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Irreversible Electroporation Ablation Combined With Anti-PD(L)1 Therapy for Locally Advanced Pancreatic Cancer

A Retrospective Study on the Efficacy of Irreversible Electroporation Ablation Combined With Anti-PD(L)1 Therapy for Locally Advanced Pancreatic Cancer

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06677762
Enrollment
55
Registered
2024-11-07
Start date
2024-11-10
Completion date
2025-06-30
Last updated
2024-11-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic Cancer

Keywords

Pancreatic cancer, irreversible electroporation, PD-(L)1

Brief summary

Pancreatic cancer is a highly lethal malignant tumor of the digestive tract, especially local advanced pancreatic cancer (LAPC), which often loses the opportunity for surgical resection at the time of diagnosis. LAPC patients are often accompanied by tumor invasion of key anatomical structures such as major blood vessels, and traditional treatment methods such as radiotherapy and chemotherapy can slow down the progression of the disease, but the effect is limited, and the overall survival rate is still very low. There is a lack of effective treatment options for LAPC, especially in local control and prolonging survival, which exists a major limitation. The surgical resection rate is low in LAPC, and the postoperative recurrence rate is high, and traditional radiotherapy and chemotherapy are difficult to completely eliminate the tumor. Immunotherapy has achieved breakthroughs in other tumors such as melanoma and non-small cell lung cancer, but the effect is limited in pancreatic cancer due to the immunosuppressive state of the tumor microenvironment (TME), which limits the efficacy of immunotherapy. In addition, the high invasiveness and rapid progression of pancreatic cancer further aggravates the treatment challenge. Recent studies have shown that local ablation techniques such as irreversible electroporation (IRE) ablation not only can effectively ablate local tumors, but also may destroy the structural integrity of tumor cells, release tumor-associated antigens, and enhance the anti-tumor effect of the immune system. Therefore, IRE ablation may provide local control of pancreatic cancer for patients. At the same time, the combination of immune checkpoint inhibitors such as anti-PD(L)1 inhibitors may enhance the immune response in the tumor microenvironment and further improve the therapeutic effect. This combined treatment regimen is expected to overcome the limitations of single therapy and provide a new treatment strategy for local advanced pancreatic cancer.

Interventions

PROCEDUREIrreversible electroporation

Irreversible electroporation ablation is an interventional ablation method, while anti-PD(L)1 is an immunotherapy.

Sponsors

Ruijin Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* The pathological diagnosis is local advanced pancreatic cancer that cannot be removed by surgery; * Received IRE ablation treatment alone or in combination with anti-PD-1 or anti-PD-L1 immune inhibitors; * Aged 18 years or older, gender is not limited, ECOG score 0-2; * Have complete medical records and imaging follow-up records; * At least 6 months of follow-up data.

Exclusion criteria

* Patients with other malignant tumors or severe immune system disorders; * Patients who cannot complete follow-up or have missing data; * Patients who have previously received immunotherapy without effect; * Patients with severe organ dysfunction or who cannot tolerate further - - treatment.

Design outcomes

Primary

MeasureTime frameDescription
OS,Overall SurvivalFrom the time of treatment to the death from any cause, assessed up to 35 monthsThe patient received treatment until death.
PFS,Progress Free SurvivalFrom the time of treatment to tumor progression or date of death from any cause, whichever came first, assessed up to 35 monthsTime of progression or death of the patient

Secondary

MeasureTime frameDescription
ORR,Objective response rateFrom the time of treatment to tumor response or date of death from any cause, whichevercame first, assessed up to 35 monthsThe proportion of patients whose tumor size decreases to a predetermined value and can maintain that minimum value for the required duration.

Contacts

Primary ContactZhongmin Wang Wang
wzm11896@rjh.com.cn13901848333
Backup ContactXiaoyu Liu Liu
lxy12931@rjh.com.cn15121013042

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026