Abstract 1176P
Background
The optimal duration of immunotherapy (ITH) for patients(pts) with unresectable/metastatic melanoma has not been defined and de-escalation strategies are under debate. Drug holidays are defined as intentional cessation of immunotherapy for period of time, in pts with therapy benefits, till potential progression (PD). While avails of drug holidays include reduction of toxicity and treatment cost as well as increased quality of pts' life, there are also potential risks including PD. Our study aimed to describe disease control upon drug holidays in melanoma pts treated with palliative ITH.
Methods
Pts with advanced unresectable/metastatic melanoma were treated with anti-PD1-based ITH. Patients were referred for drug holidays after ≥12 months of ITH. Pts who stopped the treatment due to toxicity were excluded from analysis. During study patients had imaging every 3 months. Primary endpoint was overall survival (OS), and secondary endpoints were median duration of drug holiday, 2nd progression-free survival (PFS2) after PD on drug holidays.
Results
175 patients (80F/95M) treated for advanced unresectable/metastatic melanoma were referred for drug holidays. 116(67.4%) were BRAF-negative melanoma patients. 84 pts were treated with nivolumab, 6 with nivolumab+ipilimumab, 85 with pembrolizumab; and 152(86.9%) were treated in first line. Patients treated for ≥24 months(m) before drug holidays had significantly longer OS (p=0.003) and longer PFS till disease PD on drug holidays(p=0.00053) in multivariate analysis. PFS was dependent on best response before drug holidays with the longest in CR group (p=0.011). The median duration of drug holidays was 17 m (IQR: 8-24). At the median follow-up of 48 m (95%CI: 45-51), median OS was not reached, and 5-year OS rate was 89% (95%CI: 83-96). At ITH retreatment objective response was 64% and PFS2 rate at 1-year was 69% (95%CI: 48-99). At the time of analysis 141 pts were still on drug holidays and 11 died due to melanoma PD.
Conclusions
For melanoma pts drug holidays may be offered to ITH responders. The majority of melanoma patients on drug holidays are progression-free at 24m after ITH discontinuation. ITH rechallenge allows achieving disease control after initial progression on drug holidays.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
A.M. Czarnecka: Financial Interests, Personal, Invited Speaker: BMS, MSD, Novartis, Pierre Fabre. P. Teterycz: Financial Interests, Personal, Other, travel grant: Sanofi. L. GalusR. Dziura, B. Cybulska-Stopa: Financial Interests, Personal, Speaker’s Bureau: BMS, Roche, MSD, Novartis, Pierre Fabre. J. Mackiewicz: Financial Interests, Personal, Speaker’s Bureau: BMS, GSK, Roche, MSD, Novartis, Pierre Fabre. M. Ziętek: Financial Interests, Personal, Speaker’s Bureau: BMS, MSD, Novartis. P. Rutkowski: Financial Interests, Personal, Invited Speaker, Honoraria for Lectures: MSD, BMS, Pierre Fabre; Financial Interests, Personal, Advisory Board: MSD, BMS, Pierre Fabre, Merck, Sanofi, Blueprint Medicines, Philogen; Financial Interests, Personal, Invited Speaker: Merck, Sanofi, Novartis, AstraZeneca; Financial Interests, Institutional, Research Grant, research grant for ISS: Pfizer; Financial Interests, Institutional, Funding, research grant for institution: BMS; Non-Financial Interests, Member of Board of Directors: Polish Society of Surgical Oncology; Non-Financial Interests, Member of Board of Directors, President: Polish Oncological Society. All other authors have declared no conflicts of interest.
Resources from the same session
1139P - Final results of a phase II study of pembrolizumab as first-line treatment in advanced cutaneous squamous cell carcinomas (CSCCs)
Presenter: Eve Maubec
Session: Poster session 13
1140P - Cemiplimab versus historical systemic treatments for locally advanced (la) or metastatic (m) cutaneous squamous cell carcinomas (CSCC): Results from the French study TOSCA
Presenter: Emilie Gerard
Session: Poster session 13
1141P - Early discontinuation of cemiplimab in patients with advanced cutaneous squamous cell carcinoma
Presenter: Elena Croce
Session: Poster session 13
1142P - Personalized decision making in cutaneous squamous cell carcinoma: Integrating a clinico-pathological model for absolute metastatic risk into the staging systems
Presenter: Marlies Wakkee
Session: Poster session 13
1143P - Changes in peripheral and local tumor immunity after cemiplimab treatment early describe clinical outcomes in patients with cutaneous squamous cell carcinoma
Presenter: Daniela Esposito
Session: Poster session 13
1144P - High-plex spatial profiling of cutaneous squamous cell carcinoma to identify biomarkers associated with clinical outcomes: The cMIC study
Presenter: Rahul Ladwa
Session: Poster session 13
1145P - Clinical characteristics and survival of patients with advanced Merkel cell carcinoma (MCC) treated with avelumab: Analysis of a prospective German MCC registry (MCC TRIM)
Presenter: Juergen Becker
Session: Poster session 13
1146P - Updated results from POD1UM-201: A phase II study of retifanlimab in patients with advanced or metastatic Merkel cell carcinoma (MCC)
Presenter: Giovanni Grignani
Session: Poster session 13
1148P - Avelumab as second-line or later (2L+) treatment (tx) in patients (pts) with metastatic Merkel cell carcinoma (mMCC): Real-world tx patterns in France
Presenter: Astrid Blom Fily
Session: Poster session 13