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Early cervical cancer
Abstract
Early cervical cancer includes a broad range of disease, from clinically undetectable microinvasive cancer to large, bulky tumors that replace the entire cervix. Further subgrouping of this category is therefore necessary to define the optimal treatment approach for individual cases. The International Federation of Gynecology and Obstetrics (FIGO) staging system stratifies stage I tumors into two broad categories, stage IA (microinvasive) and stage IB (gross tumor). Management of women with stage IA disease is controversial. In the United States, patients with stromal invasion of less than 3 mm and no lymphvascular involvement are usually treated conservatively with simple hysterectomy. In selected patients who desire fertility, cone biopsy with negative surgical margins is also considered. Patients with invasion of more than 3 mm or lymphvascular space involvement are at risk for pelvic lymph node metastasis and are most often treated with radical hysterectomy and pelvic lymphadenectomy. Stage IB1 cervical cancer is managed by either radical surgery or radiotherapy with equivalent recurrence and survival rates. In patients with tumors less than 4 cm in diameter, the decision between radical surgery and radiotherapy is guided by patients' overall health and treatment preferences. For younger women, radical surgery is preferred because ovarian function can be preserved and vaginal stenosis secondary to radiation can be avoided. Radiation therapy is preferred for women who may not tolerate radical surgery. We always prefer primary radiation therapy for patients with tumors larger than 4 cm in diameter. Recent data convincingly demonstrate that the addition of cisplatin-based chemotherapy significantly improves overall survival rates in cervical cancer patients who undergo radiation therapy.
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“The CC cases were diagnosed at locally advanced stages (FIGO IIA1, FIGO IIIC and FIGO IIA1) (Fig. S6A), which are not suitable for hysterectomy, radical trachelectomy, or exenteration alone [26].”
From Combining Mitomycin C with inhibition of BAD phosphorylation enhances apoptotic cell death in advanced cervical cancer (2024) · cites this paper as [26]
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Research works printed but not linked: 10
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Sanderson, S., Tatt, I. D., & Higgins, J. P. (2007) · International Journal of Epidemiology · doi:10.1093/ije/dym018 · Cited by 1,531
Wang, L., Zhang, X., Chen, S., Ye, Q., Basappa, B., Zhu, T., Lobie, P. E., & Pandey, V. (2024) · Translational Oncology · doi:10.1016/j.tranon.2024.102103 · Cited by 8
“S6A), which are not suitable for hysterectomy, radical trachelectomy, or exenteration alone [26].”
Metadata
- Authors
- Lu, K. H., & Burke, T. W.
- Affiliations
- The University of Texas MD Anderson Cancer Center (US)
- Venue
- Current Treatment Options in Oncology
- Published
- 2000-04
- Volume
- 1
- Issue
- 2
- Pages
- 147-155
- ISSN
- 1527-2729 (ISSN-L)
- 1534-6277
- OpenAlex
- W2067348107
- Cited by
- 25
- References
- 0
- Citations by year
- 2026: 2 · 2025: 1 · 2024: 1 · 2020: 1 · 2019: 1 · 2018: 1 · 2016: 2 · 2013: 1 · 2012: 2
- FWCI
- 0.00
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Current Treatment Options in Oncology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Obstetrics and Gynecology › Endometrial and Cervical Cancer Treatments
- Health Sciences › Medicine › Epidemiology › Cervical Cancer and HPV Research
- Health Sciences › Medicine › Oncology › Ovarian cancer diagnosis and treatment
- Keywords
- early-stage cervical cancer, FIGO staging, stage IA cervical cancer, stage IB cervical cancer, microinvasive cervical cancer, radical hysterectomy, pelvic lymphadenectomy, conization, fertility-sparing treatment, radiotherapy, cisplatin-based chemotherapy, lymph node metastasis, ovarian preservation, vaginal stenosis
- MeSH terms
- Antineoplastic Agents, Uterine Cervical Neoplasms, Clinical Trials as Topic, Combined Modality Therapy, Female, Humans, Hysterectomy, Neoplasm Staging, Prognosis, Radiotherapy, Immunotherapy, Active
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