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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.

Fertility preservation and treatment in pregnancy

Oncology and palliative care · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

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Maternal or obstetric deterioration

Haemorrhage, sepsis, venous thromboembolism, airway or neurological compromise, fetal distress, preterm labour or severe treatment toxicity during pregnancy requires immediate maternal stabilisation and obstetric assessment.

Action: Use ABCDE care with pregnancy-appropriate positioning and resuscitation, call the relevant acute oncology and obstetric teams together, investigate the suspected emergency without withholding necessary imaging, and make treatment or delivery decisions in a senior multidisciplinary setting.

Synopsis

Protect reproductive options before gonadotoxic treatment and deliver time-critical cancer care during pregnancy through coordinated oncology, fertility, fetal-medicine, obstetric, neonatal and psychosocial planning.

  • Ask about future fertility and pregnancy possibility at diagnosis, before surgery, systemic treatment or radiotherapy closes an option; record the patient's values without assuming them from age, parity, sex or relationship status.
  • First-line fertility triage assesses treatment urgency, ovarian or testicular reserve, expected gonadotoxicity and safe time available; urgent referral runs in parallel with cancer staging rather than after it.
  • Embryo or oocyte cryopreservation is the established option for many post-pubertal patients with ovaries when a short delay is oncologically safe; sperm cryopreservation is preferred before gonadotoxic treatment for patients producing sperm.
  • Ovarian-tissue cryopreservation can be considered when treatment cannot wait for stimulation or for selected prepubertal patients, but requires a specialist service and disease-specific assessment of malignant-cell reseeding risk.
  • Gonadotrophin-releasing hormone agonist ovarian suppression may reduce ovarian failure during some chemotherapy but is an adjunct, not a substitute for proven cryopreservation when that is feasible.
  • Cancer imaging and treatment during pregnancy are selected by gestation, tumour biology and maternal benefit; necessary maternal diagnosis should not be abandoned because of fetal radiation anxiety.
  • Avoid methotrexate, tamoxifen and other known teratogens during pregnancy; most cytotoxic chemotherapy is avoided in the first trimester, while selected regimens can be used after organogenesis through a specialist protocol.
  • Plan the final treatment dose and delivery interval to allow marrow recovery, avoid elective iatrogenic prematurity where possible, and agree neonatal assessment, breastfeeding compatibility and postpartum treatment restart before birth.

Key red flags

A new cancer diagnosis in pregnancy must not be deferred automatically until after delivery; delay may reduce the chance of cure.

Fever after systemic anticancer treatment is suspected neutropenic sepsis irrespective of pregnancy and needs immediate empirical antibiotics.

Breathlessness, pleuritic pain, unilateral leg swelling or collapse raises pregnancy- and cancer-associated venous thromboembolism risk and requires urgent assessment.

Pelvic pain, vaginal bleeding, fluid loss, reduced fetal movement or contractions needs same-day maternity triage alongside oncology review.

Any planned gonadotoxic treatment, pelvic radiotherapy or reproductive-organ surgery creates a time-limited fertility discussion before treatment starts.

Acute pregnancy complication

Bleeding, contractions, reduced fetal movement, hypertension or sepsis needs immediate maternity assessment while cancer complications are evaluated in parallel.

Investigation priorities

01
First-line reproductive and treatment assessmentFirst stepFirst line

Define pregnancy status, treatment urgency, expected gonadotoxicity and the patient's reproductive goals before therapy.

Management branches

Before treatmentPreserve options without losing cancer control

A reproductive-age or prepubertal patient is offered potentially gonadotoxic treatment.

  1. Explain the estimated treatment-specific risk, ask what future biological parenthood means to the patient and obtain consent for urgent fertility referral and storage decisions.
  2. Send a complete referral with diagnosis, stage, proposed regimen, start deadline, infection and blood-count constraints, and whether ovarian stimulation or a procedure is oncologically safe.
  3. Choose sperm, oocyte, embryo or tissue preservation with the specialist team, document limitations and legal storage consent, and confirm that treatment start remains owned by oncology.

Key medicines

Goserelin ovarian suppressionWhen selected as an adjunct, give goserelin 3.6 mg by subcutaneous implant every 28 days, starting before or as close as feasible to chemotherapy and continuing through the gonadotoxic course under the oncology protocol.It does not guarantee fertility and must not replace oocyte or embryo discussion. Exclude pregnancy, explain vasomotor and bone effects and coordinate timing in hormone-sensitive cancer with the treating oncologist.
Cytotoxic chemotherapy after organogenesisUse the full maternal, body-surface-area-based disease regimen selected by the specialist MDT after the first trimester; do not empirically reduce dose because of pregnancy and stop sufficiently before planned delivery for marrow recovery.Avoid during first-trimester organogenesis where possible. Review placental transfer, fetal growth, maternal pharmacokinetics, neutropenia and delivery timing agent by agent; this is not a single interchangeable regimen.
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Sources and review status4 sources · checked 27 Aug 2026 · clinical review pending+
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

  • NICE CG156 fertility problems recommendationsCryopreservation and fertility preservation before gonadotoxic treatment.
  • RCR protection of pregnant patients during diagnostic imagingUK justification, optimisation, dose assessment and communication for ionising imaging during pregnancy.
  • NHS England fertility preservation service specificationSpecialist fertility service and preservation pathway context.
  • NICE BNF prescribing in pregnancyUK medicine risk assessment and prescribing principles during pregnancy.

Editorial contact: Doctor’s Passport editorial team. Source-check date is separate from clinical approval. Report a content problem · Content changes

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom