Sentinel Lymph Node Biopsy for Melanoma: American Society of Clinical Oncology and Society of Surgical Oncology Joint Clinical Practice Guideline
The American Society of Clinical Oncology (ASCO) and Society of Surgical Oncology (SSO) sought to provide an evidence-based guideline on the use of lymphatic mapping and sentinel lymph node (SLN) biopsy in staging patients with newly diagnosed melanoma. A comprehensive systematic review of the liter...
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Published in | Journal of clinical oncology Vol. 30; no. 23; pp. 2912 - 2918 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Alexandria, VA
American Society of Clinical Oncology
10.08.2012
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Subjects | |
Online Access | Get full text |
ISSN | 0732-183X 1527-7755 1527-7755 |
DOI | 10.1200/JCO.2011.40.3519 |
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Abstract | The American Society of Clinical Oncology (ASCO) and Society of Surgical Oncology (SSO) sought to provide an evidence-based guideline on the use of lymphatic mapping and sentinel lymph node (SLN) biopsy in staging patients with newly diagnosed melanoma.
A comprehensive systematic review of the literature published from January 1990 through August 2011 was completed using MEDLINE and EMBASE. Abstracts from ASCO and SSO annual meetings were included in the evidence review. An Expert Panel was convened to review the evidence and develop guideline recommendations.
Seventy-three studies met full eligibility criteria. The evidence review demonstrated that SLN biopsy is an acceptable method for lymph node staging of most patients with newly diagnosed melanoma.
SLN biopsy is recommended for patients with intermediate-thickness melanomas (Breslow thickness, 1 to 4 mm) of any anatomic site; use of SLN biopsy in this population provides accurate staging. Although there are few studies focusing on patients with thick melanomas (T4; Breslow thickness, > 4 mm), SLN biopsy may be recommended for staging purposes and to facilitate regional disease control. There is insufficient evidence to support routine SLN biopsy for patients with thin melanomas (T1; Breslow thickness, < 1 mm), although it may be considered in selected patients with high-risk features when staging benefits outweigh risks of the procedure. Completion lymph node dissection (CLND) is recommended for all patients with a positive SLN biopsy and achieves good regional disease control. Whether CLND after a positive SLN biopsy improves survival is the subject of the ongoing Multicenter Selective Lymphadenectomy Trial II. |
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AbstractList | The American Society of Clinical Oncology (ASCO) and Society of Surgical Oncology (SSO) sought to provide an evidence-based guideline on the use of lymphatic mapping and sentinel lymph node (SLN) biopsy in staging patients with newly diagnosed melanoma.PURPOSEThe American Society of Clinical Oncology (ASCO) and Society of Surgical Oncology (SSO) sought to provide an evidence-based guideline on the use of lymphatic mapping and sentinel lymph node (SLN) biopsy in staging patients with newly diagnosed melanoma.A comprehensive systematic review of the literature published from January 1990 through August 2011 was completed using MEDLINE and EMBASE. Abstracts from ASCO and SSO annual meetings were included in the evidence review. An Expert Panel was convened to review the evidence and develop guideline recommendations.METHODSA comprehensive systematic review of the literature published from January 1990 through August 2011 was completed using MEDLINE and EMBASE. Abstracts from ASCO and SSO annual meetings were included in the evidence review. An Expert Panel was convened to review the evidence and develop guideline recommendations.Seventy-three studies met full eligibility criteria. The evidence review demonstrated that SLN biopsy is an acceptable method for lymph node staging of most patients with newly diagnosed melanoma.RESULTSSeventy-three studies met full eligibility criteria. The evidence review demonstrated that SLN biopsy is an acceptable method for lymph node staging of most patients with newly diagnosed melanoma.SLN biopsy is recommended for patients with intermediate-thickness melanomas (Breslow thickness, 1 to 4 mm) of any anatomic site; use of SLN biopsy in this population provides accurate staging. Although there are few studies focusing on patients with thick melanomas (T4; Breslow thickness, > 4 mm), SLN biopsy may be recommended for staging purposes and to facilitate regional disease control. There is insufficient evidence to support routine SLN biopsy for patients with thin melanomas (T1; Breslow thickness, < 1 mm), although it may be considered in selected patients with high-risk features when staging benefits outweigh risks of the procedure. Completion lymph node dissection (CLND) is recommended for all patients with a positive SLN biopsy and achieves good regional disease control. Whether CLND after a positive SLN biopsy improves survival is the subject of the ongoing Multicenter Selective Lymphadenectomy Trial II.RECOMMENDATIONSSLN biopsy is recommended for patients with intermediate-thickness melanomas (Breslow thickness, 1 to 4 mm) of any anatomic site; use of SLN biopsy in this population provides accurate staging. Although there are few studies focusing on patients with thick melanomas (T4; Breslow thickness, > 4 mm), SLN biopsy may be recommended for staging purposes and to facilitate regional disease control. There is insufficient evidence to support routine SLN biopsy for patients with thin melanomas (T1; Breslow thickness, < 1 mm), although it may be considered in selected patients with high-risk features when staging benefits outweigh risks of the procedure. Completion lymph node dissection (CLND) is recommended for all patients with a positive SLN biopsy and achieves good regional disease control. Whether CLND after a positive SLN biopsy improves survival is the subject of the ongoing Multicenter Selective Lymphadenectomy Trial II. The American Society of Clinical Oncology (ASCO) and Society of Surgical Oncology (SSO) sought to provide an evidence-based guideline on the use of lymphatic mapping and sentinel lymph node (SLN) biopsy in staging patients with newly diagnosed melanoma. A comprehensive systematic review of the literature published from January 1990 through August 2011 was completed using MEDLINE and EMBASE. Abstracts from ASCO and SSO annual meetings were included in the evidence review. An Expert Panel was convened to review the evidence and develop guideline recommendations. Seventy-three studies met full eligibility criteria. The evidence review demonstrated that SLN biopsy is an acceptable method for lymph node staging of most patients with newly diagnosed melanoma. SLN biopsy is recommended for patients with intermediate-thickness melanomas (Breslow thickness, 1 to 4 mm) of any anatomic site; use of SLN biopsy in this population provides accurate staging. Although there are few studies focusing on patients with thick melanomas (T4; Breslow thickness, > 4 mm), SLN biopsy may be recommended for staging purposes and to facilitate regional disease control. There is insufficient evidence to support routine SLN biopsy for patients with thin melanomas (T1; Breslow thickness, < 1 mm), although it may be considered in selected patients with high-risk features when staging benefits outweigh risks of the procedure. Completion lymph node dissection (CLND) is recommended for all patients with a positive SLN biopsy and achieves good regional disease control. Whether CLND after a positive SLN biopsy improves survival is the subject of the ongoing Multicenter Selective Lymphadenectomy Trial II. |
Author | R. Dirk Noyes Charles M. Balch Theodore Y. Kim Sandra L. Wong Sanjiv S. Agarwala Matias E. Valsecchi Timothy J. Akhurst Gary H. Lyman Patricia Hurley Donald L. Weaver Lynn M. Schuchter Janice N. Cormier Mark Gorman Alistair Cochran Kelly M. McMasters |
Author_xml | – sequence: 1 givenname: Sandra L. surname: Wong fullname: Wong, Sandra L. organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria – sequence: 2 givenname: Charles M. surname: Balch fullname: Balch, Charles M. organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria – sequence: 3 givenname: Patricia surname: Hurley fullname: Hurley, Patricia organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria – sequence: 4 givenname: Sanjiv S. surname: Agarwala fullname: Agarwala, Sanjiv S. organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria – sequence: 5 givenname: Timothy J. surname: Akhurst fullname: Akhurst, Timothy J. organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria – sequence: 6 givenname: Alistair surname: Cochran fullname: Cochran, Alistair organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria – sequence: 7 givenname: Janice N. surname: Cormier fullname: Cormier, Janice N. organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria – sequence: 8 givenname: Mark surname: Gorman fullname: Gorman, Mark organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria – sequence: 9 givenname: Theodore Y. surname: Kim fullname: Kim, Theodore Y. organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria – sequence: 10 givenname: Kelly M. surname: McMasters fullname: McMasters, Kelly M. organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria – sequence: 11 givenname: R. Dirk surname: Noyes fullname: Noyes, R. Dirk organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria – sequence: 12 givenname: Lynn M. surname: Schuchter fullname: Schuchter, Lynn M. organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria – sequence: 13 givenname: Matias E. surname: Valsecchi fullname: Valsecchi, Matias E. organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria – sequence: 14 givenname: Donald L. surname: Weaver fullname: Weaver, Donald L. organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria – sequence: 15 givenname: Gary H. surname: Lyman fullname: Lyman, Gary H. organization: Sandra L. Wong, University of Michigan, Ann Arbor, MI; Charles M. Balch, University of Texas Southwestern, Dallas; Janice N. Cormier, University of TexasMDAnderson Cancer Center, Houston, TX; Patricia Hurley, American Society of Clinical Oncology, Alexandria, VA; Sanjiv S. Agarwala, St Luke's Cancer Center, Bethlehem; Lynn M. Schuchter, University of Pennsylvania; Matias E. Valsecchi, Thomas Jefferson University, Philadelphia, PA; Timothy J. Akhurst, Peter MacCallum Cancer Institute, Melbourne, Victoria |
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Cites_doi | 10.1097/00008390-199508000-00008 10.1111/j.1610-0387.2007.06569.x 10.1038/jid.2009.328 10.1245/ASO.2003.03.055 10.1200/JCO.2001.19.16.3635 10.1016/j.jaad.2008.09.067 10.1200/JCO.2001.19.16.3622 10.1097/00008390-199412000-00009 10.1245/s10434-011-1979-6 10.1016/S0140-6736(08)61033-8 10.1002/jso.21876 10.1001/archsurg.2010.115 10.1200/JCO.2010.33.1884 10.1016/j.yasu.2007.05.015 10.6004/jnccn.2009.0023 10.1007/BF02574479 10.1200/JCO.1999.17.3.976 10.1245/ASO.2004.03.044 10.1001/archsurg.1989.01410090061014 10.1002/jso.20084 10.1002/cncr.24660 10.1245/ASO.2006.03.058 10.1056/NEJMoa060992 10.1245/ASO.2003.10.001 10.1200/JCO.2009.23.4799 10.1097/01.sla.0000181092.50141.fa 10.1007/s10434-000-0160-4 10.1200/JCO.2009.27.1627 10.1002/(SICI)1097-0142(19981015)83:8<1664::AID-CNCR23>3.0.CO;2-G 10.1007/BF02574492 10.2105/AJPH.86.4.538 10.1245/ASO.2006.02.021 10.1245/s10434-009-0836-3 10.1046/j.1445-2197.2003.02748.x 10.1097/00000658-199412000-00009 |
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Title | Sentinel Lymph Node Biopsy for Melanoma: American Society of Clinical Oncology and Society of Surgical Oncology Joint Clinical Practice Guideline |
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