CC BY-NC-ND 4.0 · Gesundheitswesen 2023; 85(S 03): S197-S204
DOI: 10.1055/a-2132-6797
Originalarbeit

Assessment of the Potential of Concentrating Cancer Care in Hospitals With Certification Through Survival Analysis

Article in several languages: English | deutsch
Veronika Bierbaum
1   Zentrum für Evidenzbasierte Gesundheitsversorgung, Universitätsklinikum Carl Gustav Carus, Dresden, Germany
,
Jochen Schmitt
1   Zentrum für Evidenzbasierte Gesundheitsversorgung, Universitätsklinikum Carl Gustav Carus, Dresden, Germany
,
Monika Klinkhammer-Schalke
2   Tumorzentrum Regensburg (TZR), Zentrum für Qualitätssicherung und Versorgungsforschung der Universität Regensburg, Regensburg, Germany
,
Olaf Schoffer
1   Zentrum für Evidenzbasierte Gesundheitsversorgung, Universitätsklinikum Carl Gustav Carus, Dresden, Germany
› Author Affiliations
Fundings Innovationsfonds — 01VSF17020
 

Abstract

Background Certification programs seek to improve the quality of complex interdisciplinary models of care such as cancer treatment through structuring the process of care in accordance with evidence-based guidelines. In Germany, the German Cancer Society (Deutsche Krebsgesellschaft, DKG) provides a certification programme for cancer care that covers more than one thousand centers. In a recent retrospective cohort study, it has been shown on a large, nationwide data set based on data from a statutory health insurance and selected clinical cancer registries, that there is a benefit in survival for cancer patients who have received initial treatment in hospitals certified by the DKG. Here, we deduce two absolute measures from the relative benefit in survival with the aim to quantify this benefit if all patients had been treated in a certified center.

Methods The WiZen study analysed survival of adult patients insured by the AOK with a cancer diagnosis between 2009 and 2017 in certified hospitals vs. non-certified hospitals. Besides Kaplan-Meier-estimators, Cox regression with shared frailty was used for 11 types of cancer in total, adjusting for patient-specific information such as demographic characteristics and comorbidities as well as hospital characteristics and temporal trend. Based on this regression, we predict adjusted survival curves that directly address the certification effect. From the adjusted survivals, we calculated years of life lost (YLL) and number needed to treat (NNT), along with a difference in deaths 5 years after diagnosis.

Results Based on our estimate for the 537,396 patients that were treated in a non-certified hospital included in the WiZen study, corresponding to 68,7% of the study population, we find a potential of 33,243 YLL per year in Germany based on the size of the German population as of 2017. The potential to avoid death cases 5 years from diagnosis totals 4,729 per year in Germany.

Conclusion While Cox regression is an important tool to evaluate the benefit that arises from variables with a potential impact on survival such as certification, its direct results are not well suited to quantify this benefit for decision makers in health care. The estimated years of life lost and the number of deaths that could have been avoided 5 years from diagnosis avoid mis-interpretation of the hazard ratios commonly used in survival analysis and should help to inform key stakeholders in health care without specialist background knowledge in statistics. Our measures, directly adressing the effect of certification, can furthermore be used as a starting point for health-economic calculations. Steering the care of cancer patients primarily to certified hospitals would have a high potential to improve outcomes.


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Introduction

According to the National Cancer Plan, all cancer patients should receive treatment in accordance with evidence-based treatment guidelines [1]. With this aim, the German Cancer Society (Deutsche Krebsgesellschaft, DKG) has, as of 2003, established a certification programme that focuses on structuring the entire process of care in an evidence-based, guideline-adherent manner and is currently the largest in Europe [2] [3]. In order to obtain a DKG certificate, hospitals need to meet a specified set of professional and quality requirements based on S3-guidelines [2]. These requirements cover the entire process of oncological care. Structural requirements include e. g. multidisciplinary communication, psychooncological support, as well as connection to the outpatient sector, social care, and rehabilitation. Certified hospitals need to file annual reports via entity specific surveys and indicator sheets covering key figures, part of which are quality indicators as defined in S3-guidelines to retain the certificate. Requirements, surveys and indicator sheets are publicly available via the DKG website.

Hospitals that do not hold a certificate may meet the same structural requirements for cancer therapy, but are not obliged to do so. It is hence reasonable to assume that the measures required to meet certification criteria ultimately improve outcomes. The aim of the “WiZen”- study whose results serve as a basis for this article was to provide reliable evidence about the effectiveness of certification: The “WiZen Study” (Wirksamkeit der Versorgung in onkologischen Zentren/Effectiveness of care in oncological centres), funded by the Innovation Fund of the Joint Federal Committee (Gemeinsamer Bundesausschuss, G‑BA, Funding number: 01VSF17020), provides a large and comprehensive analysis of survival in hospitals certified by the DKG vs. non-certified hospitals on the basis of nationwide AOK data and data from several clinical cancer registries. The study finds that - irrespective of the entity - treatment in a certified hospital increases the chances of survival of patients with incident cancer [4] [5] [6], consolidating previous evidence on beneficial effects of certification both nationally [7] [8] [9] [10] and internationally [11] [12] [13] [14] [15]. The statutory health insurance AOK was covering, as of 2017, a total population of around 22 million adults. The study contains cohorts of patients with incident cancer for 11 entities in total ranging from 10,596 patients (cervical carcinoma) to 172,901 patients (lung carcinoma) in the years 2009–2017. Survival analysis was conducted for eleven entities separately, including Kaplan-Meier-estimates and Cox regression with shared frailty. These entities were colon and rectal cancer, lung cancer, pancreatic cancer, breast cancer, ovarian, endometrial and cervical cancer, prostate cancer, head and neck cancers and brain tumors, defined via ICD-10 codes, see Supporting [Table 1]. For each entitity, a set of covariates was considered that consisted of patients’ demographic information (age, sex), disease-related information (distant metastasis, secondary malignoma, comorbidities) and hospital-level information (hospital status – teaching, university hospital, and ownership, as well as number of beds) and the calendar year of treatment to take into account effects of medical progress. The relative survival advantages were between 3 and 26 percent for the 11 entities and cohorts studied ([Fig. 1]).

Zoom Image
Fig. 1 Adjusted hazard ratios (95% confidence intervals) of overall survival for treatment in DKG-certified vs. non-certified hospitals for the eleven entifies considered.

Table 1 Analysis of Life Years Lost per year for the tumour entities investigated.

Entity

n (non-certified)

proportion (%) (non-certified)

Difference in area between survival functions

Difference for non- certified population (YLL)

Potentially lost life years YLL/yr in Germany (year of reference, 2017)

Colon cancer

68,826

62.7

0.21

14,495

5,114

Rectal cancer

29,370

57.1

0.24

7,042

2,484

Pancreatic cancer

39,892

88.0

0.17

6,649

2,346

Breast cancer

52,451

36.5

0.29

15,465

5,456

Cervical cancer

16,031

77.1

0.32

5,078

1,791

Endometrial cancer

7,769

73.3

0.38

2,984

1,053

Ovarian cancer

24,222

80.5

0.13

3,116

1,099

Lung cancer

139,115

80.0

0.05

7,152

2,523

Prostate cancer

57,112

70.0

0.25

14,305

5,047

Brain tumors

58,032

92.5

0.19

11,304

3,988

Head and neck cancers

44,576

84.5

0.15

6,642

2,343

total

537,396

-

-

33,243

Across entities, less than half of patients with incident cancer were treated in certified hospitals during the study period (2009–2017) and the proportion of patients treated in certified hospitals was 31.3% during the observation period. The proportion of patients who have been not been treated in a certified hospital ranges from 36.5 (breast cancers) to 92.5 per cent (brain cancers), [Fig. 2].

Zoom Image
Fig 2 Proportion of patients that have/have not received treatment in a DKG-certified hospital per entity, along with the number of patients in each entity.

Given that, as a result of the WiZen study, the certification effect showed a benefit in survival across entities, the question arises what this benefit would have encompassed had all patients been treated in a certified center. While survival analysis constitutes a powerful tool to evaluate effect of treatments for diseases such as cancer its direct results are not well suited to quantify this benefit:

Cox regression addresses the effect of multiple variables upon the survival time, and is hence suited to quantify the effect of certification. However, results of a Cox regression are typically presented in terms of Hazard ratios, i. e. the relative impact a given variable has on the (time-dependent) hazard with respect to a given reference level, e. g. presence vs. absence of a covariate. The hazard ratio constitutes a relative measure whereas in many settings the impact on a given population in terms of absolute numbers is required. This is particularly true for patients, who can interpret an absolute risk or chance such as the number needed to treat (NNT) much better than a relative risk or hazard ratio. For health policy makers, quantification of the total absolute effect as characterized by Years Life Lost (YLL) is of high importance [16]. In addition, the interpretation of a hazard ratio requires a specialized background in survival analysis and calls for careful communication [17]. The hazard ratio is thus critisized for not being particularly suited to illustrate study findings to, e. g. decision makers and other stakeholders in health care and concepts to avoid using it altogether are emerging [18] [19] [20] [21].

In this article, we compute two absolute measures from adjusted survival curves that incorporate the results from Cox regression, but do not rely on solely reporting the hazard ratios. The first measure is the number needed to treat (NNT), which allows to quantify the difference in deaths after a given point in time after diagnosis between two groups. The second measure is years of life lost (YLL), which is commonly used in the communication of statistical assessment for burden of disease for e. g. cancer and diabetes by. e. g. the Robert-Koch-Institute (RKI) and the National Cancer Institute (NCI) [22] [23] [24]. We deduct both measures from survival curves as predicted by adjusted Cox regression, allowing us to focus on the cerfication effect only.

Our approach allows for combination of results from multivariate statistical analysis with a framework that we feel is suited for communication of the effectiveness of a health-care intervention with non-statisticians.


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Methods

We use Cox regression with shared frailty [25] [26] for each entity separately for a given set of covariates detailed in [4] and summarized in Table S2. The resulting hazard ratios for each covariate indicate the extent to which the prognosis changes relatively with respect to a reference level of each variable. A hazard ratio>1 indicates a poorer prognosis for the assoated variable compared to the reference level, and a hazard ratio<1 indicates a beneficial effect. The Cox regression assumes that on a baseline which is determined in the regression, the adjusted hazard behaves proportionally to the baseline hazard with respect to the hazard ratio of a specific covariate (“proportional hazards assumption”). The probability of survival (or death) is then calculated as a prediction of a survivor function, based on an exponential transformation of the adjusted hazard function . This prediction of a survivor curve, is based on the entire model result, i. e. the hazard (ratios) of all covariates as well as the baseline hazard. The prediction must be made on a model population. The model population used here is defined by the mean value over all covariates of the actual population, i. e. mean value of age group, mean value of sex m/f, mean value of oncological second disease, etc. Stratifying variables are excluded from mean calculation. The prediction based on the model results on the model population yields an adjusted survival curve. This survival function in analogy to a Kaplan-Meier-curve starts with value one at time zero and decreases over time in a non-linear fashion. Since we are interested in a survival probability in certified/non-certified centres, the survival function is computed upon stratification by certified/non-certified hospitals.

Hence, two predictions using all estimators from the model on the mean model populations are performed, for an “all certified” and an “all non-certified” case. The covariates, with the exception of certification, are therefore identical for both strata. Fig. 3 shows a schematic representation of these two predictions. From these predictions, we compute two measures, i) the number of life years lost and ii) the number needed to treat (NNT) for one additional patient to survive at least five years after diagnosis. As the survival function is time-dependent, all considerations that result in absolute measures must be supplemented with a time reference.

Life Years Lost (YLL)

The years of life lost due to initial treatment in a certified center compared to a non-certified hospital correspond to the area separated by the two survival curves. It is therefore the difference between the areas under the respective survival curves. As the time of follow-up is restricted, we introduce a cutoff to the area, which corresponds to censoring for all values that exceed cutoff. Our total observation time is nine years; we set the cutoff to eight years to account for uncertainty in the prediction towards the end of the observation time, hence estimating a lower bound of the area. This area is now rescaled with the population in the non-certified setting, pop ncert , resulting in an estimate of Years of life lost (YLL) due to the fact the hospitals were non-certified:

Note that in our variant for life years lost, we do not explicitely take into account a person’s age at onset of disease as is common in epidemiology for computation of years of life lost due to mortality. Here, the age at the onset of diagnosis is incorporated as covariate into the prediction of the survival curve and through the median population.


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NNT and avoidable deaths within 5 years of diagnosis

The number needed to treat (NNT) related to the certification effect, is given by the inverse difference in the two survival functions for a given time t surv . We set this survival time to t surv .=5 years, as the 5-year survival is an important outcome and a broadly used epidemiological measure for the burden of disease in oncology. This time period is also relevant for patients because after this time the incidence of recurrences is significantly reduced in most cases and follow-up care is usually also terminated.

where s(t) is the simulated survival at time t for stratum X. Rescaling with the population in the non-certified setting results in an estimate of the number of deaths that could have been avoided within 5 years from diagnosis:


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Results

Adjusted survival functions were computed based on Cox regression with shared frailty for each entity separately for a given set of covariates. This set was identical for each entity with the exception of comorbidities that are entity-specific as defined by clinical experts, see Supporting Table S2. Within the WiZen study, we fitted Cox regression models upon gradually increasing the sets of covariates and found that the cerfication effect does not depend substantially on the choice of model [4]. The concordance (Harrels’ C) for these models is increasing with model complexity. The increase is substantial upon adding disease-related information to the core set (certification, age, sex), and marginal upon addition of hospital-related covariates and year of diagnosis. It becomes maximal and ranges from 0.67 to 0.82 for the model including the full set of covariates across entities, Supporting Table S3. We thus compute adjusted survivals for each entity from the model with the best concordance, i. e. the one including all covariates, with hazard ratios ranging from 0.77 to 0.92 across entities, Supporting Table S4.

Life Years Lost (YLL)

The estimation of the potential of care through treatment of patients with incident cancer into certified hospitals is based on the difference of the area under the adjusted survival function of the treatment in certified hospitals and the treatment in non-certified hospitals simulated from the Cox regression (see Fig. 3). Due to the limited observation period of the WiZen study of 9 years, the period up to 8 years after diagnosis was considered as the cutoff limit. The results are therefore conservative and include only the years of life lost within this period.

Taking into account the proportion of the national population insured by AOK, which was AOK coverage 2017 =31.5% (people insured by the AOK as of July 2017: 25.990.759, German population 2017: 82.522.000, [27]), we estimate for “Life Years Lost/yr in Germany” based on the WiZen project results for the overall population in Germany from:

The following [Table 1] shows the Life Years Lost for the 11 entities examined. The number of people affected for each entity determines the benefit in survival on a population level. The total number of patients treated in a non-certified hospital ranges from 7,769 for endometrial to 139,115 patients for lung cancer. The size of the population hence adds an essential contribution to the total YLL. The size of the area between survival functions serves as a guideline to the extent of the certification effect for each entity: if the area increases the benefit in overall survival increases as well. Hence, the YLL becomes maximal for entities that have a larger benefit, but also many people affected, as is the case for e. g. breast, colon and prostate cancer in contrast to lung cancer (small effect) or endometrial cancer (less people affected).

In total, there is a potential of around 33,200 life years saved per year in Germany.


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NNT and avoidable deaths within 5 years of diagnosis

In a next step, the number needed to treat is computed based on the WiZen results. Using the population of patients treated in certified and non-certified centres, we then use the NNT which indicates the potential to avoid one death within 5 years of diagnosis to assess the potential for the total of avoided deaths within 5 years after diagnosis.

The calculation of avoidable deaths results from the difference of the survival curves after 5 years (Fig. 3), in analogy to the procedure for Life Years Lost related to the federal population 2017 as:

The results are shown in [Table 2] for each entity individually. For cancers with very low chance of (crude) survival after five years, such as pancreatic cancer and lung cancer, the difference in the survival function is small as well, reflecting the lesser (overall) chance of preventing death with fighting the most deadly cancers. In analogy to YLL, the number of avoidable deaths scales with the size of the population for each entity, and, as a consequence, a large number of people who have not been treated in a certified setting provides a larger potential for avoidable deaths 5 years post-diagosis, which we find for colon, breast, and prostate cancer. In total, approx. 4,700 deaths per year could have been avoided 5 years post diagnosis if all patients had been treated in a certified cancer.

Table 2 Analysis of potentially avoidable deaths within 5 years after diagnosis per year for the tumour entities investigated.

Entity

n (non- certified)

proportion (%) (non- certified)

crude 5-yr survival rate, non-certified

difference certified/non-certified from adjusted 5-yr-survival rate*

number needed to Treat (NNT)*

deaths 5 yrs post-diagnosis that could have been avoided/yr (Germany)*

Colon cancer

68,826

62.7

0.467

0.031

32

754

Rectal cancer

29,370

57.1

0.433

0.036

28

372

Pancreatic cancer

39,892

88.0

0.065

0.014

70

202

Breast cancer

52,451

36.5

0.719

0.046

22

859

Cervical cancer

16,031

77.1

0.357

0.046

22

258

Endometrial cancer

7,769

73.3

0.533

0.057

18

156

Ovarian cancer

24,222

80.5

0.650

0.020

51

168

Lung cancer

139,115

80.0

0.169

0.006

179

274

Prostate cancer

57,112

70.0

0.712

0.039

26

789

Brain tumors

58,032

92.5

0.480

0.027

37

555

Head and neck cancers

44,576

84.5

0.453

0.022

46

341

total

537,396

-

-

-

-

4,729

* from adjusted survival curve.


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Discussion

We illustrated how to derive Life years lost and the Number needed to treat from adjusted survival functions that were computed based on the results of the WiZen study. We have derived these measures from the cohort used in the WiZen study which includes AOK-insured patients that were diagnosed with one out of eleven types on cancers within the years 2009–2017. Based on the 537 396 patients or 68,7% of the study population in the cohort who have not received treatment in a certified hospital, we estimated a total of 33 243 YLL per year for the entire German population as of 2017. The corresponding potential to avoid death cases for as long as five years within diagnosis sums up to 4 729 per year in Germany. Both YLL and NNT depend on the entity specific survival that was estimated based on the Cox regressions, as well as the size of the population under consideration. The difference in survival curves (both in area and for the 5 year limit) tends to be smaller for cancers with overall low survival prospects, such as pancreatic cancer. Beyond this observation, we currently do not have any additional information about the range of differences, which may arise from many factors both on the cohort and on the intervention level. As the size of the population under consideration varies significantly, the greatest contribution to the total deaths that could be avoided arise from cancers that have either high incidence such as e. g. breast and colon cancer or a very low proportion of certified centers such as brain tumours. To date, we are not aware of any literature about YLL and the assesment of avoidable deaths in the context of certification, beyond the national [7] [8] [9] [10] and international [11] [12] [13] [14] [15] evidence about the benefits of structuring the process of cancer care, be it via certification or accredition.

Our findings have a set of limitations: As in any communication of statistical results, it needs to be pointed out that the estimates presented here are based on various assumptions and do, to some extent, depend on the method [28]. The rescaling from the original population that covers patients insured by the AOK,which is roughly one third of the German population, to the entire size of the population serves as a rough estimate to estimate the total YLL and the number of deaths within 5 yrs from diagnosis that could have been avoided. The validity of this extrapolation is based on the assumption that the cohort on which the survivals were predicted adequately represents the epidemiology of the disease in Germany, which we feel is a valid assumption given the large size of the cohort. Another limitation and one of the most unfortunate shortcomings of health insurance data is that these contain very litte information on important cancer-related measures such as staging and grading. The quality of the data, and hence, the model prediction could be improved by e. g. linking SHI data with data from cancer registries as evaluated in [29].

The strength of this assesment lies in that our estimates avoid the reporting, and thus potential for misinterpretation, of the hazard ratio and can be used to inform political decision makers about the extent of the benefit in survival found in the WiZen study. As our estimates provide absolute results such as the amount of deaths within five years of diagnosis, they can be used in health-economic analyses that deal with e. g. certification and cost-effectiveness [30].

Zoom Image
Fig 3 Schematic representation of the calculation of Life Years Lost, corresponding to the area between two adjusted survival curves in the period up to 8 years ("cutoff"). Also shown is the difference in survival after 5 years, as used in the calculation of avoidable deaths.

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Conclusion

For each individual entity, steering into certified centres would have a relevant effect on preventable deaths within 5 years of diagnosis. The Number Needed To Treat, i. e. the number of additional patients to be treated in a certified centre in order to avoid a death 5 years post-diagosis, also depends on the general prognosis of the entities. For example, the Number Needed To Treat is higher for cancers with a generally poor prognosis, such as lung cancer or pancreatic cancer.

Through illustrating the potential in survival benefit from certification in the past decade, our analysis provides a starting point for a broader discussion of political implications that would either foster certification and/or install a coordinated effort to steer patients into certified hospitals.


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Ethics declaration

The WiZen study was approved by the ethics committee of the TU Dresden (approval number: EK95022019, IRB 00001473, OHRP IORG0001076). Data processing and analyses was conducted in line with the Declaration of Helsinki and the General Data Protection Regulation of the European Union.


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Contributor’s Statement

None


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Zusätzliches Material

Supplementary Material

  • Literatur

  • 1 Nationaler Krebsplan (Stand 2017) https://www.bundesgesundheitsministerium.de/fileadmin/Dateien/5_Publikationen/Praevention/Broschueren/Broschuere_Nationaler_Krebsplan.pdf
  • 2 Kowalski C, Graeven U, Kalle C. et al. Shifting cancer care towards multidisciplinarity: The cancer center certification program of the German Cancer Society. BMC Cancer 2017; 17: 1-9
  • 3 Griesshammer E, Wesselmann S. European Cancer Centre Certification Programme. Gynäkologe 2019; 52: 380-385
  • 4 Schoffer O, Rößler M, Bierbaum V. et al. Ergebnisbericht zum Projekt Wirksamkeit der Versorgung in onkologischen Zentren (WiZen). Berlin: Federal Joint Committee – Innovation Committee 2022; https://innovationsfonds.g-ba.de/downloads/beschluss-dokumente/268/2022-10-17_WiZen_Ergebnisbericht.pdf, in German
  • 5 Schoffer O, Gerken M, Bierbaum V. et al. https://www.wido.de/fileadmin/Dateien/Dokumente/Publikationen_Produkte/GGW/2022/wido_ggw_0422_schoffer_et_al.pdf, in German.
  • 6 Schmitt J, Klinkhammer-Schalke M, Bierbaum V. et al. Individuals with Cancer Benefit from Treatment in Certified Hospitals: Results from the Comparative Cohort Study WiZen. Deutsches Ärzteblatt (under Revision).
  • 7 Trautmann F, Reißfelder C, Pecqueux M. et al. Evidence-based quality standards improve prognosis in colon cancer care. European Journal of Surgical Oncology 2018; 44: 1324-1330
  • 8 Völkel V, Draeger T, Gerken M. et al. Langzeitüberleben von Patienten mit Kolon- und Rektumkarzinomen: Ein Vergleich von Darmkrebszentren und nicht zertifizierten Krankenhäusern – [Long-Term Survival of Patients with Colon and Rectum Carcinomas: Is There a Difference Between Cancer Centers and Non-Certified Hospitals?]. Gesundheitswesen. 2018; 81: 801
  • 9 Roessler M, Schmitt J, Bobeth C. et al. Kleihues-van Tol K, Reissfelder C, Rau BM, Distler M, Piso P, Günster C, Klinkhammer-Schalke M, Schoffer O, Bierbaum V. Is treatment in certified cancer centers related to better survival in patients with pancreatic cancer? Evidence from a large German cohort study. BMC Cancer 2022; 22: 621
  • 10 Butea-Bocu MC, Müller G, Pucheril D. et al. Is there a clinical benefit from prostate cancer center certification? An evaluation of functional and oncologic outcomes from 22,649 radical prostatectomy patients. World Journal of Urology 2021; 39: 5-10
  • 11 Birkmeyer NJ, Goodney PP, Stukel TA. et al. Do cancer centers designated by the National Cancer Institute have better surgical outcomes?. Cancer. 2005; 103: 435-441
  • 12 Mehta R, Ejaz A, Hyer JM. et al. The impact of Dedicated Cancer Centers on outcomes among medicare beneficiaries undergoing liver and pancreatic cancer surgery. Annals of Surgical Oncology 2019; 26: 4083-4090
  • 13 Jacob A, Albert W, Jackisch T. et al. Association of certification, improved quality and better oncological outcomes for rectal cancer in a specialized colorectal unit. Int J Colorectal Dis 2021; 36: 517-533
  • 14 Reeves ME. Do Better Operative Reports Equal Better Surgery? A Comparative Evaluation of Compliance With Operative Standards for Cancer Surgery. Am Surg 2020; 86: 1281-1288
  • 15 Paulson EC, Mitra N, Sonnad S. et al. National Cancer Institute Designation Predicts Improved Outcomes in Colorectal Cancer Surgery. Annals of Surgery 2008; 248
  • 16 Hoffrage U, Koller M. Chancen und Risiken der Risikokommunikation in der Medizin.GMS Ger Med Sci 2015; 13: Doc07
  • 17 Sashegyi A, Ferry D. On the Interpretation of the Hazard Ratio and Communication of Survival Benefit. Oncologist. 2017; 22: 484
  • 18 Altman DG, Andersen PK. Calculating the number needed to treat for trials where the outcome is time to an event. BMJ. 1999; 319: 1492
  • 19 Royston P, Parmar MK. Restricted mean survival time: an alternative to the hazard ratio for the design and analysis of randomized trials with a time-to-event outcome. BMC Med Res Methodol 2013; 13: 152
  • 20 Syriopoulou E, Wästerlid T, Lambert PC. et al. Standardised survival probabilities: a useful and informative tool for reporting regression models for survival data. Br J Cancer 2022; 127: 1808-1815
  • 21 Uno H, Claggett B, Tian L. et al. Moving beyond the hazard ratio in quantifying the between-group difference in survival analysis. J Clin Oncol 2014; 32: 2380
  • 22 https://diabsurv.rki.de/Webs/Diabsurv/DE/diabetes-in-deutschland/4-37_Verlorene_Lebensjahre_YLL.html
  • 23 Wengler A, Rommel A, Plaß D. et al. Years of life lost to death—a comprehensive analysis of mortality in Germany conducted as part of the BURDEN 2020 project Dtsch Arztebl Int 2021; 118: 137
  • 24 https://progressreport.cancer.gov/end/life_lost
  • 25 Wienke A. Frailty models in survival analysis. Amsterdam, The. Netherland: CRC Press; 2010
  • 26 Balan TA, Putter H. A tutorial on frailty models. Stat. Methods Med Res 2020; 29: 3424-3454
  • 27 https://www.bundesgesundheitsministerium.de/themen/krankenversicherung/zahlen-und-fakten-zur-krankenversicherung/kennzahlen-daten-bekanntmachungen.html
  • 28 Chudasama YV, Khunti K, Gillies CL, et al. Estimates of years of life lost depended on the method used: tutorial and comparative investigation, Journal of Clinical Epidemiology, 2022, Volume 150, Pages 42-50, ISSN 0895-4356, 10.1016/j.jclinepi.2022.06.012
  • 29 Bobeth C, van Tol KK, Rößler M. et al. Methodology and Attribution Success of a Data Linkage of Clinical Registry Data with Health Insurance Data. Gesundheitswesen 2023; 85: S154-S161
  • 30 Cheng CY, Datzmann T, Hernandez D. et al. Do certified cancer centers provide more cost-effective care? A health economic analysis of colon cancer care in Germany using administrative data. Int J Cancer 2021; 149: 1744-1754

Korrespondenzadresse

Veronika Bierbaum
Universitätsklinikum Carl Gustav Carus, Zentrum für Evidenzbasierte Gesundheitsversorgung
Fetscherstr. 74
01307 Dresden
Germany   

Publication History

Article published online:
26 September 2023

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  • Literatur

  • 1 Nationaler Krebsplan (Stand 2017) https://www.bundesgesundheitsministerium.de/fileadmin/Dateien/5_Publikationen/Praevention/Broschueren/Broschuere_Nationaler_Krebsplan.pdf
  • 2 Kowalski C, Graeven U, Kalle C. et al. Shifting cancer care towards multidisciplinarity: The cancer center certification program of the German Cancer Society. BMC Cancer 2017; 17: 1-9
  • 3 Griesshammer E, Wesselmann S. European Cancer Centre Certification Programme. Gynäkologe 2019; 52: 380-385
  • 4 Schoffer O, Rößler M, Bierbaum V. et al. Ergebnisbericht zum Projekt Wirksamkeit der Versorgung in onkologischen Zentren (WiZen). Berlin: Federal Joint Committee – Innovation Committee 2022; https://innovationsfonds.g-ba.de/downloads/beschluss-dokumente/268/2022-10-17_WiZen_Ergebnisbericht.pdf, in German
  • 5 Schoffer O, Gerken M, Bierbaum V. et al. https://www.wido.de/fileadmin/Dateien/Dokumente/Publikationen_Produkte/GGW/2022/wido_ggw_0422_schoffer_et_al.pdf, in German.
  • 6 Schmitt J, Klinkhammer-Schalke M, Bierbaum V. et al. Individuals with Cancer Benefit from Treatment in Certified Hospitals: Results from the Comparative Cohort Study WiZen. Deutsches Ärzteblatt (under Revision).
  • 7 Trautmann F, Reißfelder C, Pecqueux M. et al. Evidence-based quality standards improve prognosis in colon cancer care. European Journal of Surgical Oncology 2018; 44: 1324-1330
  • 8 Völkel V, Draeger T, Gerken M. et al. Langzeitüberleben von Patienten mit Kolon- und Rektumkarzinomen: Ein Vergleich von Darmkrebszentren und nicht zertifizierten Krankenhäusern – [Long-Term Survival of Patients with Colon and Rectum Carcinomas: Is There a Difference Between Cancer Centers and Non-Certified Hospitals?]. Gesundheitswesen. 2018; 81: 801
  • 9 Roessler M, Schmitt J, Bobeth C. et al. Kleihues-van Tol K, Reissfelder C, Rau BM, Distler M, Piso P, Günster C, Klinkhammer-Schalke M, Schoffer O, Bierbaum V. Is treatment in certified cancer centers related to better survival in patients with pancreatic cancer? Evidence from a large German cohort study. BMC Cancer 2022; 22: 621
  • 10 Butea-Bocu MC, Müller G, Pucheril D. et al. Is there a clinical benefit from prostate cancer center certification? An evaluation of functional and oncologic outcomes from 22,649 radical prostatectomy patients. World Journal of Urology 2021; 39: 5-10
  • 11 Birkmeyer NJ, Goodney PP, Stukel TA. et al. Do cancer centers designated by the National Cancer Institute have better surgical outcomes?. Cancer. 2005; 103: 435-441
  • 12 Mehta R, Ejaz A, Hyer JM. et al. The impact of Dedicated Cancer Centers on outcomes among medicare beneficiaries undergoing liver and pancreatic cancer surgery. Annals of Surgical Oncology 2019; 26: 4083-4090
  • 13 Jacob A, Albert W, Jackisch T. et al. Association of certification, improved quality and better oncological outcomes for rectal cancer in a specialized colorectal unit. Int J Colorectal Dis 2021; 36: 517-533
  • 14 Reeves ME. Do Better Operative Reports Equal Better Surgery? A Comparative Evaluation of Compliance With Operative Standards for Cancer Surgery. Am Surg 2020; 86: 1281-1288
  • 15 Paulson EC, Mitra N, Sonnad S. et al. National Cancer Institute Designation Predicts Improved Outcomes in Colorectal Cancer Surgery. Annals of Surgery 2008; 248
  • 16 Hoffrage U, Koller M. Chancen und Risiken der Risikokommunikation in der Medizin.GMS Ger Med Sci 2015; 13: Doc07
  • 17 Sashegyi A, Ferry D. On the Interpretation of the Hazard Ratio and Communication of Survival Benefit. Oncologist. 2017; 22: 484
  • 18 Altman DG, Andersen PK. Calculating the number needed to treat for trials where the outcome is time to an event. BMJ. 1999; 319: 1492
  • 19 Royston P, Parmar MK. Restricted mean survival time: an alternative to the hazard ratio for the design and analysis of randomized trials with a time-to-event outcome. BMC Med Res Methodol 2013; 13: 152
  • 20 Syriopoulou E, Wästerlid T, Lambert PC. et al. Standardised survival probabilities: a useful and informative tool for reporting regression models for survival data. Br J Cancer 2022; 127: 1808-1815
  • 21 Uno H, Claggett B, Tian L. et al. Moving beyond the hazard ratio in quantifying the between-group difference in survival analysis. J Clin Oncol 2014; 32: 2380
  • 22 https://diabsurv.rki.de/Webs/Diabsurv/DE/diabetes-in-deutschland/4-37_Verlorene_Lebensjahre_YLL.html
  • 23 Wengler A, Rommel A, Plaß D. et al. Years of life lost to death—a comprehensive analysis of mortality in Germany conducted as part of the BURDEN 2020 project Dtsch Arztebl Int 2021; 118: 137
  • 24 https://progressreport.cancer.gov/end/life_lost
  • 25 Wienke A. Frailty models in survival analysis. Amsterdam, The. Netherland: CRC Press; 2010
  • 26 Balan TA, Putter H. A tutorial on frailty models. Stat. Methods Med Res 2020; 29: 3424-3454
  • 27 https://www.bundesgesundheitsministerium.de/themen/krankenversicherung/zahlen-und-fakten-zur-krankenversicherung/kennzahlen-daten-bekanntmachungen.html
  • 28 Chudasama YV, Khunti K, Gillies CL, et al. Estimates of years of life lost depended on the method used: tutorial and comparative investigation, Journal of Clinical Epidemiology, 2022, Volume 150, Pages 42-50, ISSN 0895-4356, 10.1016/j.jclinepi.2022.06.012
  • 29 Bobeth C, van Tol KK, Rößler M. et al. Methodology and Attribution Success of a Data Linkage of Clinical Registry Data with Health Insurance Data. Gesundheitswesen 2023; 85: S154-S161
  • 30 Cheng CY, Datzmann T, Hernandez D. et al. Do certified cancer centers provide more cost-effective care? A health economic analysis of colon cancer care in Germany using administrative data. Int J Cancer 2021; 149: 1744-1754

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Abb. 1 Adjustierte Hazard Ratios (95% Konfidenzintervalle) des Gesamtüberlebens für die Behandlung in DKG-zertifizierten gegenüber nicht zertifizierten Krankenhäusern für die elf betrachteten Entitäten.
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Abb. 2 Anteil der Patienten, die in einem DKG-zertifizierten Krankenhaus/nicht DKG-zertifizierten Krankenhaus behandelt wurden, sowie die Anzahl der Patienten zu jeder Entität.
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Abb. 3 Schematische Darstellung für die Berechnung der verlorenen Lebensjahre, die der Fläche zwischen zwei angepassten Überlebenskurven im Zeitraum bis zu 8 Jahren (“Cutoff”) entsprechen. Ebenfalls dargestellt ist der Unterschied in der Überlebenszeit nach 5 Jahren, wie er für die Berechnung der vermeidbaren Todesfälle verwendet wird.
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Fig. 1 Adjusted hazard ratios (95% confidence intervals) of overall survival for treatment in DKG-certified vs. non-certified hospitals for the eleven entifies considered.
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Fig 2 Proportion of patients that have/have not received treatment in a DKG-certified hospital per entity, along with the number of patients in each entity.
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Fig 3 Schematic representation of the calculation of Life Years Lost, corresponding to the area between two adjusted survival curves in the period up to 8 years ("cutoff"). Also shown is the difference in survival after 5 years, as used in the calculation of avoidable deaths.