Cohort profile: King’s Health Partners bladder cancer biobank
verfasst von:
Pinky Kotecha, Charlotte L. Moss, Deborah Enting, Cheryl Gillett, Magdalene Joseph, Debra Josephs, Sarah Rudman, Simon Hughes, Fidelma Cahill, Harriet Wylie, Anna Haire, James Rosekilly, Muhammad Shamin Khan, Rajesh Nair, Ramesh Thurairaja, Sachin Malde, Mieke Van Hemelrijck
Bladder cancer (BC) is the 9th most common cancer worldwide, but little progress has been made in improving patient outcomes over the last 25 years. The King’s Health Partners (KHP) BC biobank was established to study unanswered, clinically relevant BC research questions.
Donors are recruited from the Urology or Oncology departments of Guy’s Hospital (UK) and can be approached for consent at any point during their treatment pathway.
At present, patients with bladder cancer are approached to provide their consent to provide blood, urine and bladder tissue. They also give access to medical records and linkage of relevant clinical and pathological data across the course of their disease. Between June 2017 and June 2019, 531 out of 997 BC patients (53.3%) gave consent to donate samples and data to the Biobank. During this period, the Biobank collected fresh frozen tumour samples from 90/178 surgical procedures (of which 73 were biopsies) and had access to fixed, paraffin embedded samples from all patients who gave consent. Blood and urine samples have been collected from 38 patients, all of which were processed into component derivatives within 1 to 2 h of collection. This equates to 193 peripheral blood mononuclear cell vials; 238 plasma vials, 224 serum vials, 414 urine supernatant vials and 104 urine cell pellets. This biobank population is demographically and clinically representative of the KHP catchment area.
Conclusion
The King’s Health Partners BC Biobank has assembled a rich data and tissue repository which is clinically and demographically representative of the local South East London BC population, making it a valuable resource for future BC research.
Hinweise
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
BC
Bladder Cancer
KHP
King’s Health Partners
TWiC
Trials within cohort study
PBMC
Peripheral blood mononuclear cells
GSTT
Guy’s and St Thomas’ NHS Foundation Trust
SES
Socioeconomic Status
BCG
Bacillus Calmette-Guerin
Background
Bladder cancer is the 9th most common cancer worldwide with around 430,000 new cases diagnosed in 2012 [1]. Nevertheless, outcomes in bladder cancer have remained largely unchanged over the last 25 years and much remains unknown about this complex disease, especially with regard to disease aetiology and progression [2]. Urological biobanking can therefore provide a valuable resource to answer a number of clinically relevant research questions [2], spurring translation into practical applications and ultimately leading to improvements in public health and healthcare.
King’s Health Partners (KHP) is an Academic Health Science Centre bringing together King’s College London, Guy’s and St Thomas’ NHS Foundation Trust (GSTT), King’s College Hospital NHS Foundation Trust and the South London and Maudsley NHS Foundation Trust, as shown in Fig. 1 [3].
Fig. 1
Catchment area of King’s Health Partners (KHP). Image adapted with permission from London City Council Government Directory [3].
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The KHP Bladder Cancer Biobank was established in April 2017 as part of the overarching KHP Cancer Biobank. Bladder cancer patients are recruited from the Urology and Oncology departments of Guy’s Hospital and provide their consent to donate blood, urine, tissue surplus to diagnostic requirements and extra tissue samples just for the Biobank. Patients may be approached to give consent at any point of their treatment journey, therefore allowing the Biobank to access residual material from an earlier diagnosis. Thus, although patients only started giving their consent from June 2017, the Biobank has samples collected both before and after this date. Clinical data relevant to bladder cancer can be linked to the biobank samples and data across the entire patient treatment journey. The resource encourages translational research and provides a bridge to patient care. The Biobank samples can be used to exhaustion, creating new research data that can be re-used by investigators. In addition, there is a potential for patients of the KHP Bladder Cancer Biobank to be linked to our ongoing Trials within Cohort Study (TWiCs), the Graham Roberts Study [4], which provides a unique opportunity to answer a wide variety of research questions of a clinical, mechanistic, as well as supportive care nature in the area of bladder cancer.
The KHP Cancer Biobank is licenced by the Human Tissue Authority (reference number 12121) and is a NHS Research Ethics Committee approved Tissue Bank with generic ethical approval to supply bioresources (reference number 18/EE/0025) [5].
Because of our catchment area (Fig. 1), KHP covers a wide range of ethnic and socioeconomic backgrounds, hence providing a unique and valuable resource.
Construction and content
A recent audit of the KHP Bladder Cancer Biobank highlighted that between April 2017–June 2019, 1089 patients were seen in a bladder clinic, with 997 subsequently diagnosed with bladder cancer. 552 patients gave their consent and following exclusion due to miscoding, 531 (53.3%) were included in the KHP Bladder Cancer Biobank. Recruitment for the biobank is ongoing (Fig. 2).
Fig. 2
Data and tissue repository available in KHP Bladder Cancer biobank
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The patients who gave consent to the KHP Bladder Cancer Biobank can be considered representative of the total KHP bladder cancer population attending clinics at GSTT, therefore making the biobank an ideal platform to explore the different features of bladder cancer. The mean age of the overall bladder cancer population seen at GSTT between April 2017 and June 2019 was 70.9 years (SD: 11.6), as compared to 71.03 years (SD: 10.55) for the biobanked population (Table 1). In addition, we observed similarities in sex distribution (78.9% males in the consented population vs 74.9% in the total population) and tumour grade distribution (e.g. 62.0% Grade 3 in the consented population vs 59.6% in the total population) (Table 2).
Table 1
Demographic information of KHP Bladder Cancer Biobank from April 2017–June 2019
Variable
Consented (n = 531)
%
Age (years)
70.1 (SD: 11.6)
< 40
11
2.1
40–49
16
3.0
50–59
61
11.5
60–69
132
24.9
70–79
194
36.5
80–89
110
20.7
90–99
7
1.3
Gender
Female
112
21.1
Male
419
78.9
Ethnicity
British (White)
302
56.9
Any other White background
28
5.3
Mixed background
1
0.2
Asian background
8
1.5
Caribbean, African or Any other Black background
9
1.7
Any other Ethnic Group
5
0.9
Not Stated or Not Known
178
22.3
Socioeconomic Status
Low
419
80.58
Middle
17
3.27
High
69
13.27
Missing
15
2.88
Trial
Yes
32
6.0
No
499
94.0
Comorbidities
Mean number of comorbidities
3.02 (SD:1.82)
Hypertension
198
37.3
Diabetes
89
16.8
Other cancer
82
15.4
Hypercholesterolaemia
80
15.1
Respiratory disease
62
11.7
Cardiovascular disease
62
11.7
Chronic Kidney Disease
32
6.0
Psychiatric Disorder
23
4.3
Smoking
Yes
183
34.5
No
33
6.2
Unknown
315
59.3
Table 2
Clinical information (diagnosis and pathological) of KHP Bladder Cancer Biobank from April 2017–June 2019
Clinical variable
Consented (n = 531)
%
Diagnosis
New
342
64.4
Recurrence
189
35.6
Histology
Urothelial Cell Carcinoma
308
58.0
Papillary Urothelial Cell Carcinoma
165
31.1
Squamous Cell Carcinoma
17
3.2
Adenocarcinoma
7
1.3
Micropapillary variant
7
1.3
Plasmacytoid variant
3
0.6
Paraganglioma
4
0.8
Papilloma
1
0.2
Small cell carcinoma
3
0.6
Sarcomatoid
2
0.4
Unknown
8
1.5
Grade
G1
38
7.2
G2
125
23.5
G3
329
62.0
Unknown
39
7.3
T stage
Ta/ Tis
193
36.3
T1
133
25.0
T2
106
20.0
T3
65
12.2
T4
14
2.6
Unknown
20
3.8
N stage
N0
485
91.3
N1
24
4.5
N2
22
4.1
M stage
M0
502
94.5
M1
29
5.5
Lymphovascular invasion
Yes
42
7.9
No
489
92.1
TURBT
Yes
428
80.6
No
103
19.4
Surgery
Yes
261
49.2
No
270
50.8
Chemotherapy
Neoadjuvant
37
7.0
Adjuvant
30
5.6
Chemotherapy
20
3.8
Palliative
6
1.1
Neoadjuvant and adjuvant
2
0.4
None
436
82.1
Radiotherapy
Yes
47
8.9
No
484
91.1
Intravesical Therapy
0.0
Yes
180
33.9
Di Stasi
76
14,3
BCG
62
11.7
Mitomycin
33
6.2
BCG and mitomycin in different occasions
7
1.3
Di Stasi and mitomycin in different occasions
1
0.2
Other
1
0.2
No
351
66.1
Intravesical Therapy Failure
Yes
35
6.6
Poorly tolerated
10
1.9
No
6
1.1
Unknown
129
24.3
Not applicable
351
66.1
Laser ablation
Yes
9
1.7
No
522
98.3
Immunotherapy
Yes
17
3.2
No
514
96.8
Tissue/ biospecimen repository
The KHP Bladder Cancer biobank includes fixed, paraffin embedded samples that are surplus to diagnostic requirement from all patients who gave consent and underwent a surgical procedure. Where possible, the Biobank collects fresh tumour and normal tissue from both resections and at biopsy. The Biobank has specialist Advanced Practitioners who review all potential specimens for suitability and are trained to partially dissect a fresh specimen and take samples for research but without impacting on the diagnostic integrity. Fresh frozen tissue is validated and stored at − 80 °C until required. All procedures are fully documented, and ischaemic times recorded, generating a specific sample-related data that can be provided to users of the resource.
During the 2-year audit period, the Biobank has collected fresh frozen tumour samples from 90/178 surgical procedures (of which 73 were a biopsy). Fixed, paraffin-embedded blocks are available from all 178 surgical procedures and if the Biobank so wished, it could request access to any tissue samples taken from the 531 patients who gave their consent.
Matched whole blood samples are also collected, from which a number of derivates are obtained including peripheral blood mononuclear cells (PBMC), plasma, serum and red blood cells. The derivatives are aliquoted, frozen and stored at − 80 °C. From urine samples, derivatives of urine supernatant and urine cell pellets are also generated and similarly stored. Similar to the tissue collection, data is recorded on processing procedures and times, number of derivatives and volume per aliquot.
Both blood and urine samples have been collected for 38 patients, which have been processed into 193 peripheral blood mononuclear cell vials; 238 plasma vials, 224 serum vials, 414 urine supernatant vials and 104 urine cell pellets.
A unique biobank identifier is automatically assigned to each new sample, which links to the donor. A second Research ID number is also created at the same time, which is used by researchers. Hence, this double anonymisation system provides the biobank with inbuilt security processes which protect patient data. Moreover, this ensures the collection of comprehensive data profiles as pathological data is linked to clinical patient data.
Data repository
All the data obtained has been collected from either GSTT Electronic Patient Records or Cancer Information System, contributing to the demographic (Table 1) and clinical (Table 2) database of the Biobank.
An overview of demographic and clinic-pathological data collected for the Biobank (Table 3) is outlined below in more detail.
Table 3
Overview of demographic and clinical information collected
Cystoprostatectomy, Cystectomy, Nephrouretectomy, Uretectomy, Nephrouretectomy and cystoprostatectomy, Cystectomy and ureterectomy, Diverticulectomy, Nephrouretectomy and cystectomy, Nephrouretectomy and partial cystectomy, Ureterostomy, Urethrectomy, Exenteration, None
Chemotherapy
Neoadjuvant, Adjuvant, Chemotherapy, Palliative, Neoadjuvant and adjuvant, None
Radiotherapy
Yes, No
Intravesical therapy
Di Stasi, BCG, Mitomycin, BCG and mitomycin in different occasions, Di Stasi and mitomycin in different occasions, Other, None
Intravesical therapy failure
Yes, No
Laser ablation
Yes, No
Immunotherapy
Yes, Poorly tolerated, Unknown, No, Not Applicable
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Demographics
Demographic information includes age, gender, ethnicity and postcode (Table 1). Currently, the cohort comprises of 62.1% White, 1.5% Asian, 1.7% Black, 1.1% Mixed or other ethnic groups. The ethnic background of 178 patients (33.5%) is not stated or not known. Postcode provides an opportunity to obtain information about the social deprivation index of the patients. We observed similarities in socioeconomic status (SES) between those who gave consent to the biobank and the GSTT total bladder cancer population (80.6% of low socioeconomic status in the consented population vs 82.6% in the total population).
In addition, baseline information of the biobanked patients also provides data on comorbidities and smoking history [6], as the latter is a known risk factor for bladder cancer (Table 2).
Finally, in the demographic database we also collect data about trial participation. Of the 531 patients in the biobank, 32 (6%) are currently also enrolled in a clinical trial.
Clinical information
Diagnostic information includes whether the bladder cancer diagnosis was new or recurrent, tumour histology, Grade, TNM staging and lymphovascular invasion (Table 2). A total of 35.6% patients in the biobank had a recurrent disease. In terms of histology, 89.1% patients had urothelial cell carcinoma, of which 31% were papillary urothelial cell carcinoma. Further details can be found in Table 2 and, as described above, the biobank population is representative of total bladder cancer population.
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In addition to diagnostic information, the Bladder Cancer Biobank also contains treatment data that can be linked to samples (Table 2). For instance, 49.2% of patients had undergone a radical cystectomy.
Utility and discussion
The biobank provides a valuable resource for research. As an example, we have outlined one of the ongoing studies below.
Phenotyping γδ T cells in bladder cancer- results from a pilot study
A recent analysis of over 18,000 tumour transcriptomes found a γδ T cell transcription signature to be strongly associated with a positive prognosis in human cancers [7]. γδ T cells have also been implicated in responses to Bacillus Calmette-Guerin (BCG) therapy of non-muscle invasive bladder cancer [8, 9]. However, studies in muscle-invasive bladder cancer have been limited. This project, which was approved by the Bladder Biobank Access Committee, uses a grid culture method to expand and isolate lymphocytes from tumour and para-tumoural tissue samples selected by the Biobank from fresh cystectomy specimens. Matched blood and urine samples from bladder cancer patients are also collected by research nursing staff and processed by the biobank which supplies cell suspensions for downstream phenotyping. The presence and phenotype of γδ T cells in bladder cancer and their associations with clinical features and outcomes are currently being examined and preliminary data has already been presented [10].
An additional arm of the project examines matched urine and blood samples from patients undergoing Bacillus-Calmette Guerin therapy for non-muscle invasive bladder cancer and these samples are also processed through the Biobank. Thus far, results show a γδ T cell compartment in tumour and para-tumoural tissue with carcinoma in situ affecting γδ T cell representation in both areas. Para-tumoural tissue also shows a stage related relationship with an increased percentage of γδ T cells in para-tumoural tissue surrounding higher stage tumours.
Strengths and weakness
The KHP Bladder Cancer Biobank is a novel and valuable resource. Its size and depth allow the linkage of biospecimens and clinical data across the patient treatment journey with multidisciplinary input from both oncology and urology specialties. As detailed, the biobank is largely representative of the overall bladder cancer population of South East London. Despite this, currently a large proportion of bladder cancer patients diagnosed or treated at Guy’s Hospital are not consented to the biobank; however, this provides a further valuable opportunity to increase the sample size and tissue resources in the future. The Biobank is a resource to be utilised and can be accessed by any academic or commercial establishment who has a valid research question. Potential applicants are encouraged to apply through the KHP Cancer Biobank website.
Conclusions
The KHP Bladder Cancer Biobank has assembled a comprehensive data repository, which is demographically and clinically representative of the total bladder cancer population in the Guy’s and St Thomas Trust catchment area. With a rich data and tissue repository, the Biobank is a valuable resource for future translational research.
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Acknowledgements
The authors are grateful to all sample and data donors who participated in the KHP BCaBB Biobank.
Ethics approval and consent to participate
The KHP Cancer biobank meets the current laws and ethical guidelines associated with tissue collection and use for research. This includes having a Human Tissue Authority licence (reference 12121) and a favourable opinion from the East of England – Cambridge East Research Ethics Committee (REC Ref 18/EE/0025). No administrative permissions and/or licenses were acquired by our team to access the data used in our research.
Consent for publication
Not applicable.
Competing interests
Mieke Van Hemelrijck is a member of the editorial board for the BMC Cancer journal.
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Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Cohort profile: King’s Health Partners bladder cancer biobank
verfasst von
Pinky Kotecha Charlotte L. Moss Deborah Enting Cheryl Gillett Magdalene Joseph Debra Josephs Sarah Rudman Simon Hughes Fidelma Cahill Harriet Wylie Anna Haire James Rosekilly Muhammad Shamin Khan Rajesh Nair Ramesh Thurairaja Sachin Malde Mieke Van Hemelrijck
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Auch myeloide Immunzellen lassen sich mit chimären Antigenrezeptoren gegen Tumoren ausstatten. Solche CAR-Fresszell-Therapien werden jetzt für solide Tumoren entwickelt. Künftig soll dieser Prozess nicht mehr ex vivo, sondern per mRNA im Körper der Betroffenen erfolgen.
Frauen mit unbehandelter oder neu auftretender Hypertonie haben ein deutlich erhöhtes Risiko für Uterusmyome. Eine Therapie mit Antihypertensiva geht hingegen mit einer verringerten Inzidenz der gutartigen Tumoren einher.
Nach einer Prostatabiopsie treten häufig Probleme beim Wasserlassen auf. Ob sich das durch den periinterventionellen Einsatz von Alphablockern verhindern lässt, haben australische Mediziner im Zuge einer Metaanalyse untersucht.
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