Induction radiochemotherapy with low dose fractionation XRT in patients with advanced HNSCC.

Poster abstract

Purpose/Objective

Supported by the National Science Centre, Poland, 2020/39/O/NZ5/02625.

Induction chemotherapy (iCH) although is not a standard approach, is often used in clinical practice for patients with advanced head and neck cancer (HNSCC). Tumor regression is a potential goal of induction treatment to reduce target volume in the second stage of treatment – radiochemotherapy or radiotherapy.

In this study the most common iCH, TPF (docetaxel, cisplatin, and 5-fluoruracil) has been replaced with two-drugs regimen combined with low-dose radiation. Complementary mechanisms of action and excellent radiation sensitization of drugs together with hyperradiosensitivity (HRS) phenomenon of low-dose fractionated radiation therapy may be beneficial for patients with bulky disease. Additionally, lower toxicity could be expected for two-drugs modality. Preliminary results on effectiveness and toxicity has been presented.



Material/Methods

The group consisted of 27 patients treated due to advanced HNSCC in National Research Institute of Oncology, Gliwice branch between 2020 and 2023. There were 23 (85%) men and 4 (15%) women in the median age of 60 years. In most cases primary tumor site was oropharynx followed by hypopharynx and CUP in 17 (63%), 7 (26%) and 3 (11%) cases respectively. All patients presented advanced stage - III stage in 16 cases (59%) and IV stage in 11 cases (41%). HPV- positive tumors were found in 13 (48%) patients. There were 2 cycles of iCHT consisting of carboplatin (AUC 6) and paclitaxel (75 mg/m2) combined with low-dose radiotherapy 2 x 0.5 Gy on days 1, 8 and 15. Additionally, two doses of 0.5 Gy was given on day 2. CT ,MRI and PET-CT scans were performed to estimate the staging of the cancer, all according to the 8th edition of the TNM classification for malignant tumors. 

The volume of the primary tumor and metastatic lymph nodes were estimated in cm3 before and after induction radiochemotherapy with low dose fractionation radiotherapy to  analyze the potential value of tumor volume regression . After ICHRTL, all patients were qualified for the second stage of treatment - radiochemotherapy in 24 cases and radiotherapy in 3 cases, respectively. To investigate the presence of HRS effect, fibroblasts were irradiated in vitro with doses ranging from 0.1 to 4 Gy (6-MV X-ray beam) and cell radiosensitivity was estimated by flow cytometry-based clonogenic survival assay and RIANS test (pATM and H2AX foci assays). 


Results

Clinical and experimental data will be presented.The mean volumes of tumor and metastatic lymph nodes among 27 patients before ICHRTL were 32.5 cm3 (Vt) and 45.1 cm3 (Vn) , respectively. After ICHRTL, these mean values were 17.2 cm3 (Vt) and 22.2 cm3 (Vn). Wilcoxon test analize showed significant decrease in T volume (Vt) and N volume (Vn) before and after iCHRTL (p=0.003) and p=0.00008) respectively. Due to complications 16 patients (60%) did not receive the full dose of chemotherapy and radiotherapy (ICHRTL). Leukopenia and neutropenia occurred in 12 (44%) and 11 (40%) patients respectively. Poor drug tolerance (vomiting, nausea, abdominal pain) was observed in 3 (11%) patients, and renal failure in 1 (4%) patient.  Among normal skin fibroblasts assessed from 21 patients two demonstrated HRS effect.   

 


Conclusion

The use of ICHRTL in patients with advanced HNSCC is a low-toxicity and effective method. The obtained regression of tumor volume (Vt) and metastatic lymph nodes (Vn)  in most patients managed to reduce the high dose area  in the second stage of treatment (radiotherapy/radiochemotherapy). Further observations are needed to estimate the potential role  of  decrease in T volume (Vt) and N volume (Vn) after ICHRTL on the expected survival of patients.  

Authors
1Urszula Kacorzyk, 2Barbara Bobek-Billewicz, 1Katarzyna Drosik - Rutowicz, 3Dorota Słonina, 3Gabriela Winiarska, 1Marek Kentnowski, 1Agata Bieleń, 4Piotr Paul, 4Ewa Chmielik, 5Anna Hebda, 3Agnieszka Mazurek, 1Krzysztof Składowski, 1Tomasz Rutkowski, 6Adam Gądek, 7Wojciech Fidyk, 8Jolanta Mrochem - Kwarciak, 1Natalia Amrogowicz, 1Andrzej Wygoda, 1Bolesław Pilecki, 1Dominika Leś, 1Paweł Polanowski, 3Monika Pietrowska, 3Małgorzata Oczko-Wojciechowska, 6Paulina Leszczyńska
1National Research Institute of Oncology, Gliwice branch, Radiation and Clinical Oncology Department, Gliwice, Poland. 2National Research Institute of Oncology, Gliwice branch, Radiology and Diagnostic Imaging Department, Gliwice, Poland. 3National Research Institute of Oncology, Gliwice branch, Center for Translational Research and Molecular Biology of CancerRadiation and Clinical Oncology Department, Gliwice, Poland. 4National Research Institute of Oncology, Gliwice branch, Tumor Pathology Department, Gliwice, Poland. 5National Research Institute of Oncology, Gliwice branch, Radiotherapy Department, Gliwice, Poland. 6National Research Institute of Oncology, Gliwice branch, Radiotherapy Planning Department, Gliwice, Poland. 7National Research Institute of Oncology, Gliwice branch, Department of Bone Marrow Transplantation and Oncohematology, Gliwice, Poland. 8National Research Institute of Oncology, Gliwice branch, Analytics and Clinical Biochemistry Department, Gliwice, Poland
Bibliographic references

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