Abstract 3336
Background
The Thoracic Oncology Centre of the University Hospital Zürich, founded in 2011, is certified by the German Cancer Society, and is one of 17 multidisciplinary organ-based centres of the CCCZ. All treatment recommendations are made at a multidisciplinary tumor board. Since 1980, all new cancer cases among the population of both cantons Zurich and Zug, are registered in the KKR.
Methods
The aim of the current study is to quantify the mortality risk of patients with NSCLC and identify differences on survival time and other factors between patients receiving their primary treatment at the CCCZ and those treated elsewhere and registered by KKR. Association of sex, histology, stage and age at initial diagnosis to survival as well as differential effect on survival between CCCZ and KKR are also explored. Imputation of last follow-up date of KKR by the database cut-off date (7 August 2018) was used, to address possible underestimation of survival due to missingness in this centre.
Results
Patients included 848 primary cases from the CCCZ and 1761 cases from the KKR diagnosed between January 1, 2011 and December 31, 2015. A comparable median follow-up time of 57 months and 56 months for CCCZ and KKR patients, respectively, was calculated. OS is significantly superior for CCCZ patients as compared to KKR patients (median: 36.0m, 95%CI:[31.0, 45.0] versus 12.0m, 95%CI:[11.0, 13.0];HR=1.71 [95% CI 1.54, 1.90] p < 0.001). This difference remained significant when examined in the subgroups of gender, age (≤65 and >65y), UICC stage (I/II, III, IV), and histology (squamous, adenocarcinoma). The effect of treatment outside or within the CCCZ on patients’ survival remained significant (HR = 1.42 [95% CI 1.27, 1.57]; p < 0.001) in multivariate analysis adjusting for sex, histology, UICC stage and age at diagnosis, all factors with a significant effect on OS.
Conclusions
Our analysis provides further evidence of the importance of the volume of experience and the availability of a multidisciplinary organisation and research environment, as delivered by a comprehensive cancer centre, on the outcome of patients with all stages of NSCLC.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Comprehensive Cancer Center Zürich.
Funding
Has not received any funding.
Disclosure
R.A. Stahel: Advisory / Consultancy: I have received honoraria as a consultant at advisory boards from AbbVie, AstraZeneca, Boehringer Ingelheim, MSD, Pfizer, Roche and Takeda.; Speaker Bureau / Expert testimony: I have received honoraria as a speaker from AstraZeneca, Boehringer Ingelheim, MSD and Roche.; Honoraria (self): Roche and Takeda; Research grant / Funding (institution), ETOP trials (president and scientific chair): AstraZeneca, BMS, Boehringer Ingelheim, Genentech, MSD, Roche, and Pfizer. All other authors have declared no conflicts of interest.
Resources from the same session
3620 - Safety, efficacy, PK and PD biomarker results of the first-in-human study of mutant isocitrate dehydrogenase 1 (mIDH1) inhibitor BAY 1436032 in patients (pts) with mIDH1 advanced solid tumours
Presenter: Wolfgang Wick
Session: Poster Display session 1
Resources:
Abstract
5465 - Proof of concept clinical study by US-guided intratumor injection of VCN-01, an oncolytic adenovirus expressing hyaluronidase in patients with pancreatic cancer
Presenter: Manuel Hidalgo
Session: Poster Display session 1
Resources:
Abstract
2555 - A Phase 1a/b first-in-human, open-label, dose-escalation, safety, PK and PD study of TP-0903 in solid tumors
Presenter: John Sarantopoulos
Session: Poster Display session 1
Resources:
Abstract
3533 - First in human phase 1/2a study of PEN-866, a Heat Shock Protein 90 (HSP90) ligand – SN38 conjugate for patients with advanced solid tumors: Phase 1 results
Presenter: Johanna Bendell
Session: Poster Display session 1
Resources:
Abstract
4114 - A Phase I Open-Label, Non-Randomized Study of Recombinant Super-Compound Interferon (rSIFN-co) In Patients with Advanced Solid Tumors
Presenter: Amanda Seet
Session: Poster Display session 1
Resources:
Abstract
2537 - Evaluation of Pharmacodynamic (PD) Biomarkers in Advanced Cancer Patients Treated with Oxidative Phosphorylation (OXPHOS) Inhibitor, OPC-317 (OPC)
Presenter: Jie Qing Eu
Session: Poster Display session 1
Resources:
Abstract
5764 - Pharmacokinetic (PK) assessment of BT1718: A phase 1/2a study of BT1718, a first in class Bicycle Toxin Conjugate (BTC), in patients (pts) with advanced solid tumours
Presenter: Natalie Cook
Session: Poster Display session 1
Resources:
Abstract
2683 - A phase I open label dose escalation trial evaluating VT1021 in patients with advanced solid tumors.
Presenter: Wael Harb
Session: Poster Display session 1
Resources:
Abstract
3609 - Interim Results from Trial of SL-801, a Novel XPO-1 Inhibitor, in Patients with Advanced Solid Tumors
Presenter: Judy Wang
Session: Poster Display session 1
Resources:
Abstract
3485 - Phase 1 Trial of Fruquintinib in Patients with Advanced Solid Tumors: Results of the Dose Escalation Phase
Presenter: Andrea Wang-Gillam
Session: Poster Display session 1
Resources:
Abstract