Curative and palliative multimodal treatment concepts for soft tissue sarcomas
Author:
Publisher
Springer Science and Business Media LLC
Subject
Oncology,Hematology
Link
https://link.springer.com/content/pdf/10.1007/s00761-022-01288-4.pdf
Reference42 articles.
1. Ardoino I, Miceli R, Berselli M et al (2010) Histology-specific nomogram for primary retroperitoneal soft tissue sarcoma. Cancer 116:2429–2436
2. Italiano A, Le Cesne A, Mendiboure J et al (2014) Prognostic factors and impact of adjuvant treatments on local and metastatic relapse of soft-tissue sarcoma patients in the competing risks setting. Cancer 120:3361–3369
3. Gronchi A, Ferrari S, Quagliuolo V et al (2017) Histotype-tailored neoadjuvant chemotherapy versus standard chemotherapy in patients with high-risk soft-tissue sarcomas (ISG-STS 1001): an international, open-label, randomised, controlled, phase 3, multicentre trial. Lancet Oncol 18:812–822
4. Issels RD, Lindner LH, Verweij J et al (2010) Neo-adjuvant chemotherapy alone or with regional hyperthermia for localised high-risk soft-tissue sarcoma: a randomised phase 3 multicentre study. Lancet Oncol 11:561–570
5. Woll PJ, Reichardt P, Le Cesne A et al (2012) Adjuvant chemotherapy with doxorubicin, ifosfamide, and lenograstim for resected soft-tissue sarcoma (EORTC 62931): a multicentre randomised controlled trial. Lancet Oncol 13:1045–1054
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