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Colposcopy and Treatment of Cervical Intraepithelial Neoplasia - RHO

Colposcopy and Treatment of Cervical Intraepithelial Neoplasia - RHO

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An introduction to invasive cancer <strong>of</strong> the uterine cervix<br />

choice once the disease has spread beyond the confines<br />

<strong>of</strong> the cervix <strong>and</strong> vaginal fornices, when surgery is not<br />

effective. The management <strong>of</strong> cervical cancer with<br />

radiotherapy may <strong>of</strong>ten involve a combination <strong>of</strong><br />

external radiotherapy (for the entire pelvis) <strong>and</strong><br />

intracavitary irradiation (to the central part <strong>of</strong> the<br />

disease). The addition <strong>of</strong> intracavitory irradiation to<br />

external beam radiotherapy is associated with improved<br />

disease control <strong>and</strong> survival, as compared to external<br />

radiotherapy alone for locally advanced disease such as<br />

stage IIB <strong>and</strong> III.<br />

Women with microinvasive cancer (stage IA) may be<br />

treated with conization or total hysterectomy or<br />

extended hysterectomy. Those with stage IB <strong>and</strong> IIA<br />

cancer may be treated with radical (Wertheim’s)<br />

hysterectomy, <strong>and</strong> pelvic lymphadenectomy or with<br />

intracavitary radiotherapy, or with a combination <strong>of</strong><br />

external radiotherapy <strong>and</strong> intracavitary radiotherapy.<br />

In selected cases <strong>of</strong> small (< 2 cm) stage IB carcinoma,<br />

radical trachelectomy combined with laparoscopic<br />

lymphadenectomy, to salvage the reproductive<br />

function <strong>of</strong> the patient, can be performed.<br />

Radiotherapy <strong>and</strong> surgery produce similar results for<br />

early invasive cancer (stages IB <strong>and</strong> IIA). Stage IIB <strong>and</strong><br />

III cancers are treated with a combination <strong>of</strong> external<br />

<strong>and</strong> intracavitary radiotherapy. Women with stage IV<br />

disease are treated palliatively with external<br />

radiotherapy <strong>and</strong>/or with chemotherapy.<br />

Concomitant chemotherapy with cisplatin has<br />

improved the results <strong>of</strong> radiotherapy in advanced<br />

cervical cancer. R<strong>and</strong>omized clinical trials have shown<br />

a significant gain in overall <strong>and</strong> disease free survival<br />

for cisplatin-based therapy given concurrently with<br />

radiotherapy (Thomas, 2000; Green et al., 2001). A<br />

significant benefit <strong>of</strong> chemo-radiation on both local <strong>and</strong><br />

distant recurrence has been observed. The absolute<br />

benefit with combined therapy in overall survival was<br />

16%. Based on this evidence, concurrent chemotherapy<br />

with radiotherapy is emerging as the new st<strong>and</strong>ard <strong>of</strong><br />

care for advanced cervical cancer.<br />

Clinical stage <strong>of</strong> disease at presentation is the single<br />

most important predictor <strong>of</strong> long-term survival; survival<br />

rates also decline with advancing age. Other factors<br />

influencing survival include general health <strong>and</strong><br />

nutritional status. Anaemic patients respond poorly to<br />

treatment; as do those with HIV-seropositive disease.<br />

Several clinical <strong>and</strong> population-based studies have<br />

demonstrated consistently high five-year survival<br />

associated with stage I disease (> 75%), with rapidly<br />

decreasing survival with advanced stages <strong>of</strong> disease<br />

(< 10% in stage IV) (Delgado et al., 1990; Fagundes et<br />

al., 1992; Kosary et al., 1994; Gatta et al., 1998;<br />

Sankaranarayanan et al., 1998; Denton et al., 2000). In<br />

a large series <strong>of</strong> cervical cancer patients treated by<br />

radiation therapy, the frequency <strong>of</strong> distant metastases<br />

(most frequently to para-aortic lymph nodes, lung,<br />

abdominal cavity, liver <strong>and</strong> gastrointestinal tract) was<br />

shown to increase with increasing stage <strong>of</strong> disease from<br />

3% in stage IA to 75% in stage IVA (Fagundes et al.,<br />

1992). In a study <strong>of</strong> 1028 patients treated with radical<br />

surgery, survival rates correlated consistently with<br />

tumour volume (Burghardt et al., 1992). Five-year<br />

survival rates ranged between 91% for patients with<br />

tumours <strong>of</strong> < 2.5 cm 3 <strong>and</strong> 70% for those with tumours <strong>of</strong><br />

10-50 cm 3 . The three-year disease-free survival ranged<br />

from 94.6% for stage I tumours 5 mm to 59.5% for<br />

stage I tumours 21 mm (Delgado et al., 1990).<br />

Advanced clinical stages are associated with increasing<br />

frequency <strong>of</strong> vascular invasion <strong>and</strong> spread to pelvic <strong>and</strong><br />

para-aortic lymph nodes <strong>and</strong> distant metastases.<br />

27

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