Real-life clinical benefit of oral metronomic cyclophosphamide administration in elderly and heavily pretreated epithelial ovarian cancer patients

被引:0
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作者
Attianese, Daniela [1 ]
Massobrio, Roberta [1 ]
Giorgi, Margherita [1 ]
Villa, Michela [3 ]
Fuso, Luca [1 ]
Badellino, Enrico [3 ]
Bellero, Marco [4 ]
Ferrero, Annamaria [1 ,2 ]
机构
[1] Univ Torino, Mauriziano Umberto Hosp 1, Acad Div Gynecol & Obstet, Turin, Italy
[2] Univ Torino, Dept Surg Sci, Turin, Italy
[3] Cardinal Massaia Hosp, Div Gynecol & Obstet, Asti, Italy
[4] Mauriziano Umberto I Hosp, Pharmacol Div, Turin, Italy
关键词
Oral metronomic cyclophosphamide; Elderly; Ovarian cancer; Clinical benefit; PRIMARY PERITONEAL; CHEMOTHERAPY; RECURRENT; SURVIVAL; REGIMEN; WOMEN; 2ND;
D O I
10.1007/s00404-024-07670-4
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
PurposeOral metronomic cyclophosphamide (OMC) implicates the daily administration of low doses of chemotherapy. Its antitumor activity combined with an oral administration route and a good toxicity profile makes OMC an attractive option for heavily pretreated patients. We retrospectively evaluated OMC's clinical benefit and objective response in recurrent ovarian cancer patients.MethodsThis is a retrospective observational study involving patients treated with OMC (50 mg daily) from 2017 to 2022 at the Academic Division Gynaecology, Mauriziano Hospital, Torino, Italy. Clinical benefit assessment included CA125 response, radiological response, and reported symptomatic improvement. Toxicities were reported using Common Terminology Criteria for Adverse Events version 5.0.ResultsThirty-eight patients (average age 72, range 49-88) were included. 90% had FIGO stage III/IV at diagnosis and 64% underwent >= 3 previous lines of chemotherapy. Before OMC, 79% had ECOG 1 or 2. 8.6% of patients had a partial response (PR), and 40% a stable disease (SD). Median duration of response was 7.4 months. After 3 months on OMC, 51% experienced symptom improvement, and 53.3% experienced Ca125 reduction or stabilization. 66.7% of patients older than 75 responded to treatment; in 40% of cases, responses lasted >= 6 months (p = 0.08). No G3-4 hematological toxicities occurred. Nausea and fatigue G1-G2 were reported in 5 (13%) and 13 (34%) cases, respectively.ConclusionOMC is a feasible therapeutic option for recurrent ovarian cancer, providing satisfying clinical responses with a good toxicity profile, even in elderly and heavily pretreated patients with a suboptimal performance status.
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收藏
页码:2183 / 2190
页数:8
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