| Literature DB >> 29094224 |
Cristina Meazza1, Graziella Cefalo2, Maura Massimino3, Primo Daolio4, Ugo Pastorino5, Paolo Scanagatta5, Carlo Morosi6, Marta Podda3, Andrea Ferrari3, Monica Terenziani3, Filippo Spreafico3, Michela Casanova3, Antonina Parafioriti7, Paola Collini8, Lorenza Gandola6, Stefano Bastoni4, Veronica Biassoni3, Elisabetta Schiavello3, Stefano Chiaravalli3, Nadia Puma3, Luca Bergamaschi3, Roberto Luksch3.
Abstract
To improve the poor prognosis for children with metastatic osteosarcoma (OS), interleukin-2 (IL-2) was added to the standard treatment due to its capacity to activate lymphocytes and differentiate lymphocyte subsets into lymphokine-activated killer (LAK) cells that are capable of recognizing and killing various tumor cells. This study concerns a cohort of unselected patients aged < 18 years with metastatic OS, who were treated with IL-2, high-dose methotrexate, doxorubicin, cisplatin, ifosfamide, LAK reinfusion, and surgery, between 1995 and 2010. Thirty-five patients aged 4-17 years were involved. Thirty-two of the 35 patients underwent surgery on their primary tumor, and 25 had surgery on lung metastases too. Twenty-seven patients received IL-2 plus LAK reinfusion. The median follow-up was 130 months (77-228), and the 3-year event-free and overall survival rates were 34.3 and 45.0%, respectively. Eleven patients remained alive, all of whom achieved a complete surgical removal of the primary tumor and lung metastases (1 patient did not receive lung resections due to complete lung metastases remission). Patients who had a complete surgical remission of the primary and metastatic sites and who responded well to chemotherapy had a better event-free survival. These results confirm the importance of complete surgical remission and point to a noteworthy (though still be ameliorate) survival rate in our series of patients, underling a potential role for immunotherapy with IL-2 and LAK/NK cell activation.Entities:
Keywords: Chemotherapy; Children; IL-2; Lung metastases; Osteosarcoma; Surgery
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Year: 2017 PMID: 29094224 DOI: 10.1007/s12032-017-1052-9
Source DB: PubMed Journal: Med Oncol ISSN: 1357-0560 Impact factor: 3.064