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Re: Is pregnancy safe for a melanoma patient post treatment?

Forums General Melanoma Community Is pregnancy safe for a melanoma patient post treatment? Re: Is pregnancy safe for a melanoma patient post treatment?

    FertilityDoc
    Participant

    I gathered some iformation for you from the NIH.  See below.  I hope this is helpful to you

    Kevin

    Should women who previously were diagnosed with
    melanoma avoid pregnancy?

    The issue here is whether pregnancy activates micrometastatic
    disease. There is no convincing evidence
    that pregnancy activates or stimulates dormant micrometastatic
    disease, although anecdotal case reports
    certainly suggest that this may happen in some cases. One
    of the difficulties in addressing this question is that it is
    impossible to know prospectively which patients are harboring
    micrometastases. One author noted similar fiveand
    ten-year survival rates for 115 patients who were
    pregnant with melanoma compared with 330 female
    melanoma patients who were never pregnant during or after
    their diagnosis.’ The pregnant group, however, had a
    higher frequency of lymph node involvement at the time
    of diagnosis. A better survival was actually noted for 71
    patients who were pregnant within a year before or five
    years after a diagnosis of melanoma, but the control group
    consisted of only 31 women who did not get pregnant
    during a similar interval and who actually had higher
    stage disease.47 In another study, women diagnosed with
    melanoma before getting pregnant were compared with
    women diagnosed after completing all pregnancies.39 The
    latter group actually appeared to do worse at five years,
    although statistical comparison was not provided. In a retrospective
    study conducted at Duke University, 43
    women with stage I melanoma who became pregnant
    within the next five years had prognoses similar to those
    of 337 women who did not get pregnant, both in terms of
    relapse and disease-free survival.9
    There is no evidence that nulliparous women as a
    group differ from parous women as a group, in terms of
    prognosis from the time of a subsequent diagnosis of
    melanoma while pregnant. In a study that compared 85
    women diagnosed with melanoma before their first pregnancy
    with 143 women who had completed all pregnancies,
    melanoma developed in 68 between pregnancies and
    in 92 during pregnancy, and there was no difference in
    these groups.39 Two other small studies also found no difference
    in prognosis for nulliparous as opposed to parous
    women,4M42 although the studies were small in scope. The
    only trials that address the issue of the importance of subsequent
    pregnancy on prognosis have failed to identify
    parity as an important variable in multivariate analysis.39
    In the absence of definitive data, many authorities have
    recommended that women avoid pregnancy for two to
    five years after a diagnosis of melanoma, mainly because
    that is the time period during which most recurrences are
    diagnosed.’944149 In one study, such patients who did become
    pregnant were actually used as controls to compare
    with patients who were being diagnosed with melanoma
    for the first time while pregnant.37

    Should women who previously were diagnosed with
    melanoma during a pregnancy avoid subsequent pregnancy?
    Historically, there has been great concern regarding
    the risk of subsequent pregnancy in women who were initially
    diagnosed with melanoma during a previous pregnancy,
    based on the presumption that these melanomas in
    particular may be influenced adversely by growth factors
    and hormones secreted during pregnancy. Earlier observers
    felt strongly that pregnancy worsened the prognosis
    in this group of patients.2549 There is no objective
    evidence that this group is at higher risk with subsequent
    pregnancy, however. Despite this, the consensus is to recommend
    the deferral of subsequent pregnancy for two to
    three years in women in whom a primary melanoma developed
    during pregnancy.7

    Is there a risk of transplacental metastases to the fetus:?

    There definitely is a risk of transplacental transmission
    of melanoma from mother to fetus, but fortunately
    this risk is low.  Placental involvement itself is indicative
    of widespread hematogenous dissemination in the
    mother, but placental involvement does not necessarily
    mean that the newborn baby will have melanoma. Of 35
    cases of placental or fetal involvement with cancer following
    pregnancy, one study found that 11 were due to
    melanoma, the most common cancer associated with this
    phenomenon, followed by leukemia or lymphoma. Of
    the 11 melanoma patients, the placenta was involved in 7
    and the fetus in 6. Two of the infants with melanoma underwent
    spontaneous regression of disease after delivery.
    It has been suggested that only 25% of infants with placental
    metastatic melanoma will actually die of metastatic
    melanoma, and it is almost always manifest at the time
    of delivery and then fails to regress spontaneously after
    delivery. The implications of these observations are that
    women diagnosed with metastatic melanoma during
    pregnancy need not abort their fetus out of a fear of
    transplacental spread, and active therapy for a fetus born
    in the setting of placental metastases is not warranted.

     

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