Cervical cancer natural history, complications and prognosis: Difference between revisions
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:::* Bilateral disease | :::* Bilateral disease | ||
:::* Clinical stage | :::* Clinical stage | ||
:* Other prognostic factors are include:<ref name="KangKim2011">{{cite journal|last1=Kang|first1=Woo Dae|last2=Kim|first2=Cheol Hong|last3=Cho|first3=Moon Kyoung|last4=Kim|first4=Jong Woon|last5=Cho|first5=Hye Yon|last6=Kim|first6=Yoon Ha|last7=Choi|first7=Ho Sun|last8=Kim|first8=Seok Mo|title=HPV-18 is a poor prognostic factor, unlike the HPV viral load, in patients with stage IB–IIA cervical cancer undergoing radical hysterectomy|journal=Gynecologic Oncology|volume=121|issue=3|year=2011|pages=546–550|issn=00908258|doi=10.1016/j.ygyno.2011.01.015}}</ref> | :* Other prognostic factors are include:<ref name="KangKim2011">{{cite journal|last1=Kang|first1=Woo Dae|last2=Kim|first2=Cheol Hong|last3=Cho|first3=Moon Kyoung|last4=Kim|first4=Jong Woon|last5=Cho|first5=Hye Yon|last6=Kim|first6=Yoon Ha|last7=Choi|first7=Ho Sun|last8=Kim|first8=Seok Mo|title=HPV-18 is a poor prognostic factor, unlike the HPV viral load, in patients with stage IB–IIA cervical cancer undergoing radical hysterectomy|journal=Gynecologic Oncology|volume=121|issue=3|year=2011|pages=546–550|issn=00908258|doi=10.1016/j.ygyno.2011.01.015}}</ref><ref name="pmid8093678">{{cite journal |vauthors=Maiman M, Fruchter RG, Guy L, Cuthill S, Levine P, Serur E |title=Human immunodeficiency virus infection and invasive cervical carcinoma |journal=Cancer |volume=71 |issue=2 |pages=402–6 |date=January 1993 |pmid=8093678 |doi= |url=}}</ref> | ||
::* [[Human immunodeficiency virus]] (HIV) status: Women with [[HIV]] have more aggressive and advanced disease and a poorer prognosis. | ::* [[Human immunodeficiency virus]] (HIV) status: Women with [[HIV]] have more aggressive and advanced disease and a poorer prognosis. | ||
::* C-myc overexpression: A study of patients with known invasive [[squamous carcinoma]] of the cervix found that overexpression of the [[C-myc oncogene]] was associated with a poorer prognosis. | ::* C-myc overexpression: A study of patients with known invasive [[squamous carcinoma]] of the cervix found that overexpression of the [[C-myc oncogene]] was associated with a poorer prognosis. | ||
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Common complications of cervical cancer include pain, vaginal bleeding, fistula and renal failure. Prognosis is generally good, and the 5 year survival rate of patients with cervical cancer is approximately 70%.
Natural history
Cervical cancer is the most common cancer mainly among women in developing countries, there is an estimate of almost 260 000 deaths annually, about 80% occurred in developing countries. Infection by high risk strain of oncogenic HPV types is an established cause of neoplastic lesions of the cervix, vagina and vulva, anus, penis and oropharynx. HPV 16 and 18, are the most common cause of approximately 70% of all cervical cancers worldwide. HPV is highly transmissible through direct skin to skin contact and intercourse, women with persistent high-risk HPV infections are at greatest risk for developing cervical cancer. Since the identification of HPV as main cause of cervical cancer, prevention strategies had been developed by the introduction of HPV testing in screening and utilizing HPV vaccines in preadolescent girls and young women whom are at greater risk. The most important risk factors associated with the infection by HPV are sexual intercourse at early age at the start of the first sexual relationships, having high number of sexual partners throughout life, or women being with men having multiple sexual partners. Male circumcision and use of condoms are factors that can reduce, but not preventing the transmission of human papilloma virus.[1]
Complications
Advanced stage of cervical cancer can cause varieties of complications, some of these are include:[2]
- Pain
- Vaginal hemorrhage
- Enterovaginal, rectovaginal, and vesico- or ureterovaginal fistulas
- Renal failure and/or uremia
- Malnutrition
- Anemia
- Mental depression
Prognosis
The prognosis for patients with cervical cancer is Prognosis is generally good, and the 5 year survival rate of patients with cervical cancer is approximately 67.9%, this is heavily because of annual screening wiht Pap smear and introduction of new preventive methods like HPV vaccination to decrease the mortality and incidence rates. Majority of cervical cancer cases can be detected early through the use of screening by Pap test and HPV DNA testing.
Prognosis of cervical cancer depends upon the clinical stage of the disease and distant metastasis.[3][4][5]
These prognostic factors that affecting survival rate are include:[6]
- Patient age
- Maximum tumor diameter of ≥6 cm
- Pelvic lymph node enlargement, and distant metastasis
- Pretreatment hemoglobin level
- Concurrent chemoradiotherapy, increases survival rate significantly in patients with advanced stage of cervical cancer in comparison with those receiving radiation therapy alone.
- Performance status
- Bilateral disease
- Clinical stage
- Human immunodeficiency virus (HIV) status: Women with HIV have more aggressive and advanced disease and a poorer prognosis.
- C-myc overexpression: A study of patients with known invasive squamous carcinoma of the cervix found that overexpression of the C-myc oncogene was associated with a poorer prognosis.
- Number of cells in S phase: The number of cells in S phase may also have prognostic significance in early cervical carcinoma.
- HPV-18 DNA: HPV-18 DNA has been found to be an independent adverse molecular prognostic factor. Two studies have shown a worse outcome when HPV-18 was identified in cervical cancers of patients undergoing radical hysterectomy and pelvic lymphadenectomy.
- A polymorphism in the Gamma-glutamyl hydrolase enzyme, which is related to folate metabolism, has been shown to decrease response to cisplatin, and as a result is associated with poorer outcomes.
Refrences
- ↑ Castellsagué, Xavier (2008). "Natural history and epidemiology of HPV infection and cervical cancer". Gynecologic Oncology. 110 (3): S4–S7. doi:10.1016/j.ygyno.2008.07.045. ISSN 0090-8258.
- ↑ Schmitz, Herbert E.; Isaacs, John H. (1957). "Complications of Advanced Cervical Cancer and Their Management". Radiology. 69 (3): 324–329. doi:10.1148/69.3.324. ISSN 0033-8419.
- ↑ Yuan, Chiou-Chung; Wang, Peng-Hui; Lai, Chiung-Ru; Tsu, En-Jie; Yen, Ming-Shyen; Ng, Heung-Tat (1999). "Recurrence and Survival Analyses of 1,115 Cervical Cancer Patients Treated with Radical Hysterectomy". Gynecologic and Obstetric Investigation. 47 (2): 127–132. doi:10.1159/000010076. ISSN 0378-7346.
- ↑ B.K., Vishma; B., Prakash; Kulkarni, Praveen; M., Renuka (2016). "Survival and prognostic factors for cervical cancer: a hospital based study in Mysuru, India". International Journal of Community Medicine and Public Health: 218–223. doi:10.18203/2394-6040.ijcmph20151566. ISSN 2394-6032.
- ↑ Jung, Kyu-Won; Won, Young-Joo; Kong, Hyun-Joo; Oh, Chang-Mo; Shin, Aesun; Lee, Jin-Soo (2013). "Survival of Korean Adult Cancer Patients by Stage at Diagnosis, 2006-2010: National Cancer Registry Study". Cancer Research and Treatment. 45 (3): 162–171. doi:10.4143/crt.2013.45.3.162. ISSN 1598-2998.
- ↑ Endo, Daisuke; Todo, Yukiharu; Okamoto, Kazuhira; Minobe, Shinichiro; Kato, Hidenori; Nishiyama, Noriaki (2015). "Prognostic factors for patients with cervical cancer treated with concurrent chemoradiotherapy: a retrospective analysis in a Japanese cohort". Journal of Gynecologic Oncology. 26 (1): 12. doi:10.3802/jgo.2015.26.1.12. ISSN 2005-0380.
- ↑ Kang, Woo Dae; Kim, Cheol Hong; Cho, Moon Kyoung; Kim, Jong Woon; Cho, Hye Yon; Kim, Yoon Ha; Choi, Ho Sun; Kim, Seok Mo (2011). "HPV-18 is a poor prognostic factor, unlike the HPV viral load, in patients with stage IB–IIA cervical cancer undergoing radical hysterectomy". Gynecologic Oncology. 121 (3): 546–550. doi:10.1016/j.ygyno.2011.01.015. ISSN 0090-8258.
- ↑ Maiman M, Fruchter RG, Guy L, Cuthill S, Levine P, Serur E (January 1993). "Human immunodeficiency virus infection and invasive cervical carcinoma". Cancer. 71 (2): 402–6. PMID 8093678.