Evidence for Cervical Brachytherapy in Cervical Cancer
Brachytherapy is an essential and irreplaceable component of definitive radiation therapy for cervical cancer, with strong evidence demonstrating that omitting it compromises survival outcomes. 1, 2
Critical Role in Treatment
Brachytherapy must be included as part of definitive radiation therapy for all patients with intact cervical cancer who are not surgical candidates. 1 The evidence is unequivocal:
- Definitive radiation therapy should consist of pelvic external beam radiation combined with intracavitary brachytherapy, administered at high doses (≥80-90 Gy) within a short timeframe (<55 days) 3
- The decline in brachytherapy use has been directly associated with negative impacts on survival, even in the era of modern external beam techniques 2
- Conformal external beam therapies such as IMRT or SBRT should NOT be used as routine alternatives to brachytherapy for treatment of central disease in patients with an intact cervix 1, 2
Survival and Local Control Data
The historical evidence demonstrates excellent outcomes when brachytherapy is properly incorporated:
- Local control rates of 88-95% for stage IB, 70-80% for stage IIB, and 30-40% for stage III 3
- 5-year survival rates exceeding 80% for stage IB, 65% for stage IIB, and 40% for stage III 3
- In early-stage disease (IB-IIA), radiation therapy (including brachytherapy) achieved 83% overall survival and 74% disease-free survival at 5 years, comparable to radical surgery but with lower severe morbidity (12% vs 28%) 3
Technical Requirements and Dosing
The total doses from brachytherapy and external beam radiation to point A must reach at least 80 Gy for small tumors and ≥85 Gy for larger tumors. 1, 4 Key technical parameters include:
- Point A dosing remains the standard based on extensive experience and tumor control results 1
- For limited-stage disease, the combination must deliver 60 Gy to the central pelvis and 45-50 Gy to the lateral pelvic area 1
- Pelvic sidewall dose recommendations are 50-55 Gy for early lesions and 55-65 Gy for advanced disease 4
- Bladder and rectal doses should be kept below 80 Gy and 75 Gy LDR equivalent doses, respectively 4
Treatment Timing: A Critical Factor
The entire radiation course (including both external beam and brachytherapy) must be completed within 8 weeks. 1, 5 This timing is crucial because:
- Extending treatment beyond 6-8 weeks results in approximately 0.5-1% decrease in pelvic control and cause-specific survival for each extra day of delay 1
- Brachytherapy should be initiated toward the latter part of external beam treatment, after sufficient tumor regression has occurred to permit satisfactory applicator geometry 1, 6
- Initial EBRT of 40-45 Gy to the whole pelvis is necessary to obtain tumor shrinkage before optimal intracavitary placements 1
Applicator Selection
Intracavitary brachytherapy using an intrauterine tandem combined with vaginal colpostats (ovoids, ring, or cylinder) is the standard technique. 1, 5 Important considerations:
- Applicator selection should be based on patient and tumor anatomy 1
- Interstitial brachytherapy should only be used in rare cases when tumor geometry renders intracavitary brachytherapy infeasible, and only by individuals and institutions with appropriate experience 1, 5, 4
- Precise applicator placement is essential for improved local control and reduced morbidity 5
Image-Guided Brachytherapy
Modern 3D image-guided techniques represent an evolution in brachytherapy delivery:
- Current 3D image-guided techniques optimize implant dose coverage of tumor while potentially reducing dose to adjacent bladder, rectum, and bowel structures 1, 7
- CT or MRI-guided adaptive brachytherapy is evolving as the preferred method 2
- When implementing 3D image-guided approaches, traditional point A dosing must not be abandoned to avoid underdosing tumors 1
- MRI remains the gold standard for soft tissue assessment, with 86% agreement with surgical pathology for tumor size 1
Specific Clinical Scenarios
Stage IA2 Disease
- For patients with surgical contraindications, brachytherapy may represent an alternative option 3
- For highly selected very early disease (stage IA2), brachytherapy alone without external beam radiation may be an option 1
Adjuvant Setting After Surgery
- Vaginal brachytherapy is clearly indicated when there is a positive vaginal margin after hysterectomy 3, 6
- Vaginal brachytherapy may be added as a boost to external beam radiation in high-risk scenarios, particularly with margin concerns 3, 6
- For patients with positive pelvic nodes, positive surgical margins, and/or positive parametrium, postoperative pelvic radiation with concurrent cisplatin-containing chemotherapy with or without vaginal brachytherapy is recommended 3
Integration with Chemotherapy
Concurrent cisplatin-based chemotherapy should be administered during external beam radiotherapy for most patients with cervical cancer. 1 The evidence shows:
- Meta-analysis of 18 randomized trials demonstrated an absolute 5-year survival benefit of 8% for overall disease-free survival, 9% for locoregional disease-free survival, and 7% for metastases-free survival 3
- This benefit applies to all stages of locally advanced disease 3
Common Pitfalls to Avoid
- Never substitute IMRT or SBRT for brachytherapy in patients with intact cervix undergoing curative-intent treatment 1, 2
- Do not allow treatment delays beyond 8 weeks total duration, as each day of delay reduces outcomes 1, 5
- Do not abandon point A dosing when using image-guided techniques, as this risks underdosing the tumor 1
- Ensure adequate total dose of at least 80-85 Gy to point A; suboptimal dosing compromises local control 1, 4
Access Considerations
With careful care coordination, external beam radiation therapy and brachytherapy can be successfully delivered at different treatment centers without compromising treatment time and outcomes in areas where access to brachytherapy may be limited. 2