Evaluation of the Attitude of Pre Menopausal Women With Breast Cancer Faced With the Risk of Fertility Loss Caused by Chemotherapy
1 oktober 2020 uppdaterad av: Latin American Cooperative Oncology Group
Evaluation of the Attitude of Pre Menopausal Women With Breast Cancer Faced With the Risk
To evaluate the attitude of pre menopausal women with breast cancer faced with the risk of loss of fertility caused by chemotherapy using EORTC's Fertility Questionnaire.
Studieöversikt
Status
Avslutad
Betingelser
Detaljerad beskrivning
To characterize the attitude of pre menopausal patients with breast cancer regarding the risks of infertility based on the following variables:
- Age at diagnosis
- Number of children
- Will of having children
- Marital status
- Scholarity
- Period of time from the diagnosis
- Time of the last menstruation period
- Chemotherapy administration
- Clinical staging at the diagnosis
- Pathological evaluation
- Documentation of the cancer therapy
Studietyp
Observationell
Inskrivning (Faktisk)
343
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
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São Paulo, Brasilien
- Hospital Perola Byington
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Rio Grande Do Sul
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Porto Alegre, Rio Grande Do Sul, Brasilien
- CPO - Pucrs
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Porto Alegre, Rio Grande Do Sul, Brasilien
- HCPA
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-
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Havana, Kuba
- Instituto Nacional de Oncologia y Radiobiologia
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Toluca de Lerdo, Mexiko
- Cenro Oncologico Estatal ISSEMYM
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Surquillo, Peru
- INEN
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Puerto Cabello, Venezuela
- Hospital de Clínicas San Agustín
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-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år till 40 år (Vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Kvinna
Testmetod
Icke-sannolikhetsprov
Studera befolkning
Pre menopausal women diagnosed with breast cancer prior treatment
Beskrivning
Inclusion Criteria:
- Women with age ≥ 18 and ≤ 40
- Indication of (neo) adjuvant chemotherapy
- Prior chemotherapy treatment
- Patients with menstrual periods in the last 6 months
- In use of contraceptive methods
- Without breast cancer recurrence
- Capacity to read and understand the informed consent
Exclusion Criteria:
- Patients which received or with indication of definitive ovarian suppression (surgery and/or radiotherapy), except temporary pharmacological ovarian suppression
- Patients whom initiated chemotherapy treatment before entering the study
- Altered state of mind, dementia, or any other psychiatry problem that can interfere in the comprehension or interpretation of the informed consent.
- Previous diagnosis of infertility
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
Kohorter och interventioner
Grupp / Kohort |
|---|
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Pre menopausal women with breast cancer
Pre menopausal women with breast cancer prior treatment in face of infertility evoked by chemotherapy
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
|---|---|
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To analyze the number of pre-menopausal patients diagnosed with breast cancer that did not agree in receiving chemotherapy due to the risk of infertility
Tidsram: Baseline and 1 year after after the first interview
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Baseline and 1 year after after the first interview
|
Sekundära resultatmått
Resultatmått |
Tidsram |
|---|---|
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Civilstånd
Tidsram: Baslinje
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Baslinje
|
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Infertility risk for breast cancer patients after accepting chemotherapy
Tidsram: Baseline and 1 year after the first interview
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Baseline and 1 year after the first interview
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Minimal percentage of cure necessary for patients accept the chemotherapy treatment
Tidsram: Baseline and 1 year after the first interview
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Baseline and 1 year after the first interview
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Age when diagnosed
Tidsram: Baseline and 1 year after the first interview
|
Baseline and 1 year after the first interview
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Number of children
Tidsram: Baseline and 1 year after the first interview
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Baseline and 1 year after the first interview
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Desire to have kids
Tidsram: Baseline and 1 year after the first interview
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Baseline and 1 year after the first interview
|
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Scholarity
Tidsram: Baseline
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Baseline
|
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Period of time since the diagnosis
Tidsram: Baseline
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Baseline
|
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Chemotherapy scheme administration
Tidsram: Baseline and 1 year after the first interview
|
Baseline and 1 year after the first interview
|
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Period of time from the last menstruation period
Tidsram: Baseline and 1 year after the first interview
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Baseline and 1 year after the first interview
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Description of quality of life of patients with the EORTC QLQ-BR23
Tidsram: Baseline and 1 year after the first interview
|
Baseline and 1 year after the first interview
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Samarbetspartners
Utredare
- Studierektor: Gustavo Werutsky, MD, Latin American Cooperative Oncology Group
Publikationer och användbara länkar
Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.
Allmänna publikationer
- Jemal A, Siegel R, Xu J, Ward E. Cancer statistics, 2010. CA Cancer J Clin. 2010 Sep-Oct;60(5):277-300. doi: 10.3322/caac.20073. Epub 2010 Jul 7. Erratum In: CA Cancer J Clin. 2011 Mar-Apr;61(2):133-4.
- Benson JR, Jatoi I, Keisch M, Esteva FJ, Makris A, Jordan VC. Early breast cancer. Lancet. 2009 Apr 25;373(9673):1463-79. doi: 10.1016/S0140-6736(09)60316-0.
- Cardoso F, Loibl S, Pagani O, Graziottin A, Panizza P, Martincich L, Gentilini O, Peccatori F, Fourquet A, Delaloge S, Marotti L, Penault-Llorca F, Kotti-Kitromilidou AM, Rodger A, Harbeck N; European Society of Breast Cancer Specialists. The European Society of Breast Cancer Specialists recommendations for the management of young women with breast cancer. Eur J Cancer. 2012 Dec;48(18):3355-77. doi: 10.1016/j.ejca.2012.10.004. Epub 2012 Oct 29.
- Colleoni M, Rotmensz N, Robertson C, Orlando L, Viale G, Renne G, Luini A, Veronesi P, Intra M, Orecchia R, Catalano G, Galimberti V, Nole F, Martinelli G, Goldhirsch A. Very young women (<35 years) with operable breast cancer: features of disease at presentation. Ann Oncol. 2002 Feb;13(2):273-9. doi: 10.1093/annonc/mdf039.
- Vallejos Sologuren C, Gómez HL, et al. Clinicopathologic and outcome variables of worse prognosis in premenopausal patients (pts) age 35 and younger. 2010 Breast Cancer Symposium. Abstract 65
- Reichman BS, Green KB. Breast cancer in young women: effect of chemotherapy on ovarian function, fertility, and birth defects. J Natl Cancer Inst Monogr. 1994;(16):125-9.
- Senkus E, Gomez H, Dirix L, Jerusalem G, Murray E, Van Tienhoven G, Westenberg AH, Bottomley A, Rapion J, Bogaerts J, Di Leo A, Neskovic-Konstantinovic Z. Attitudes of young patients with breast cancer toward fertility loss related to adjuvant systemic therapies. EORTC study 10002 BIG 3-98. Psychooncology. 2014 Feb;23(2):173-82. doi: 10.1002/pon.3384. Epub 2013 Aug 29.
- Gradishar WJ, Schilsky RL. Ovarian function following radiation and chemotherapy for cancer. Semin Oncol. 1989 Oct;16(5):425-36. No abstract available.
- Stearns V, Schneider B, Henry NL, Hayes DF, Flockhart DA. Breast cancer treatment and ovarian failure: risk factors and emerging genetic determinants. Nat Rev Cancer. 2006 Nov;6(11):886-93. doi: 10.1038/nrc1992. Epub 2006 Oct 12.
- Dnistrian AM, Schwartz MK, Fracchia AA, Kaufman RJ, Hakes TB, Currie VE. Endocrine consequences of CMF adjuvant therapy in premenopausal and postmenopausal breast cancer patients. Cancer. 1983 Mar 1;51(5):803-7. doi: 10.1002/1097-0142(19830301)51:53.0.co;2-v.
- Moore HCF, et al. Phase III trial (Prevention of Early Menopause Study [POEMS]-SWOG S0230) of LHRH analog during chemotherapy (CT) to reduce ovarian failure in earlystage, hormone receptor-negative breast cancer: An international Intergroup trial of SWOG, IBCSG, ECOG, and CALGB (Alliance). J Clin Oncol 32:5s, 2014 (suppl; abstr LBA505)
- Brandberg Y, Michelson H, Nilsson B, Bolund C, Erikstein B, Hietanen P, Kaasa S, Nilsson J, Wiklund T, Wilking N, Bergh J; Scandinavian Breast Group Study 9401. Quality of life in women with breast cancer during the first year after random assignment to adjuvant treatment with marrow-supported high-dose chemotherapy with cyclophosphamide, thiotepa, and carboplatin or tailored therapy with Fluorouracil, epirubicin, and cyclophosphamide: Scandinavian Breast Group Study 9401. J Clin Oncol. 2003 Oct 1;21(19):3659-64. doi: 10.1200/JCO.2003.07.020.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 maj 2015
Primärt slutförande (Faktisk)
15 juni 2020
Avslutad studie (Faktisk)
15 juni 2020
Studieregistreringsdatum
Först inskickad
27 januari 2016
Först inskickad som uppfyllde QC-kriterierna
8 augusti 2016
Första postat (Uppskatta)
11 augusti 2016
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
5 oktober 2020
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
1 oktober 2020
Senast verifierad
1 oktober 2020
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- LACOG 0414
Plan för individuella deltagardata (IPD)
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OBESLUTSAM
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