as a chemotherapy regimen 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 or Bevacizumab + FOLFIRI5-fluorouracilParticipants will receive either cetuximab or bevacizumab along with FOLFIRI as a chemotherapy regimen 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 or Bevacizumab + FOLFIRILeucovorin calcium/LevoleucovorinParticipants will receive either cetuximab or bevacizumab along with FOLFIRI as a chemotherapy regimen 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 or Bevacizumab + FOLFIRIIrinotecanParticipants will receive either cetuximab or bevacizumab along with FOLFIRI as a chemotherapy regimen 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 + FOLFIRILeucovorin calcium/LevoleucovorinParticipants will receive amivantamab along with FOLFIRI (consisting of 5-fluorouracil, leucovorin calcium \[folinic acid\] or levoleucovorin, and irinotecan) as a chemotherapy regimen 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 2 years 1 month

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.

Overall Survival (OS)Up to 4 years 4 months

OS is defined as the time from the date of randomization to the date of participant's death due to any cause.

Secondary Outcome Measures
NameTimeMethod
Progression Free Survival After Subsequent Therapy (PFS2)Up to 4 years 4 months

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

Objective Response Rate as Assessed by InvestigatorUp to 4 years 4 months

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

Objective Response Rate (ORR) as Assessed by BICRUp to 4 years 4 months

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

Progression Free Survival as Assessed by InvestigatorUp to 4 years 4 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 investigator.

Duration of Response (DoR) as Assessed by BICRUp to 4 years 4 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.

Duration of Response as Assessed by InvestigatorUp to 4 years 4 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 investigator.

Disease Control Rate (DCR) as Assessed by BICRUp to 4 years 4 months

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

Disease Control Rate as Assessed by InvestigatorUp to 4 years 4 months

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

Time to Treatment FailureUp to 4 years 4 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 4 years 4 months

Curative resection (R0) rate is defined as the percentage of randomized participants who underwent curative surgery.

Number of Participants with Adverse Events (AEs) by SeverityUp to 4 years 4 months

An AE is any untoward medical occurrence in a participant administered a pharmaceutical (investigational or non investigational) product. An AE does not necessarily have a causal relationship with the treatment. Severity of AEs will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) v5.0. by using standard grades as follows: Grade 1: Mild; asymptomatic or mild symptoms; Grade 2: Moderate; minimal, local or noninvasive intervention indicated; Grade 3: Severe 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 4 years 4 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 4 years 4 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 4 years 4 months

Time to worsening in symptoms and functioning as measured by EORTC QLQ-C30 score will be reported. 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.

Change From Baseline in European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C29) ScoreFrom baseline up to 4 years 4 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-C29 ScoreUp to 4 years 4 months

Time to worsening in symptoms and functioning as measured by EORTC QLQ-CR29 will be reported. 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. Change from baseline in the EORTC QLQ-CR29 score will be reported.

Overall Side Effect Burden as Measured by European Organisation for Research and Treatment of Cancer (EORTC) Item 168 Scale ScoreUp to 4 years 4 months

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 indicates severe symptoms.

Trial Locations

Locations (168)

Assuta MC

🇮🇱

Tel Aviv, Israel

Jolimont

🇧🇪

Haine Saint Paul La Louviere, Belgium

Az Groeninge

🇧🇪

Kortrijk, Belgium

Universitair Ziekenhuis Leuven

🇧🇪

Leuven, Belgium

Fundacao Pio XII

🇧🇷

Barretos, Brazil

Fundacao Universidade de Caxias do Sul

🇧🇷

Caxias do Sul, Brazil

Fundacao Doutor Amaral Carvalho

🇧🇷

Jau, Brazil

Hospital Santa Izabel Santa Casa de Misericordia da Bahia

🇧🇷

Salvador, 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

Peking University First Hospital

🇨🇳

Beijing, China

Centrul Medical Unirea SRL

🇷🇴

Brasov, Romania

Hosp. Clinico Univ. de Valencia

🇪🇸

Valencia, Spain

Istituto Dei Tumori Di Milano

🇮🇹

Milano, Italy

Ironwood Cancer and Research Center

🇺🇸

Chandler, Arizona, United States

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

University of Colorado Denver Anschultz Medical Campus

🇺🇸

Aurora, Colorado, United States

Eastern Connecticut Hematology & Oncology Assoc.

🇺🇸

Norwich, Connecticut, United States

Mount Sinai Medical Center Campus

🇺🇸

Miami Beach, Florida, United States

AdventHealth Cancer Institute

🇺🇸

Orlando, Florida, United States

Grady Memorial Hospital

🇺🇸

Atlanta, Georgia, United States

Winship Cancer Institute Emory University

🇺🇸

Atlanta, Georgia, United States

Mary Bird Perkins Cancer Center

🇺🇸

Baton Rouge, Louisiana, United States

MedStar Franklin Square Medical Center

🇺🇸

Baltimore, Maryland, United States

Cancer And Hematology Centers of Western Michigan PC

🇺🇸

Grand Rapids, Michigan, United States

Hattiesburg Clinic

🇺🇸

Hattiesburg, Mississippi, United States

Washington University School Of Medicine

🇺🇸

Saint Louis, Missouri, United States

Nebraska Cancer Specialists

🇺🇸

Omaha, Nebraska, United States

Astera Cancer Care

🇺🇸

East Brunswick, New Jersey, United States

New York Cancer and Blood Specialists

🇺🇸

Shirley, New York, United States

Fox Chase Cancer Center

🇺🇸

Philadelphia, Pennsylvania, United States

Tennessee Oncology

🇺🇸

Nashville, Tennessee, United States

MD Anderson Cancer Center

🇺🇸

Houston, Texas, United States

Scott And White Memorial Hospital

🇺🇸

Temple, Texas, United States

Providence Regional Cancer System

🇺🇸

Lacey, Washington, United States

Concord Hospital

🇦🇺

Concord, Australia

Warringal Private Hospital

🇦🇺

Heidelberg, Australia

Queen Elizabeth Hospital

🇦🇺

South Woodville, Australia

Western Health Sunshine Hospital

🇦🇺

St Albans, Australia

Institut Jules Bordet

🇧🇪

Anderlecht, Belgium

UZ Antwerpen

🇧🇪

Edegem, Belgium

AZ Maria Middelares

🇧🇪

Gent, Belgium

Beijing Friendship Hospital Capital Medical University

🇨🇳

Beijing, China

Beijing Cancer Hospital

🇨🇳

Beijing, China

West China Hospital of Sichuan University

🇨🇳

Chengdu, China

Ganzhou Cancer Hospital

🇨🇳

Ganzhou, China

Sun Yat Sen University Cancer Center

🇨🇳

Guangzhou, China

The Sixth Affiliated Hospital Sun Yat sen University

🇨🇳

Guangzhou, China

Guangdong Provincial People's Hospital

🇨🇳

Guangzhou, China

The Second Affiliated Hospital of Zhejiang University

🇨🇳

Hangzhou, China

Zhejiang Cancer Hospital

🇨🇳

Hangzhou, China

Huizhou Central People's Hospital

🇨🇳

Huizhou, China

Gansu Provincial Cancer Hospital

🇨🇳

Lanzhou, China

The First Affiliated Hospital of NanChang University

🇨🇳

Nanchang, China

Fudan University Shanghai Cancer Center

🇨🇳

Shanghai, China

Tianjin Medical University Cancer Institute and Hospital

🇨🇳

Tianjin, China

Hubei Cancer Hospital

🇨🇳

Wuhan, China

Institut Sainte Catherine

🇫🇷

Avignon Cedex 9, France

Hopital Haut Leveque

🇫🇷

Pessac, France

CHU De Poitiers

🇫🇷

Poitiers Cedex, France

Charite Universitatsmedizin Berlin Campus Virchow Klinikum

🇩🇪

Berlin, Germany

Krankenhaus NorthWest

🇩🇪

Frankfurt am Main, Germany

Klinikum der Universitaet Muenchen

🇩🇪

Munich, Germany

Prince Of Wales Hospital

🇭🇰

Shatin, Hong Kong

Markhot Ferenc Oktatokorhaz es Rendelointezet

🇭🇺

Eger, Hungary

Pecsi Tudomanyegyetem

🇭🇺

Pecs, Hungary

Rajiv Gandhi Cancer Institute and Research Centre

🇮🇳

Delhi, India

Asian Institute Of Gastroenterology

🇮🇳

Hyderabad, India

B P Poddar Hospital and Medical research Limited

🇮🇳

Kolkata, India

Tata Memorial Hospital

🇮🇳

Mumbai, India

Deenanath Mangeshkar Hospital and Research Centre

🇮🇳

Pune, India

Christian medical

🇮🇳

Vellore, India

Yitzhak Shamir Medical Center

🇮🇱

Beer Yaakov, Israel

Rambam Medical Center

🇮🇱

Haifa, Israel

Hadassah Medical Center

🇮🇱

Jerusalem, Israel

Rabin Medical Center

🇮🇱

Petach Tikva, Israel

Sheba Medical Center

🇮🇱

Ramat Gan, Israel

Tel Aviv Sourasky Medical Center

🇮🇱

Tel Aviv Yafo, Israel

Istituto Oncologico Veneto - IRCCS

🇮🇹

Padova, Italy

Azienda Ospedaliero Universitaria Pisana

🇮🇹

Pisa, Italy

Istituto Clinico Humanitas

🇮🇹

Rozzano, Italy

Azienda Sanitaria Universitaria Friuli Centrale ASU FC

🇮🇹

Udine, Italy

Chiba Cancer Center

🇯🇵

Chiba, Japan

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

Kindai University Hospital

🇯🇵

Osaka Sayama shi, Japan

National Hospital Organization Osaka National Hospital

🇯🇵

Osaka-Shi, Japan

Osaka University Hospital

🇯🇵

Suita-shi, Japan

The Cancer Institute Hospital of JFCR

🇯🇵

Tokyo, Japan

Kyungpook National University Chilgok Hospital

🇰🇷

Daegu, Korea, Republic of

Korea University Anam Hospital

🇰🇷

Seoul, 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 Mary s Hospital

🇰🇷

Seoul, Korea, Republic of

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

Institut Kanser Negara Clinical Research Center

🇲🇾

Putrajaya, Malaysia

Centro Oncologico de Chihuahua

🇲🇽

Chihuahua, Mexico

Centro Oncologico Personalizado Cope S De R L De C V

🇲🇽

Ciudad de Mexico, Mexico

Actualidad Basada En La Investigacion Del Cancer

🇲🇽

Guadalajara, Mexico

Oncocenter

🇲🇽

Puebla, Mexico

Cuidados Oncologicos

🇲🇽

Queretaro, Mexico

Health Pharma Queretaro SA de CV

🇲🇽

Queretaro, Mexico

Meander Medisch Centrum

🇳🇱

Amersfoort, Netherlands

Radboud University Medical Center

🇳🇱

Nijmegen, Netherlands

Erasmus MC

🇳🇱

Rotterdam, Netherlands

ETZ TweeSteden

🇳🇱

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

Narodowy Instytut Onkologii im Marii Sklodowskiej Curie Panstwowy Instytut Badawczy

🇵🇱

Warszawa, Poland

Pan American Center for Oncology Trials LLC

🇵🇷

San Juan, Puerto Rico

Ponderas Academic Hospital

🇷🇴

Bucuresti, Romania

Clinica de Oncologie Sf Nectarie

🇷🇴

Craiova, Romania

Hosp. de La Santa Creu I Sant Pau

🇪🇸

Barcelona, Spain

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

Sahlgrenska Universitetssjukhuset

🇸🇪

Gothenburg, Sweden

Skanes universitetssjukhus

🇸🇪

Lund, Sweden

Sodersjukhuset

🇸🇪

Stockholm, Sweden

Karolinska Universitetssjukhuset

🇸🇪

Stockholm, Sweden

Uppsala University

🇸🇪

Uppsala, Sweden

Chang Gung Memorial Hospital

🇨🇳

Kaohsiung City, Taiwan

Kaohsiung Medical University Chung Ho Memorial Hospital

🇨🇳

Kaohsiung, Taiwan

Taichung Veterans General Hospital

🇨🇳

Taichung, Taiwan

National Cheng Kung University Hospital

🇨🇳

Tainan, Taiwan

National Taiwan University Hospital

🇨🇳

Taipei, Taiwan

Taipei Veterans General Hospital

🇨🇳

Taipei, Taiwan

Linkou Chang Gung Memorial Hospital

🇨🇳

Taoyuan, Taiwan

Ramathibodi Hospital

🇹🇭

Bangkok, Thailand

Siriraj Hospital

🇹🇭

Bangkok, Thailand

Chiang Mai University

🇹🇭

Chiang Mai, Thailand

Songklanagarind hospital

🇹🇭

Songkhla, Thailand

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

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

Royal Marsden Hospital

🇬🇧

London, United Kingdom

Mount Vernon Cancer Centre

🇬🇧

Northwood, United Kingdom

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