Leiomyosarcoma: Does Location of Primary Help to Determine the Best Systemic Therapy Options?

Author:

Novotny Jan Philipp,George SuzanneORCID

Funder

Deutsche Forschungsgemeinschaft

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Oncology

Reference47 articles.

1. George S, Serrano C, Hensley ML, Ray-Coquard I. Soft Tissue and uterine leiomyosarcoma. J Clin Oncol. 2018;36(2):144–50.

2. Martin-Liberal J. Leiomyosarcoma: principles of management. Intractable Rare Dis Res. 2013;2(4):127–9.

3. Howlader NNA, Krapcho M, Miller D, Brest A, Yu M, Ruhl J, Tatalovich Z, Mariotto A, Lewis DR, Chen HS, Feuer EJ, Cronin KA (eds). SEER cancer statistics review, 1975–2017, National Cancer Institute. Bethesda, MD, https://seer.cancer.gov/csr/1975_2017/, based on November 2019 SEER data submission, posted to the SEER web site, April 2020.

4. Kleinerman RA, Tucker MA, Abramson DH, Seddon JM, Tarone RE, Fraumeni JF Jr. Risk of soft tissue sarcomas by individual subtype in survivors of hereditary retinoblastoma. J Natl Cancer Inst. 2007;99(1):24–31.

5. Ognjanovic S, Olivier M, Bergemann TL, Hainaut P. Sarcomas in TP53 germline mutation carriers: a review of the IARC TP53 database. Cancer. 2012;118(5):1387–96.

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