Sacituzumab Govitecan for Second and Subsequent Line Palliative Treatment of Patients with Triple-Negative Breast Cancer: A Polish Real-World Multicenter Cohort Study

被引:0
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作者
Puskulluoglu, Miroslawa [1 ]
Pieniazek, Malgorzata [2 ,3 ]
Las-Jankowska, Manuela [4 ,5 ]
Streb, Joanna [6 ]
Ziobro, Marek [1 ]
Pacholczak-Madej, Renata [7 ,8 ,9 ]
Kilian-Van Miegem, Paulina [10 ]
Rudzinska, Agnieszka [1 ]
Grela-Wojewoda, Aleksandra [1 ]
Lacko, Aleksandra [2 ,3 ]
Jarzab, Michal [11 ]
Polakiewicz-Gilowska, Anna [11 ]
机构
[1] Mar Sklodowska Curie Natl Res Inst Oncol, Krakow Branch, Dept Clin Oncol, Krakow, Poland
[2] Wroclaw Med Univ, Dept Oncol, Plac Hirszfelda 12, PL-53413 Wroclaw, Poland
[3] Lower Silesian Comprehens Canc Ctr, Plac Hirszfelda 12, PL-53413 Wroclaw, Poland
[4] Nicolaus Copernicus Univ Torun, Oncol Ctr, Ludw Rydygier Coll Medicum Bydgoszcz, Surg Oncol, PL-85067 Bydgoszcz, Poland
[5] Prof Franciszek Lukaszczyk Mem Hosp, Oncol Ctr, Dept Clin Oncol, PL-85796 Bydgoszcz, Poland
[6] Jagiellonian Univ, Med Coll, Dept Oncol, PL-31008 Krakow, Poland
[7] Jagiellonian Univ, Med Coll, Dept Anat, Swietej Anny 12, PL-31008 Krakow, Poland
[8] Mar Sklodowska Curie Natl Res Inst Oncol, Krakow Branch, Dept Gynecol Oncol, Garncarska St 11, PL-31115 Krakow, Poland
[9] Dist Hosp, Dept Chemotherapy, Szpitalna St 22, PL-34200 Sucha Beskidzka, Poland
[10] Oncol Ctr Prof F Lukaszczyk Bydgoszcz, Chemotherapy Outpatient Clin, PL-85796 Bydgoszcz, Poland
[11] Mar Sklodowska Curie Natl Res Inst Oncol, Gliwice Branch, Breast Canc Unit, PL-44102 Gliwice, Poland
关键词
Triple-negative breast cancer; Metastases; Sacituzumab govitecan; Real-world study; Poland;
D O I
10.1007/s40487-024-00307-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
IntroductionSacituzumab govitecan (SG) is approved for patients with previously treated metastatic or locally advanced triple-negative breast cancer (TNBC), as per the ASCENT trial results. Real-world studies (RWSs) cover more diverse patients than clinical trials, offering crucial data for healthcare policies. This study aimed to investigate the safety and efficacy of SG in real-world Polish patients with previously treated metastatic TNBC.MethodsIn this ambispective multicenter cohort study, we collected demographic and clinical data. Premedication, adjustments in SG dosage, and treatment regimen adhered to the product's characteristics.ResultsWe included 79 female patients. The median age at SG initiation was 53 years; 32% of patients were initially diagnosed with a non-TNBC subtype. The median number of previous palliative lines was 2. Seven patients presented with brain metastases. The median overall survival was 10.3 months, and the median progression-free survival (PFS) was 4.4 months. The overall response rate was 35%, with a median time to response of 2 months. SG was discontinued by 70% of patients, primarily due to disease progression (95%). Treatment delays due to adverse events (AEs) occurred in 67% and dose reductions in 25% of patients, with neutropenia being the most common. Grade >= 2 AEs included neutropenia (43%), anemia (10.1%), and diarrhea (4%). A longer interval between breast cancer diagnosis and SG initiation or between metastasis diagnosis and SG initiation correlated with improved PFS, likely reflecting the disease's biological aggressiveness rather than treatment efficacy.ConclusionIn this RWS, SG demonstrated effectiveness and safety in patients with previously treated metastatic TNBC, consistent with ASCENT trial outcomes. Further research is needed to explore the efficacy of SG in different patient populations and healthcare systems.
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收藏
页码:787 / 801
页数:15
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