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Outcomes with adjuvant anti-PD-1 therapy in patients with sentinel lymph node-positive melanoma without completion lymph node dissection.
Eroglu, Zeynep; Broman, Kristy K; Thompson, John F; Nijhuis, Amanda; Hieken, Tina J; Kottschade, Lisa; Farma, Jeffrey M; Hotz, Meghan; Deneve, Jeremiah; Fleming, Martin; Bartlett, Edmund K; Sharma, Avinash; Dossett, Lesly; Hughes, Tasha; Gyorki, David E; Downs, Jennifer; Karakousis, Giorgos; Song, Yun; Lee, Ann; Berman, Russell S; van Akkooi, Alexander; Stahlie, Emma; Han, Dale; Vetto, John; Beasley, Georgia; Farrow, Norma E; Hui, Jane Yuet Ching; Moncrieff, Marc; Nobes, Jenny; Baecher, Kirsten; Perez, Matthew; Lowe, Michael; Ollila, David W; Collichio, Frances A; Bagge, Roger Olofsson; Mattsson, Jan; Kroon, Hidde M; Chai, Harvey; Teras, Jyri; Sun, James; Carr, Michael J; Tandon, Ankita; Babacan, Nalan Akgul; Kim, Younchul; Naqvi, Mahrukh; Zager, Jonathan; Khushalani, Nikhil I.
Afiliação
  • Eroglu Z; Department of Cutaneous Oncology, Moffitt Cancer Center, Tampa, Florida, USA zeynep.eroglu@moffitt.org.
  • Broman KK; University of South Florida, Tampa, Florida, USA.
  • Thompson JF; Department of Cutaneous Oncology, Moffitt Cancer Center, Tampa, Florida, USA.
  • Nijhuis A; University of South Florida, Tampa, Florida, USA.
  • Hieken TJ; Melanoma Institute Australia, North Sydney, New South Wales, Australia.
  • Kottschade L; Melanoma Institute Australia, North Sydney, New South Wales, Australia.
  • Farma JM; Department of Surgery, Mayo Clinic, Rochester, New York, USA.
  • Hotz M; Department of Surgery, Mayo Clinic, Rochester, New York, USA.
  • Deneve J; Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania, USA.
  • Fleming M; Department of Surgical Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania, USA.
  • Bartlett EK; Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
  • Sharma A; Department of Surgery, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
  • Dossett L; Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Hughes T; Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Gyorki DE; Department of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
  • Downs J; Department of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
  • Karakousis G; Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
  • Song Y; Division of Cancer Surgery, Peter MacCallum Cancer Centre, Melbourne, Victoria, Australia.
  • Lee A; Department of Surgery, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Berman RS; Department of Surgery, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • van Akkooi A; Department of Surgery, New York University, New York, New York, USA.
  • Stahlie E; Department of Surgery, New York University, New York, New York, USA.
  • Han D; Department of Surgical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Vetto J; Department of Surgical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Beasley G; Division of Surgical Oncology, Oregon Health and Science University, Portland, Oregon, USA.
  • Farrow NE; Division of Surgical Oncology, Oregon Health and Science University, Portland, Oregon, USA.
  • Hui JYC; Department of Surgery, Duke University, Durham, North Carolina, USA.
  • Moncrieff M; Department of Surgery, Duke University, Durham, North Carolina, USA.
  • Nobes J; Department of Surgery, University of Minnesota, Minneapolis, Minnesota, USA.
  • Baecher K; Norfolk and Norwich University Hospital, Norwich, UK.
  • Perez M; Norfolk and Norwich University Hospital, Norwich, UK.
  • Lowe M; Department of Surgery, Emory University, Atlanta, Georgia, USA.
  • Ollila DW; Department of Surgery, Emory University, Atlanta, Georgia, USA.
  • Collichio FA; Department of Surgery, Emory University, Atlanta, Georgia, USA.
  • Bagge RO; Department of Surgery, University of North Carolina, Chapel Hill, North Carolina, USA.
  • Mattsson J; Department of Medicine, University of North Carolina, Chapel Hill, North Carolina, USA.
  • Kroon HM; Department of Surgery, Sahlgrenska Center for Cancer Research, University of Gothenburg, Gothenburg, Sweden.
  • Chai H; Department of Surgery, Sahlgrenska Center for Cancer Research, University of Gothenburg, Gothenburg, Sweden.
  • Teras J; Department of Surgery, Royal Adelaide Hospital, University of Adelaide, Adelaide, South Australia, Australia.
  • Sun J; Department of Surgery, Royal Adelaide Hospital, University of Adelaide, Adelaide, South Australia, Australia.
  • Carr MJ; North Estonia Medical Centre Foundation, Tallinn, Estonia.
  • Tandon A; Department of Cutaneous Oncology, Moffitt Cancer Center, Tampa, Florida, USA.
  • Babacan NA; Department of Cutaneous Oncology, Moffitt Cancer Center, Tampa, Florida, USA.
  • Kim Y; University of South Florida, Tampa, Florida, USA.
  • Naqvi M; Department of Cutaneous Oncology, Moffitt Cancer Center, Tampa, Florida, USA.
  • Zager J; Department of Biostatistics and Bioinformatics, Moffitt Cancer Center, Tampa, Florida, USA.
  • Khushalani NI; Department of Biostatistics and Bioinformatics, Moffitt Cancer Center, Tampa, Florida, USA.
J Immunother Cancer ; 10(8)2022 08.
Article em En | MEDLINE | ID: mdl-36002183
ABSTRACT
Until recently, most patients with sentinel lymph node-positive (SLN+) melanoma underwent a completion lymph node dissection (CLND), as mandated in published trials of adjuvant systemic therapies. Following multicenter selective lymphadenectomy trial-II, most patients with SLN+ melanoma no longer undergo a CLND prior to adjuvant systemic therapy. A retrospective analysis of clinical outcomes in SLN+ melanoma patients treated with adjuvant systemic therapy after July 2017 was performed in 21 international cancer centers. Of 462 patients who received systemic adjuvant therapy, 326 patients received adjuvant anti-PD-1 without prior immediate (IM) CLND, while 60 underwent IM CLND. With median follow-up of 21 months, 24-month relapse-free survival (RFS) was 67% (95% CI 62% to 73%) in the 326 patients. When the patient subgroups who would have been eligible for the two adjuvant anti-PD-1 clinical trials mandating IM CLND were analyzed separately, 24-month RFS rates were 64%, very similar to the RFS rates from those studies. Of these no-CLND patients, those with SLN tumor deposit >1 mm, stage IIIC/D and ulcerated primary had worse RFS. Of the patients who relapsed on adjuvant anti-PD-1, those without IM CLND had a higher rate of relapse in the regional nodal basin than those with IM CLND (46% vs 11%). Therefore, 55% of patients who relapsed without prior CLND underwent surgery including therapeutic lymph node dissection (TLND), with 30% relapsing a second time; there was no difference in subsequent relapse between patients who received observation vs secondary adjuvant therapy. Despite the increased frequency of nodal relapses, adjuvant anti-PD-1 therapy may be as effective in SLN+ pts who forego IM CLND and salvage surgery with TLND at relapse may be a viable option for these patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Linfonodo Sentinela / Melanoma Tipo de estudo: Observational_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Linfonodo Sentinela / Melanoma Tipo de estudo: Observational_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article