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BACKGROUND: Patients with trivial branch duct intraductal papillary mucinous neoplasm (BD IPMN) which remain s stable over 5 years reportedly do not have an increased risk of developing pancreatic cancer (PC) compared to the general population. In these patients, d iscontinuation of surveillance seems feasible . However, prospective studies to confirm the safety of this approach are lacking.
AIM: To assess whether current surveillance policies for stable, trivial BD IPMN can be discontinued safely after 5 years of follow up .
METHODS: TRIVIAL is an international prospective multicenter single arm trial exploring discontinuation of surveillance in patients with at least 5 years stable trivial BD IPMN. The trial will include 394 adult patients at least 70 years of age with BD IPMN ≤ 30 millimeter without worrisome features or high risk stigmata during 5 years. The primary endpoint is rate of PC and futile surgery (i.e., surgery for low grade dysplasia IPMN or other non malignant pathology) during 5 year follow up. The predefined target is a rate of 1% and below 3%.
STRENGTHS: The burden for patients to participate in this trial is negligible. P atients will only be asked to answer self reported digital surveys once per year during five years . The potential benefits for patients are twofold: the psychological impact of potentially unnecessary surveillance will be spared to patients , whereas the socio economic burden of repeated imaging will be avoided. Moreover, the study will provide data contributing to the development of new, evidence based surveillance strateg ies At the end of follow up patients undergo MRCP to assess disease course (i.e., development of worrisome features, high risk stigmata, PC).
LIMITATIONS: The most prominent risk of IPMN is the development of pancreatic cancer However this risk will not be omitted fully by the TRIVIAL trial eligibility criteria as participants still have the same risk as the general population. This requires adequate counselling
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Single-arm, discontinuation of follow-up |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Discontinuation of surveillance | Other | The intervention is discontinuation of current surveillance policies which consist of annual imaging with MRI/MRCP and clinical assessment. |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of pancreatic cancer | Primary endpoint is pancreatic cancer (PC), including IPMN derived PC high grade dysplasia (HGD) or concurrent PC, confirmed by pathology (e.g., surgery, fine needle biopsy), at 5 years follow up. Concurrent PC is defined as invasive PC that develops independently from the associated IPMN with a non dilated , segment of the pancreatic duct present between the two lesions. Therefore, a clear distinction will be made on what type of PC occurred (i.e., IPMN derived, HGD, concurrent PC). | Through study completion at 5 years after inclusion |
| Incidence of futile surgery | Futile surgery is defined as surgery for IPMN with low grade dysplasia (LGD) confirmed at final pathology, or other non malignant diagnosis (i.e., pseudocysts , serous cystadenoma). | Through study completion at 5 years after inclusion |
| Measure | Description | Time Frame |
|---|---|---|
| Pancreatic cancer related mortality | Through study completion at 5 years after inclusion | |
| All causes mortality | Through study completion at 5 years after inclusion | |
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Inclusion Criteria:
Exclusion Criteria:
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All consecutive patients of ≥70 years of age with trivial BD IPMN ≤30 millimeters that have been stable for at least 5 years are eligible for inclusion.
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| ID | Term |
|---|---|
| D010190 | Pancreatic Neoplasms |
| ID | Term |
|---|---|
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D004701 | Endocrine Gland Neoplasms |
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| Time to progression or surgery |
in months |
| Through study completion at 5 years after inclusion |
| Incidence of low grade and high grade dysplasia at pathology | Through study completion at 5 years after inclusion |
| Incidence of individual worrisome and high risk features and of individual relative and absolute indications | Through study completion at 5 years after inclusion |
| Incidence of pancreatic surgery | Through study completion at 5 years after inclusion |
| Serum CA 19.9 value | in U/L | At baseline and through study completion at 5 years after inclusion |
| Cyst growth | mm/year | Through study completion at 5 years after inclusion |
| Adjusted Charlson comorbidity index (ACCI) | At baseline and through study completion at 5 years after inclusion |
| Rate of misdiagnosis (only in resected patients) patients) | Through study completion at 5 years after inclusion |
| Incidence of additional follow up and diagnostic work up | Through study completion at 5 years after inclusion |
| Incidence of symptoms suspect for PC during follow up | Through study completion at 5 years after inclusion |
| D004066 |
| Digestive System Diseases |
| D010182 | Pancreatic Diseases |
| D004700 | Endocrine System Diseases |