Skip to main content
Erschienen in: Journal of Genetic Counseling 2/2013

01.04.2013 | Original Research

Life Events may Contribute to Family Communication About Cancer Risk Following BRCA1/2 Testing

verfasst von: Julie Lapointe, Claudia Côté, Karine Bouchard, Béatrice Godard, Jacques Simard, Michel Dorval

Erschienen in: Journal of Genetic Counseling | Ausgabe 2/2013

Einloggen, um Zugang zu erhalten

Abstract

We assessed whether certain life events contributed to the communication about cancer risk within families who have undergone BRCA1/2 testing. We also explored what type of resources participants would have valued to help in supporting family communication about genetic information. Two hundred and forty-six individuals (218 women, 28 men) who received a BRCA1/2 genetic test result 3 to 10 years earlier (mean of 6.4 years) participated in a telephone interview. Participants were asked about the occurrence of a number of life events (cancer diagnosis, death, uptake of prophylactic surgery, and providing care to a family member with cancer) in their family since their BRCA1/2 test result disclosure and, for each occurrence, whether it fostered family communication about cancer risk. A total of 182 participants (74 %) reported that they or one of their relatives received a cancer diagnosis, 176 (72 %) reported that someone died in their family, and 73 (30 %) stated that they or one of their relatives undertook a prophylactic surgery. During this period, 109 participants (44 %) also provided care for a family member who had cancer. Among participants who reported these life events, family communication was fostered by these events in proportions varying from 50 % (death) to 69 % (cancer diagnosis). Our results indicate that life events may contribute to family communication about cancer risk. Further research is needed to determine whether these events provide a “window of opportunity” to reach family members, address their needs and concerns about cancer, update family cancer history, and introduce genetic counseling and risk assessment.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
Zurück zum Zitat Ardern-Jones, A., Kenen, R., Lynch, E., Doherty, R., & Eeles, R. (2010). Is no news good news? Inconclusive genetic test results in BRCA1 and BRCA2 from patients and professionals’ perspectives. Hereditary Cancer in Clinical Practice, 8(1), 1.PubMedPubMedCentralCrossRef Ardern-Jones, A., Kenen, R., Lynch, E., Doherty, R., & Eeles, R. (2010). Is no news good news? Inconclusive genetic test results in BRCA1 and BRCA2 from patients and professionals’ perspectives. Hereditary Cancer in Clinical Practice, 8(1), 1.PubMedPubMedCentralCrossRef
Zurück zum Zitat Carlsson, C., & Nilbert, M. (2007). Living with hereditary non-polyposis colorectal cancer; experiences from and impact of genetic testing. Journal of Genetic Counseling, 16(6), 811–820.PubMedCrossRef Carlsson, C., & Nilbert, M. (2007). Living with hereditary non-polyposis colorectal cancer; experiences from and impact of genetic testing. Journal of Genetic Counseling, 16(6), 811–820.PubMedCrossRef
Zurück zum Zitat Crotser, C. B., & Dickerson, S. S. (2010). Women receiving news of a family BRCA1/2 mutation: messages of fear and empowerment. Journal of Nursing Scholarship, 42(4), 367–378.PubMedCrossRef Crotser, C. B., & Dickerson, S. S. (2010). Women receiving news of a family BRCA1/2 mutation: messages of fear and empowerment. Journal of Nursing Scholarship, 42(4), 367–378.PubMedCrossRef
Zurück zum Zitat DeMarco, T. A., & McKinnon, W. C. (2007). Life after BRCA1/2 testing: family communication and support issues. Breast Disease, 27(1), 127–136.CrossRef DeMarco, T. A., & McKinnon, W. C. (2007). Life after BRCA1/2 testing: family communication and support issues. Breast Disease, 27(1), 127–136.CrossRef
Zurück zum Zitat Dorval, M., Bouchard, K., Maunsell, E., Plante, M., Chiquette, J., Camden, S., et al. (2008). Health behaviors and psychological distress in women initiating BRCA1/2 genetic testing: comparison with control population. Journal of Genetic Counseling, 17(4), 314–326.PubMedCrossRef Dorval, M., Bouchard, K., Maunsell, E., Plante, M., Chiquette, J., Camden, S., et al. (2008). Health behaviors and psychological distress in women initiating BRCA1/2 genetic testing: comparison with control population. Journal of Genetic Counseling, 17(4), 314–326.PubMedCrossRef
Zurück zum Zitat Douglas, H. A., Hamilton, R. J., & Grubs, R. E. (2009). The effect of BRCA gene testing on family relationships: a thematic analysis of qualitative interviews. Journal of Genetic Counseling, 18(5), 418–435.PubMedCrossRef Douglas, H. A., Hamilton, R. J., & Grubs, R. E. (2009). The effect of BRCA gene testing on family relationships: a thematic analysis of qualitative interviews. Journal of Genetic Counseling, 18(5), 418–435.PubMedCrossRef
Zurück zum Zitat Forrest, K., Simpson, A. J., Wilson, B. J., Teijlingen, E. R. V., McKee, L., Haites, N., et al. (2003). To tell or not to tell: barriers and facilitators in family communication about genetic risk. Clinical Genetics, 64(4), 317–326.CrossRefPubMed Forrest, K., Simpson, A. J., Wilson, B. J., Teijlingen, E. R. V., McKee, L., Haites, N., et al. (2003). To tell or not to tell: barriers and facilitators in family communication about genetic risk. Clinical Genetics, 64(4), 317–326.CrossRefPubMed
Zurück zum Zitat Foster, C., Eeles, R., Ardern-Jones, A., Moynihan, C., & Watson, M. (2004). Juggling roles and expectations: dilemmas faced by women talking to relatives about cancer and genetic testing. Psychology & Health, 19(4), 439–455.CrossRef Foster, C., Eeles, R., Ardern-Jones, A., Moynihan, C., & Watson, M. (2004). Juggling roles and expectations: dilemmas faced by women talking to relatives about cancer and genetic testing. Psychology & Health, 19(4), 439–455.CrossRef
Zurück zum Zitat Gaff, C. L., Clarke, A. J., Atkinson, P., Sivell, S., Elwyn, G., Iredale, R., et al. (2007). Process and outcome in communication of genetic information within families: a systematic review. European Journal of Human Genetics, 15(10), 999–1011.PubMedCrossRef Gaff, C. L., Clarke, A. J., Atkinson, P., Sivell, S., Elwyn, G., Iredale, R., et al. (2007). Process and outcome in communication of genetic information within families: a systematic review. European Journal of Human Genetics, 15(10), 999–1011.PubMedCrossRef
Zurück zum Zitat Gallo, A. M., Angst, D. B., & Knafl, K. A. (2009). Disclosure of genetic information within families: how nurses can facilitate family communication. American Journal of Nursing, 109(4), 65–69.PubMedCrossRef Gallo, A. M., Angst, D. B., & Knafl, K. A. (2009). Disclosure of genetic information within families: how nurses can facilitate family communication. American Journal of Nursing, 109(4), 65–69.PubMedCrossRef
Zurück zum Zitat Geer, K. P., Ropka, M. E., Cohn, W. F., Jones, S. M., & Miesfeldt, S. (2001). Factors influencing patients’ decisions to decline cancer genetic counseling services. Journal of Genetic Counseling, 10(1), 25–40.PubMedCrossRef Geer, K. P., Ropka, M. E., Cohn, W. F., Jones, S. M., & Miesfeldt, S. (2001). Factors influencing patients’ decisions to decline cancer genetic counseling services. Journal of Genetic Counseling, 10(1), 25–40.PubMedCrossRef
Zurück zum Zitat Hamilton, R. J., Bowers, B. J., & Williams, J. K. (2005). Disclosing genetic test results to family members. Journal of Nursing Scholarship, 37(1), 18–24.PubMedCrossRef Hamilton, R. J., Bowers, B. J., & Williams, J. K. (2005). Disclosing genetic test results to family members. Journal of Nursing Scholarship, 37(1), 18–24.PubMedCrossRef
Zurück zum Zitat Harris, J. N., Hay, J., Kuniyuki, A., Asgari, M. M., Press, N., & Bowen, D. J. (2010). Using a family systems approach to investigate cancer risk communication within melanoma families. Psycho-Oncology, 19(10), 1102–1111.PubMedPubMedCentralCrossRef Harris, J. N., Hay, J., Kuniyuki, A., Asgari, M. M., Press, N., & Bowen, D. J. (2010). Using a family systems approach to investigate cancer risk communication within melanoma families. Psycho-Oncology, 19(10), 1102–1111.PubMedPubMedCentralCrossRef
Zurück zum Zitat Hughes, C., Lerman, C., Schwartz, M., Peshkin, B. N., Wenzel, L., Narod, S. A., et al. (2002). All in the family: evaluation of the process and content of sisters’ communication about BRCA1 and BRCA2 genetic test results. American Journal of Medical Genetics, 107(2), 143–150.PubMedCrossRef Hughes, C., Lerman, C., Schwartz, M., Peshkin, B. N., Wenzel, L., Narod, S. A., et al. (2002). All in the family: evaluation of the process and content of sisters’ communication about BRCA1 and BRCA2 genetic test results. American Journal of Medical Genetics, 107(2), 143–150.PubMedCrossRef
Zurück zum Zitat Iredale, R., Brain, K., Gray, J., & France, E. (2003). The information and support needs of women at high risk of familial breast and ovarian cancer: how can cancer genetic services give patients what they want? Familial Cancer, 2(2), 119–121.PubMedCrossRef Iredale, R., Brain, K., Gray, J., & France, E. (2003). The information and support needs of women at high risk of familial breast and ovarian cancer: how can cancer genetic services give patients what they want? Familial Cancer, 2(2), 119–121.PubMedCrossRef
Zurück zum Zitat Kenen, R., Arden-Jones, A., & Eeles, R. (2004). Healthy women from suspected hereditary breast and ovarian cancer families: the significant others in their lives. European Journal of Cancer Care, 13(2), 169–179.PubMedCrossRef Kenen, R., Arden-Jones, A., & Eeles, R. (2004). Healthy women from suspected hereditary breast and ovarian cancer families: the significant others in their lives. European Journal of Cancer Care, 13(2), 169–179.PubMedCrossRef
Zurück zum Zitat Koehly, L. M., Peterson, S. K., Watts, B. G., Kempf, K. K. G., Vernon, S. W., & Gritz, E. R. (2003). A social network analysis of communication about hereditary nonpolyposis colorectal cancer genetic testing and family functioning. Cancer Epidemiology Biomarkers & Prevention, 12(4), 304–313. Koehly, L. M., Peterson, S. K., Watts, B. G., Kempf, K. K. G., Vernon, S. W., & Gritz, E. R. (2003). A social network analysis of communication about hereditary nonpolyposis colorectal cancer genetic testing and family functioning. Cancer Epidemiology Biomarkers & Prevention, 12(4), 304–313.
Zurück zum Zitat Lawsin, C., Duhamel, K., Itzkowitz, S., Brown, K., Lim, H., & Jandorf, L. (2009). An examination of the psychosocial factors influencing colorectal cancer patients’ communication of colorectal cancer patient risk with their siblings. Cancer Epidemiology, Biomarkers & Prevention, 18(11), 2907–2912.CrossRef Lawsin, C., Duhamel, K., Itzkowitz, S., Brown, K., Lim, H., & Jandorf, L. (2009). An examination of the psychosocial factors influencing colorectal cancer patients’ communication of colorectal cancer patient risk with their siblings. Cancer Epidemiology, Biomarkers & Prevention, 18(11), 2907–2912.CrossRef
Zurück zum Zitat Lea, D. H., Kaphingst, K. A., Bowen, D., Lipkus, I., & Hadley, D. W. (2011). Communicating genetic and genomic information: health literacy and numeracy considerations. Public Health Genomics, 14(4–5), 279–289.PubMedCrossRef Lea, D. H., Kaphingst, K. A., Bowen, D., Lipkus, I., & Hadley, D. W. (2011). Communicating genetic and genomic information: health literacy and numeracy considerations. Public Health Genomics, 14(4–5), 279–289.PubMedCrossRef
Zurück zum Zitat McBride, C. M., Puleo, E., Pollak, K. I., Clipp, E. C., Woolford, S., & Emmons, K. M. (2008). Understanding the role of cancer worry in creating a “teachable moment” for multiple risk factor reduction. Social Science & Medicine, 66(3), 790–800.CrossRef McBride, C. M., Puleo, E., Pollak, K. I., Clipp, E. C., Woolford, S., & Emmons, K. M. (2008). Understanding the role of cancer worry in creating a “teachable moment” for multiple risk factor reduction. Social Science & Medicine, 66(3), 790–800.CrossRef
Zurück zum Zitat McKinnon, W., Naud, S., Ashikaga, T., Colletti, R., & Wood, M. (2007). Results of an intervention for individuals and families with BRCA mutations: a model for providing medical updates and psychosocial support following genetic testing. Journal of Genetic Counseling, 16(4), 433–456.PubMedCrossRef McKinnon, W., Naud, S., Ashikaga, T., Colletti, R., & Wood, M. (2007). Results of an intervention for individuals and families with BRCA mutations: a model for providing medical updates and psychosocial support following genetic testing. Journal of Genetic Counseling, 16(4), 433–456.PubMedCrossRef
Zurück zum Zitat Mellon, S., Berry-Bobovski, L., Gold, R., Levin, N., & Tainsky, M. A. (2006). Communication and decision-making about seeking inherited cancer risk information: findings from female survivor-relative focus groups. Psycho-Oncology, 15(3), 193–208.PubMedCrossRef Mellon, S., Berry-Bobovski, L., Gold, R., Levin, N., & Tainsky, M. A. (2006). Communication and decision-making about seeking inherited cancer risk information: findings from female survivor-relative focus groups. Psycho-Oncology, 15(3), 193–208.PubMedCrossRef
Zurück zum Zitat Mesters, I., van den Borne, H., McCormick, L., Pruyn, J., de Boer, M., & Imbos, T. (1997). Openness to discuss cancer in the nuclear family: scale, development, and validation. Psychosomatic Medicine, 59, 269–279.PubMedCrossRef Mesters, I., van den Borne, H., McCormick, L., Pruyn, J., de Boer, M., & Imbos, T. (1997). Openness to discuss cancer in the nuclear family: scale, development, and validation. Psychosomatic Medicine, 59, 269–279.PubMedCrossRef
Zurück zum Zitat Nycum, G., Avard, D., & Knoppers, B. (2009). Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information. European Journal of Human Genetics, 17(7), 872–880.PubMedPubMedCentralCrossRef Nycum, G., Avard, D., & Knoppers, B. (2009). Factors influencing intrafamilial communication of hereditary breast and ovarian cancer genetic information. European Journal of Human Genetics, 17(7), 872–880.PubMedPubMedCentralCrossRef
Zurück zum Zitat Pho, K., Geller, A., & Schroy, P. C., 3rd. (2000). Lack of communication about familial colorectal cancer risk associated with colorectal adenomas (United States). Cancer Causes and Control, 11(6), 543–546.PubMedCrossRef Pho, K., Geller, A., & Schroy, P. C., 3rd. (2000). Lack of communication about familial colorectal cancer risk associated with colorectal adenomas (United States). Cancer Causes and Control, 11(6), 543–546.PubMedCrossRef
Zurück zum Zitat Riley, B. D., Culver, J. O., Skrzynia, C., Senter, L. A., Peters, J. A., Costalas, J. W., et al. (2011). Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the national society of genetic counselors. Journal of Genetic Counseling. doi:https://doi.org/10.1007/s10897-011-9462-x.PubMedCrossRef Riley, B. D., Culver, J. O., Skrzynia, C., Senter, L. A., Peters, J. A., Costalas, J. W., et al. (2011). Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the national society of genetic counselors. Journal of Genetic Counseling. doi:https://​doi.​org/​10.​1007/​s10897-011-9462-x.PubMedCrossRef
Zurück zum Zitat Rolland, J. S., & Williams, J. K. (2005). Toward a biopsychosocial model for 21st-century genetics. Family Process, 44(1), 3–24.PubMedCrossRef Rolland, J. S., & Williams, J. K. (2005). Toward a biopsychosocial model for 21st-century genetics. Family Process, 44(1), 3–24.PubMedCrossRef
Zurück zum Zitat Schroy, P. C., 3rd, Lal, S. K., Wilson, S., Heeren, T., & Farraye, F. A. (2005). Deficiencies in knowledge and familial risk communication among colorectal adenoma patients. Journal of Clinical of Gastroenterology, 39(4), 298–302.CrossRef Schroy, P. C., 3rd, Lal, S. K., Wilson, S., Heeren, T., & Farraye, F. A. (2005). Deficiencies in knowledge and familial risk communication among colorectal adenoma patients. Journal of Clinical of Gastroenterology, 39(4), 298–302.CrossRef
Zurück zum Zitat Schwarz, N., & Oyserman, D. (2001). Asking questions about behavior: cognition, communication, and questionnaire construction. American Journal of Evaluation, 22(2), 127–160.CrossRef Schwarz, N., & Oyserman, D. (2001). Asking questions about behavior: cognition, communication, and questionnaire construction. American Journal of Evaluation, 22(2), 127–160.CrossRef
Zurück zum Zitat Segal, J., Esplen, M. J., Toner, B., Baedorf, S., Narod, S., & Butler, K. (2004). An investigation of the disclosure process and support needs of BRCA1 and BRCA2 carriers. American Journal of Medical Genetics Part A, 125A(3), 267–272.PubMedCrossRef Segal, J., Esplen, M. J., Toner, B., Baedorf, S., Narod, S., & Butler, K. (2004). An investigation of the disclosure process and support needs of BRCA1 and BRCA2 carriers. American Journal of Medical Genetics Part A, 125A(3), 267–272.PubMedCrossRef
Zurück zum Zitat Simard, J., Dumont, M., Moisan, A.-M., Gaborieau, V., Vezina, H., Durocher, F., et al. (2007). Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer. Journal of Medical Genetics, 44(2), 107–121.PubMedCrossRef Simard, J., Dumont, M., Moisan, A.-M., Gaborieau, V., Vezina, H., Durocher, F., et al. (2007). Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer. Journal of Medical Genetics, 44(2), 107–121.PubMedCrossRef
Zurück zum Zitat Sinicrope, P. S., Patten, C. A., Clark, L. P., Brockman, T. A., Frost, M. H., Petersen, L. R., et al. (2009). Adult daughters’ reports of breast cancer risk reduction and early detection advice received from their mothers: an exploratory study. Psycho-Oncology, 18(2), 169–178.PubMedPubMedCentralCrossRef Sinicrope, P. S., Patten, C. A., Clark, L. P., Brockman, T. A., Frost, M. H., Petersen, L. R., et al. (2009). Adult daughters’ reports of breast cancer risk reduction and early detection advice received from their mothers: an exploratory study. Psycho-Oncology, 18(2), 169–178.PubMedPubMedCentralCrossRef
Zurück zum Zitat Tercyak, K. P., Peshkin, B. N., DeMarco, T. A., Brogan, B. M., & Lerman, C. (2002). Parent-child factors and their effect on communicating BRCA1/2 test results to children. Patient Education and Counseling, 47(2), 145–153.CrossRefPubMed Tercyak, K. P., Peshkin, B. N., DeMarco, T. A., Brogan, B. M., & Lerman, C. (2002). Parent-child factors and their effect on communicating BRCA1/2 test results to children. Patient Education and Counseling, 47(2), 145–153.CrossRefPubMed
Zurück zum Zitat Tercyak, K. P., Peshkin, B. N., Demarco, T. A., Patenaude, A. F., Schneider, K. A., Garber, J. E., et al. (2007). Information needs of mothers regarding communicating BRCA1/2 cancer genetic test results to their children. Genetic Testing, 11(3), 249–255.PubMedPubMedCentralCrossRef Tercyak, K. P., Peshkin, B. N., Demarco, T. A., Patenaude, A. F., Schneider, K. A., Garber, J. E., et al. (2007). Information needs of mothers regarding communicating BRCA1/2 cancer genetic test results to their children. Genetic Testing, 11(3), 249–255.PubMedPubMedCentralCrossRef
Zurück zum Zitat Trepanier, A., Ahrens, M., McKinnon, W., Peters, J., Stopfer, J., Grumet, S. C., et al. (2004). Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. Journal of Genetic Counseling, 13(2), 83–114.PubMedCrossRef Trepanier, A., Ahrens, M., McKinnon, W., Peters, J., Stopfer, J., Grumet, S. C., et al. (2004). Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. Journal of Genetic Counseling, 13(2), 83–114.PubMedCrossRef
Zurück zum Zitat van den Nieuwenhoff, H. W. P., Mesters, I., Gielen, C., & de Vries, N. K. (2007). Family communication regarding inherited high cholesterol: why and how do patients disclose genetic risk? Social Science & Medicine, 65(5), 1025–1037.CrossRef van den Nieuwenhoff, H. W. P., Mesters, I., Gielen, C., & de Vries, N. K. (2007). Family communication regarding inherited high cholesterol: why and how do patients disclose genetic risk? Social Science & Medicine, 65(5), 1025–1037.CrossRef
Zurück zum Zitat van Oostrom, I., Meijers-Heijboer, H., Duivenvoorden, H. J., Bröcker-Vriends, A. H. J. T., van Asperen, C. J., Sijmons, R. H., et al. (2007). Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study. Clinical Genetics, 71(1), 35–42.PubMedCrossRef van Oostrom, I., Meijers-Heijboer, H., Duivenvoorden, H. J., Bröcker-Vriends, A. H. J. T., van Asperen, C. J., Sijmons, R. H., et al. (2007). Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study. Clinical Genetics, 71(1), 35–42.PubMedCrossRef
Zurück zum Zitat Walker, G. A., & Shostak, J. (2010). Common statistical methods for clinical research with SAS examples (3rd ed.). Cary, NC: SAS Publishing. Walker, G. A., & Shostak, J. (2010). Common statistical methods for clinical research with SAS examples (3rd ed.). Cary, NC: SAS Publishing.
Zurück zum Zitat Wilson, B. J., Forrest, K., Van Teijlingen, E. R., McKee, L., Haites, N., Matthews, E., et al. (2004). Family communication about genetic risk: the little that is known. Community Genetics, 7, 15–24.PubMed Wilson, B. J., Forrest, K., Van Teijlingen, E. R., McKee, L., Haites, N., Matthews, E., et al. (2004). Family communication about genetic risk: the little that is known. Community Genetics, 7, 15–24.PubMed
Zurück zum Zitat Wiseman, M., Dancyger, C., & Michie, S. (2010). Communicating genetic risk information within families: a review. Familial Cancer, 9(4), 691–703.PubMedCrossRef Wiseman, M., Dancyger, C., & Michie, S. (2010). Communicating genetic risk information within families: a review. Familial Cancer, 9(4), 691–703.PubMedCrossRef
Metadaten
Titel
Life Events may Contribute to Family Communication About Cancer Risk Following BRCA1/2 Testing
verfasst von
Julie Lapointe
Claudia Côté
Karine Bouchard
Béatrice Godard
Jacques Simard
Michel Dorval
Publikationsdatum
01.04.2013
Verlag
Springer US
Erschienen in
Journal of Genetic Counseling / Ausgabe 2/2013
Print ISSN: 1059-7700
Elektronische ISSN: 1573-3599
DOI
https://doi.org/10.1007/s10897-012-9531-9

Weitere Artikel der Ausgabe 2/2013

Journal of Genetic Counseling 2/2013 Zur Ausgabe

Mammakarzinom: Brustdichte beeinflusst rezidivfreies Überleben

26.05.2024 Mammakarzinom Nachrichten

Frauen, die zum Zeitpunkt der Brustkrebsdiagnose eine hohe mammografische Brustdichte aufweisen, haben ein erhöhtes Risiko für ein baldiges Rezidiv, legen neue Daten nahe.

Mehr Lebenszeit mit Abemaciclib bei fortgeschrittenem Brustkrebs?

24.05.2024 Mammakarzinom Nachrichten

In der MONARCHE-3-Studie lebten Frauen mit fortgeschrittenem Hormonrezeptor-positivem, HER2-negativem Brustkrebs länger, wenn sie zusätzlich zu einem nicht steroidalen Aromatasehemmer mit Abemaciclib behandelt wurden; allerdings verfehlte der numerische Zugewinn die statistische Signifikanz.

Blutdrucksenkung könnte Uterusmyome verhindern

Frauen mit unbehandelter oder neu auftretender Hypertonie haben ein deutlich erhöhtes Risiko für Uterusmyome. Eine Therapie mit Antihypertensiva geht hingegen mit einer verringerten Inzidenz der gutartigen Tumoren einher.

„Übersichtlicher Wegweiser“: Lauterbachs umstrittener Klinik-Atlas ist online

17.05.2024 Klinik aktuell Nachrichten

Sie sei „ethisch geboten“, meint Gesundheitsminister Karl Lauterbach: mehr Transparenz über die Qualität von Klinikbehandlungen. Um sie abzubilden, lässt er gegen den Widerstand vieler Länder einen virtuellen Klinik-Atlas freischalten.

Update Gynäkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert – ganz bequem per eMail.