TY - JOUR
T1 - Nature and management of melanoma recurrences following adjuvant anti-PD-1 based therapy
AU - Woodford, Rachel
AU - McKeown, Janet
AU - Hoeijmakers, Lotte L.
AU - Mangana, Johanna
AU - Dimitriou, Florentia
AU - Allayous, Clara
AU - Zaman, Farzana
AU - Aya, Francisco
AU - Marsiglio, John
AU - Goodman, Rachel
AU - Rayson, Victoria
AU - Placzke, Joanna
AU - Kessels, Jolien
AU - Ramalyte, Egle
AU - Haque, Waqas
AU - Wilson, Isabella
AU - Trojaniello, Claudia
AU - Benannoune, Naima
AU - Roberts-Thomson, Rachel
AU - Robert, Caroline
AU - Blank, Christian U.
AU - Dummer, Reinhard
AU - Lebbe, Celeste
AU - Haydon, Andrew
AU - Arance, Ana
AU - Hu-Lieskovan, Siwen
AU - Johnson, Douglas B.
AU - Mcarthur, Grant A.
AU - Rutkowski, Piotr
AU - Neyns, Bart
AU - Sullivan, Ryan J.
AU - Weber, Jeffrey
AU - Carlino, Matteo S.
AU - Ascierto, Paolo A.
AU - Lo, Serigne
AU - Long, Georgina V.
AU - Menzies, Alexander M.
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2024/11/1
Y1 - 2024/11/1
N2 - Introduction: Approximately 50 % of resected stage II-IV melanoma patients develop recurrent disease by 5 years despite adjuvant anti-PD-1 therapy. Data to define best management of recurrences is lacking. Methods: This was a multicentre, international, retrospective cohort study. Patients with resected stage II-IV melanoma who commenced adjuvant anti-PD-1-based therapy before January 2022 and later recurred were identified. Data on demographics, disease characteristics, recurrence patterns, management and outcomes were collected. Results: 711 patients from 17 sites were included. Median age was 60 [range 16–92], 64 % were male, 2 % stage II, 91 % were stage III, 7 % stage IV. Median time to recurrence was 6.2 months (0–68.5) and median follow up time from recurrence was 19.8 months (range 0.2–73.1). 63 % recurred on anti-PD-1 therapy, 36 % off therapy [3 % < 6 months, 33 % > 6 months]. Initial recurrences were locoregional (LR) alone in 44 %, distant alone (DR) in 43 %, and 11 % in both sites. LR recurrences were managed with local therapy, alone (62 %) or with “second adjuvant” anti-PD-1 (14 %) or BRAF/MEK therapy (23 %); 12 m RFS2 was 25 %, 29 % and 69 % respectively (p = 0.0045). Definitive systemic therapy at first recurrence was given in 16 % LR and 86 % DR, with best outcomes for anti-CTLA4 + anti-PD-1 and trial combinations (24 m PFS 63 % and 69 %, respectively). The 24 m OS for the entire cohort was 65 %. Conclusion: Most recurrences following adjuvant anti-PD-1 based therapy occur early and while still on drug. Outcomes are poor, regardless of site, timing of recurrence, and subsequent treatment.
AB - Introduction: Approximately 50 % of resected stage II-IV melanoma patients develop recurrent disease by 5 years despite adjuvant anti-PD-1 therapy. Data to define best management of recurrences is lacking. Methods: This was a multicentre, international, retrospective cohort study. Patients with resected stage II-IV melanoma who commenced adjuvant anti-PD-1-based therapy before January 2022 and later recurred were identified. Data on demographics, disease characteristics, recurrence patterns, management and outcomes were collected. Results: 711 patients from 17 sites were included. Median age was 60 [range 16–92], 64 % were male, 2 % stage II, 91 % were stage III, 7 % stage IV. Median time to recurrence was 6.2 months (0–68.5) and median follow up time from recurrence was 19.8 months (range 0.2–73.1). 63 % recurred on anti-PD-1 therapy, 36 % off therapy [3 % < 6 months, 33 % > 6 months]. Initial recurrences were locoregional (LR) alone in 44 %, distant alone (DR) in 43 %, and 11 % in both sites. LR recurrences were managed with local therapy, alone (62 %) or with “second adjuvant” anti-PD-1 (14 %) or BRAF/MEK therapy (23 %); 12 m RFS2 was 25 %, 29 % and 69 % respectively (p = 0.0045). Definitive systemic therapy at first recurrence was given in 16 % LR and 86 % DR, with best outcomes for anti-CTLA4 + anti-PD-1 and trial combinations (24 m PFS 63 % and 69 %, respectively). The 24 m OS for the entire cohort was 65 %. Conclusion: Most recurrences following adjuvant anti-PD-1 based therapy occur early and while still on drug. Outcomes are poor, regardless of site, timing of recurrence, and subsequent treatment.
KW - Adjuvant
KW - Anti-PD-1 therapy
KW - Distant recurrence
KW - Immunotherapy
KW - Immunotherapy resistance
KW - Locoregional recurrence
KW - Melanoma
KW - Recurrent disease
UR - http://www.scopus.com/inward/record.url?scp=85205430095&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2024.115055
DO - 10.1016/j.ejca.2024.115055
M3 - Article
AN - SCOPUS:85205430095
SN - 0959-8049
VL - 212
JO - European Journal of Cancer
JF - European Journal of Cancer
M1 - 115055
ER -