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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00007775naa a2200985 4500
001oai:lup.lub.lu.se:770bbf34-e18f-4407-803a-7a3c439a7090
003SwePub
008170811s2017 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/770bbf34-e18f-4407-803a-7a3c439a70902 URI
024a https://doi.org/10.1056/NEJMoa16132102 DOI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Faries, B.u Saint John's Health Center4 aut
2451 0a Completion dissection or observation for sentinel-node metastasis in melanoma
264 1c 2017
300 a 12 s.
520 a BACKGROUND Sentinel-lymph-node biopsy is associated with increased melanoma-specific survival (i.e., survival until death from melanoma) among patients with node-positive intermediatethickness melanomas (1.2 to 3.5 mm). The value of completion lymph-node dissection for patients with sentinel-node metastases is not clear. METHODS In an international trial, we randomly assigned patients with sentinel-node metastases detected by means of standard pathological assessment or a multimarker molecular assay to immediate completion lymph-node dissection (dissection group) or nodal observation with ultrasonography (observation group). The primary end point was melanoma-specific survival. Secondary end points included disease-free survival and the cumulative rate of nonsentinel-node metastasis. RESULTS Immediate completion lymph-node dissection was not associated with increased melanomaspecific survival among 1934 patients with data that could be evaluated in an intention-Totreat analysis or among 1755 patients in the per-protocol analysis. In the per-protocol analysis, the mean (-SE) 3-year rate of melanoma-specific survival was similar in the dissection group and the observation group (86-1.3% and 86-1.2%, respectively; P = 0.42 by the logrank test) at a median follow-up of 43 months. The rate of disease-free survival was slightly higher in the dissection group than in the observation group (68-1.7% and 63-1.7%, respectively; P = 0.05 by the log-rank test) at 3 years, based on an increased rate of disease control in the regional nodes at 3 years (92-1.0% vs. 77-1.5%; P<0.001 by the log-rank test); these results must be interpreted with caution. Nonsentinel-node metastases, identified in 11.5% of the patients in the dissection group, were a strong, independent prognostic factor for recurrence (hazard ratio, 1.78; P = 0.005). Lymphedema was observed in 24.1% of the patients in the dissection group and in 6.3% of those in the observation group. CONCLUSIONS Immediate completion lymph-node dissection increased the rate of regional disease control and provided prognostic information but did not increase melanoma-specific survival among patients with melanoma and sentinel-node metastases.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Cancer och onkologi0 (SwePub)302032 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Cancer and Oncology0 (SwePub)302032 hsv//eng
700a Thompson, J. F.u University of California, Los Angeles4 aut
700a Cochran, Alistair J.u Jonsson Comprehensive Cancer Center4 aut
700a Andtbacka, R. H.u Huntsman Cancer Institute4 aut
700a Mozzillo, Nicolau Saint John's Health Center4 aut
700a Zager, J. S.u H. Lee Moffitt Cancer Center & Research Institute4 aut
700a Jahkola, Tiinau Helsinki University Central Hospital4 aut
700a Bowles, T. L.u Intermountain Medical Center4 aut
700a Testori, Au European Institute of Oncology4 aut
700a Beitsch, P. D.u Dallas Surgical Group4 aut
700a Hoekstra, H Ju University Medical Center Groningen4 aut
700a Moncrieff, M.u Norfolk and Norwich University Hospital NHS Trust4 aut
700a Ingvar, C.u Lund University,Lunds universitet,Kirurgi, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Lunds Melanomstudiegrupp,Forskargrupper vid Lunds universitet,Surgery (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine,Lund Melanoma Study Group,Lund University Research Groups,Skåne University Hospital4 aut0 (Swepub:lu)kir-cin
700a Wouters, M. W. J. M.u Netherlands Cancer Institute4 aut
700a Sabel, M. S.u University of Michigan4 aut
700a Levine, E. A.u Wake Forest University4 aut
700a Agnese, D.u Ohio State University4 aut
700a Henderson, Mu Peter MacCallum Cancer Centre4 aut
700a Dummer, R.u University of Zurich4 aut
700a Rossi-Alvarez, Cu University of Padova4 aut
700a Neves, R. I.u Penn State Hershey Cancer Institute4 aut
700a Trocha, S. D.u Saint Louis University School of Medicine4 aut
700a Wright, Alan Fu Tom Baker Cancer Centre4 aut
700a Byrd, D. R.u University of Washington4 aut
700a Matter, M.u Lausanne University Hospital4 aut
700a Hsueh, E.u Tom Baker Cancer Centre4 aut
700a MacKenzie-Ross, A.u Guy's and St Thomas' NHS Foundation Trust4 aut
700a Johnson, D. B.4 aut
700a Terheyden, P.u University Medical Center Schleswig-Holstein4 aut
700a Berger, A. C.u Thomas Jefferson University4 aut
700a Huston, T. L.u Sunnybrook Health Sciences Centre4 aut
700a Wayne, J. D.u Vanderbilt University4 aut
700a Smithers, B. M.u Princess Alexandra Hospital4 aut
700a Neuman, H. B.u Fox Chase Cancer Center4 aut
700a Schneebaum, S.u Greenville Health System Cancer Center (GHS)4 aut
700a Gershenwald, Jeffrey Eu Klinikum Nürnberg4 aut
700a Ariyan, C. E.u Stony Brook University4 aut
700a Desai, D. C.u St. Luke's University Health Network4 aut
700a Jacobs, L. L.u Memorial Sloan-Kettering Cancer Center4 aut
700a McMasters, K. M.u Roswell Park Cancer Institute4 aut
700a Gesierich, A.u Northwestern University4 aut
700a Hersey, Pu University of Wisconsin-Madison4 aut
700a Bines, S. D.u Rush University Medical Center Chicago4 aut
700a Kane, J. M.u Tel Aviv Sourasky Medical Center – Ichilov Hospital4 aut
700a Barth, R. J.u Dartmouth-Hitchcock Medical Center4 aut
700a McKinnon, G.u Johns Hopkins University School of Medicine4 aut
700a Farma, J. M.u University of Louisville4 aut
700a Schultz, E.u Hospital Clínic of Barcelona4 aut
700a Vidal-Sicart, Sergiu Anderson Medical Center4 aut
700a Hoefer, R. A.u Dartmouth-Hitchcock Medical Center4 aut
700a Lewis, Melanie J.u Sentara CarePlex Hospital4 aut
700a Scheri, R.u Newcastle Melanoma Unit4 aut
700a Kelley, M. C.u Istituto Nazionale Tumori IRCCS - Fondazione G Pascale, Napoli4 aut
700a Nieweg, Omgo E.u University of Sydney4 aut
700a Noyes, R. D.u Huntsman Cancer Institute4 aut
700a Hoon, Dave S. B.u Saint John's Health Center4 aut
700a Wang, H. J.u University of California, Los Angeles4 aut
700a Elashoff, D. A.u University of California, Los Angeles4 aut
700a Elashoff, R. M.u University of California, Los Angeles4 aut
710a Saint John's Health Centerb University of California, Los Angeles4 org
773t New England Journal of Medicineg 376:23, s. 2211-2222q 376:23<2211-2222x 0028-4793
856u http://dx.doi.org/10.1056/NEJMoa1613210y FULLTEXT
8564 8u https://lup.lub.lu.se/record/770bbf34-e18f-4407-803a-7a3c439a7090
8564 8u https://doi.org/10.1056/NEJMoa1613210

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