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Updated: Aug 10, 2025

An Orthotopic Resectional Mouse Model of Pancreatic Cancer
Published on: September 24, 2020
CA19-9 Response to First-Line Neoadjuvant FOLFIRINOX and Second-Line Gemcitabine/Nab-Paclitaxel for Patients with
Sam Z Thalji1, Mandana Kamgar2, Ben George2
1Department of Surgery, Division of Surgical Oncology, LaBahn Pancreatic Cancer Program, Medical College of Wisconsin, Milwaukee, WI, USA.
For operable pancreatic cancer, a lack of CA19-9 response to first-line FOLFIRINOX may predict high response to second-line gemcitabine/nab-paclitaxel. This highlights the importance of monitoring treatment response early.
Area of Science:
- Oncology
- Gastroenterology
- Medical Oncology
Background:
- Response to second-line neoadjuvant therapy in operable pancreatic cancer is not well-studied.
- This study investigates carbohydrate antigen 19-9 (CA19-9) response to first-line and second-line chemotherapy regimens.
Purpose of the Study:
- To evaluate the efficacy of first-line (1L) and second-line (2L) neoadjuvant chemotherapy in operable pancreatic cancer (PC).
- To assess the role of CA19-9 response in predicting treatment outcomes for PC patients.
Main Methods:
- Identified operable PC patients with elevated CA19-9 (≥35 U/mL) and normal bilirubin (<2 mg/dL) receiving 1L FOLFIRINOX (FFX).
- Patients were restaged after 2 months; response determined by tumor size reduction on CT or ≥50% CA19-9 decline with preserved performance status.
- Subsequent treatment involved continuing FFX or switching to gemcitabine/nab-paclitaxel (GnP) for total neoadjuvant therapy.
Main Results:
- Of 108 patients receiving 1L FFX, 76 (70%) continued FFX and 32 (30%) switched to GnP.
- Among patients switching to GnP, 27 had no response to 1L FFX; 26 (96%) responded to 2L GnP.
- After 4 months, CA19-9 response rates were 82% for FFX continuation versus 97% for GnP switch (p=0.04).
Conclusions:
- Lack of biochemical response (CA19-9) to 2 months of 1L FFX may identify a subgroup with a high response rate to 2L GnP.
- Assessing treatment response at 2-month intervals is crucial for optimizing neoadjuvant therapy in operable pancreatic cancer.
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