The impact of neoadjuvant therapy in patients with left-sided resectable pancreatic cancer: an international multicenter study
Articolo
Data di Pubblicazione:
2025
Abstract:
Background: Left-sided pancreatic cancer is associated with worse overall survival (OS) compared with right-sided pancreatic cancer. Although neoadjuvant therapy is currently seen as not effective in patients with resectable pancreatic cancer (RPC), current randomized trials included mostly patients with right-sided RPC. The purpose of this study was to assess the association between neoadjuvant therapy and OS in patients with left-sided RPC compared with upfront surgery.Patients and methods: This was an international multicenter retrospective study including consecutive patients after left-sided pancreatic resection for pathology-proven RPC, either after neoadjuvant therapy or upfront surgery in 76 centers from 18 countries on 4 continents (2013-2019). The primary endpoint was OS from diagnosis. Time-dependent Cox regression analysis was carried out to investigate the association of neoadjuvant therapy with OS, adjusting for confounders at the time of diagnosis. Adjusted OS probabilities were calculated.Results: Overall, 2282 patients after left-sided pancreatic resection for RPC were included of whom 290 patients (13%) received neoadjuvant therapy. The most common neoadjuvant regimens were (m)FOLFIRINOX (38%) and gemcitabine-nab-paclitaxel (22%). After upfront surgery, 72% of patients received adjuvant chemotherapy, mostly a single-agent regimen (74%). Neoadjuvant therapy was associated with prolonged OS compared with upfront surgery (adjusted hazard ratio 0.69, 95% confidence interval 0.58-0.83) with an adjusted median OS of 53 versus 37 months (P = 0.0003) and adjusted 5-year OS rates of 47% versus 35% (P = 0.0001) compared with upfront surgery. Interaction analysis demonstrated a stronger effect of neoadjuvant therapy in patients with a larger tumor (P-interaction = 0.003) and higher serum carbohydrate antigen 19-9 (CA19-9; P-interaction = 0.005). In contrast, the effect of neoadjuvant therapy was not enhanced for splenic artery (P-interaction = 0.43), splenic vein (P-interaction = 0.30), retroperitoneal (P-interaction = 0.84), and multivisceral (P-interaction = 0.96) involvement.Conclusions: Neoadjuvant therapy in patients with left-sided RPC was associated with improved OS compared with upfront surgery. The impact of neoadjuvant therapy increased with larger tumor size and higher serum CA19-9 at diagnosis. Randomized controlled trials on neoadjuvant therapy specifically in patients with left-sided RPC are needed.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
CA19-9; neoadjuvant therapy; pancreatic adenocarcinoma; pancreatic body/tail; resectable; tumor size
Elenco autori:
Rangelova, E; Stoop, T F; Van Ramshorst, T M E; Ali, M; Van Bodegraven, E A; Javed, A A; Hashimoto, D; Steyerberg, E; Banerjee, A; Jain, A; Sauvanet, A; Serrablo, A; Giani, A; Giardino, A; Zerbi, A; Arshad, A; Wijma, A G; Coratti, A; Zironda, A; Socratous, A; Rojas, A; Halimi, A; Ejaz, A; Oba, A; Patel, B Y; Björnsson, B; Reames, B N; Tingstedt, B; Goh, B K P; Payá-Llorente, C; Del Pozo, C D; González-Abós, C; Medin, C; Van Eijck, C H J; De Ponthaud, C; Takishita, C; Schwabl, C; Månsson, C; Ricci, C; Thiels, C A; Douchi, D; Hughes, D L; Kilburn, D; Flanking, D; Kleive, D; Silva, D S; Edil, B H; Pando, E; Moltzer, E; Kauffman, E F; Warren, E; Bozkurt, E; Sparrelid, E; Thoma, E; Verkolf, E; Ausania, F; Giannone, F; Hüttner, F J; Burdio, F; Souche, F R; Berrevoet, F; Daams, F; Motoi, F; Saliba, G; Kazemier, G; Roeyen, G; Nappo, G; Butturini, G; Ferrari, G; Kito Fusai, G; Honda, G; Sergeant, G; Karteszi, H; Takami, H; Suto, H; Matsumoto, I; Mora-Oliver, I; Frigerio, I; Fabre, J M; Chen, J; Sham, J G; Davide, J; Urdzik, J; De Martino, J; Nielsen, K; Okano, K; Kamei, K; Okada, K; Tanaka, K; Labori, K J; Goodsell, K E; Alberici, L; Webber, L; Kirkov, L; De Franco, L; Miyashita, M; Maglione, M; Gramellini, M; Ramera, M; Amaral, M J; Ramaekers, M; Truty, M J; Van Dam, M A; Stommel, M W J; Petrikowski, M; Imamura, M; Hayashi, M; D'Hondt, M; Brunner, M; Hogg, M E; Zhang, C; Suárez-Muñoz, M Á; Luyer, M D; Unno, M; Mizuma, M; Janot, M; Sahakyan, M A; Jamieson, N B; Busch, O R; Bilge, O; Belyaev, O; Franklin, O; Sánchez-Velázquez, P; Pessaux, P; Holka, P S; Ghorbani, P; Casadei, R; Sartoris, R; Schulick, R D; Grützmann, R; Sutcliffe, R; Mata, R; Patel, R B; Takahashi, R; Rodriguez Franco, S; Cabús, S S; Hirano, S; Gaujoux, S; Festen, S; Kozono, S; Maithel, S K; Chai, S M; Yamaki, S; Van Laarhoven, S; Mieog, J S D; Murakami, T; Codjia, T; Sumiyoshi, T; Karsten, T M; Nakamura, T; Sugawara, T; Boggi, U; Hartman, V; De Meijer, V E; Bartholomä, W; Kwon, W; Koh, Y X; Cho, Y; Takeyama, Y; Inoue, Y; Nagakawa, Y; Kawamoto, Y; Ome, Y; Soonawalla, Z; Uemura, K; Wolfgang, C L; Jang, J Y; Padbury, R; Satoi, S; Messersmith, W; Wilmink, J W; Abu Hilal, M; Besselink, M G; Del Chiaro, M
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