RecruitingPhase IIIEN originalPancreatic cancerEarly / localized

Neoadjuvant vs Upfront Surgery for Resectable Pancreatic Cancer and Periampullary Cancer

⚠️

This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

Adjuvant chemotherapy after surgery significantly improved the survival of pancreatic cancer (PC) patients, but there is a problem that only about 50% of patients start adjuvant chemotherapy after pancreatectomy. Neoadjuvant chemotherapy might control potential metastatic lesions which are not being detected in early disease status and improve the R0 resection rate. In addition, it prevents futile surgery by selecting patients with rapid progression of disease. Furthermore, compared to chemotherapy administered after surgery, more patients can complete the planned chemotherapy schedule in neoadjuvant setting. There are still few studies worldwide that prospectively explored the efficacy of neoadjuvant chemotherapy in resectable PC and periampullary cancer and the administration of neoadjuvant therapy in resectable PC depends on individual clinical judgment. Therefore, systematic and prospective clinical trials are essential to standardize treatment protocol in resectable PC and periampullary Cancer. This randomized controlled trial compares neoadjuvant chemotherapy followed by surgery versus upfront surgery for patients with clearly resectable pancreatic head cancer and periampullary cancer. The study aims to determine if neoadjuvant chemotherapy improves overall survival compared to immediate surgery followed by adjuvant chemotherapy.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • •Potwierdzony histologicznie lub cytologicznie rak głowy trzustki lub rak okolic brodawki dwunastnicznej
  • •Nowotwór w stadium operacyjnym bez rozrostu na główne naczynia krwionośne
  • •Brak widocznych przerzutów (rozsiania) nowotworu
  • •Dobry stan zdrowotny pacjenta (ECOG 0-1)
  • •Prawidłowe funkcjonowanie wątroby, nerek i szpiku kostnego
  • •Zgoda pacjenta na udział w badaniu
  • •Brak wcześniejszej operacji trzustki lub chemioterapii raka trzustki
  • •Liczba leukocytów, płytek krwi i hemoglobina w wymaganym zakresie

✗ Disqualifies

  • •Nowotwór w stadium granicznym lub zaawansowanym
  • •Rak ciała lub ogona trzustki
  • •Przerzuty do odległych narządów
  • •Wcześniejsza chemioterapia, operacja lub radioterapia raka trzustki
  • •Poważne choroby uniemożliwiające operację lub chemioterapię
  • •Ciąża lub karmienie piersią
  • •Inne nowotwory złośliwe w ostatnich 5 latach
  • •Poważna operacja lub uraz w ciągu ostatnich 28 dni

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Maximum age
75 Years
Last updated (source)
September 11, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (1)

Liver and GIT hospital , Minia University

Minya, Egypt

Trial contact

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 9/12/2026.

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