Evaluation of the safety and effectiveness of the combination of gemcitabine monochemotherapy and high-intensity focused ultrasound therapy in the treatment of patients with adenogenic pancreatic cancer
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Keywords

high-intensity focused ultrasound therapy
HIFU-therapy
adenogenic pancreatic cancer
life expectancy
pain syndrome
gemcitabine

How to Cite

Moskvicheva , L., Kornietskaya А., & Bolotina, L. (2022). Evaluation of the safety and effectiveness of the combination of gemcitabine monochemotherapy and high-intensity focused ultrasound therapy in the treatment of patients with adenogenic pancreatic cancer. Voprosy Onkologii, 68(6), 780–785. https://doi.org/10.37469/0507-3758-2022-68-6-780-785

Abstract

Aim. Improvement of the results of treatment for pancreatic cancer patients who are not eligible to radical surgical intervention.

Material and methods. We present the safety and efficacy results of combined treatment that includes gemcitabine monochemotherapy and high-intensity focused ultrasound therapy (HIFU-therapy) for 35 patients with stage II–IV adenogenic pancreatic cancer with functional status ECOG 0-2, which was conducted in 2017–2020 on the basis of P.A. Herzen Moscow Oncology Research Institute ― the branch of the National Medical Research Center of Radiology. Gemcitabine monochemotherapy was performed at a dosage of 750–1000 mg/m2 on the 1st, 8th, and 15th days every 4 weeks. HIFU-therapy was performed with a device with an ultrasound flow intensity of 2 kW/cmwithin 30–45 minutes, in the scope of 3–8 sessions per course, with acoustic power of 300–600 W.

Results. Partial response of the primary tumor, according to the RECIST criteria, was achieved in 22.9% of patients after 6 courses of combined treatment; the disease control rate comprised 68.6%.

A decrease in the pain severity, as compared to the baseline, was registered in 58.3% of patients (6.29±0.38 vs. 4.88±0.39 according to the VAS; p=0.001). The pain control rate was 95.8%.

The median of the overall survival of patients reached 16 months; the median time to progression reached 9 months. 1-, 2- and 3-year overall survival was 71,4%, 17,1%, and 5,7% respectively; a 1-year time to progression was 25,7%.

Grade 3–4 adverse events were detected in 25.7% of patients, local complications of HIFU therapy ― in 34.3% of patients.

Conclusion. The combination of gemcitabine monochemotherapy and HIFU therapy is well tolerated by patients with pancreatic cancer with ECOG 0-2 functional status. It is characterized by relatively low toxicity and manageable local complications that do not require treatment interruption. Combined treatment performed for patients with pancreatic cancer at stages II–IV provides a statistically significant reduction of the level of abdominal pain syndrome by 6 months of treatment and demonstrates promising long-term results.

Aim. Improvement of the results of treatment for pancreatic cancer patients who are not eligible to radical surgical intervention.

Material and methods. We present the safety and efficacy results of combined treatment that includes gemcitabine monochemotherapy and high-intensity focused ultrasound therapy (HIFU-therapy) for 35 patients with stage II–IV adenogenic pancreatic cancer with functional status ECOG 0-2, which was conducted in 2017–2020 on the basis of P.A. Herzen Moscow Oncology Research Institute ― the branch of the National Medical Research Center of Radiology. Gemcitabine monochemotherapy was performed at a dosage of 750–1000 mg/m2 on the 1st, 8th, and 15th days every 4 weeks. HIFU-therapy was performed with a device with an ultrasound flow intensity of 2 kW/cmwithin 30–45 minutes, in the scope of 3–8 sessions per course, with acoustic power of 300–600 W.

Results. Partial response of the primary tumor, according to the RECIST criteria, was achieved in 22.9% of patients after 6 courses of combined treatment; the disease control rate comprised 68.6%.

A decrease in the pain severity, as compared to the baseline, was registered in 58.3% of patients (6.29±0.38 vs. 4.88±0.39 according to the VAS; p=0.001). The pain control rate was 95.8%.

The median of the overall survival of patients reached 16 months; the median time to progression reached 9 months. 1-, 2- and 3-year overall survival was 71,4%, 17,1%, and 5,7% respectively; a 1-year time to progression was 25,7%.

Grade 3–4 adverse events were detected in 25.7% of patients, local complications of HIFU therapy ― in 34.3% of patients.

Conclusion. The combination of gemcitabine monochemotherapy and HIFU therapy is well tolerated by patients with pancreatic cancer with ECOG 0-2 functional status. It is characterized by relatively low toxicity and manageable local complications that do not require treatment interruption. Combined treatment performed for patients with pancreatic cancer at stages II–IV provides a statistically significant reduction of the level of abdominal pain syndrome by 6 months of treatment and demonstrates promising long-term results.

https://doi.org/10.37469/0507-3758-2022-68-6-780-785
pdf (Русский)

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