Evidence map›Paper›PMID 42597043›Full record

ArticlePregnancy (Hoboken, N.J.)2026

Society for Maternal-Fetal Medicine Consult Series #76: Cancer in pregnancy.

Society for Maternal‐Fetal Medicine (SMFM), Moti Gulersen, Clarissa Bonanno, Justin S Brandt, Stephanie Pierce, Elyce H Cardonick, SMFM Publications Committee

Abstract read
In one paragraph

Article in Pregnancy (Hoboken, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Society for Maternal‐Fetal Medicine (SMFM)
Moti Gulersen
Clarissa Bonanno
Justin S Brandt
Stephanie Pierce
Elyce H Cardonick
SMFM Publications Committee

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Approximately one in 1000 pregnancies is complicated by the diagnosis of cancer each year, and the incidence of cancer among reproductive-age individuals is increasing. Management of a pregnant person with cancer can be complex and warrants a multidisciplinary approach to care. Recent data have demonstrated reassuring outcomes for pregnant persons and their offspring after treatment of many types of cancer in pregnancy. Treatment of cancer in pregnancy must be individualized based on the specific type and stage of cancer, gestational age at diagnosis, and the patient's desire to continue the pregnancy. This document aims to aid clinicians by summarizing the principles of diagnosing cancer in pregnancy and counseling patients about their reproductive and treatment options. It provides current, evidence-based recommendations for the medical and obstetrical management of patients with cancer. The following are the Society for Maternal-Fetal Medicine recommendations: (1) we suggest that ultrasonography and non-contrast magnetic resonance imaging (MRI) be used as first-line imaging techniques in the evaluation of a pregnant person with suspected cancer (GRADE 2B); (2) although non-contrast MRI and ultrasonography are first-line diagnostic imaging modalities in pregnancy, we recommend that computed tomography (CT) with or without contrast, gadolinium contrast for MRI, and fluorine-18-fluorodeoxyglucose positron emission tomography plus CT (18-FDG-PET/CT) not be withheld from a pregnant person if clinically indicated (GRADE 1C); (3) we recommend initiating thromboprophylaxis for all patients with active hematological or gynecological cancers during pregnancy and considering thromboprophylaxis for all patients with nonhematological or nongynecological cancers during pregnancy, based on individual risk factors (GRADE 1C); (4) we recommend that surgery for the treatment of cancer not be delayed or withheld from a pregnant patient at any gestational age in pregnancy (GRADE 1C); (5) we recommend that chemotherapy generally be administered after 12 weeks of gestation, provided that the patient desires to continue the pregnancy and that delaying treatment until after 12 weeks of gestation is not expected to significantly change the pregnant patient's prognosis compared with initiating treatment immediately after diagnosis (GRADE 1C); (6) to improve long-term neurodevelopmental outcomes of children exposed to chemotherapy in utero, we suggest avoiding clinician-initiated preterm delivery when possible (GRADE 2C); (7) we recommend intravenous methylprednisolone, 62.5 mg (corresponding to 10 mg of dexamethasone), or oral prednisolone, 30 mg (corresponding to 6 mg of dexamethasone), as first-line therapy for chemotherapy-induced nausea when corticosteroids are indicated (GRADE 1B); (8) we recommend serial fetal growth surveillance every 3-4 weeks in pregnancies with an active cancer diagnosis, regardless of treatment (GRADE 1C); (9) we recommend initiation of antenatal fetal surveillance starting at 32 weeks of gestation in pregnancies with an active cancer diagnosis, regardless of treatment, unless indicated earlier for maternal or fetal reasons (GRADE 1C); (10) we recommend that planned delivery prior to 37 weeks of gestation in pregnant patients with cancer generally be avoided unless indicated for medical or obstetrical reasons (GRADE 1C); (11) we recommend that chemotherapy treatment generally be stopped by 34 weeks of gestation to allow 3-4 weeks for recovery of myelosuppression before spontaneous labor or planned delivery, except for weekly paclitaxel, which can be administered up to 35 or 36 weeks, as only 1-2 weeks are necessary for recovery before delivery (GRADE 1C); (12) we recommend that the mode of delivery be determined by routine obstetrical indications for most patients with cancer in pregnancy (GRADE 1C); (13) we recommend a placental pathology examination in all cases of cancer during pregnancy, regardless of cancer type or treatment (GRADE 1C); (14) we recommend that cancer be considered as part of the differential diagnosis for pregnant patients with multiple chromosomal aneuploidies or single autosomal monosomy detected by cell-free DNA screening that is discordant with fetal findings (GRADE 1C).

Indexed as

cancerchemotherapycounselingdeliveryimagingmalignancymaternal‐fetal medicinepregnancythromboprophylaxis

Identifiers

PMID42597043
PMCPMC13344446

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.