Skip to main content Accessibility help
×
Hostname: page-component-cd9895bd7-lnqnp Total loading time: 0 Render date: 2024-12-26T06:29:56.888Z Has data issue: false hasContentIssue false

3 - Chemotherapy in the treatment of pregnant women with cancer

from SECTION 1 - Epidemiology, Genetics and Basic Principles of Chemotherapy and Radiotherapy

Published online by Cambridge University Press:  05 October 2014

Elyce Cardonick
Affiliation:
Robert Wood Johnson Medical School
Sean Kehoe
Affiliation:
John Radcliffe Hospital, Oxford
Eric Jauniaux
Affiliation:
University College Hospital, London
Pierre Martin-Hirsch
Affiliation:
Royal Preston Hospital
Philip Savage
Affiliation:
Charing Cross Hospital, London
Get access

Summary

Introduction

A malignancy is currently diagnosed in approximately 1 per 1000 pregnant women and, as women delay pregnancy to older maternal ages, physicians can expect to increasingly encounter the difficult dilemma of managing cancer during pregnancy. The most common malignancies occurring in pregnant women are breast cancer, lymphoma and melanoma. It is estimated that 7—14% of premenopausal breast cancers occur in pregnancy and 3% of women with Hodgkin's disease are pregnant at diagnosis.

A number of key issues must be considered regarding the treatment of a malignancy in pregnancy. The decision on whether or not to use chemotherapy must take into account the effect of a treatment delay on maternal survival, and the benefits of maternal treatment during pregnancy must be weighed against the fetal risks from in utero treatment exposure.

There is a lack of data to help make these difficult decisions. To date, 447 reports of women receiving chemotherapy during pregnancy have been published: 343 have previously been summarised in a review in Lancet Oncology. These and the 104 additional cases published since that review are described in this chapter.

Chemotherapy, teratogenicity and gestational age

The potential teratogenicity of a drug is dependent on the fetal stage of development at exposure, the dosage and the characteristics that affect placental transfer. High lipid solubility, low molecular weight, non-ionisation and loose binding to plasma proteins favour transfer of drug from mother to fetus.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2008

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure no-reply@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×