Locally Advanced Pancreatic AdenocarcinomaROBINNCT07241663
Surgery for Locally Unresectable Pancreatic Cancer
An observational study of Locally Advanced Pancreatic Adenocarcinoma, run by Azienda Ospedaliera di Padova at 1 site in Italy.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Locally Advanced Pancreatic Adenocarcinoma
- What is being tested?
- Questionnaire
- How many people
- 150 participants
- Where
- 1 siteItaly
- Study dates
- 1 Jan 2025to 31 Dec 2028
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patient with hystologically proved locally advanced pancreatic adenocarcinoma
Who may be able to join
- Patients older than 18 years
- Patients able to give informed consent
- Histologically confirmed pancreatic adenocarcinoma
- LAPC stage according to NCCN10 at diagnosis (Figure 1)
- Received at least 4 months of induction chemotherapy
- RECIST 1.1 stable disease (SD) or partial response (PR) after induction therapy
- Patient considered eligible for radical resection by local MDT
Who cannot join
- Informed consent withdrawal
- Presence of tumor characteristics precluding surgery
- Presence of patient significant comorbidities precluding surgery
- Unavailable pre-induction therapy abdominal imaging
- Pathological confirmation of any tumor different from PDAC
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Italy1 site, 1 recruiting
- Recruiting
UOC Chirurgia Generale 2, Azienda Ospedale di Padova, Padova, Italy 35128
Padova
Giovanni Marchegiani, MD, PhD, Professor, +390498212259, giovanni.marchegiani@unipd.it
Giampaolo Perri, MD, PhD, +390498212259, giampaolo.perri@unipd.it
About this study
Official title: Conversion Surgery for Locally Unresectable Pancreatic Cancer - International Multi-center Observational Trial (ROBIN= suRgery for lOcally unresectaBle pancreatIc Cancer)
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.
Read the detailed description
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:
- Most of the available literature consists of retrospective studies, without intention-to-treat design and with clear selection bias for best responders after induction therapy, who are selected for surgery. Other studies reported similar survival outcomes in non-resected LAPC patients who had a good radiographic and serologic response after first line chemotherapy. While standard dose RT appeared ineffective in patients who have not undergone resection, RT with dose intensification and ablative intent might enable improvements in local control in LAPC patients, and SBRT seems to successfully achieve local control while also improving QoL.
- Most series considered locally advanced and borderline resectable PC as a single entity or did not distinguish between arterial resection of common hepatic artery (CHA)/celiac trunk (CA) or superior mesenteric artery (SMA), despite clear differences in terms of prognosis and perioperative complexity. Surgery for LAPC is feasible and safe only at high-volume centers with dedicated programs, and arterial resections are technically demanding procedures with a long learning curve (esteemed around 15 procedures).
- Quality of life (QoL) and patient reported outcomes (PROMS) were seldom verified and put in the context of the relatively modest survival of resected LAPC patients. Despite improvements in recent years, arterial divestment or resections may not only increase significantly perioperative morbidity and mortality, but also imply life-long consequences such as diarrhea, due to nerve plexus dissection, and diabetes, as total pancreatectomy is often required. Despite its technical complexity, there is no high-level evidence supporting the benefit of aggressive surgery for LAPC after induction chemotherapy.
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.
- Being tested
- Questionnaire
- Keywords
- Pancreatic cancer, Coversion Surgery Pancreatic Cancer, Quality of Life, Locally advanced PDAC, Unresectable Pancreatic Cancer, Neoadjuvant therapy for pancreatic cancer
- Medical subject headings
- Pancreatic Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
QuestionnaireOther
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.
What is being measured
The primary outcome is the main question the study is designed to answer.
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.
Measured: From enrollment to the end of study period, set at 2 years
Secondary outcomes (2)
Disease-specific survival (DSS)
Measured: 2 year from enrollment
Recurrence-free survival (RFS)
Measured: 2 year from enrollment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Nov 2025
- Study start1 Jan 2025
- Primary completion31 Dec 2026 (estimated)
- Study completion31 Dec 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Locally Advanced Pancreatic AdenocarcinomaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 150 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Azienda Ospedaliera di Padova
- Sponsor type
- University, hospital or other
- Collaborators
- University of Padova
- Responsible party
- Principal investigator, Prof. Umberto Cillo, Azienda Ospedaliera di Padova
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07241663
- Sponsor's protocol ID
- AOP3371
- Other IDs
- 6096/AO/24
- Acronym
- ROBIN
- Status last verified
- Nov 2025
- First submitted
- 17 Nov 2025
- Last updated
- 26 Nov 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 26 Nov 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Conversion Surgery for Locally Unresectable Pancreatic Cancer - International Multi-center Observational Trial (ROBIN= suRgery for lOcally unresectaBle pancreatIc Cancer)
- ClinicalTrials.gov ID
- NCT07241663
- Acronym / sponsor ID
- ROBIN / AOP3371
- Keywords
- Pancreatic cancer, Coversion Surgery Pancreatic Cancer, Quality of Life, Locally advanced PDAC, Unresectable Pancreatic Cancer, Neoadjuvant therapy for pancreatic cancer
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 150 participants (estimated)
- Lead sponsor
- Azienda Ospedaliera di PadovaUniversity, hospital or other
- Collaborators
- University of Padova
- Study start
- 1 Jan 2025 (actual)
- Primary completion
- 31 Dec 2026 (estimated)
- Study completion
- 31 Dec 2028 (estimated)
- First posted
- 21 Nov 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
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:
- Most of the available literature consists of retrospective studies, without intention-to-treat design and with clear selection bias for best responders after induction therapy, who are selected for surgery. Other studies reported similar survival outcomes in non-resected LAPC patients who had a good radiographic and serologic response after first line chemotherapy. While standard dose RT appeared ineffective in patients who have not undergone resection, RT with dose intensification and ablative intent might enable improvements in local control in LAPC patients, and SBRT seems to successfully achieve local control while also improving QoL.
- Most series considered locally advanced and borderline resectable PC as a single entity or did not distinguish between arterial resection of common hepatic artery (CHA)/celiac trunk (CA) or superior mesenteric artery (SMA), despite clear differences in terms of prognosis and perioperative complexity. Surgery for LAPC is feasible and safe only at high-volume centers with dedicated programs, and arterial resections are technically demanding procedures with a long learning curve (esteemed around 15 procedures).
- Quality of life (QoL) and patient reported outcomes (PROMS) were seldom verified and put in the context of the relatively modest survival of resected LAPC patients. Despite improvements in recent years, arterial divestment or resections may not only increase significantly perioperative morbidity and mortality, but also imply life-long consequences such as diarrhea, due to nerve plexus dissection, and diabetes, as total pancreatectomy is often required. Despite its technical complexity, there is no high-level evidence supporting the benefit of aggressive surgery for LAPC after induction chemotherapy.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patient with hystologically proved locally advanced pancreatic adenocarcinoma
Key inclusion criteria (7 listed)
- Patients older than 18 years
- Patients able to give informed consent
- Histologically confirmed pancreatic adenocarcinoma
- LAPC stage according to NCCN10 at diagnosis (Figure 1)
- Received at least 4 months of induction chemotherapy
Key exclusion criteria (5 listed)
- Informed consent withdrawal
- Presence of tumor characteristics precluding surgery
- Presence of patient significant comorbidities precluding surgery
- Unavailable pre-induction therapy abdominal imaging
- Pathological confirmation of any tumor different from PDAC
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| QuestionnaireEach 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. | Other | – |
Primary outcome
HRQoL deterioration-free survival
Time frame: From enrollment to the end of study period, set at 2 years
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.
2 secondary outcomes
Disease-specific survival (DSS)
Time frame: 2 year from enrollment
Recurrence-free survival (RFS)
Time frame: 2 year from enrollment
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 Nov 2025.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
UOC Chirurgia Generale 2, Azienda Ospedale di Padova, Padova, Italy 35128
Padova, Italy
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Locally Advanced Pancreatic Adenocarcinoma, run by Azienda Ospedaliera di Padova at 1 site in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 26 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
HRQoL deterioration-free survival (time frame: From enrollment to the end of study period, set at 2 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Nov 2025.