August 04, 2015
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Assisted reproduction feasible for women with breast cancer history

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Women with a history of breast cancer can utilize assisted reproductive technology to become pregnant without any detriment to their cancer outcome, according to study results.

Perspective from Nanette Santoro, MD

Although previous studies have shown pregnancy to be safe following breast cancer, many women become infertile following systemic treatment.

According to study background, between 6% and 10% of women with breast cancer have the disease during their reproductive age. Those women who face infertility often inquire about assisted reproductive technology (ART) — such as ovulation induction associated with intercourse or intra-uterine insemination, controlled ovarian stimulation with gonadotropins for in vitro fertilization, or intra-cytoplasmic sperm injection and egg donation.

Hatem A. Azim, Jr., MD, associate scientific director of the BrEAST Data Centre at the Jules Bordet Institute in Brussels, Belgium, and colleagues sought to evaluate the effect of ART on recurrence and death rates in patients previously treated for breast cancer who subsequently became pregnant.

Hatem A. Azim, Jr., MD

Hatem A. Azim

“Given the rising trend of delaying childbearing and the toxicity induced by anti-cancer medication on ovarian function, natural conception is challenging and sometimes not feasible and thus a lot of cancer survivors would need to consider assisted reproduction in order to become pregnant,” Azim told HemOnc Today. “However, the safety of this approach in already-treated breast cancer patients is unknown. In this study, we addressed — for the first time — the feasibility and safety of assisted reproduction in women who have already been diagnosed and treated for breast cancer.”

The investigators evaluated data from 198 women aged 18 to 45 years who were diagnosed with breast cancer between 2000 and 2009 and who later became pregnant. Researchers divided patients into two cohorts: those who used ART to achieve pregnancy following their systemic therapy for breast cancer (n = 25; 34 pregnancies) and those who became pregnant spontaneously (n = 173, 247 pregnancies).

Fewer women in the ART cohort had histological grade 3 tumors (36% vs. 59%; P = .033).

Approximately 90% of the entire population had received primary adjuvant chemotherapy and more than half of them had endocrine-sensitive disease. Patients in the ART cohort were older than the spontaneous group at diagnosis (mean: 33.7 years vs. 31.4 years; P = .009) as well as at time of conception (38 years vs. 35 years; P < .001).

ART patients experienced more miscarriages than the spontaneous group (23.5% vs. 12.6%). Seventy-seven percent of the spontaneous cohort and 76% of the ART cohort achieved full-term pregnancies.

After a mean follow-up between conception and last follow-up of 5.25 years in the spontaneous group and 4.16 years in the ART group, researchers observed no difference in breast cancer outcome between the two groups.

The researchers acknowledged they had a lack of information on the fertility drugs used and the protocols for in vitro fertilization or egg donation or the hormone levels achieved. Also, there was no assessment on the patients’ parity and fertility history, which may have influenced decisions for subsequent pregnancies and how to become pregnant after treatment.

Finally, the study design was limited statistically to estimate the impact of ART on the risk for recurrence, although the researchers wrote it is often difficult to conduct a prospective study powered to address such questions.

“We believe that this study would provide physicians with more reassurances when faced with women with history of breast cancer to consider assisted reproduction in order to conceive,” Azim said. “Based on our study, this approach does not appear to increase the risk for breast cancer recurrence and thus should not be discouraged, especially in women who have received adequate adjuvant therapy.” – by Anthony SanFilippo

For more information:

Hatem A. Azim, Jr., MD, can be reached at the Jules Bordet Institute, Boulevard de Waterloo 121, 1000 Brussels, Belgium; email: hatem.azim@bordet.be

Disclosure: The researchers report no relevant financial disclosures.