Abstract

Exocrine pancreatic cancers include common type pancreatic ductal adenocarcinoma and cystic neoplasms, which account for 85% and 10% of cases, respectively. The remaining 5% are rare histotypes, comprising adenosquamous carcinoma, acinar cell carcinoma, signet ring cell carcinoma, medullary carcinoma, pancreatoblastoma, hepatoid carcinoma, undifferentiated carcinoma and its variant with osteoclast-like giant cells, solid pseudopapillary carcinoma, and carcinosarcoma. Due to their low incidence, little knowledge is available on their clinical and molecular features as well as on treatment choices. The national initiative presented here aims at the molecular characterization of series of rare histotypes for which therapeutic and follow-up data are available. A nationwide Italian Rare Pancreatic Cancer (IRaPaCa) task force whose first initiative is a multicentric retrospective study involving 21 Italian cancer centers to retrieve histologic material and clinical and treatment data of at least 100 patients with rare exocrine pancreatic cancers has been created. After histologic revision by a panel of expert pathologists, DNA and RNA from paraffin tissues will be investigated by next-generation sequencing using molecular pathway-oriented and immune-oriented mutational and expression profiling panels constructed availing of the information from the International Cancer Genome Consortium. Bioinformatic analysis of data will drive validation studies by immunohistochemistry and in situ hybridization, as well as nanostring assays. We expect to gather novel data on rare pancreatic cancer types that will be useful to inform the design of therapeutic choices.

Highlights

  • Exocrine pancreatic cancers include common type pancreatic ductal adenocarcinoma and cystic neoplasms, which account for 85% and 10% of cases, respectively

  • Common type pancreatic ductal adenocarcinoma (PDAC) accounts for 85% of exocrine pancreatic cancers

  • According to World Health Organization classification, the remaining exocrine pancreatic cancers are represented by rare histotypes, comprising pancreatic adenosquamous carcinoma, pancreatic acinar cell carcinoma, solid pseudopapillary carcinoma, undifferentiated carcinoma and its variant with osteoclast-like giant cells (UCOGC), signet ring cell carcinoma, medullary carcinoma, pancreatoblastoma, hepatoid carcinoma, and carcinosarcoma.[1]

Read more

Summary

Introduction

Exocrine pancreatic cancers include common type pancreatic ductal adenocarcinoma and cystic neoplasms, which account for 85% and 10% of cases, respectively. The remaining 5% are rare histotypes, comprising adenosquamous carcinoma, acinar cell carcinoma, signet ring cell carcinoma, medullary carcinoma, pancreatoblastoma, hepatoid carcinoma, undifferentiated carcinoma and its variant with osteoclast-like giant cells, solid pseudopapillary carcinoma, and carcinosarcoma Due to their low incidence, little knowledge is available on their clinical and molecular features as well as on treatment choices. According to World Health Organization classification, the remaining exocrine pancreatic cancers are represented by rare histotypes, comprising pancreatic adenosquamous carcinoma, pancreatic acinar cell carcinoma, solid pseudopapillary carcinoma, undifferentiated carcinoma and its variant with osteoclast-like giant cells (UCOGC), signet ring cell carcinoma, medullary carcinoma, pancreatoblastoma, hepatoid carcinoma, and carcinosarcoma.[1] Due to the low incidence of these malignancies, their clinical features are usually reported only in case reports or in small series of retrospective observational studies.[2,3] Notably, patients with these rare pancreatic cancers are excluded from clinical trials. The clinical dilemma in the management of patients with rare pancreas cancers at advanced stage is as follows: Do chemotherapy regimens recommended for PDAC have a clinical activity or should other therapeutic approaches (different chemotherapy combinations, targeted therapies, immunotherapy) be considered?

Objectives
Methods
Findings
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call