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Excess of early onset multiple myeloma in endometrial cancer probands and their relatives suggests common susceptibility.

Excess of early onset multiple myeloma in endometrial cancer probands and their relatives suggests common susceptibility. Research Abstract Details 

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  • Excess of early onset multiple myeloma in endometrial cancer probands and their relatives suggests common susceptibility. Abstract Text:

    israel zighelboimIsrael Zighelboim,sheri babbSheri Babb,feng gaoFeng Gao,matthew a powellMatthew A Powell,david g mutchDavid G Mutch,paul j goodfellowPaul J Goodfellow,

    OBJECTIVE: Determine whether there is an association between uterine cancer and multiple myeloma. METHODS: Data on second malignancies were obtained for 368 uterine corpus cancer patients treated between 1992 and 2005. Detailed family histories were devised for 192 probands. Diagnoses of multiple myelomas, lymphomas and leukemias in family members were medical record verified. The frequency of multiple myeloma among uterine cancer patients was compared to the female age-adjusted incidence rate of multiple myeloma obtained from the SEER database. The crude rate of multiple myeloma (as well as Hodgkin's, non-Hodgkin's lymphomas and leukemias) among first-degree relatives of patients with uterine cancer was compared to the age-adjusted incidence rate of multiple myeloma in the general population. Descriptive statistics were used to evaluate disease and cohort characteristics. A P value less than 0.05 was considered statistically significant. RESULTS: Two of 368 uterine cancer patients were also diagnosed with multiple myeloma, both at age 50. The observed incidence of multiple myeloma in this cohort (543 per 100,000; 95% CI: 66-1962 per 100,000) represents a 120-fold increase based on predicted incidence (P=0.00014). The frequency of multiple myeloma in first-degree relatives was 2/1351 (148 per 100,000; 95% CI: 14.8-533 per 100,000) which represents a 27-fold increase compared to the general population (P=0.0026). The frequencies of leukemias and lymphomas in these family members on the other hand were not significantly increased (P=0.152 and P=0.218). CONCLUSION: This specific excess frequency of early onset multiple myeloma in endometrial cancer probands and their relatives suggests shared susceptibility.

    Excess of early onset multiple myeloma in endometrial cancer probands and their relatives suggests common susceptibility. Publishing Authors By Initials

    i zighelboimI Zighelboim,s babbS Babb,f gaoF Gao,ma powellMA Powell,dg mutchDG Mutch,pj goodfellowPJ Goodfellow,

    For similar investigative techniques: genetic techniques: pedigree research abstracts see: investigative techniques: genetic techniques: pedigree research

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    Excess of early onset multiple myeloma in endometrial cancer probands and their relatives suggests common susceptibility. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Gynecologic oncology

    VOLUME: 105

    Page Numbers: 390-4

    Journal Abbreviation:

    ISSN: 0090-8258

    DAY: 1

    MONTH: 03

    YEAR: 2007

    Excess of early onset multiple myeloma in endometrial cancer probands and their relatives suggests common susceptibility. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 365304

    Excess of early onset multiple myeloma in endometrial cancer probands and their relatives suggests common susceptibility. Keywords Mesh Terms:

    KEYWORDS: Pedigree

    MESH TERMS: genetics

    Chemical & Substance for Abstract: Excess of early onset multiple myeloma in endometrial cancer probands and their relatives suggests common susceptibility. Information

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    Grant and Affiliation Information for Excess of early onset multiple myeloma in endometrial cancer probands and their relatives suggests common susceptibility.

    AFFILIATION: Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Washington University School of Medicine and Siteman Cancer Center, 4911 Barnes Jewish Plaza, Box 8064, St. Louis, MO 63110, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NCI

    GRANT: R01 CA71754

    ACRONYM: CA

    MEDLINETA: Gynecol Oncol

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