Mamma-Studien: Target - Therapie | ||||||||||||||||||||||||||||||||||||||||
allgemeines |
Während die klassische Chemotherapie Tumorzellen direkt abtötet oder hemmt, ist die Target - Therapie auf spezielle molekularbiologische Funktionen ausgerichtet. | |||||||||||||||||||||||||||||||||||||||
ALTTO |
NeoSHERE |
GeparQuinto |
CHER-LOB |
NOAH(9) |
HERA | |||||||||||||||||||||||||||||||||||
PHARE |
COMPLETE | |||||||||||||||||||||||||||||||||||||||
Sunitinib |
IMPALA |
Randomisierte, multizentrische klinische Prüfung der Phase III zu Sunitinib (SU 011248) oder Capecitabin bei Patientinnen mit fortgeschrittenen Mammakarzinom, bei denen eine Therapie mit Taxanen und Anthracyclinen versagt hat oder bei denen nach Versagen vonTaxanen eine weitere Anthracyclinbehandlung nicht angezeigt ist | ||||||||||||||||||||||||||||||||||||||
SUN 1099 | Capecitabin mit und ohne Sunitinib bei metastasiertem Mammakarzinom. | |||||||||||||||||||||||||||||||||||||||
Gefitinib |
EORTC 10021 |
Anastrazol +- Gefitinib | ||||||||||||||||||||||||||||||||||||||
Bevacizumab |
| |||||||||||||||||||||||||||||||||||||||
Everolismus |
| |||||||||||||||||||||||||||||||||||||||
COX-2 |
| |||||||||||||||||||||||||||||||||||||||
PARP-IH |
| |||||||||||||||||||||||||||||||||||||||
CDK4/6 |
| |||||||||||||||||||||||||||||||||||||||
Trop-2 |
| |||||||||||||||||||||||||||||||||||||||
Teil von |
Mamma - Karzinom: Studien | Mamma - Karzinom: StudienMamma - Karzinom | Gynäkologische Onkologie | |||||||||||||||||||||||||||||||||||||
Quellen |
1.) Piccart-Gebhart MJ, et al.: Trastuzumab after adjuvant chemotherapy in HER2-positive breast cancer. NEJM 353(2005):1659-1672 2.) Romond EH, et al.: Trastuzumab plus adjuvant chemotherapy for operable HER2-positive breast cancer. NEJM 353(2005):1673-1684 3.) Joensuu H, et al.: Adjuvant docetaxel or vinorelbine with or without trastuzumab for breast cancer. NEJM 354(2006):809-820 4.) Smith I, et al.: 2-Year follow-up of trastuzumab after adjuvant chemotherapy in HER2-positive breast cancer: a randomised controlled trial. Lancet 369(2007):29-36 5.) Tan-Chiu E, et al.: Assessment of cardiac dysfunction in a randomized trial comparing doxorubicin and cyclophosphamide followed by paclitaxel, with or without trastuzumab as adjuvant therapy in node-positive, human epidermal growth factor receptor 2-overexpressing breast cancer: NSABP B-31. JCO 23(2005):7811-7819 6.) Gianni L, et al: Efficacy and safety of neoadjuvant pertuzumab and trastuzumab in women with locally advanced, inflammatory, or early HER2-positive breast cancer (NeoSphere): A randomised multicentre, open-label, phase 2 trial. Lancet Oncol 13(2012):25-32 7.) Untch M, et al: Lapatinib vs trastuzumab in combination with neoadjuvant anthracycline-taxine-based chemotherapy: Primary efficacy endpoint analysis of the GEPARQUINTO STUDY (GBG 44). San Antonio Breast Cancer Symposium, 8.-12.12.2010, Abstr S3-1 8.) Guarneri V, et al: Preoperative chemotherapy plus trastuzumab, lapatinib, or both in human epidermal growth factor receptor 2–positive operable breast cancer: Results of the randomized phase II CHER-LOB study. JCO 30(2012):1989-1995 9.) Gianni L, et al: Neoadjuvant chemotherapy with trastuzumab followed by adjuvant trastuzumab versus neoadjuvant chemotherapy alone, in patients with HER2-positive locally advanced breast cancer (the NOAH trial): A randomised controlled superiority trial with a parallel HER2-negative cohort. Lancet 375(2010):377-384 |
|||||||||||||||||||||||||||||||||||||||
Impressum Zuletzt geändert am 30.07.2021 19:10