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Tumor-Infiltrating Lymphocyte Therapy or Ipilimumab in Advanced Melanoma

Authors :
Maartje W. Rohaan
Troels H. Borch
Joost H. van den Berg
Özcan Met
Rob Kessels
Marnix H. Geukes Foppen
Joachim Stoltenborg Granhøj
Bastiaan Nuijen
Cynthia Nijenhuis
Inge Jedema
Maaike van Zon
Saskia Scheij
Jos H. Beijnen
Marten Hansen
Carlijn Voermans
Inge M. Noringriis
Tine J. Monberg
Rikke B. Holmstroem
Lidwina D.V. Wever
Marloes van Dijk
Lindsay G. Grijpink-Ongering
Ludy H.M. Valkenet
Alejandro Torres Acosta
Matthias Karger
Jessica S.W. Borgers
Renske M.T. ten Ham
Valesca P. Retèl
Wim H. van Harten
Ferry Lalezari
Harm van Tinteren
Astrid A.M. van der Veldt
Geke A.P. Hospers
Marion A.M. Stevense-den Boer
Karijn P.M. Suijkerbuijk
Maureen J.B. Aarts
Djura Piersma
Alfons J.M. van den Eertwegh
Jan-Willem B. de Groot
Gerard Vreugdenhil
Ellen Kapiteijn
Marye J. Boers-Sonderen
W. Edward Fiets
Franchette W.P.J. van den Berkmortel
Eva Ellebaek
Lisbet R. Hölmich
Alexander C.J. van Akkooi
Winan J. van Houdt
Michel W.J.M. Wouters
Johannes V. van Thienen
Christian U. Blank
Aafke Meerveld-Eggink
Sebastian Klobuch
Sofie Wilgenhof
Ton N. Schumacher
Marco Donia
Inge Marie Svane
John B.A.G. Haanen
Guided Treatment in Optimal Selected Cancer Patients (GUTS)
Medical Biochemistry
CCA - Cancer Treatment and Quality of Life
AII - Cancer immunology
Landsteiner Laboratory
General Internal Medicine
Health Technology & Services Research
Health Technology Assessment (HTA)
Medical Oncology
Erasmus MC other
Surgery
Interne Geneeskunde
MUMC+: MA Medische Oncologie (9)
RS: GROW - R3 - Innovative Cancer Diagnostics & Therapy
Source :
New England Journal of Medicine, 387(23), 2113-2125. MASSACHUSETTS MEDICAL SOC, The New England Journal of Medicine, 387, 2113-2125, New England journal of medicine, 387(23), 2113-2125. Massachussetts Medical Society, Rohaan, M W, Borch, T H, Van Den Berg, J H, Met, Ö, Kessels, R, Geukes Foppen, M H, Stoltenborg Granhøj, J, Nuijen, B, Nijenhuis, C, Jedema, I, Van Zon, M, Scheij, S, Beijnen, J H, Hansen, M, Voermans, C, Noringriis, I M, Monberg, T J, Holmstroem, R B, Wever, L D V, Van Dijk, M, Grijpink-Ongering, L G, Valkenet, L H M, Torres Acosta, A, Karger, M, Borgers, J S W, Ten Ham, R M T, Retèl, V P, Van Harten, W H, Lalezari, F, Van Tinteren, H, Van Der Veldt, A A M, Hospers, G A P, Stevense-Den Boer, M A M, Suijkerbuijk, K P M, Aarts, M J B, Piersma, D, Van Den Eertwegh, A J M, De Groot, J W B, Vreugdenhil, G, Kapiteijn, E, Boers-Sonderen, M J, Fiets, W E, Van Den Berkmortel, F W P J, Ellebaek, E, Hölmich, L R, Van Akkooi, A C J, Van Houdt, W J, Wouters, M W J M, Van Thienen, J V, Blank, C U, Meerveld-Eggink, A, Klobuch, S, Wilgenhof, S, Schumacher, T N, Donia, M, Svane, I M & Haanen, J B A G 2022, ' Tumor-Infiltrating Lymphocyte Therapy or Ipilimumab in Advanced Melanoma. ', New England Journal of Medicine, vol. 387, no. 23, pp. 2113-2125 . https://doi.org/10.1056/NEJMoa2210233, The New England journal of medicine, 387(23), 2113-2125. Massachussetts Medical Society, New England Journal of Medicine, 387(23), 2113-2125. MASSACHUSETTS MEDICAL SOCIETY, The New England Journal of Medicine, 387, 23, pp. 2113-2125
Publication Year :
2022
Publisher :
MASSACHUSETTS MEDICAL SOC, 2022.

Abstract

Item does not contain fulltext BACKGROUND: Immune checkpoint inhibitors and targeted therapies have dramatically improved outcomes in patients with advanced melanoma, but approximately half these patients will not have a durable benefit. Phase 1-2 trials of adoptive cell therapy with tumor-infiltrating lymphocytes (TILs) have shown promising responses, but data from phase 3 trials are lacking to determine the role of TILs in treating advanced melanoma. METHODS: In this phase 3, multicenter, open-label trial, we randomly assigned patients with unresectable stage IIIC or IV melanoma in a 1:1 ratio to receive TIL or anti-cytotoxic T-lymphocyte antigen 4 therapy (ipilimumab at 3 mg per kilogram of body weight). Infusion of at least 5×10(9) TILs was preceded by nonmyeloablative, lymphodepleting chemotherapy (cyclophosphamide plus fludarabine) and followed by high-dose interleukin-2. The primary end point was progression-free survival. RESULTS: A total of 168 patients (86% with disease refractory to anti-programmed death 1 treatment) were assigned to receive TILs (84 patients) or ipilimumab (84 patients). In the intention-to-treat population, median progression-free survival was 7.2 months (95% confidence interval [CI], 4.2 to 13.1) in the TIL group and 3.1 months (95% CI, 3.0 to 4.3) in the ipilimumab group (hazard ratio for progression or death, 0.50; 95% CI, 0.35 to 0.72; P

Details

Language :
English
ISSN :
15334406 and 00284793
Volume :
387
Issue :
23
Database :
OpenAIRE
Journal :
New England Journal of Medicine
Accession number :
edsair.doi.dedup.....edf28a71e5a16116e2b0f59cdac9485a