Cancer Treatment During Pregnancy and Maternal and Infant Outcomes: A Descriptive Cohort Study Using a Japanese Claims Database - Scorecard - MDSpire
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Cancer Therapy in Pregnancy and Outcomes for Mothers and Infants: A Descriptive Cohort Study Based on Japanese Claims Data

  • By

  • Masami Tsuchiya

  • Tomofumi Ishikawa

  • Takamasa Sakai

  • Satoko Hori

  • Taku Obara

  • October 16, 2026

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Clinical Scorecard: Cancer Therapy in Pregnancy and Outcomes for Mothers and Infants: A Descriptive Cohort Study Based on Japanese Claims Data

At a Glance

CategoryDetail
ConditionClinical topic addressed by the source article: Cancer Therapy in Pregnancy and Outcomes for Mothers and Infants
Key MechanismsDescriptive claims-based study characterizing cancer treatment during pregnancy and maternal and infant outcomes; outcomes were stratified by prescription of EPhMRA L01/L02 anticancer agents.
Target PopulationJapanese mother–infant-linked live-birth pregnancies with estimated gestational age of 22–42 weeks and required claims follow-up; 500 had cancer diagnosed before delivery.
Care SettingJMDC mother–infant-linked claims from Japanese employment-based health insurance societies, covering inpatient and outpatient care from January 2005 through December 2024.

Key Highlights

  • The descriptive cohort included 241,891 pregnancies, including 500 with cancer diagnosed before delivery and 236,002 pregnancies without a malignant neoplasm diagnosis.
  • Sixteen cancer pregnancies had at least one anticancer agent prescribed from cancer diagnosis through delivery; 484 were classified as unexposed to these agents.
  • Anticancer agents were defined as drugs in EPhMRA groups L01 and L02, and outcomes were stratified by this exposure.
  • The internal reference group was a background benchmark and was not intended for causal inference.
  • The supplied article excerpt describes study design and methods but does not provide outcome results.

Guideline-Based Recommendations

Diagnosis

    Management

      Monitoring & Follow-up

      • The cohort required infant observation for at least 6 months after birth or until death during that interval.

      Risks

        Patient & Prescribing Data

        Anticancer agents were defined as EPhMRA groups L01 and L02. The supplied excerpt does not provide further treatment-modality or regimen details.

        Clinical Best Practices

        • Interpret the internal reference group as a background benchmark, not a comparator intended for causal inference.
        • The study classified exposure by prescription of EPhMRA L01/L02 anticancer agents from cancer diagnosis through delivery; other treatment modalities were described separately.
        • The supplied excerpt describes study design and methods but does not provide outcome findings.

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        Original Source(s)

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