The project proposes a prospective multicenter study to evaluate the incorporation of deep regional hyperthermia into the standard of care neoadjuvant chemotherapy (mFOLFIRINOX/NABPACLITAXEL) followed by radiotherapy in borderline and locally advanced ductal adenocarcinoma pancreatic cancer. Although current treatments, based on induction chemotherapy followed by surgery or radiotherapy in selected patients, have improved survival and resection rates, overall survival remains poor. Hyperthermia is a therapeutic intensification strategy with a solid biological basis. By controlling tumor heating (39-43°C), it enhances the efficacy of chemotherapy and radiation therapy by improving tumor oxygenation, increasing perfusion, and inhibiting DNA damage repair, without adding significant systemic toxicity. The available clinical evidence, although based mainly on retrospective and small studies, suggests that the combination of HRP with multimodal treatments improves local control, favors conversion to surgery, and may prolong survival while maintaining a favorable safety profile. The protocol contemplates the initial administration of induction chemotherapy (preferably mFOLFIRINOX or, alternatively, gemcitabine with nab-paclitaxel)plus hyperthermia followed by multidisciplinary reevaluation. Patients who deemed resectable will undergo surgery and adjuvant chemoradiotherapy and hyperthermia. Patients without metastatic progression who remain unresectable will receive SBRT in five fractions along with sessions of deep regional hyperthermia. Subsequently, the possibility of surgery will be assessed again and a standardized follow-up will be carried out with clinical, radiological, biochemical and pathological evaluation when appropriate. The main objective of the study is to determine the impact of this strategy on overall survival. Secondary objectives will be to evaluate progression-free survival, local control, conversion rate to surgery, proportion of R0 resections, tumor response, safety, tolerability, and feasibility of treatment. With this, the study aims to provide prospective evidence on the role of hyperthermia as a therapeutic intensification strategy in localized pancreatic cancer.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
60
Hyperthermia plus neoadjuvant chemotherapy/radiotherapy Arm Description: Hyperthermia plus neoadjuvant chemotherapy (mFOLFIRINOX/nab Paclitaxel) followed by a) surgically resectable: Hyperthermia plus adjuvant chenmotherapy+/-radiotherapy b) surgically non-resectable: hyperthermia plus SBRT
Hospital Universitario de Gran Canaria Dr Negrín
Las Palmas de Gran Canaria, Las Palmas, Spain
Hospital Universitario Quirón Salud
Málaga, Malaga, Spain
overall survival
Time from included in the study to death for any cause
Time frame: one year
Progression Free Survival
Time from included in the study to disease progression
Time frame: one year
Objective response rate (ORR)
according to RECIST 1.1.
Time frame: 6 months
disease control rate (DCR),
according to RECIST 1.1.
Time frame: 6 months
Biochemical response using CEA and CA 19-9.
Modifications CEA and CA19.9 values
Time frame: 6 months
Conversion rate to surgery.
Resectabiity after neoadjuvant treatment
Time frame: 6 months
R0 resection rate
Rate of complete resection in surgically treated patients
Time frame: 7 months
Pathological response, including ypTNM and GRT.
Pathological confirmed response after neoadjuvant treatment
Time frame: 7 months
Local progression-free survival as first cause of failure
Time from included in the study to local progression after treatment as first site of failure
Time frame: one year
Acute and late toxicity chemotherapy and radiotherapy
Acute and late toxicity of treatment according to CTCAE v5.0.
Time frame: Acute: one month. Late: 12 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.