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O&G VivasGynaecological oncology — cervical

O&G Vivas · Gynaecological oncology — cervical

Cervical cancer — structured oral station (12 minutes)

FRANZCOG oral-format station on cervical cancer: the candidate assigns the FIGO 2018 stage with the IB subgroups and IIIC nodal substages, defends the chemoradiotherapy regimen with weekly cisplatin, explains the LACC-driven return to open surgery, and counsels honestly on prognosis. Scored against the eight published RANZCOG oral domains.

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FRANZCOGMRCOGABOGFRCSCMRCPI
Prompt
You are the gynaecology registrar in clinic. A 38-year-old woman, para 2, presents with three months of postcoital bleeding and has not had cervical screening for eight years. Speculum examination shows a 3 cm friable exophytic lesion on the ectocervix; bimanual suggests parametrial induration but a mobile cervix. A directed biopsy confirms squamous cell carcinoma. The examiner will ask you to stage the tumour with FIGO 2018, defend the management, discuss the surgical-versus-chemoradiotherapy watershed, and counsel the patient on prognosis and follow-up.

Station format

4 minutes reading, 12 minutes examination, 20 marks, global scoring. The eight published RANZCOG oral domains apply to every station: history and examination; investigations and interpreting results; treatment and management; clinical knowledge; complex, urgent or unusual clinical presentations; rapport with patient, support person or colleague; respect; communication skills. You are marked on how you behave, not only what you know. [1]

Reveal the examiner script and model responsesShowHide

Opening prompt — "Stage this tumour using FIGO 2018 and tell me why."

Model response — assign the stage with the verbatim definitions: [1]

  • "This is Stage IIIC1 (r) — a 3.5 cm tumour with parametrial invasion and an enlarged right external iliac lymph node on MRI."
  • "Under FIGO 2018, the tumour alone would be Stage IIB (parametrial invasion); the pelvic nodal disease upstages it to IIIC1, which is pelvic lymph node metastasis only. IIIC2 would be para-aortic."
  • "The 'r' notation records that the nodal status was determined by imaging — radiological — rather than surgical pathology ('p')."[1]

Probe 1 — "What is the standard treatment for this stage?"

  • "Concurrent chemoradiotherapy. EBRT to the whole pelvis, with para-aortic field extension if nodes were involved; intracavitary brachytherapy to a total combined dose per protocol; plus weekly cisplatin as a radiosensitiser per the current protocol (confirm exact doses, fractionation and cycles against the current statement)." [2][5]
  • "The CCCMAC meta-analysis of 18 randomised trials showed a 6 percent absolute 5-year survival benefit over radiotherapy alone. Surgery is not appropriate for Stage IIIC disease."

Probe 2 — "She is 38 and asks whether surgery could be offered to preserve her ovaries. How do you answer?"

  • "For Stage IIIC1, surgery is not the treatment — chemoradiotherapy is curative-intent and superior to surgery for this stage. However, because the ovaries would be in the radiation field, I would offer ovarian transposition high into the paracolic gutters, out of the radiation field, to preserve ovarian function, given her young age."[1][2][5]

Probe 3 — "If instead her tumour were 1.5 cm Stage IB1 and she wished to preserve fertility, what would change?"

  • "For a 1.5 cm Stage IB1 tumour, radical trachelectomy with pelvic lymphadenectomy is the fertility-sparing option of choice. The cervix and parametrium are removed with pelvic lymphadenectomy, followed by anastomosis of the uterus to the vaginal end, allowing future pregnancy."
  • "Live-birth rates are around 68 percent thereafter, but over half deliver preterm after radical trachelectomy — thorough counselling and close obstetric monitoring." [4]
  • "For the radical hysterectomy candidate with early disease, the open abdominal approach is now the standard after LACC, which showed minimally-invasive radical hysterectomy had lower disease-free survival (86 vs 97 percent at 4.5 years) and higher recurrence." [3]

Probe 4 — Communication probe: "She asks what her chances are. What do you say?"

This is a scored communication domain — demonstrate it out loud: [1]

  • "I would be honest and precise, and sit at her eye level: 'Stage IIIC1 cervical cancer is serious but treatable with curative intent. Nodal disease confers a worse prognosis than node-negative disease, and tumour over 4 cm raises pelvic recurrence — but in locally advanced disease, 5-year survival was 73 percent with chemoradiotherapy versus 58 percent with radiotherapy alone. The treatment is demanding — weeks of daily radiotherapy plus weekly chemotherapy — but it gives you the best chance of cure. I will support you through every step, and we will have a dedicated team including a cancer nurse, a dietitian, and a counsellor.'"[1][5]

Probe 5 — "Two years later she has a central pelvic recurrence. What are the options?"

  • "Investigate with imaging (MRI pelvis, PET-CT) and biopsy to confirm recurrence and exclude distant disease."[1]
  • "For an isolated central pelvic recurrence after chemoradiotherapy in a fit patient, pelvic exenteration (anterior, posterior, or total) may be curative — 5-year survival 30 to 60 percent, operative mortality under 10 percent. This is a major undertaking and requires careful selection, counselling, and a multidisciplinary approach."[5]
  • "For recurrent disease not amenable to exenteration, systemic therapy with the GOG-240 triplet (cisplatin, paclitaxel, bevacizumab) plus pembrolizumab for PD-L1-positive disease is the standard."[6]
Obstetrics & Gynaecology Pro

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You have read the opening of this viva. The complete unit — every section and its primary-source references — is part of the Obstetrics & Gynaecology fellowship library.

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References6ShowHide
  1. [1]Bhatla N, Berek JS, Cuello Fredes M, et al. Revised FIGO staging for carcinoma of the cervix uteri. Int J Gynaecol Obstet, 2019.PMID 30656645
  2. [2]Chemoradiotherapy for Cervical Cancer Meta-Analysis Collaboration (CCCMAC). Reducing uncertainties about the effects of chemoradiotherapy for cervical cancer: a systematic review and meta-analysis of individual patient data from 18 randomized trials. J Clin Oncol, 2008.PMID 19001332
  3. [3]Ramirez PT, Frumovitz M, Pareja R, et al. Minimally Invasive versus Abdominal Radical Hysterectomy for Cervical Cancer. N Engl J Med, 2018.PMID 30380365
  4. [4]Sidonie M, et al. Oncologic, pregnancy, and reproductive outcomes of fertility-sparing surgery in early-stage cervical cancer: a systematic review. Surg Oncol, 2026.PMID 42114502
  5. [5]Bhatla N, Aoki D, Sharma DN, Sankaranarayanan R Cancer of the cervix uteri: 2025 update. Int J Gynaecol Obstet, 2025.PMID 40908766
  6. [6]Tewari KS, Sill MW, Penson RT, Huang H, Ramondetta LM, Landrum LM, Oaknin A, Reid TJ, Leitao MM, Michael HE, DiSaia PJ, Copeland LJ, Creasman WT, Stehman FB, Brady MF, Burger RA, Thigpen JT, Birrer MJ, Waggoner SE, Moore DH, Look KY, Koh WJ, Monk BJ Bevacizumab for advanced cervical cancer: final overall survival and adverse event analysis of a randomised, controlled, open-label, phase 3 trial (Gynecologic Oncology Group 240). Lancet, 2017.PMID 28756902
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