Translating Evidence into Practice: Primary Cutaneous Melanoma Guidelines. Sentinel Lymph Node Biopsy

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American Academy of Dermatology 2018 Annual Meeting San Diego, CA, February 17, 2018 Translating Evidence into Practice: Primary Cutaneous Melanoma Guidelines. Sentinel Lymph Node Biopsy Christopher Bichakjian, MD Professor of Dermatology Chief, Division of Cutaneous Surgery and Oncology Director, Multidisciplinary Melanoma Program Michigan Medicine, University of Michigan

Disclosures I do not have any relationships with industry Member, National Comprehensive Cancer Network (NCCN), Melanoma Clinical Practice Guidelines

2011 Guidelines of Care for Melanoma The Dark Ages

Sentinel Lymph Node Biopsy AAD recommendations Impact AJCC 8 th Ed staging Contrast with current NCCN guidelines Future/new role of SLNB

Sentinel Lymph Node Biopsy Sentinel Lymph Node Afferent Lymphatic Vessel Primary Melanoma

Sentinel Lymph Node Biopsy AAD: Status of SLN is most important prognostic indicator for disease-specific survival in patients with primary cutaneous melanoma. Bichakjian CK, et al. J Am Acad Dermatol. 2011;65:1032-47

Melanoma-specific Survival by SLN Status MSLT-I 85.1±1.5% 62.1±4.8% HR 3.09 (95% CI 2.21-4.49) Gershenwald JE, et al. J Clin Oncol. 1999;17:976-83, Morton DL, et al. N Engl J Med. 2014;370(7):599-609

While there is interest in newer prognostic molecular techniques such as gene expression profiling to differentiate melanomas at low versus high risk for metastasis, routine (baseline) prognostic genetic testing of primary cutaneous melanomas (before or following sentinel lymph node biopsy [SLNB]) is not recommended outside of a clinical study (trial).

2011 AAD Guidelines of Care Sentinel Lymph Node Biopsy (SLNB) for Primary Cutaneous Melanoma Tis/T1a, SLNB is not recommended T1b 0.76-1.00 mm thickness, discuss SLNB T1b 0.75 mm thickness, SLNB should not be considered unless other adverse parameters in addition to ulceration and mitotic rate are present, such as angiolymphatic invasion, positive deep margin, or young age > 1.o mm thickness, SLNB should be considered Bichakjian CK, et al. J Am Acad Dermatol. 2011;65:1032-47

8 th Edition AJCC T-Classification T Class. Thickness (mm) Ulceration Status Stage (cn0) SLN Positivity Stage (pn0) T1 < 0.8 a - without ulceration IA <5% IA T1 < 0.8 0.8 1.0 T2 >1.0 2.0 b - with ulceration b w/ or w/o ulceration a - without ulceration b - with ulceration IB 5-10% IA IB 10% IB IIA IIA T3 >2.0 4.0 a - without ulceration b - with ulceration IIA IIB IIA IIB T4 > 4.0 a - without ulceration b - with ulceration IIB IIC IIB IIC Amin, M.B., Edge, S.B., Greene, F.L., et al. (Eds.) AJCC Cancer Staging Manual. 8th Ed. New York: Springer; 2017

Transition to risk based recommendations If risk of positive sentinel lymph node is: <5%, NCCN does not recommend SLNB Clinical stage IA, T1a, without other adverse features, including positive deep margin. 5-10%, NCCN recommends discussing and considering SLNB Clinical stage IB, T1b (or T1a with adverse features) 10%, NCCN recommends discussing and offering SLNB

Indication for Sentinel Lymph Node Biopsy for Cutaneous Melanoma in 2018 Prognosis Consider additional surgery (completion lymph node dissection) DeCOG-SLT MSLT-2 Consider adjuvant systemic therapy

Multicenter Selective Lymphadenectomy Trial-II

Multicenter Selective Lymphadenectomy Trial-II 1934 patients with nodal metastasis determined by pathological assessment or RT-PCR (~12%) Randomized to completion lymph node dissection (CLND) vs active nodal basin surveillance Clinical and ultrasound exam q4 mos x yrs 1-2; q6 mos yrs 3-5 46.6% trunk, 39.7% extremities, 13.7% head and neck Immediate completion lymph node dissection: Increased rate of regional disease control Provided prognostic information (non-sentinel node positivity) Did not increase melanoma-specific survival

MSLT-II Considerations Tumor burden bias Location morbidity of nodal recurrence Reliability of active nodal basin surveillance Prognostic information (stage IIIA) Adjuvant systemic therapy separate discussion