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O&G TopicsGynaecological oncology — cancer in pregnancy

O&G · Gynaecological oncology — cancer in pregnancy

Gynaecological cancer in pregnancy

Also known as Cancer in pregnancy · Cervical cancer in pregnancy · Ovarian cancer in pregnancy · Chemotherapy in pregnancy · Gynaecological malignancy in pregnancy

Exam-exhaustive FRANZCOG fellowship reference on gynaecological cancer in pregnancy — cervical cancer (fertility- and pregnancy-preserving strategy, neoadjuvant chemotherapy), the adnexal mass in pregnancy (IOTA/ESGO imaging, surgery in the second trimester), the trimester safety of chemotherapy (first-trimester malformation risk, long-term child outcomes), timing of treatment versus delivery, the contraindicated agents, and the ESGO/INCIP and ASCO guideline framework. ANZ-primary (RANZCOG), globally tagged to ESMO, ESGO/INCIP, ASCO.

high18 referencesUpdated 1 Aug 202611 min readVerification in progress

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FRANZCOGMRCOGABOGFRCSCMRCPI

Red flags

  • Chemotherapy before 12 weeks carries a high major-malformation rate — the first trimester is avoided; after 12 weeks the malformation rate approximates the background population rate
  • Iatrogenic preterm delivery, not chemotherapy, is the dominant driver of child cognitive harm — do not deliver early without a reason
  • Methotrexate, hormonal therapies, HER2-targeted agents, VEGF and PARP inhibitors, antibody-drug conjugates and all cellular therapies are contraindicated in pregnancy regardless of gestational age
  • A cervical lesion in pregnancy is cancer until biopsy proves otherwise; an adnexal mass is cancer until IOTA/ESGO imaging and markers are interpreted for pregnancy
  • Final chemotherapy must be timed so delivery does not fall during maternal haematological nadir
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Practise this topic8 MCQs with explanations

Target exams

FRANZCOGMRCOGABOGFRCSCMRCPI

Red flags

  • Chemotherapy before 12 weeks carries a high major-malformation rate — the first trimester is avoided; after 12 weeks the malformation rate approximates the background population rate
  • Iatrogenic preterm delivery, not chemotherapy, is the dominant driver of child cognitive harm — do not deliver early without a reason
  • Methotrexate, hormonal therapies, HER2-targeted agents, VEGF and PARP inhibitors, antibody-drug conjugates and all cellular therapies are contraindicated in pregnancy regardless of gestational age
  • A cervical lesion in pregnancy is cancer until biopsy proves otherwise; an adnexal mass is cancer until IOTA/ESGO imaging and markers are interpreted for pregnancy
  • Final chemotherapy must be timed so delivery does not fall during maternal haematological nadir
One-line fellowship answer

Gynaecological cancer in pregnancy is managed by a multidisciplinary team aiming for standard oncological treatment that preserves maternal prognosis while protecting the fetus. The rules that make it safe: stage with ultrasound and MRI (no gadolinium) under ALARA; give chemotherapy only after the first trimester (before 12 weeks the major-malformation rate is high); never give methotrexate, hormonal therapies, HER2-targeted agents, VEGF/PARP inhibitors, antibody-drug conjugates or cellular therapies; plan delivery at or after 37 weeks with the final chemotherapy dose timed to avoid maternal nadir; and avoid iatrogenic preterm delivery, because prematurity — not chemotherapy — is what harms the child.[1][2][4]

She is 23 weeks pregnant and your colposcopy just confirmed an invasive squamous carcinoma of the cervix. In the next hour you will not make a single decision alone — you will activate a multidisciplinary team, you will weigh her prognosis against her baby's survival, and you will resist the two impulses that wreck these cases: deferring treatment as if the cancer will wait, and delivering early as if prematurity is harmless. Neither is true. Cancer in pregnancy is the discipline where obstetrics and oncology must think as one.[1][14]

Scope and why it is its own topic

Cancer is diagnosed in approximately one in every thousand pregnant women, and its incidence is rising as childbearing is delayed into the years when cancer becomes more common.[6][7] Of the gynaecological cancers, cervical cancer is the commonest malignancy diagnosed in pregnancy; ovarian malignancy in pregnancy is uncommon and, in young women, is more often borderline or germ-cell than high-grade epithelial. The framework is unified by a single principle, stated in the ESGO/INCIP guideline: treatment during pregnancy should adhere to standard oncological management as much as possible to optimise maternal prognosis, always taking fetal wellbeing into account, and always within a multidisciplinary team.[1][7]

The decision space is defined by three variables — tumour type and stage, gestational age, and the patient's values — and the answer is almost never "treat now at any cost" or "wait and see." It is "what standard treatment can I safely deliver now, and what must wait until fetal maturation?"[1][2]

The numbers that anchor the decision

~1 in 1000Cancer in pregnancyincidence, rising with delayed childbearing
21.7%Major malformation, chemo before 12 wkvs ~3% after 12 weeks (background)
≥37 weeksDelivery targetfinal chemo dose timed to avoid maternal nadir
normal9-year neurodevelopmentno excess harm vs unexposed children
[2] [4] [6]
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References18ShowHide
  1. [1]Amant F, Planchamp F, Berveiller P, et al. ESGO/INCIP Guidelines for the management of patients with gynecological cancers during pregnancy Int J Gynecol Cancer, 2025.PMID 40707270
  2. [2]Loren AW, Lacchetti C, Amant F, et al. Management of Cancer During Pregnancy: ASCO Guideline J Clin Oncol, 2026.PMID 41380115
  3. [3]Peccatori FA, Azim HA Jr, Orecchia R, et al. Cancer, pregnancy and fertility: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up Ann Oncol, 2013.PMID 23813932
  4. [4]van Gerwen M, Maggen C, Cardonick E, et al. Association of Chemotherapy Timing in Pregnancy With Congenital Malformation JAMA Netw Open, 2021.PMID 34106263
  5. [5]Amant F, Van Calsteren K, Halaska MJ, et al. Long-term cognitive and cardiac outcomes after prenatal exposure to chemotherapy in children aged 18 months or older: an observational study Lancet Oncol, 2012.PMID 22326925
  6. [6]Van Assche IA, Huis In 't Veld EA, Van Calsteren K, et al. Cognitive and Behavioral Development of 9-Year-Old Children After Maternal Cancer During Pregnancy: A Prospective Multicenter Cohort Study J Clin Oncol, 2023.PMID 36634293
  7. [7]Wolters V, Heimovaara J, Maggen C, et al. Management of pregnancy in women with cancer Int J Gynecol Cancer, 2021.PMID 33649001
  8. [8]Maggen C, Wolters VERA, Van Calsteren K, et al. Impact of chemotherapy during pregnancy on fetal growth J Matern Fetal Neonatal Med, 2022.PMID 36202393
  9. [9]Cardonick EH, Gringlas MB, Hunter K, et al. Development of children born to mothers with cancer during pregnancy: comparing in utero chemotherapy-exposed children with nonexposed controls Am J Obstet Gynecol, 2015.PMID 25434835
  10. [10]Fruscio R, Trozzi R, Galimberti S, et al. Epithelial ovarian cancer and borderline tumors during pregnancy: a report from the International Network on Cancer, Infertility, and Pregnancy Int J Gynecol Cancer, 2025.PMID 39971439
  11. [11]Timmerman D, Planchamp F, Bourne T, et al. ESGO/ISUOG/IOTA/ESGE Consensus Statement on preoperative diagnosis of ovarian tumors Ultrasound Obstet Gynecol, 2021.PMID 33794043
  12. [12]Gaughran JE, Naji O, Al Sabbagh MQ, et al. Is Ultrasound a Reliable and Reproducible Method for Assessing Adnexal Masses in Pregnancy? A Systematic Review Cureus, 2021.PMID 34849310
  13. [13]Karam A, Feldman N, Holschneider CH Neoadjuvant cisplatin and radical cesarean hysterectomy for cervical cancer in pregnancy Nat Clin Pract Oncol, 2007.PMID 17534393
  14. [14]Salani R, Billingsley CC, Crafton SM Cancer and pregnancy: an overview for obstetricians and gynecologists Am J Obstet Gynecol, 2014.PMID 24316272
  15. [15]Avilés A, Neri N, Nambo MJ Hematological malignancies and pregnancy: treat or no treat during first trimester Int J Cancer, 2012.PMID 22511239
  16. [16]Avilés A, Neri N, Nambo MJ Long-term evaluation of cardiac function in children who received anthracyclines during pregnancy Ann Oncol, 2006.PMID 16272162
  17. [17]Maggen C, Dierickx D, Cardonick E, et al. Maternal and neonatal outcomes in 80 patients diagnosed with non-Hodgkin lymphoma during pregnancy: results from the International Network on Cancer, Infertility and Pregnancy Br J Haematol, 2021.PMID 32945547
  18. [18]LeJeune CL, Janovska N, Wakatsuki A, et al. Analysis of indocyanine green-guided sentinel lymph node mapping for cervical cancer during pregnancy Int J Gynecol Cancer, 2026.PMID 42424759

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PreviousPost-molar gestational trophoblastic neoplasia: FIGO 2000 staging and WHO prognostic score, risk-stratified chemotherapy, hCG surveillance and the near-universal cureGynaecological oncology — gestational trophoblastic diseaseNextGynaecological cancer in pregnancy — diagnostic, treatment-timing and delivery frameworkGynaecological oncology — cancer in pregnancy