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Armando Santoro

Researcher at Humanitas University

Publications -  961
Citations -  56759

Armando Santoro is an academic researcher from Humanitas University. The author has contributed to research in topics: Medicine & Cancer. The author has an hindex of 93, co-authored 847 publications receiving 48505 citations. Previous affiliations of Armando Santoro include Aix-Marseille University & University of Milan.

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Assessment of tumor response in malignant pleural mesothelioma.

TL;DR: The use of FDG-PET for prediction of response and, more importantly, of survival outcomes of MPM patients is promising and warrants validation in large prospective series, and computer-assisted techniques for CT measurement are being developed.
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Stereotactic body radiation therapy: A promising chance for oligometastatic breast cancer

TL;DR: SBRT is a safe and feasible alternative treatment of liver and lung oligometastases from breast cancer, in selected patients not amenable to surgery, with good local control and survival rate.
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Multidisciplinary treatment of malignant pleural mesothelioma.

TL;DR: There have been several major advances in the management of patients with MPM, including more accurate staging and patient selection, improvements in surgical techniques and postoperative care, novel chemotherapy regimens with definite activity such as antifolate (pemetrexed or raltitrexed)-platinum combinations, and new radiotherapy techniques such as intensity-modulated radiation therapy.
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Median sternotomy and multiple lung resections for metastatic sarcomas.

TL;DR: In this article, a new treatment plan consisting of early bilateral lung exploration and resection through median sternotomy in all cases of sarcoma with resectable lung metastases, including synchronous or previously resected ones, was adopted.
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Metastatic colorectal cancer: integrating irinotecan into combination and sequential chemotherapy.

TL;DR: The question of how best to sequence combination chemotherapy was addressed in a recent trial in which patients were randomized to receive either an irinotecan-based combination with 5-FU/FA (FOLFIRI) followed by an oxaliplatin- based combination (F OLFOX), or the two regimens in the reverse order.