Abstract 842P
Background
Advanced-stage ENKTL is characterized by its low prevalence, poor prognosis, and inconclusive optimal therapy. This study investigated the treatment of newly diagnosed advanced-stage ENKTLs.
Methods
Newly diagnosed stage III/IV ENKTL patients from two large Chinese cancer centers in the last 10-15 years were retrospectively analyzed.
Results
With a median follow-up of 75.03 (range, 0.33-292.13) months, the median overall survival (OS) for the 195 newly diagnosed stage Ⅲ/Ⅳ ENKTL patients was 19.43 (range, 0.33-292.13) months, and estimated 1-, 2-, 3-, and 5-year OS were 59.5%, 46.3%, 41.8%, and 35.1%, respectively. First-line multi-modality therapy prolonged OS compared to single-modality therapy (P<0.001). Chemotherapy (CT)+radiotherapy (RT) compared to CT alone (P=0.007), and hematopoietic stem cell transplantation (HSCT) compared to non-HSCT (P<0.001) both significantly improved OS. For patients ≤60 years yet ineligible for HSCT, other therapies with complete remission led to comparable OS (P=0.141) with no significant differences in baseline features. Patients treated with chidamide maintenance therapy (MT) achieved a median progression-free survival (PFS) of 55.83 (range, 53.27-92.33) months and a median OS of 60.65 (range, 53.70-95.70) months. Non-anthracycline (ANT)- compared to ANT-, asparaginase (ASP)- compared to non-ASP-, and gemcitabine (GEM)- compared to non-GEM-based CT regimens, led to prolonged PFS (P=0.031; P=0.005; P=0.009) and OS (P=0.010; P=0.086; P=0.003), respectively. GEM+ASP combinations slightly improved PFS and OS compared to regimens containing GEM or ASP alone (P>0.05). GEM+ASP combinations led to significantly superior PFS (P=0.058[log-rank], P=0.036[Breslow]) and OS (P=0.008) compared to ANT+ASP regimens. First-line intensive therapy, including CT, RT, HSCT, and chidamide MT, was therefore proposed and could improve long-term survival for advanced-stage ENKTLs.
Conclusions
We propose the first-line intensive therapy for newly diagnosed advanced-stage ENKTLs, including CT, RT, HSCT, and chidamide MT. GEM+ASP combinations appear to yield the optimal efficacy and survival. RT, consolidative HSCT, or chidamide MT are recommended.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Chinese Geriatric Oncology Society Scientific Research Fund (CGOS-06-2014-1-1-01600).
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1000P - Real-world clinical outcomes of cabozantinib (cabo) as a second-line (2L) treatment for advanced hepatocellular carcinoma (aHCC)
Presenter: Daniel Ahn
Session: Poster session 18
1001P - Patients’ prioritization of treatment goals in hepatocellular carcinoma (HCC): A global qualitative observational study (PERIDOT)
Presenter: Marcus-Alexander Wörns
Session: Poster session 18
1002P - Efficacy and safety of tislelizumab combined with TKIs and FOLFOX4-HAIC in conversion therapy of unresectable hepatocellular carcinoma
Presenter: Kai Tan
Session: Poster session 18
1003P - Efficacy and safety of triple combination therapy with transarterial chemoembolization (TACE), tyrosine kinase inhibitor (TKI), and immune checkpoint inhibitor (ICI) versus dual combination therapy in unresectable hepatocellular carcinoma (uHCC): A systematic review and meta-analysis
Presenter: Omar Maaño
Session: Poster session 18
1004P - Comparative efficacy of systemic sequential regorafenib after sorafenib or lenvatinib treatment failure for advanced hepatocellular carcinoma: A retrospective, multi-center, real-world study
Presenter: Danjun Song
Session: Poster session 18
1005P - Atezolizumab plus bevacizumab combined with transarterial chemoembolization and hepatic arterial infusion chemotherapy for unresectable hepatocellular carcinoma with high tumor burden
Presenter: Jiliang Qiu
Session: Poster session 18
1006P - Associations of online search trends and prescription trends for hepatocellular carcinoma drugs
Presenter: Philipp Berning
Session: Poster session 18
1007P - Network meta-analysis (NMA) of lenvatinib vs key comparators in first-line unresectable hepatocellular carcinoma (uHCC)
Presenter: David Trueman
Session: Poster session 18