Aleiomyosarcoma(LMS) is a rare malignant (cancerous)smooth muscle tumor.[1]The word is fromleio-'smooth'myo-'muscle' andsarcoma'tumor ofconnective tissue'. Thestomach,bladder,uterus,blood vessels,andintestinesare examples of hollow organs made up ofsmooth muscleswhere LMS can be located; however, the uterus and abdomen are the most common sites.[2]

Leiomyosarcoma
Other namesLMS
Leiomyosarcoma of theadrenal vein.Coronal view of abdominal MRI. Tumor (arrow) extends from the superior pole of the right kidney to the right atrium.
SpecialtyHematologyandOncology

Although leiomyosarcomas are rare, they belong to the more common types ofsoft-tissue sarcoma,representing 10–20% of new cases.[2]This type of cancer is more frequently diagnosed in adults as compared to children.[2]LMSs are seen in adults more often than they are seen in children.[3]When considering LMS specifically in the context of the uterus, it affects approximately 6 individuals per 1 million people in the United States each year.[2]LMSs are resistant cancers, meaning they are generally not very responsive tochemotherapyor radiation. The best outcomes occur when the tumor tissue can be removed surgically at an early stage, while it is small and has not yet spread from the original site (it remainsin situ).[4]

Mechanism

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Smooth muscle cells make up theinvoluntary muscles,which are found in most parts of the body, including the uterus, stomach and intestines, the walls of all blood vessels, and the skin. These are the areas where LMSs originate from.[5]LMSs also often develop in theretroperitoneal region[3]which consists of the suprarenal glands, the kidney, and ureter. Just as it is not known what truly causes most sarcomas, LMSs have similarly complex karyotypes and it is suggested that because of the complexity, genomic instability might be the cause.[3]

Uterine leiomyosarcomas come from the smooth muscle in the muscle layer of the uterus.[6]Cutaneous leiomyosarcomas derive from thepilo-erectormuscles in the skin. Gastrointestinal leiomyosarcomas might come from smooth muscle in the GI tract, or alternatively, from a blood vessel. At most other primary sites—retroperitoneal extremity (in the abdomen, behind the intestines), truncal, abdominal organs, etc.—leiomyosarcomas appear to grow from the muscle layer of a blood vessel (thetunica media). Thus, a leiomyosarcoma can have a primary site of origin anywhere in the body from a blood vessel.[4]

The tumors are usually hemorrhagic and soft and microscopically marked by pleomorphism, abundant (15–30 per 10 high-power fields) abnormal mitotic figures, and coagulative tumor cell necrosis. The differential diagnosis, which includes spindle cell carcinoma, spindle cellmelanoma,fibrosarcoma,malignantperipheral nerve sheath tumorand evenbiphenotypic sinonasal sarcoma,is wide.

Diagnosis

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Gross pathologyof uterine leiomyosarcoma showing hemorrhagic, necrotic and cystic areas upon sectioning
Histopathologyof leiomyosarcoma shows variable atypia, often with cytoplasmic vacuoles at both ends of nuclei, and frequent mitoses.[7]

To diagnose LMS, a physical exam may be performed by one’s physician, imaging tests such as MIT, CT and PET scans can be performed, or tissue biopsies can also be completed where the histopathology of the removed tissue sample is examined.[1]Because LMS is a widespread disease, the symptoms vary based on the location of the tumor and also, the size.[2]Some of the symptoms include nausea and vomiting, palpable lumps, pain, bleeding and unintentional weight loss.[2]

Treatment

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Surgery, with as wide a margin of removal as possible, has generally been the most effective and preferred way to attack LMS. If surgical margins are narrow or not clear of tumor, however, or in some situations where tumor cells were left behind, chemotherapy or radiation has been shown to give a clear survival benefit.[8]While LMS tends to be resistant to radiation and chemotherapy, each case is different and results can vary widely.

For metastatic (widespread) disease, chemotherapy and targeted therapies are the first choices. Chemotherapy regimens include:doxorubicin/ifosfamideand doxorubicin combination/gemcitabineanddocetaxel/trabectedin;[9]pazopanibis the targeted therapy used in metastatic leiomyosarcoma as second line and is well tolerated.[10]

LMS of uterine origin often responds to hormonal treatments.[11][12]As of 2020, several clinical trials for uterine LMS are active.[13]

Uterine leiomyomas vs uterine leiomyosarcomas

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Leiomyomasare benign smooth muscle tumors that have overlapping features with leiomyosarcomas. Although both originate from smooth muscle, it is important to note that leiomyomas do not mature to become leiomyosarcomas.[14]Leiomyomas are seen in pre-menopausal women and are symptomatic 20–50% of the time, while leiomyosarcomas, the most common uterine sarcomas, are seen in older post-menopausal women[15]with 40-60 being the peak age incidence.[16]Since leiomyomas are benign and mostly asymptomatic, minimally invasive treatment modalities are used to treat them.[15]For this same reason, it is crucial to distinguish them from LMSs before surgical procedures to ensure that laparoscopic procedures or diagnosis delay will not lead to heightened morbidity given the poor prognosis of LMS.[15]For example, the FDA has warned against using morcellation for benign leiomyomas as those with unsuspected sarcomas are at risk of cancer spread.[17]

Notable cases

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People who have had leiomyosarcoma include:

See also

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References

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  1. ^ab"Leiomyosarcoma - Overview - Mayo Clinic".www.mayoclinic.org.Retrieved2023-10-04.
  2. ^abcdef"Leiomyosarcoma - NCI".www.cancer.gov.2020-06-22.Retrieved2023-10-04.
  3. ^abcKumar, Vinay; Abbas, Abul K.; Aster, Jon C. (2021). "Chapter 26: Bones, Joints, and Soft Tissue Tumors".Robbins & Cotran Pathologic Basis of Disease(10th ed.). Jeremy Bowes. p. 1208.ISBN978-0-323-53113-9.
  4. ^ab"Basic info".Leiomyosarcoma.info.Archived fromthe originalon 2009-04-30.
  5. ^Kumar, Vinay; Abbas, Abul K.; Aster, Jon C. (2021). "Chapter 26: Bones, Joints, and Soft Tissue Tumors".Robbins & Cotran Pathologic Basis of Disease(10th ed.). Jeremy Bowes. p.1213.ISBN978-0-323-53113-9.
  6. ^Sue Ghosh; Jonathan Hecht; Tanaz Ferzandi; Christopher Awtrey (2007)."Leiomyosarcoma of the Uterus (ULMS): A Review".The Liddy Shriver Sarcoma Initiative.Retrieved1 February2016.
  7. ^Vijay Shankar, M.D."Soft tissue - Smooth muscle - Leiomyosarcoma - general".Pathology Outlines.Topic Completed: 1 November 2012. Revised: 11 September 2019
  8. ^"About Chemotherapy".Leiomyosarcoma.info.August 2002. Archived fromthe originalon 2009-06-25.
  9. ^Rastogi, Sameer; Bakhshi, Sameer (2016). "Trabectedin in Soft Tissue Sarcoma: Have We Hit the Bull's-eye?".Journal of Clinical Oncology.34(29): 3582–3583.doi:10.1200/jco.2015.65.7130.PMID27458287.
  10. ^Rastogi, Sameer; Sharma, Aparna; Vanidassane, Ilavarasi; Aggarwal, Aditi; Mridha, Asitranjan; Pandey, Rambha; Dhamija, Ekta; Barwad, Adarsh (2019)."Pazopanib efficacy and toxicity in a metastatic sarcoma cohort: Are Indian patients different?".Indian Journal of Cancer.56(3): 207–210.doi:10.4103/ijc.IJC_105_18.PMID31389382.S2CID198168573.
  11. ^Abu-Rustum, N. R.; Curtin, J. P.; Burt, M.; Jones, W. B. (1997). "Regression of uterine low-grade smooth-muscle tumors metastatic to the lung after oophorectomy".Obstetrics and Gynecology.89(5 Pt 2): 850–852.doi:10.1016/S0029-7844(97)00033-1.PMID9166348.S2CID23049718.
  12. ^Hardman, M. P.; Roman, J. J.; Burnett, A. F.; Santin, A. D. (2007). "Metastatic Uterine Leiomyosarcoma Regression Using an Aromatase Inhibitor".Obstetrics & Gynecology.110(2 Pt 2): 518–520.doi:10.1097/01.AOG.0000267533.56546.c2.PMID17666649.S2CID24257210.
  13. ^"Uterine Sarcoma Clinical Trials".National Cancer Institute.
  14. ^Kumar, Vinay; Abbas, Abul K.; Aster, Jon C. (2021). "Chapter 26: Bones, Joints, and Soft Tissue Tumors".Robbins & Cotran Pathologic Basis of Disease(10th ed.). Jeremy Bowes. p.1014.ISBN978-0-323-53113-9
  15. ^abcSun, S.; Bonaffini, P. A.; Nougaret, S.; Fournier, L.; Dohan, A.; Chong, J.; Smith, J.; Addley, H.; Reinhold, C. (October 2019)."How to differentiate uterine leiomyosarcoma from leiomyoma with imaging".Diagnostic and Interventional Imaging.100(10): 619–634.doi:10.1016/j.diii.2019.07.007.ISSN2211-5684.PMID31427216.
  16. ^Kumar, Vinay; Abbas, Abul K.; Aster, Jon C. (2021). "Chapter 26: Bones, Joints, and Soft Tissue Tumors".Robbins & Cotran Pathologic Basis of Disease(10th ed.). Jeremy Bowes. p.1015.ISBN978-0-323-53113-9
  17. ^Health, Center for Devices and Radiological (2020-12-30)."UPDATE: Perform Only Contained Morcellation When Laparoscopic Power Morcellation Is Appropriate: FDA Safety Communication".FDA.
  18. ^"Leicester legend Weller mourned".BBC Online. 2004-11-13.Retrieved2010-05-14.
  19. ^"Jordan treated for cancer".BBC Online. 2002-08-11.Retrieved2009-10-30.
  20. ^Gillespie, Kerry (2008-04-12)."'Can't ever give up hope,' Basrur says ".The Toronto Star.Retrieved2010-01-08.
  21. ^Brown, Stacia."Diana Sands: What Was and What Could've Been".Archived fromthe originalon 6 December 2017.Retrieved25 May2017.
  22. ^"That's My Time".Irwinbarker.com.Archived fromthe originalon 2008-10-02.Retrieved5 March2015.In Irwin's own words: 'Cancer has my body but not my spirit, and I'll continue to make jokes, not so much about cancer, but in spite of it.'
  23. ^Fiona Hackett (2009-11-27)."Former player Linda Uttley".waspsfc.co.uk.Retrieved2022-02-28.
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