Pancreatic cancer (PC) is one of the few types of cancer with increasing incidence and mortality rates.
1 In 2017, the number of annual deaths in the European Union due to PC will exceed the number of death due to breast cancer.
2 Resection is the only chance for prolonged survival; unfortunately only 15–20% of PC patients are eligible for resection due to advanced or metastatic disease at diagnosis.
3 Tumor/node/metastases (TNM) stage I and II PC are generally considered eligible for resection.
4 The European Society of Medical Oncology (ESMO) guidelines, during the study period and most recent, state that patients with a borderline resectable or locally advanced tumor should be treated with neoadjuvant chemotherapy (neo-ACT) in clinical trials whenever possible and that adjuvant chemotherapy (ACT) is considered as standard of care after curative resection for PC.
5,
6 Recently, the ESPAC-4 trial showed a survival benefit in patients treated with adjuvant gemcitabine and capecitabine compared with gemcitabine alone.
7 Despite advances in (neo)-ACT, the median survival for patients with an initial resectable tumor is only 23.3 (range 12–54) months.
8
Previous studies have reported variations in incidence, mortality and survival in PC between countries.
9–12 The EUropean REgistration of Cancer CAre (EURECCA) consortium, established by the European CanCer Organisation (ECCO), aims to investigate differences in treatment and to improve cancer care through Europe.
13 International comparisons of (neo-)ACT and outcome in surgically treated patients with PC are sparse. Therefore, the purpose of this study was to describe and compare (neo-)ACT and outcome of patients who underwent tumor resection for resectable (TNM stage I and II) pancreatic adenocarcinoma in the EURECCA Pancreas consortium.
Materials and Methods
Study Design and Data Preparation
This is an observational cohort study of eight partners (registries) in the EURECCA Pancreas consortium [national: Belgium (BE), The Netherlands (NL), Slovenia (SLO), Ukraine (UA), and Bulgaria (BG); regional: Catalonia (Spain) (CAT(E)) and Munich (Germany) (MU(D); and single center: Milan (Italy) (MIL(I))] who shared their anonymized dataset. Detailed description of the registries is provided in Table S1 (Supplementary). The American Joint Committee on Cancer and International Union Against Cancer TNM 7th Edition classification were used to describe stage.
4,
14 In case pathology TNM variables were not informative (missing or X), clinical TNM variables were used as replacement. In case clinical TNM variables also were not informative (missing or X), pathology TNM variables were considered to be “0.” The 3rd edition of the International Classification of Disease for Oncology was used for topographical and morphological (i.e., pathologic diagnosis) coding.
15 Age was categorized as < 65 years, 65–75 years, and > 75 years. Overall survival (OS) was calculated from date of surgery until date of death (event) or last follow-up (censored). Ninety-day mortality was calculated to distinguish surgery-related from disease-related death.
16
Patient Selection
All patients with pancreatic tumors (included codes: C25.0–C25.9; excluded: C25.4), diagnosed in 2012–2013 (present in all registries), undergoing tumor resection, for adenocarcinoma (included codes: 8140-8380, 8500-8585; excluded: 8150-8158, 8240-8249), stage I and II were included.
15 Patients with a history of other malignancies were not excluded, because PC is most often determinative for the prognosis. BG could not confirm tumor resection and was only used in descriptive statistics in Table S2 (Supplementary). SLO and UA were not included in analyses of neo-ACT, because no information was available. CAT(E) and UA were not included in analyses of ACT, because no information was available.
Statistical Analyses
Statistical analyses were performed using SPSS Inc. for Windows (version 23.0). Numerical data are reported as mean [standard deviation (SD)] and compared using the one-way ANOVA test. Categorical data are reported as absolute numbers (percentages) and compared using the Chi square test. Multivariable logistics regression analyses (adjusted for sex, age group, and stage) where performed for neo-ACT, ACT, and 90-day mortality. Kaplan–Meier curves, log-rank tests, and multivariable Cox regression analyses (adjusted for sex, age group, stage) where used to compare OS. For multivariable comparisons between registries, BE (national) and CAT(E) (regional) were used as reference groups (first in alphabetic order). For reasons of bias, comparisons were performed separately per registry type: national, regional, and single-center registries. To assess the risk of missing data bias, sensitivity analyses were conducted by adding patients with “unknown” stage to the original analyses. To assess the influence of 90-day mortality on the use of ACT, multivariable sensitivity analysis was performed with 90-day mortality as covariate. To assess the influence of use of (neo-)ACT on OS, multivariable sensitivity analysis was performed with (neo-)ACT as covariates. The original results were considered robust if the sensitivity analyses showed similar results. P < 0.05 was considered statistically significant for all analyses.
Discussion
The main purpose of this study was to describe and compare (neo–)ACT and outcomes of patients who underwent tumor resection for stage I and II pancreatic adenocarcinoma in the EURECCA consortium. There were some differences in the use of neo-ACT. Although the ESMO guidelines—during the study period and most recently—recommended the use of ACT, variations were observed in OR for ACT usage between national registries.
6 Also, large variations in 90-day mortality and OS were observed between the registries included in this study.
Previous studies from the EURECCA consortium showed variations in the use of chemo(radiation)therapy in colon, rectal, and breast cancer patients.
17–19 The observed variations in neo-ACT, but mainly ACT, between the registries in this study are in concordance with a recent large-scale international study of resected PC patients.
20 A possible explanation for the variations can be differences in adherence to (inter)national guidelines.
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19 Also, cultural, socioeconomic, and healthcare differences may play a role in the use of (neo-)ACT.
21–23 The observation that few patients received neo-ACT was probably due to the statement by the ESMO guidelines (during the study period) that neo-ACT should be used in clinical trial settings.
6 Clinical trials are more easily accessible in specialized centers, which explains the greater use of neo-ACT in the (specialized) single-center registry compared with the national and regional registries. A recent meta-analysis has shown the benefit of neo-ACT over upfront surgery.
24 An interesting international comparison would be how these results are implemented in more recent practice. A complicated postoperative course can delay or omit the use of ACT.
25 In a sensitivity analyses with 90-day mortality added to the multivariable analyses for the use of ACT, we confirmed that differences in 90-day mortality were not of influence on the differences in the use of ACT between the registries. The use of ACT decreased per ascending age group and patients in the age group > 75 years showed a significant worse OS in multivariable analyses in the national, regional, and single-center registries. As previously investigated, elderly patients are at higher risk of postoperative complications.
26 Although centralization improved outcome of pancreatic surgery in elderly patients in a recent study, further research is needed to gain knowledge on this matter.
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Variations in 90-day mortality were observed between the national registries, even after adjustment for sex, age group, and stage. Multiple studies have shown a lower postoperative mortality after pancreatic surgery in high- compared with low-volume hospitals.
28,
29 In our study this could not be assessed, because the annual hospital volumes were not available. Nonetheless, BE and MU(D) showed a high 90-day mortality and centralization of pancreatic surgery was not (yet) implemented over there during the study period. Caution has to be taken with this statement as detailed information about perioperative treatment, likely to affect 90-day mortality, was not available.
This study showed a better survival in patients receiving ACT compared with naïve patients in the national, regional, and single-center registries. This can be explained by confounding by indication (fit patients with a good prognosis are generally more likely to receive ACT), and therefore a justifiable comparison is not possible. The recent ESPAC-4 trial (2017) showed a significant better survival for patients treated with adjuvant gemcitabine and capecitabine compared with gemcitabine alone (28.0 (95% CI = 23.5–31.5 months vs. 25.5 (95% CI = 22.7–27.9) months) after resection for PC.
7 Considering the randomized ESPAC-trial has strict inclusion criteria (e.g., full recovery after surgery, creatinine clearance ≥ 50 mL/min) and our study is mainly population-based, the results are largely comparable. Still, direct comparison is hampered by the differences in study design. In a sensitivity analyses with (neo-)ACT added to the multivariable analyses for OS, we confirmed that differences in ACT were not of influence on the differences in OS between the registries. Definite conclusions cannot be drawn from this sensitivity analysis, because immortal time bias and confounding by indication cannot be ruled out.
Our study has several limitations. First, caution has to be taken with interpretation of the results as differences in (unmeasured) patient characteristics (e.g., patient selection for tumor resection) might have been of influence. Nevertheless, analyses were adjusted for important factors (sex, age group, stage) and still showed differences between the registries. Second, due to inherent differences between national, regional, and single-center registries, which also explain the observed inter-registry-type variations, analyses had to be performed separately per registry type and lowered the statistical power (e.g., multivariable analyses for 90-day mortality was not possible in the single-center registry). Third, due to missing data this study excluded some patients (e.g., unknown stage or tumor resection) and registries (e.g., SLO and UA did not provide data on neo-ACT, CAT(E), and UA did not provide data on ACT and the dataset from BG could not confirm tumor resection) from certain analyses. A possible explanation for this is that the provided datasets may originally have been established for other intentions (e.g., Cancer Registry or Clinical/Surgical Audit) and thus focused on completeness of certain (other) variables. Although most included registries are surgically driven and therefore very comparable, this probably introduced missing data bias.
30 Sensitivity analyses with patients with unknown stage added to the analyses confirmed the robustness of the results of this study. Still, variables, such as stage and tumor resection, are pivotal when investigating treatment and outcome in cancer patients. Future registration should focus on completeness and uniform use of definitions as previously stated by other member of the EURECCA consortium.
13,
17 Nonetheless, this study is the first to describe and compare (neo-)ACT and outcome of patients undergoing tumor resection for pancreatic adenocarcinoma stage I and II in eight different European registries.
Acknowledgment
The authors thank Dr. De Schutter and Mrs. Verbeeck (Belgian Cancer Registry, Brussels, Belgium), Dr. Manchon-Wals (Cancer Plan, Barcelona), and the Munich Cancer Registry for the collection of data. The authors also thank the registration team of the Netherlands Comprehensive Cancer Organisation (IKNL) for the collection of data for the Netherlands Cancer Registry as well as IKNL staff for scientific advice. Furthermore, the authors thank Prof. Zerbi (Pancreatic Surgery Unit, Department of Surgery, Humanitas University, Milan, Italy) for revising the manuscript.