New chemo combo may offer older pancreatic cancer patients a better-tolerated option
NCT ID NCT05360732
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether switching between two chemotherapy drugs (FOLFOX and FOLFIRI) can reduce side effects in people aged 65 and older with metastatic pancreatic cancer. The goal is to find a treatment that is easier to tolerate than the standard three-drug regimen. 37 participants will be monitored for toxicity and how long they live without the cancer getting worse.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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37 people
The number who actually took part.
- Started
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Apr 2022
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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65 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age 65 years or older 2. The treating physician will use their discretion when assessing if the patient is eligible for this treatment. 3. Patients must have newly diagnosed and previously untreated, histologically or cytologically confirmed adenocarcinoma of the pancreas, with at least one site of metastatic disease (local recurrences after surgery allowed), with lesions that are measurable by RECIST v1.1 criteria. In patients with mixed histology tumors, the predominant feature must be adenocarcinoma. 4. Eastern Cooperative Oncology Group Performance status of 0-2. 5. Previous surgery, adjuvant chemotherapy and/or radiation therapy will be allowed, provided radiation therapy is completed at least 2 weeks prior to signing consent and adjuvant therapy was administered more than 6 months prior to signing consent. 6. Patients must have bone marrow and organ function as defined below: * Absolute Neutrophil Count ≥ 1,500/μL * Platelets ≥ 100,000/μL * Total Bilirubin ≤2 X ULN * AST(SGOT)/ALT(SGPT)/ o Alkaline Phasphatase ≤3 X ULN o Or ≤5x ULN if liver metastasis present * Creatinine ≤2.0 mg/dL And * eGFR (using Cockcroft Gault equation) \> 40ml/min 7. Patients must be fluent in English and must be able and willing to undergo Comprehensive Geriatric Assessment 8. Chemotherapy is harmful to the human fetus. For this reason, sexually active males with partners of childbearing potential must agree to use an accepted and effective method of contraception prior to study entry and for the duration of the study. 9. Patients must demonstrate ability to understand and the willingness to sign a written informed consent document. 10. Men and women, regardless of race, ethnic group or sexual orientation are eligible for this study. Exclusion Criteria: 1\. Endocrine or acinar pancreatic carcinoma 2 Patients who have had any systemic chemotherapy in the metastatic or locally advanced inoperable setting (adjuvant or neoadjuvant therapy is allowed) 3 Patients who have received radiation therapy within 2 weeks of signing consent. 4 Patients who are currently receiving or have previously received any other investigational therapy for metastatic pancreatic cancer. 5 Patients with known brain metastases - treated or untreated, are excluded from this study because of their poor prognosis and frequent development of progressive neurological dysfunction that would confound the evaluation of neurologic and other adverse events. 6 Any patients with immune deficiency are at increased risk of lethal infections when treated with marrow-suppressive therapy, known HIV-positive patients and those with known active or inactive hepatitis B, untreated HCV or treated HCV without a documented sustained virologic response are excluded from the study. 7 Patients with uncontrolled intercurrent illness including, but not limited to, ongoing or active bacterial infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements. 8 Patients with evidence of active malignancy within 2 years of enrollment without definitive treatment. Patients with localized prostate cancer status-post surgical resection or definitive radiation, localized ER/PR+/HER2- breast cancer status-post definitive local treatment with a low OncotypeDx® on adjuvant hormonal therapy, or local skin cancers that were previously resected will be eligible for inclusion. Patients with a history of in situ cancers treated with definitive local therapy will also be eligible. 9 Patients with grade 3 or higher baseline sensory neuropathy 10 Patients with chronic diarrhea (\>4 bowel movements/day) unresolved despite best supportive care for greater than 2 weeks. 11 Patients with any of the following results on the Comprehensive Geriatric Assessment: * \>2 falls in the past month * BMI \<18
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Fox Chase Cancer Center
Philadelphia, Pennsylvania, 19111, United States
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Other studies related to the condition(s) this trial covers.
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