Does systemic chemotherapy improve outcome in breast cancer patients with carcinomatous meningitis?

2004 ◽  
Vol 2 (3) ◽  
pp. 134
Author(s):  
A Niwinska ◽  
H Rudnicka ◽  
J Giermek ◽  
A Jagiello-Gruszfeld ◽  
T Pienkowski
2013 ◽  
Vol 46 (15) ◽  
pp. 1585-1589 ◽  
Author(s):  
G. Hofmann ◽  
M. Balic ◽  
N. Dandachi ◽  
M. Resel ◽  
W. Schippinger ◽  
...  

2019 ◽  
Vol 37 (15_suppl) ◽  
pp. e18129-e18129
Author(s):  
Sonya Davey ◽  
Surbhi Grover ◽  
Dipho Irene I Setlhako ◽  
Tlotlo Bathethi Ralefala ◽  
Patrick Manshimba ◽  
...  

e18129 Background: Cancer drug stockouts occur at high frequencies globally, however their clinical effects are understudied in sub-Saharan Africa (SSA). We aim to describe prescription patterns and cost of systemic chemotherapy in cancer patients in Botswana during periods of stockout. Methods: Using a retrospective cohort study of the ten most common solid tumor malignancies treated with systemic chemotherapy at Princess Marina Hospital (PMH), Gaborone in 2016, we conducted a subset analysis of suboptimal events, defined as a cycle with ≥ 7 days delay or therapy switch from initiated guideline regimen, that occurred during drug stockout vs non-stockout periods. We estimated financial cost of therapy per cycle using Management Sciences for Health International Price Indicator Guide. Chi-squared and Wilcoxon rank sum were used for comparisons. Results: 167/378 patients contributed to 320 suboptimal events. 63% (201/320) of events occurred during a drug stockout, of which 43%, 43% and 14% were delays, switches, or both, respectively. There were significantly more delays (56% vs 44%, p < .0001) and switches (75% vs 26%, p < .0001) during stockout periods vs no stockout. The majority of switches during drug stockouts occurred in breast cancer patients receiving curative therapy: 48% (20/42) were “paclitaxel + trastuzumab” ($4673) to “paclitaxel alone” ($35) in HER2 positive patients resulting in a 99% cost decrease; and 29% (12/42) were paclitaxel ($35) to docetaxel ($108) resulting in a 209% cost increase per cycle switched. Colon cancer patients receiving palliative-intent therapy were the second most frequent patients with therapy switches during stockout periods: 42% (8/19) were “capecitabine + oxaliplatin” ($259) to “capecitabine alone” ($105) resulting in a 59% cost decrease. Conclusions: Breast cancer patients form the majority of patients treated with systemic chemotherapy at PMH and experienced the most delays and switches in therapy during drug stockout periods. Changes in drug prescription patterns during stockout periods may be associated with switches leading to inferior but less costly regimens, and in some cases costly regimens with higher toxicity. Interventions that minimize cancer drug stockouts are imperative and further studies to understand impact of stockout on survival are needed in SSA.


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