scholarly journals Low-dose metronomic chemotherapy as an efficient treatment option in metastatic breast cancer—results of an exploratory case–control study

2020 ◽  
Vol 182 (2) ◽  
pp. 389-399
Author(s):  
S. Krajnak ◽  
C. Schnatz ◽  
K. Almstedt ◽  
W. Brenner ◽  
F. Haertner ◽  
...  
2019 ◽  
Vol 37 (15_suppl) ◽  
pp. e12578-e12578
Author(s):  
Marco Johannes Battista ◽  
Carola Schnatz ◽  
Katrin Almstedt ◽  
Walburgis Brenner ◽  
Anne-Sophie Heimes ◽  
...  

e12578 Background: There is a growing importance of low-dose metronomic chemotherapy (LDMC) in metastatic breast cancer (MBC). In this retrospective case-control-analysis we compared the efficacy of LDMC and conventional chemotherapy in MBC. Methods: Each LDMC patient receiving oral cyclophosphamide (CTX) (50 mg daily) and methotrexate (MTX) (2.5 mg every other day) was matched with two patients who received conventional chemotherapy. Age, number of chemotherapy lines and metastatic lesions as well as hormone receptor (HR) status were considered as matching criteria. Primary endpoint was disease control rate greater than 24 weeks (DCR). Secondary endpoints were DCR in subgroups (number of chemotherapy lines, number of different metastatic lesions and HR status), progression-free survival (PFS) and duration of response (DoR). Results: A total of 35 cases and 70 controls entered the study. 31% patients with LDMC and 26% patients with conventional chemotherapy showed DCR (p = 0.644). Among younger patients DCR was 41% in LDMC vs. 30% in the control group (p = 0.534). In addition, DCR was achieved in 35% vs. 27% patients with ≤ 2 chemotherapy lines (p = 0.560) and in 36% vs. 20% patients with ≤ 2 different metastatic lesions (p = 0.168), respectively. In the triple negative group 30% LDMC vs. 5% control patients showed DCR (p = 0.095). PFS was 12.0 vs. 13.5 weeks (p = 0.415), DoR was 26.5 vs. 20.5 weeks (p = 0.628), respectively. Conclusions: In this retrospective case-control study we demonstrated a similar efficacy of LDMC compared to conventional chemotherapy in the treatment of MBC. Moreover, no significant differences were found in the subgroups studied. Therefore, the concept of LDMC may also be a treatment option in both younger and non-heavily pre-treated MBC patients who do not need rapid remission.


1996 ◽  
Vol 8 (6) ◽  
pp. 367-370 ◽  
Author(s):  
A. Ezzat ◽  
M.A. Raja ◽  
J. Berry ◽  
F.E. Zwaan ◽  
A. Jamshed ◽  
...  

2015 ◽  
Vol 33 (15_suppl) ◽  
pp. e11567-e11567 ◽  
Author(s):  
Mirela Souto ◽  
Andrea Shimada ◽  
Caroline Chaul Barbosa ◽  
Manuel Cruz Abrahao ◽  
Artur Katz

2015 ◽  
Vol 77 (2) ◽  
pp. 365-374 ◽  
Author(s):  
Herman Andres Perroud ◽  
Carlos Maria Alasino ◽  
Maria Jose Rico ◽  
Leandro Ernesto Mainetti ◽  
Francisco Queralt ◽  
...  

Breast Care ◽  
2018 ◽  
Vol 13 (4) ◽  
pp. 272-276 ◽  
Author(s):  
Slavomir Krajnak ◽  
Marco Battista ◽  
Walburgis Brenner ◽  
Katrin Almstedt ◽  
Tania Elger ◽  
...  

Background: Low-dose metronomic chemotherapy (LDMC) is increasingly used in metastatic breast cancer (MBC). In this retrospective analysis, we examined the therapeutic effects and side effects of LDMC in a cohort of MBC patients. Methods: Patients with MBC were included when LDMC with oral cyclophosphamide (CTX) and methotrexate (MTX) was administered between 2009 and 2015. The primary endpoint was disease control rate (DCR) ≥ 24 weeks after the start of LDMC. Secondary endpoints were duration of progression-free survival (PFS), rates of discontinuation due to side effects, and DCR with regard to subgroups. Results: Retrospective data of 35 patients were available for this analysis. 31% patients achieved DCR. The median PFS was 12 weeks. 9% of patients discontinued LDMC due to adverse events. DCR was 37% in the first 2 lines and 25% in further lines of therapy. 22% of patients with multiple metastases and 35% with ≤2 different metastatic sites achieved DCR. DCR was achieved in 33% of hormone receptor(HR)-positive patients and 27% of HR-negative patients. Conclusion: The DCR of 31% is in line with the results of previous phase II studies. LDMC was well tolerated. Subgroup analysis was not able to identify a group in which LDMC was more efficient.


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