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O&G VivasGynaecological oncology — cancer in pregnancy

O&G Vivas · Gynaecological oncology — cancer in pregnancy

Gynaecological cancer in pregnancy — structured oral station (12 minutes)

FRANZCOG oral-format station on gynaecological cancer in pregnancy: the imaging approach (non-contrast MRI first-line, do not withhold CT or PET, no abdominal shielding), the three cervical cancer management paths, the 14-week and 35-week chemotherapy windows with contraindicated agents, the delivery recommendations, and honest counselling on fetal outcomes. Scored against the eight published RANZCOG oral domains.

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Prompt
You are the gynaecology registrar in clinic. A 32-year-old woman at 14 weeks gestation, para 1, is referred after an abnormal cervical screening result and a friable, bleeding lesion on the ectocervix at her booking visit. A directed punch biopsy confirms moderately differentiated squamous cell carcinoma. She wishes to continue this pregnancy. The examiner will ask you to outline the imaging approach, describe the management options, defend the chemotherapy windows, and counsel the patient on fetal outcomes and delivery.

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 — "How do you stage her cervical cancer in pregnancy?"

Model response — name the imaging approach: [1][2]

  • "Non-contrast MRI is the first-line cross-sectional modality for local staging — tumour size, parametrial invasion, and nodal status — without ionising radiation."
  • "If I need to stage for distant disease, CT or PET-CT should not be withheld when clinically indicated — the diagnostic information outweighs the fetal dose at staged doses."
  • "I would not use abdominal shielding during CT — it is no longer recommended because it increases scatter dose internally and degrades image quality (LeJeune 2025)."[1][2]

Probe 1 — "She is 14 weeks and wishes to continue the pregnancy. What are her management options?"

  • "This is a stage IB1 or higher cervical cancer diagnosed in the early second trimester, and she wishes to continue — so the three options are: (1) termination and definitive treatment; (2) neoadjuvant platinum chemotherapy after 14 weeks to bridge to delivery, then definitive chemoradiotherapy or surgery postpartum; or (3) caesarean-radical-hysterectomy at term." [1][5]
  • "If her tumour were stage IA1 without lymphovascular space invasion, she could be managed conservatively with definitive surgery after delivery. The determining factors are the FIGO stage, the gestational age, the tumour biology, and her values — this is an MDT decision with her at the centre."[1]

Probe 2 — "When would you give chemotherapy, and which agents must you avoid?"

  • "I would start chemotherapy after 14 weeks — organogenesis is complete, so the teratogenic risk falls to near-background — and stop by 35 weeks to allow marrow recovery before delivery. I would not give it within 3 weeks of planned delivery." [1]
  • "The four contraindicated agents are: tamoxifen — teratogenic; trastuzumab — oligohydramnios and fetal renal injury; checkpoint inhibitors — they disrupt the fetomaternal immune tolerance that sustains pregnancy; and bevacizumab — third-trimester wound healing impairment and bleeding."[1]

Probe 3 — "Will the chemotherapy harm her baby's development?"

  • "The long-term news is reassuring. The Korakiti (2020) systematic review found generally normal neurodevelopment in children exposed to chemotherapy in utero." [3]
  • "The main driver of adverse neonatal outcome is iatrogenic preterm birth, not the chemotherapy itself. So my priority is to avoid unnecessary prematurity — deliver at term where the cancer treatment allows, and time the last chemotherapy dose to leave at least 3 weeks for marrow recovery."[3]

Probe 4 — Communication: "She asks what her chances are and whether she can deliver normally. What do you say?"

This is a scored communication domain — demonstrate it out loud: [1][4]

  • "I would sit at her eye level and say: 'The most important thing is that being pregnant does not make your cancer worse — when we treat it properly, your prognosis is the same as if you were not pregnant. We have a plan that protects both you and your baby: chemotherapy after 14 weeks is safe for the baby's development, and the evidence shows children exposed in the womb develop normally. For delivery, because of where your cancer is, I would recommend a caesarean — it protects the cervix and lets us do any surgery needed at the same time. We will plan this together with our maternal-fetal medicine, gynae-oncology and neonatal teams, and you will have a dedicated team supporting you at every step.'"[1][4]

Probe 5 — "How would you deliver her, and what must you remember at delivery?"

  • "I would plan a caesarean delivery, because cervical cancer — especially after biopsy or conisation — makes the cervix unsuitable for vaginal delivery. If she is near term, a caesarean-radical-hysterectomy may be appropriate." [1]
  • "At delivery I must send the placenta to pathology in every case — placental metastasis, though rare, must be sought and documented. I would also arrange for the neonate to be assessed and monitored for marrow recovery if she had recent chemotherapy."[1]
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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References5ShowHide
  1. [1]Amant F, Berveiller P, Boere IA, et al. Gynecologic cancers in pregnancy: guidelines based on a third international consensus meeting. Ann Oncol, 2019.PMID 31435648
  2. [2]LeJeune CL, Nougaret S, Massera RT, et al. Abdominal shielding not recommended for diagnostic imaging with ionising radiation during pregnancy. Lancet Oncol, 2025.PMID 41167213
  3. [3]Korakiti AM, Zografos E, van Gerwen M, et al. Long-Term Neurodevelopmental Outcome of Children after in Utero Exposure to Chemotherapy. Cancers (Basel), 2020.PMID 33287323
  4. [4]Amant F, von Minckwitz G, Han SN, et al. Prognosis of women with primary breast cancer diagnosed during pregnancy: results from an international collaborative study. J Clin Oncol, 2013.PMID 23610117
  5. [5]LeJeune CL, Van Calsteren K, Amant F A multidisciplinary management approach to cervical cancer during pregnancy. Lancet, 2026.PMID 41720126
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