An observational study in Locally Advanced Pancreatic Adenocarcinoma, sponsored by Azienda Ospedaliera di Padova. Recruiting at 1 site in Italy. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-11-26.
Sponsored by Azienda Ospedaliera di Padova · Observational
Pancreatic cancer is a severe disease often diagnosed at an advanced stage, when surgery is not possible. New chemotherapy treatments can sometimes shrink the tumor and make surgery an option. This study aims to understand if surgery after such treatments can improve survival and quality of life in selected patients treated at expert centers.
Pancreatic cancer (PC) has a rising incidence and remains associated with one of the mostchallenging prognosis in oncology, with a 5-years survival around 11% and merely 4% of patients alive at 10 years. About one third of PC patients is diagnosed with locally advanced (LAPC) stage of disease, with a primary tumor that is considered unresectable (in the absence of metastatic disease) due to the local involvement of major vessels and is typically treated with palliative chemotherapy or best supportive care, with the aim to prolong survival while maintaining acceptable quality of life (QoL). However, the introduction of novel induction chemotherapy regimens has improved the clinical outcome of these patients in recent years. The preferred induction regimen for patients with favorable performance status (ECOG 0-1) has become modified 5-fluorouracil, leucovorin, irinotecan, and oxaliplatin [(m)FOLFIRINOX], with gemcitabine + nab-paclitaxel (GEMNabP) as a more tolerable alternative. In this scenario, the resection of apparently unresectable PC following induction chemotherapy, although somewhat controversial, has emerged as an important development for selected patients. In this regard, the National Comprehensive Cancer Network (NCCN) guidelines recommends 4 to 6 months of induction combination chemotherapy followed by conventional radiotherapy (CRT) or stereotactic body radiation therapy (SBRT) for selected patients without systemic metastases, followed by consideration for surgical resection if feasible, with adjuvant chemotherapy if clinically indicated. Surgical resection can be usually achieved in about 25% of LAPC patients after chemotherapy with modern regimens, and in the context of multidisciplinary management at high-volume centers with high expertise. Resection is associated with encouraging results in terms of median overall survival (OS), reaching 20 to 40 months, and with 5-years survival around 20%. To achieve surgical radicality, venous resection, arterial divestment or even arterial resection could be necessary. In recent multicentric series, patients receiving R0 portal vein (PV)/superior mesenteric vein (SMV) resection had a median OS of 24 months and a 20% 5-year OS 16, and patients requiring major arterial reconstruction and/or periarterial divestment had in-hospital mortality rates of 4-5%, median OS of 13.7-20.1 months, and 5-year OS of 12.5-13.7%. Despite the encouraging survival outcomes, based on both remarkable advances in surgical technique at high-volume centers and the use of modern combination chemotherapy regimens and chemo-radiation, aggressive surgery for LAPC after induction chemotherapy remains a controversial topic for several aspects:
The aim of the present study is to evaluate survival and QoL outcomes in a cohort of patients affected by LAPC and selected for surgical exploration and radical resection after disease non progression during induction chemotherapy at leading expert centers.
3,896 studies on the registry are indexed under Pancreatic Neoplasms; 1,007 are open to participants now.
This study's planned enrollment of 150 is below the median of 200 across 740 observational studies indexed under Pancreatic Neoplasms.
Browse Pancreatic Neoplasms studies →Azienda Ospedaliera di Padova is the lead sponsor of 38 studies on the registry; 13 are open to participants now.
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Patient with hystologically proved locally advanced pancreatic adenocarcinoma
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).
Your pathology report is the document that shows this.
The standard rules for measuring tumours on CT or MRI scans, to tell whether a cancer is shrinking, stable or growing during treatment.
“Measurable disease per RECIST 1.1” usually means at least one tumour 10 mm or more at its longest on a CT scan, or a lymph node 15 mm or more across its short axis.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Histologically or cytologically confirmed
The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).
Your pathology report is the document that shows this.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
RECIST
The standard rules for measuring tumours on CT or MRI scans, to tell whether a cancer is shrinking, stable or growing during treatment.
“Measurable disease per RECIST 1.1” usually means at least one tumour 10 mm or more at its longest on a CT scan, or a lymph node 15 mm or more across its short axis.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Each enrolled patient will complete quality of life questionnaires, specifically the EORTC QLQ-C30, PAN26, and EQ-5D, at different time points: at enrollment and every 2-3 months after surgery, for up to 2 years.
HRQoL deterioration-free survival
The primary outcome is HRQoL deterioration-free survival, defined as the time from surgery until definite HRQoL score deterioration and including death from any cause as an event.
Time frame: From enrollment to the end of study period, set at 2 years
Disease-specific survival (DSS)
Time frame: 2 year from enrollment
Recurrence-free survival (RFS)
Time frame: 2 year from enrollment
Plan to share: No
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Azienda Ospedaliera di Padova