Pregnant women are excluded from this study; breastfeeding should be discontinued Patients who are pregnant or breastfeeding are excluded from the study Women who are pregnant or breastfeeding (unless the patient is willing to interrupt breastfeeding during study treatment administration and then resume months after study discontinuation); women of childbearing potential must not consider getting pregnant during the study Not pregnant or nursing, with negative serum pregnancy test; pregnant women are excluded from this study; breastfeeding should be discontinued; timeline: within weeks prior to enrollment Pregnant women are excluded from this study; breastfeeding must be discontinued Pregnant or breastfeeding women will be excluded from participation in this trial Patients may not be pregnant or nursing; pregnant women are excluded from this study; a negative pregnancy test must be documented days or less prior to registration; breastfeeding must be discontinued prior to registration for this clinical trial Pregnant women and women who are breastfeeding are excluded from this study Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; breastfeeding should be discontinued prior to the first dose of study drug and women should refrain from nursing throughout the treatment period and for months following the last dose of study drug Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; breastfeeding should be discontinued Women must not be pregnant or breastfeeding; pregnant women are excluded from this study Inability or refusal to practice effective contraception during therapy or the presence of pregnancy or active breastfeeding; pregnant or breastfeeding women will be excluded from participation in this trial Pregnant women and women who are breastfeeding are excluded from this study Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; in nursing mothers, breastfeeding should be discontinued Pregnant women or lactating women who are breastfeeding are excluded from this study Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant or breastfeeding women are excluded from this study Pregnant women and breastfeeding mothers are excluded Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded; breastfeeding should be discontinued Patients who are pregnant or breastfeeding will be excluded from the study Pregnant women are excluded from this study; breastfeeding should be discontinued Women must not be pregnant or breastfeeding; pregnant women are excluded from this study Pregnant women are excluded; breastfeeding should be discontinued Pregnant and breastfeeding women are excluded. Pregnant or breastfeeding women are excluded from this study Women who are pregnant or breastfeeding are excluded from the study Pregnant women are excluded; breastfeeding should be discontinued prior to study entry Pregnant women are excluded from this study; breastfeeding should be discontinued PHASE I STUDY ELIGIBILITY CRITERIA:\r\nPregnant and breastfeeding women are excluded from this study Pregnant or breastfeeding women are excluded from this study Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; breastfeeding should be discontinued for the duration of active study therapy Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant or breastfeeding women are excluded from this study Pregnant or breastfeeding women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; breastfeeding should also be avoided Pregnant women are excluded from this study; breastfeeding should be discontinued while on study; patients who become pregnant while on study will be removed from the study once the pregnancy is confirmed Pregnant and breastfeeding women are excluded from this study Pregnant women are excluded from this study; breastfeeding should also be avoided Patients who are pregnant or breastfeeding are excluded from the study Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; breastfeeding should be discontinued prior to the first dose of study drug and women should refrain from nursing throughout the treatment period and for months following the last dose of study drug Pregnant women are excluded; breastfeeding should be discontinued prior to the first dose of study drug and women should refrain from nursing throughout the treatment period and for months following the last dose of study drug Pregnant or nursing (lactating) women; NOTE: Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; breastfeeding should also be avoided Pregnant women are excluded from this study; breastfeeding should be discontinued prior to treatment with dabrafenib/trametinib Pregnant or lactating women are excluded from this study; breastfeeding must be discontinued for eligibility Women must not be pregnant or breastfeeding; pregnant women are excluded from this study Women must not be pregnant or breastfeeding; breastfeeding must be discontinued or the subject is not eligible for the study PHASE II: Women must not be pregnant or breastfeeding; breastfeeding must be discontinued or the subject is not eligible for the study Pregnant and breastfeeding women are excluded from this study Pregnant women are excluded from this study; breastfeeding should be discontinued prior to beginning treatment Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded; breastfeeding should be discontinued prior to entry onto the study Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant or breastfeeding women; women desiring to become pregnant within the timeframe of the study are also excluded. Pregnant women are excluded from this study; breastfeeding should be discontinued prior to starting study treatment Pregnant women are excluded from this study; breastfeeding should be discontinued upon start of protocol therapy Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; breastfeeding should be discontinued if patient wishes to participate in study Pregnant women are excluded from this study; breastfeeding should be discontinued prior to entry onto the study Pregnant women or women who are breastfeeding are excluded from this study Pregnant women are excluded from this study; breastfeeding is not allowed during study treatment Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; breastfeeding should be discontinued prior to entry onto the study Pregnant women are excluded from this study; breastfeeding should be discontinued at least two weeks prior to the start of PF- dosing Pregnant women and women who are breastfeeding are excluded from this study Pregnancy or breastfeeding; a pregnancy test must be performed within days prior to ibrutinib initiation in women of childbearing potential; pregnant women are excluded; breastfeeding must be discontinued Pregnant or breastfeeding women are excluded from this study; breastfeeding should be discontinued Pregnant or nursing women; breastfeeding must be discontinued prior to treatment Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study and women who become pregnant while on study must be immediately discontinued; women who are breastfeeding will not be eligible for study participation Pregnant women (admittedly, an unlikely event) are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; breastfeeding should be discontinued by nursing mothers who agree to participate in the study Pregnant and breastfeeding women are excluded from this study Pregnant and breastfeeding women are not eligible for thyroidectomy and so are excluded from this study Pregnant women are excluded from this study; breastfeeding should be discontinued Pregnant women are excluded from this study; breastfeeding should be discontinued Participants who are breastfeeding are excluded Pregnant or intention to get pregnant, or breastfeeding; pregnant women are excluded from this study; women who are breastfeeding will be excluded Pregnant or lactating women are excluded from this study; breastfeeding must be discontinued for the duration of study participation and for days after the last dose of the study agent Pregnant women are excluded from this study; breastfeeding should be discontinued Participants who are breastfeeding are excluded Pregnant women are excluded from this study; breastfeeding should be discontinued Women who are pregnant, as well as those women who are breastfeeding, will be excluded from this study; as part of their routine preoperative testing, all women of child bearing age receive a pregnancy test; the research staff will follow up on these results in order to determine eligibility; women who have had a hysterectomy or have not had menses for > months will not be required to undergo a pregnancy test; breastfeeding women will be excluded from this study Pregnant women are excluded from this study; breastfeeding mothers are also excluded from this study Pregnant and breastfeeding women are excluded from this study Pregnant women are excluded from this study; breastfeeding should be discontinued prior to treatment with ALA Pregnant women and women who are breastfeeding are excluded from this study Pregnant women are excluded from this study; breastfeeding must be discontinued.