TY - JOUR
T1 - Active surveillance of patients who have sentinel node positive melanoma
T2 - An international, multi-institution evaluation of adoption and early outcomes after the Multicenter Selective Lymphadenectomy Trial II (MSLT-2)
AU - Broman, Kristy Kummerow
AU - Hughes, Tasha
AU - Dossett, Lesly
AU - Sun, James
AU - Kirichenko, Dennis
AU - Carr, Michael J.
AU - Sharma, Avinash
AU - Bartlett, Edmund K.
AU - Nijhuis, Amanda A.G.
AU - Thompson, John F.
AU - Hieken, Tina J.
AU - Kottschade, Lisa
AU - Downs, Jennifer
AU - Gyorki, David E.
AU - Stahlie, Emma
AU - van Akkooi, Alexander
AU - Ollila, David W.
AU - Frank, Jill
AU - Song, Yun
AU - Karakousis, Giorgos
AU - Moncrieff, Marc
AU - Nobes, Jenny
AU - Vetto, John
AU - Han, Dale
AU - Farma, Jeffrey M.
AU - Deneve, Jeremiah L.
AU - Fleming, Martin D.
AU - Perez, Matthew C.
AU - Lowe, Michael C.
AU - Olofsson Bagge, Roger
AU - Mattsson, Jan
AU - Lee, Ann Y.
AU - Berman, Russell S.
AU - Chai, Harvey
AU - Kroon, Hidde M.
AU - Teras, Juri
AU - Teras, Roland M.
AU - Farrow, Norma E.
AU - Beasley, Georgia
AU - Hui, Jane Yuet Ching
AU - Been, Lukas
AU - Kruijff, Schelto
AU - Kim, Youngchul
AU - Naqvi, Syeda Mahrukh Hussnain
AU - Sarnaik, Amod A.
AU - Sondak, Vernon K.
AU - Zager, Jonathan S.
N1 - Funding Information:
John F. Thompson reports personal fees from Bristol‐Meyers Squibb Australia and Merck Sharp & Dohme Australia and personal fees and travel support from GlaxoSmithKline and Provectus Inc, outside the submitted work. Tina J. Hieken reports grants from Genentech, outside the submitted work. David E. Gyorki reports personal fees from Amgen, outside the submitted work. Alexander van Akkooi reports grants and personal fees from Amgen, Bristol‐Myers Squibb, and Novartis; and personal fees from 4SC, Merck‐Pfizer, MSD‐Merck, and Sanofi, outside the submitted work. Jeffrey M. Farma reports personal fees from Novartis and Delcath, outside the submitted work. Roger Olofsson Bagge reports grants from Astra Zeneca and personal fees from Amgen, BD/Bard, Bristol‐Myers Squibb, Merck Sharp & Dohme, Novartis, Roche, and Sanofi Genzyme, outside the submitted work. Georgia Beasley reports grants form Istari Oncology and personal fees from Sanofi‐Regeneron, outside the submitted work. Amod A. Sarnaik reports grants from Provectus Inc and grants and personal fees from Iovance Biotherapeutics, outside the submitted work. Vernon K. Sondak reports personal fees from Array, Bristol‐Myers Squibb, Genentech/Roche, Merck, Novartis, Regeneron, Replimune, Pfizer, and Polynoma, outside the submitted work. Jonathan S. Zager reports grants from Amgen, Delcath Systems, Philogen, and Provectus; grants and personal fees from Castle Biosciences and Novartis, and personal fees from Array Biopharma, Merck, and Sun Pharma, outside the submitted work. The remaining authors made no disclosures.
Funding Information:
This work was supported in part by the Biostatistics and Bioinformatics Shared Resource at the H. Lee Moffitt Cancer Center and Research Institute, a National Cancer Institute‐designated comprehensive cancer center (P30‐CA076292).
Publisher Copyright:
© 2021 American Cancer Society
PY - 2021/7/1
Y1 - 2021/7/1
N2 - Background: For patients with sentinel lymph node (SLN)-positive cutaneous melanoma, the Second Multicenter Selective Lymphadenectomy trial demonstrated equivalent disease-specific survival (DSS) with active surveillance using nodal ultrasound versus completion lymph node dissection (CLND). Adoption and outcomes of active surveillance in clinical practice and in adjuvant therapy recipients are unknown. Methods: In a retrospective cohort of SLN-positive adults treated at 21 institutions in Australia, Europe, and the United States from June 2017 to November 2019, the authors evaluated the impact of active surveillance and adjuvant therapy on all-site recurrence-free survival (RFS), isolated nodal RFS, distant metastasis-free survival (DMFS), and DSS using Kaplan-Meier curves and Cox proportional hazard models. Results: Among 6347 SLN biopsies, 1154 (18%) were positive and had initial negative distant staging. In total, 965 patients (84%) received active surveillance, 189 (16%) underwent CLND. Four hundred thirty-nine patients received adjuvant therapy (surveillance, 38%; CLND, 39%), with the majority (83%) receiving anti–PD-1 immunotherapy. After a median follow-up of 11 months, 220 patients developed recurrent disease (surveillance, 19%; CLND, 22%), and 24 died of melanoma (surveillance, 2%; CLND, 4%). Sixty-eight patients had an isolated nodal recurrence (surveillance, 6%; CLND, 4%). In patients who received adjuvant treatment without undergoing prior CLND, all isolated nodal recurrences were resectable. On risk-adjusted multivariable analyses, CLND was associated with improved isolated nodal RFS (hazard ratio [HR], 0.36; 95% CI, 0.15-0.88), but not all-site RFS (HR, 0.68; 95% CI, 0.45-1.02). Adjuvant therapy improved all-site RFS (HR, 0.52; 95% CI, 0.47-0.57). DSS and DMFS did not differ by nodal management or adjuvant treatment. Conclusions: Active surveillance has been adopted for most SLN-positive patients. At initial assessment, real-world outcomes align with randomized trial findings, including in adjuvant therapy recipients. Lay Summary: For patients with melanoma of the skin and microscopic spread to lymph nodes, monitoring with ultrasound is an alternative to surgically removing the remaining lymph nodes. The authors studied adoption and real-world outcomes of ultrasound monitoring in over 1000 patients treated at 21 centers worldwide, finding that most patients now have ultrasounds instead of surgery. Although slightly more patients have cancer return in the lymph nodes with this strategy, typically, it can be removed with delayed surgery. Compared with up-front surgery, ultrasound monitoring results in the same overall risk of melanoma coming back at any location or of dying from melanoma.
AB - Background: For patients with sentinel lymph node (SLN)-positive cutaneous melanoma, the Second Multicenter Selective Lymphadenectomy trial demonstrated equivalent disease-specific survival (DSS) with active surveillance using nodal ultrasound versus completion lymph node dissection (CLND). Adoption and outcomes of active surveillance in clinical practice and in adjuvant therapy recipients are unknown. Methods: In a retrospective cohort of SLN-positive adults treated at 21 institutions in Australia, Europe, and the United States from June 2017 to November 2019, the authors evaluated the impact of active surveillance and adjuvant therapy on all-site recurrence-free survival (RFS), isolated nodal RFS, distant metastasis-free survival (DMFS), and DSS using Kaplan-Meier curves and Cox proportional hazard models. Results: Among 6347 SLN biopsies, 1154 (18%) were positive and had initial negative distant staging. In total, 965 patients (84%) received active surveillance, 189 (16%) underwent CLND. Four hundred thirty-nine patients received adjuvant therapy (surveillance, 38%; CLND, 39%), with the majority (83%) receiving anti–PD-1 immunotherapy. After a median follow-up of 11 months, 220 patients developed recurrent disease (surveillance, 19%; CLND, 22%), and 24 died of melanoma (surveillance, 2%; CLND, 4%). Sixty-eight patients had an isolated nodal recurrence (surveillance, 6%; CLND, 4%). In patients who received adjuvant treatment without undergoing prior CLND, all isolated nodal recurrences were resectable. On risk-adjusted multivariable analyses, CLND was associated with improved isolated nodal RFS (hazard ratio [HR], 0.36; 95% CI, 0.15-0.88), but not all-site RFS (HR, 0.68; 95% CI, 0.45-1.02). Adjuvant therapy improved all-site RFS (HR, 0.52; 95% CI, 0.47-0.57). DSS and DMFS did not differ by nodal management or adjuvant treatment. Conclusions: Active surveillance has been adopted for most SLN-positive patients. At initial assessment, real-world outcomes align with randomized trial findings, including in adjuvant therapy recipients. Lay Summary: For patients with melanoma of the skin and microscopic spread to lymph nodes, monitoring with ultrasound is an alternative to surgically removing the remaining lymph nodes. The authors studied adoption and real-world outcomes of ultrasound monitoring in over 1000 patients treated at 21 centers worldwide, finding that most patients now have ultrasounds instead of surgery. Although slightly more patients have cancer return in the lymph nodes with this strategy, typically, it can be removed with delayed surgery. Compared with up-front surgery, ultrasound monitoring results in the same overall risk of melanoma coming back at any location or of dying from melanoma.
KW - active surveillance
KW - cohort studies
KW - cutaneous malignant melanoma
KW - follow-up studies
KW - immunotherapy
KW - lymph node excision
KW - metastatic melanoma
KW - sentinel lymph node
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U2 - 10.1002/cncr.33483
DO - 10.1002/cncr.33483
M3 - Article
C2 - 33826754
AN - SCOPUS:85103626704
SN - 0008-543X
VL - 127
SP - 2251
EP - 2261
JO - Cancer
JF - Cancer
IS - 13
ER -