Abstract 1460P
Background
Nearly half of patients (pts) with esophagogastric cancer (EGC) treated with curative intent experience disease recurrence. Survival is poor and palliative systemic therapy (ST) offers limited benefit. Thus far, it is unknown whether the effectiveness of treatment with curative intent is associated with the outcomes of first-line ST.
Methods
Pts with metachronous metastatic EGC initially treated for nonmetastatic disease (2015–2017) with i) neoadjuvant chemoradiotherapy and resection (nCRT), ii) perioperative chemotherapy (PC), iii) definitive chemoradiotherapy (dCRT), and subsequently with first-line ST, were identified from the Netherlands Cancer Registry. Effectiveness of curative treatment was assessed by the time to treatment failure (TTF, above or below the median), and, if applicable by pathological response (complete/subtotal or partial/no). Outcomes of first-line ST were assessed by TTF and overall survival (OS) from start of first-line ST. Associations were analyzed using Kaplan Meier curves and multivariable Cox proportional hazards models.
Results
We identified 468 pts. Pts in the nCRT (n=275) and PC group (n=81) with a TTF of the curative treatment longer than the median TTF, had a significantly longer first-line TTF, which also translated into a longer OS for pts in the nCRT group: 5.8 vs 8.6 months (HR 1.39 95% CI 1.08-1.80; Table). Outcomes of first-line ST were not significantly different between pts with good or poor pathological response in the nCRT and PC group. TTF of dCRT (n=112) was not associated with outcomes of first line ST. Table: 1460P
Multivariable cox regression analyses of time to treatment failure and overall survival since start of first-line systemic therapy
Curative treatment | N | TTF first-line ST | OS | |||||||
Median (months) | HR | 95%CI | P | Median (months) | HR | 95%CI | P | |||
nCRT | 275 | |||||||||
TTF (months) | ||||||||||
=/> 15.3 | 138 | 5.1 | 8.6 | |||||||
< 15.3 | 137 | 4.0 | 1.41 | 1.06-1.76 | 0.01 | 5.8 | 1.39 | 1.08-1.80 | 0.01 | |
Pathological response | ||||||||||
Good | 94 | 4.6 | 7.3 | |||||||
Poor | 173 | 4.4 | 1.02 | 0.77-1.34 | 0.90 | 6.7 | 1.09 | 0.83-1.42 | 0.54 | |
PC | 81 | |||||||||
TTF (months) | ||||||||||
=/> 19.6 | 41 | 6.4 | 10.3 | |||||||
< 19.6 | 40 | 3.6 | 2.00 | 1.23-3.25 | 0.01 | 7.3 | 1.22 | 0.77-1.93 | 0.45 | |
Pathological response | ||||||||||
Good | 14 | 7.6 | 12.1 | |||||||
Poor | 56 | 3.7 | 1.63 | 0.82-3.25 | 0.16 | 7.2 | 1.54 | 0.79-2.99 | 0.20 | |
dCRT | 112 | |||||||||
TTF (months) | ||||||||||
=/> 5.1 | 56 | 3.6 | 5.4 | |||||||
< 5.1 | 56 | 3.7 | 0.90 | 0.60-1.35 | 0.61 | 7.0 | 0.84 | 0.56-1.26 | 0.40 |
Conclusions
We demonstrated a positive correlation between the effectiveness of nCRT and PC and outcomes of first-line ST. When discussing the effectiveness of first-line ST with metachronous metastatic EGC pts, the time to recurrence after curative treatment may be an important consideration, while this may not be applicable for pathological response.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
UMC Utrecht.
Funding
Has not received any funding.
Disclosure
R.H.A. Verhoeven: Financial Interests, Institutional, Advisory Board, Consultancy: Daiichi Sankyo; Financial Interests, Institutional, Research Grant: Bristol Myers Squibb; Non-Financial Interests, Member of Board of Directors, The Dutch Upper-GI Cancer Group is the Dutch multidisciplinary research group regarding Upper-GI cancers: Dutch Upper-GI Cancer Group; Non-Financial Interests, Member of Board of Directors: International Association of Cancer Registries. H.W.M. van Laarhoven: Financial Interests, Institutional, Invited Speaker: Astellas, BeiGene, Benecke, BMS, Daiichi Sankyo, JAAP, Medtlaks, Novartis, Springer, Travel Congress Management BV; Financial Interests, Institutional, Advisory Board: Amphera, Anocca, Astellas, AstraZeneca, BeiGene, Boehringer Ingelheim, Daiichi Sankyo, Dragonfly, MSD, Servier; Financial Interests, Institutional, Other, Advices on protocol development: Myeloid; Financial Interests, Institutional, Other, Selection of articles for Framingham: Framingham; Financial Interests, Institutional, Research Grant, LyRICX study: Servier; Financial Interests, Institutional, Research Grant, TAPESTRY study: Merck; Financial Interests, Institutional, Research Grant, AUSPICIOUS study: Incyte; Financial Interests, Institutional, Research Grant, LOAD study: ORCA; Financial Interests, Institutional, Coordinating PI: Auristone; Financial Interests, Institutional, Local PI, DESTINY-GASTRIC03: AstraZeneca; Non-Financial Interests, Leadership Role, Chair upper GI Faculty: ESMO; Non-Financial Interests, Institutional, Product Samples, For all clinical study mentioned, study medication is provided: See 'research funding'. N. Haj Mohammad: Financial Interests, Institutional, Research Grant: Servier; Financial Interests, Institutional, Invited Speaker: Servier; Financial Interests, Institutional, Advisory Board: BMS, Merck, Lilly, AstraZeneca. All other authors have declared no conflicts of interest.
Resources from the same session
1525P - Nab-paclitaxel/gemcitabine with or without epigenetic targeting followed by consolidating immune targeting with durvalumab and lenalidomide in patients with advanced pancreatic ductal adenocarcinoma: Results from the SEPION/AIO-PAK-0118 phase I/II study
Presenter: Jens Siveke
Session: Poster session 18
1527P - GnP vs mFOLFIRINOX or S-IROX in metastatic pancreatic cancer: 1-year follow-up updated data from the GENERATE (JCOG1611)
Presenter: Satoshi Kobayashi
Session: Poster session 18
1528P - TCOG T5221 trial: A phase II randomized study of gemcitabine and nab-paclitaxel in combination with S- 1/LV (GASL) or oxaliplatin (GAP) as first-line treatment for metastatic pancreatic cancer
Presenter: Yung-yeh Su
Session: Poster session 18
1531TiP - TWINPEAK phase I/II study, PT886 a bispecific antibody targeting claudin 18.2 and CD47 in combination with chemotherapy and/or pembrolizumab in gastric/GEJ-carcinomas or PDAC
Presenter: Michael Overman
Session: Poster session 18
1532TiP - Zolbetuximab with gemcitabine + nab-paclitaxel (GN) in first-line treatment of Claudin 18.2–positive metastatic pancreatic cancer (mPC): Phase II, open-label, randomized study
Presenter: Wungki Park
Session: Poster session 18
1533TiP - A multicenter, open-label phase II study to evaluate the efficacy and safety of pimicotinib (CSF-1R inhibitor) in combination with chemotherapy with or without toripalimab in patients (pts) with advanced pancreatic ductal adenocarcinoma (aPDAC)
Presenter: Xiaofei Zhang
Session: Poster session 18
1534TiP - Valproic acid combinEd with Simvastatin and gemcitabine/nab-paclitaxel-based regimens in untreated metastatic Pancreatic Adenocarcinoma patients-VESPA trial
Presenter: Alfredo Budillon
Session: Poster session 18