Leiomyosarcoma Explained
A leiomyosarcoma, also known as LMS, is a rare malignant (cancerous) smooth muscle tumor.[1] The origin of the word is from leio- + myo- + sarcoma which means malignant smooth muscle tumor. The stomach, bladder, uterus, blood vessels, and intestines are examples of hollow organs made up of smooth muscles where LMS can be located; however, the uterus and abdomen are the most common sites.[2]
Although leiomyosarcomas are rare, they belong to the more common types of soft-tissue sarcoma, representing 10–20% of new cases. This type of cancer is more frequently diagnosed in adults as compared to children. 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. LMSs are resistant cancers, meaning they are generally not very responsive to chemotherapy or 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 remains in situ).[4]
Mechanism
Smooth muscle cells make up the involuntary 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 the retroperitoneal region 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.
Uterine leiomyosarcomas come from the smooth muscle in the muscle layer of the uterus.[6] Cutaneous leiomyosarcomas derive from the pilo-erector muscles 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 (the tunica 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 cell melanoma, fibrosarcoma, malignant peripheral nerve sheath tumor and even biphenotypic sinonasal sarcoma, is wide.
Diagnosis
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. Because LMS is a widespread disease, the symptoms vary based on the location of the tumor and also, the size. Some of the symptoms include nausea and vomiting, palpable lumps, pain, bleeding and unintentional weight loss.
Treatment
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.[7] 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/ifosfamide and doxorubicin combination/gemcitabine and docetaxel/trabectedin;[8] pazopanib is the targeted therapy used in metastatic leiomyosarcoma as second line and is well tolerated.[9]
LMS of uterine origin often responds to hormonal treatments.[10] [11] As of 2020, several clinical trials for uterine LMS are active.[12]
Uterine leiomyomas vs uterine leiomyosarcomas
Leiomyomas are 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.[13] 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[14] with 40-60 being the peak age incidence.[15] Since leiomyomas are benign and mostly asymptomatic, minimally invasive treatment modalities are used to treat them. 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. For example, the FDA has warned against using morcellation for benign leiomyomas as those with unsuspected sarcomas are at risk of cancer spread.[16]
Notable cases
People who have had leiomyosarcoma include:
- Leicester City footballer Keith Weller, who made over 300 appearances for the Foxes, scored 47 goals. Also, he made four appearances for England, scoring one goal.[17]
- Katie Price[18]
- Canadian public-health physician Sheela Basrur (1956–2008) developed uterine leiomyosarcoma in 2006.[19]
- American actress Diana Sands[20]
- The first year of treatment for leiomyosarcoma of Canadian comedian Irwin Barker was the subject of a 2008 television documentary, That's My Time; he died in 2010.[21]
- E. J. McGuire, long-time professional ice hockey coach, scout, and vice president of the National Hockey League Central Scouting Bureau
- Ellis Avery, American writer, two-time winner of the Stonewall Book Award
- Linda Uttley (1966–2009), English rugby union footballer in the Women's England Team, was diagnosed with leiomyosarcoma in 2007 and died in 2009 at the age of 43.[22]
- Irene Hirano Inouye, founding President of the U.S.-Japan Council, a position she held ever since she helped create the organization in 2009.
See also
External links
Notes and References
- Web site: Leiomyosarcoma - Overview - Mayo Clinic . 2023-10-04 . www.mayoclinic.org.
- Web site: 2020-06-22 . Leiomyosarcoma - NCI . 2023-10-04 . www.cancer.gov . en.
- Book: Kumar . Vinay . Robbins & Cotran Pathologic Basis of Disease . Abbas . Abul K. . Aster . Jon C. . Jeremy Bowes . 2021 . 978-0-323-53113-9 . 10th . 1208 . English . Chapter 26: Bones, Joints, and Soft Tissue Tumors.
- Web site: Basic info. Leiomyosarcoma.info. dead. https://web.archive.org/web/20090430111311/http://www.leiomyosarcoma.info/basic.htm. 2009-04-30.
- 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. .
- Web site: Leiomyosarcoma of the Uterus (ULMS): A Review. The Liddy Shriver Sarcoma Initiative. Sue Ghosh . Jonathan Hecht . Tanaz Ferzandi . Christopher Awtrey . 2007. 1 February 2016.
- Web site: About Chemotherapy . August 2002 . Leiomyosarcoma.info . dead . https://web.archive.org/web/20090625203601/http://www.leiomyosarcoma.info/chemo10therapy.htm . 2009-06-25 .
- 10.1200/jco.2015.65.7130. 27458287. Trabectedin in Soft Tissue Sarcoma: Have We Hit the Bull's-eye?. Journal of Clinical Oncology. 34. 29. 3582–3583. 2016. Rastogi. Sameer. Bakhshi. Sameer.
- 10.4103/ijc.IJC_105_18. Pazopanib efficacy and toxicity in a metastatic sarcoma cohort: Are Indian patients different?. Indian Journal of Cancer. 56. 3. 207–210. 2019. Rastogi. Sameer. Sharma. Aparna. Vanidassane. Ilavarasi. Aggarwal. Aditi. Mridha. Asitranjan. Pandey. Rambha. Dhamija. Ekta. Barwad. Adarsh. 31389382. 198168573 . free .
- 10.1016/S0029-7844(97)00033-1 . Abu-Rustum . N. R. . Curtin . J. P. . Burt . M. . Jones . W. B. . Regression of uterine low-grade smooth-muscle tumors metastatic to the lung after oophorectomy . Obstetrics and Gynecology . 89 . 5 Pt 2 . 850–852 . 1997 . 9166348. 23049718 .
- Hardman . M. P. . Roman . J. J. . Burnett . A. F. . Santin . A. D. . Metastatic Uterine Leiomyosarcoma Regression Using an Aromatase Inhibitor . 10.1097/01.AOG.0000267533.56546.c2 . Obstetrics & Gynecology . 110 . 2 Pt 2 . 518–520 . 2007 . 17666649 . 24257210 .
- Web site: Uterine Sarcoma Clinical Trials. National Cancer Institute.
- 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.
- Sun . 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 . 10.1016/j.diii.2019.07.007 . 2211-5684 . 31427216.
- 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.
- Health . Center for Devices and Radiological . 2020-12-30 . UPDATE: Perform Only Contained Morcellation When Laparoscopic Power Morcellation Is Appropriate: FDA Safety Communication . FDA . en.
- Web site: Leicester legend Weller mourned. 2010-05-14. 2004-11-13. BBC Online.
- Web site: Jordan treated for cancer. 2009-10-30. 2002-08-11. BBC Online.
- News: Gillespie . Kerry. 'Can't ever give up hope,' Basrur says . The Toronto Star. 2008-04-12 . 2010-01-08.
- Web site: Brown. Stacia. Diana Sands: What Was and What Could've Been. 25 May 2017. https://web.archive.org/web/20171206213240/http://clutchmagonline.com/2012/08/diana-sands-what-was-and-what-couldve-been/. 6 December 2017. dead.
- Web site: That's My Time . Irwinbarker.com. 5 March 2015. https://web.archive.org/web/20081002025115/http://www.irwinbarker.com/thats_my_time.shtml. 2008-10-02. 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.'.
- Web site: Former player Linda Uttley. Fiona Hackett. 2009-11-27. waspsfc.co.uk. 2022-02-28.