Cefiderocol versus standard therapy for hospital-acquired and health-care-associated Gram-negative bacterial bloodstream infection (the GAME CHANGER trial): an open-label, parallel-group, randomised trial - 07/10/25

Doi : 10.1016/S1473-3099(25)00469-4

David L Paterson, ProfFRACP ^a,^b,^c,⁎ , Helmi Sulaiman, MBBS ^d, Po-Yu Liu, MD ^e, Mark D Chatfield, MSc ^c, Mesut Yilmaz, ProfMD ^f,^af, Zeti Norfidiyati Salmuna, MPath ^g,^ac, Mohd Zulfakar Mazlan, MMed ^h,^ac, Siriluck Anunnatsiri, MD ⁱ, Rujipas Sirijatuphat, MD ^j,^ad, Darunee Chotiprasitsakul, MD ^k,^ae, David C Lye, ProfMBBS ^l,^am,^an,^ao, Jyoti Somani, MD ^m,^p, Shirin Kalimuddin, MBBS MPH ^q,^r, Abdullah T Aslan, MBBS ^c, Visanu Thamlikitkul, ProfMD ^j,^ad, Yi-Tzu Lee, ProfPhD ^s,^t, Ya-Sung Yang, ProfMD ^u,^v, Yi-Tsung Lin, PhD ^w,^x, Wan Nurliyana Wan Ramli, BAO ^y, Chien-Hao Tseng, MD ^e, Sophia Archuleta, MD ^m,^p, Yvonne Fu Zi Chan, MRCP ^q, Brian M Forde, PhD ^c,^z, Hugh Wright, FRACP ^aa, Adam G Stewart, FRACP ^c, Kay A Ramsay, PhD ^c, Weiping Ling, PhD ^a, Vicki Rossi, BSN ^c, Tiffany M Harris-Brown, MPH ^c, Patrick N A Harris, PhD ^a,^b,^c,^aa,^ab
on behalf of the
GAME CHANGER Trial Investigators^{^†}
Members listed at the end of the Article
^a ADVANCE-ID, Saw Swee Hock School of Public Health, National University of Singapore, Singapore
^b Infectious Diseases Translational Research Programme, Yong Loo Lin School of Medicine, National University of Singapore, Singapore
^c University of Queensland Centre for Clinical Research, The University of Queensland, Brisbane, QLD, Australia
^d Department of Medicine, Infectious Diseases Unit, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia
^e Division of Infectious Diseases, Taichung Veterans General Hospital, Taichung, Taiwan
^f Department of Infectious Diseases and Clinical Microbiology, School of Medicine, Istanbul Medipol University, Istanbul, Türkiye
^g Department of Medical Microbiology and Parasitology, School of Medical Sciences, Universiti Sains Malaysia, Kota Bharu, Malaysia
^h Department of Anaesthesiology and Intensive Care, School of Medical Sciences, Universiti Sains Malaysia, Kota Bharu, Malaysia
ⁱ Department of Medicine, Division of Infectious Diseases and Tropical Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand
^j Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand
^k Department of Medicine, Division of Infectious Diseases, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand
^l Department of Infectious Diseases, Tan Tock Seng Hospital, Singapore
^m Yong Loo Lin School of Medicine, National University of Singapore, Singapore
ⁿ Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore
^o Department of Infectious Diseases, National Centre for Infectious Diseases, Singapore
^p Department of Medicine, Division of Infectious Diseases, National University Hospital, Singapore
^q Department of Infectious Diseases, Singapore General Hospital, Singapore
^r Programme in Emerging Infectious Diseases, Duke–National University of Singapore Medical School, Singapore
^s Department of Emergency Medicine, Taipei Veterans General Hospital, Taipei, Taiwan
^t Faculty of Medicine, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan
^u Department of Internal Medicine, Division of Infectious Diseases and Tropical Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan
^v Institute of Preventive Medicine, National Defense Medical Center, Taipei, Taiwan
^w Department of Medicine, Division of Infectious Diseases, Taipei Veterans General Hospital, Taipei, Taiwan
^x Institute of Emergency and Critical Care Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan
^y Department of Internal Medicine, Kulliyyah of Medicine, International Islamic University Malaysia, Gambang, Malaysia
^z Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, Australia
^aa Department of Infectious Disease, Royal Brisbane & Women’s Hospital, Brisbane, QLD, Australia
^ab Pathology Queensland, Central Microbiology, Royal Brisbane & Women’s Hospital, Brisbane, QLD, Australia
^ac Department of Internal Medicine, School of Medical Sciences, Universiti Sains Malaysia, Kota Bharu, Kelantan, Malaysia
^ad Department of Research, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand
^ae Microbiology Laboratory, Department of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand
^af School of Medicine, Istanbul Medipol University, Istanbul, Türkiye

^*Correspondence to: Prof David L Paterson, ADVANCE-ID, Saw Swee Hock School of Public Health, National University of Singapore, Singapore 117549ADVANCE-IDSaw Swee Hock School of Public HealthNational University of Singapore117549Singapore

Sous presse. Épreuves corrigées par l'auteur. Disponible en ligne depuis le Tuesday 07 October 2025

Summary

Background

Bloodstream infections caused by bacteria with carbapenem resistance are associated with high mortality. Cefiderocol has broad in vitro activity against carbapenem-resistant Gram-negative bacilli. We aimed to assess whether cefiderocol was non-inferior or superior to standard-of-care antibiotics in preventing mortality in patients with bloodstream infection caused by Gram-negative bacilli.

Methods

The GAME CHANGER trial was an open-label, parallel-group, randomised clinical trial in which patients with health-care-associated or hospital-acquired Gram-negative bloodstream infection were recruited from 17 tertiary hospitals with more than 500 beds in Australia, Malaysia, Singapore, Taiwan, Thailand, and Türkiye. Adult patients (aged ≥21 years in Singapore or ≥18 years elsewhere) with positive blood cultures and Gram-negative bacilli seen on Gram stain were eligible. Participants were randomly assigned in a 1:1 ratio to cefiderocol (2 g intravenously every 8 h) or standard of care (chosen by the patient’s clinical team) using an online randomisation tool with strata defined by severity of comorbidities and region, with random permuted blocks of unequal size. Patients, treating clinicians, and site investigators were not masked to treatment. The primary outcome was all-cause mortality at 14 days after randomisation. All outcomes were analysed in participants who received at least one dose of assigned antibiotic, grew an aerobic Gram-negative bacillus from the index blood culture, and did not withdraw consent before day 14. The non-inferiority margin was 10%; superiority was to be assessed if non-inferiority was shown, and was evaluated in both the main analysis population and in patients with at least one carbapenem-resistant organism causing bloodstream infection. Missing data were handled by imputing data. The trial was registered on ClinicalTrials.gov (NCT03869437) and is closed to new participants.

Findings

513 participants were enrolled between Nov 12, 2019, and Oct 31, 2023 (210 [42%] female and 294 [58%] male). 256 patients were randomly assigned to cefiderocol and 257 were assigned to standard of care. Nine patients (six in the cefiderocol group and three in the standard-of-care group) were excluded from further analysis because they withdrew consent or their blood cultures did not grow an aerobic Gram-negative bacillus. Thus, 504 participants were included in the main analysis population. 20 (8%) of 250 patients in the cefiderocol group had died at 14 days compared with 17 (7%) of 254 patients in the standard-of-care group (absolute risk difference 1%, 95% CI –3 to 6). 127 (25%) of 504 patients had an infection with a carbapenem-resistant organism; at 14 days, nine (14%) of 64 patients in the cefiderocol group had died compared with six (10%) of 63 patients in the standard-of-care group (5%, –7 to 16). There were five treatment-emergent serious adverse events that were either probably or possibly related to the study drug (all in the cefiderocol group): delirium, stupor, rigors, abnormal liver chemistry, and rash, all of which resolved without treatment (except for the rash, which required hydrocortisone and anti-histamines).

Interpretation

Among patients with a hospital-acquired or health-care-associated Gram-negative bloodstream infection, cefiderocol resulted in non-inferior 14-day mortality compared with standard of care. Adverse events were similar between groups, although those thought to be related to the study drug only occurred in the cefiderocol group. In both the main analysis population and the carbapenem-resistant subset, cefiderocol was not superior to standard of care. This evidence suggests that cefiderocol is efficacious in patients with health-care-associated Gram-negative bloodstream infection who are at high risk of antibiotic resistance, but more evidence is required to define its efficacy when carbapenem-resistant organisms are the cause.