Adjuvant breast cancer chemotherapy during late-trimester pregnancy: not quite a standard of care
© Epstein; licensee BioMed Central Ltd. 2007
Received: 28 September 2006
Accepted: 30 May 2007
Published: 30 May 2007
Diagnosis of breast cancer during pregnancy was formerly considered an indication for abortion. The pendulum has since swung to the other extreme, with most reviews now rejecting termination while endorsing immediate anthracycline-based therapy for any pregnant patient beyond the first trimester. To assess the evidence for this radical change in thinking, a review of relevant studies in the fields of breast cancer chemotherapy, pregnancy, and drug safety was conducted.
Accumulating evidence for the short-term safety of anthracycline-based chemotherapy during late-trimester pregnancy represents a clear advance over the traditional norm of therapeutic abortion. Nonetheless, the emerging orthodoxy favoring routine chemotherapy during gestation should continue to be questioned on several grounds: (1) the assumed difference in maternal survival accruing from chemotherapy administered earlier – i.e., during pregnancy, rather than after delivery – has not been quantified; (2) the added survival benefit of adjuvant cytotoxic therapy prescribed within the hormone-rich milieu of pregnancy remains presumptive, particularly for ER-positive disease; (3) the maternal survival benefit associated with modified adjuvant regimens (e.g., weekly schedules, omission of taxanes, etc.) has not been proven equivalent to standard (e.g., post-delivery) regimens; and (4) the long-term transplacental and transgenerational hazards of late-trimester chemotherapy are unknown.
Although an incrementally increased risk of cancer-specific mortality is impossible to exclude, mothers who place a high priority on the lifelong well-being of their progeny may be informed that deferring optimal chemotherapy until after delivery is still an option to consider, especially in ER-positive, node-negative and/or last-trimester disease.
Immediate chemotherapy may be clearly indicated for pregnant breast cancer patients with unresectable primary tumors or metastatic presentations, whereas operable tumors raise a more complex conflict of interest: the mother is threatened directly by cancer recurrence and hence, indirectly, by any treatment compromise made on behalf of the fetus. Decisions made in this context tend to be less drastic for the mother than for the fetus, given that the latter has more life-years to lose, and faces health hazards that are wholly avoidable. This risk imbalance is worsened by the weaker advocacy position of the fetus, who tends not to be considered the primary 'client' in such oncologic scenarios.
A central belief underlying the new enthusiasm for gestational chemotherapy is that delay of adjuvant cancer treatment is substantially deleterious to maternal outcomes. Taken to extremes, this assumption must be valid: if adjuvant treatment is delayed until metastases appear, the opportunity for cure has been lost. Such logic likewise supports the utility of therapeutic abortion which, uniquely, permits full deployment of all adjuvant modalities according to standard time-schedules. Relevant to this, however, no survival benefit attributable to therapeutic abortion has yet been proven , despite the fact that this option enables the most standard adjuvant therapy scheduling.
At present, there are no controlled data defining the extent to which a less extreme delay in the initiation of adjuvant therapy impairs overall survival outcomes. Retrospective studies have indicated that adjuvant chemotherapy delays of up to three months have no discernible effect on prognosis [9, 10]; only in very advanced disease has delay in initiating adjuvant chemotherapy been associated with any impairment of disease-free survival , though other groups have failed to demonstrate impaired overall survival in any patient subset . Using a model that quantifies risk increments in patients deferring breast cancer chemotherapy until after delivery, Nettleton et al estimated a modest 1.5–4.0% increased risk of transforming from axillary node-negative to -positive  in late-trimester patients, assuming a typical 10–12 week delay . A large retrospective review of premenopausal patients indicated that only patients with ER-absent tumors are likely to benefit from early initiation of adjuvant chemotherapy .
While it is reasonable to believe that gestational chemotherapy confers survival benefits similar to those apparent in overviews of nonpregnant patients receiving conventional chemotherapy , such overviews only calculate average effects, and should not be extrapolated to patient subsets affected by qualitative interactions . Pregnancy represents exactly such an interaction: dramatic changes of mammary gland gene expression are induced by the presence of the fetus , reflecting corresponding changes in the tumor microenvironment. Breast cancer survival outcomes vary inversely with diagnostic proximity to earlier pregnancy [19, 20], raising the possibility of biological resistance to adjuvant treatments. Since the benefit of chemotherapy tends to be lower for hormone-driven tumors in both the adjuvant  and neoadjuvant settings [22–24], and appears similar to that of ovarian suppression in premenopausal women with hormone-dependent disease [25, 26], the question arises: for pregnant patients whose tumors express some hormone receptors, will adjuvant chemotherapy given "early" in the hormone-rich pregnancy environment necessarily be more effective than similar chemotherapy given after delivery; or could the opposite be the case?
A further worry raised by the vogue for gestational chemotherapy is the possibility that suboptimal regimens may be delivered, albeit with good intentions; in the worst of all possible worlds, such regimens could imperil the fetus without benefiting the mother. For example, Peccatori et al treated pregnant patients using weekly epirubicin 30–50 mg/m2 with the aim of maximizing therapeutic effect while minimizing fetal drug exposure . However, the adjuvant efficacy of such customized regimens – whether in pregnant or non-pregnant patients – is simply not known, though it is accepted that "low-dose" chemotherapy regimens are less effective. Other modifications of standard regimens – e.g., exclusion of antimetabolites and/or taxanes, lower dose-intensity and/or dose-density, or withholding of the humanized antibody trastuzumab – are popular in this setting, raising the question: is the administration of such 'modified' regimens during pregnancy aimed at treating the patient or the doctor? If a pregnant breast cancer patient does not receive chemotherapy of similar efficacy to that received by nonpregnant patients, should it be assumed that this deficiency will be rectified in the post-partum period – or would it be better to defer the entire treatment regimen until after delivery, at which time a more concentrated and intensive approach could plausibly improve survival benefits?
Expected vs. non-expected positive endpoints for gestational exposure to cytotoxic drugs.
Expected effects of transplacental mutagens in late-trimester pregnancies
Expected to be normal
Expected to be abnormal
Congenital malformation rate
Postnatal apgar indices
Infant sexual/genital development
Pediatric cancer rate
Adult cancer rate
Transgenerational malformation rate
Transgenerational cancer rate
Short-term cardiovascular function
Long-term cardiovascular function
A further safety-related concern is that a future pregnancy is possible, but not guaranteed. The summative risks of chemotherapy-induced infertility (say, 20%), early metastatic relapse (say, 20%) or marital problems (say, 10%) might be expected to reduce the certainty of having another baby, keeping in mind that the duration of any adjuvant hormonal therapy is likely to be five years or longer. Although it is difficult to quantify the relative net fertility outcomes of early vs. late chemotherapy in this context, it is certainly arguable that the fetus of a pregnant breast cancer patient may be, if anything, more precious to the mother than the average pregnancy, given the uncertain prognoses for both maternal survival and fecundity.
Moreover, patients may believe that the most painful choice – in this case, abortion, which is chosen in up to 50% of cases in many international series  – must be the best . Clinicians aware of the anxieties facing the patient may feel obliged to offer active intervention ("at least we're doing something"), unintentionally biasing informed consent . Patient acceptance of gestational chemotherapy may likewise have more to do with cultural norms of cooperation and punishment  than with logical consideration of all options. These concerns support reservations expressed by Barthelmes et al , Pautier et al  and Mathieu et al  about the trend towards routine immediate adjuvant chemotherapy for late-trimester breast cancer patients.
Oncologists may be less familiar than obstetricians with the ethical complexities confronting pregnant patients. Management of cancer in pregnancy is complicated by the tendencies of clinicians to equate (maternal) risk with (maternal plus fetal) benefit, to assume that immediacy of action is always best, to hold the interests of the 'client' (mother) above those of any third party (fetus), and to imply that lack of proven danger equals safety. Basing standard recommendations on such convictions is tempting, but firmer knowledge of gestational breast cancer biology, measured therapeutic benefits, and longer-term toxicity data is needed before any such standard can be scientifically endorsed . In the meantime, the debate will continue as to whether chemotherapy should be presumed 'innocent until proven guilty' or 'guilty until proven innocent': although the Hippocratic ethical maxim "First, do no harm" favors the latter from the viewpoint of the fetus, an assumption of gestational chemotherapy efficacy will favor the former from the viewpoint of the mother.
The inconvenient truth remains that gestational chemotherapy has not yet been proven to have net benefits (long-term maternal survival increments minus long-term fetal toxicities) exceeding those of delayed chemotherapy. Equally, however, there remains insufficient data to claim that delayed chemotherapy should be standard, and the issue is likely to remain unresolved. Nonetheless, deferral of chemotherapy to the post-partum period remains a valid and defensible option for oncologists to invite selected late-trimester breast cancer patients – e.g., those with hormone receptor-positive disease, node-negative staging, and/or no more than 12 weeks until delivery – to consider.
The author thanks the reviewers for constructive comments, Dr Polly Cheung for helpful discussions, and Professor Raymond Liang for support.
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