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

被引:0
|
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.
引用
收藏
页码:2183 / 2190
页数:8
相关论文
共 50 条
  • [1] CLINICAL BENEFIT OF ORAL METRONOMIC CYCLOPHOSPHAMIDE ADMINISTRATION IN HEAVILY PRETREATED RECURRENT EPITHELIAL OVARIAN CANCER
    Attianese, D.
    Badellino, E.
    Villa, M.
    Bellero, M.
    Massobrio, R.
    Fuso, L.
    Biglia, N.
    Ferrero, A.
    INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2021, 31 : A230 - A230
  • [2] Bevacizumab plus Low-Dose Metronomic Oral Cyclophosphamide in Heavily Pretreated Patients with Recurrent Ovarian Cancer
    Sanchez-Munoz, Alfonso
    Mendiola, Cesar
    Perez-Ruiz, Elisabeth
    Rodriguez-Sanchez, Cesar A.
    Miguel Jurado, Jose
    Alonso-Carrion, Lorenzo
    Ghanem, Ismael
    de Velasco, Guillermo
    Quero-Blanco, Cristina
    Alba, Emilio
    ONCOLOGY, 2010, 79 (1-2) : 98 - 104
  • [3] Pembrolizumab in combination with bevacizumab and oral metronomic cyclophosphamide for recurrent epithelial ovarian, fallopian tube, or primary peritoneal cancer: Real-life clinical experience
    Poblete, S.
    Caulkins, M. A.
    Roche, C. L.
    Loecher, A.
    Attwood, K.
    Gaulin, N.
    Mager, K.
    Frederick, P.
    Zsiros, E.
    ANNALS OF ONCOLOGY, 2022, 33 (07) : S807 - S807
  • [4] Bevacizumab plus low-dose metronomic oral cyclophosphamide in heavily pretreated recurrent ovarian cancer.
    Sanchez-Munoz, A.
    Mendiola, C.
    Rodriguez, C. A.
    Perez-Ruiz, E.
    Jurado, J. M.
    Alonso-Carrion, L.
    Ghanem, I.
    Deelasco, G.
    Quero Blanco, C.
    Alba, E.
    JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (15)
  • [5] Feasibility study of oral cyclophosphamide salvage therapy for the treatment of heavily pretreated patients with recurrent epithelial ovarian cancer
    Watanabe, Yoh
    Etoh, Tomomaro
    Koike, Eiji
    Mizuno, Yoshiaki
    Wang, Wei-Min
    Hoshiai, Hiroshi
    INTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY, 2010, 15 (05) : 468 - 471
  • [6] Feasibility study of oral cyclophosphamide salvage therapy for the treatment of heavily pretreated patients with recurrent epithelial ovarian cancer
    Yoh Watanabe
    Tomomaro Etoh
    Eiji Koike
    Yoshiaki Mizuno
    Wei-Min Wang
    Hiroshi Hoshiai
    International Journal of Clinical Oncology, 2010, 15 : 468 - 471
  • [7] BEVACIZUMAB PLUS METRONOMIC CYCLOPHOSPHAMIDE FOR HEAVILY PRETREATED OVARIAN CANCER: A SINGLE INSTITUTION EXPERIENCE
    Ghanem, I.
    Mendiola, C.
    Diaz, A.
    Velasco, G.
    Manso, L.
    Ciruelos, E.
    Manneh, R. A.
    Hoyos, S.
    Pascual, T.
    Cortes-Funes, H.
    ANNALS OF ONCOLOGY, 2012, 23 : 325 - 325
  • [8] A retrospective, real-life analysis of metronomic oral single-agent cyclophosphamide for the treatment of platinum-pretreated advanced ovarian carcinoma in Italy
    Gebbia, Vittorio
    Martorana, Federica
    Scandurra, Giuseppina
    Valerio, Maria Rosaria
    Cufari, Salvatore
    Vigneri, Paolo
    Sano, Maria Vita
    Scollo, Paolo
    JOURNAL OF ONCOLOGY PHARMACY PRACTICE, 2024, 30 (05) : 853 - 859
  • [9] METRONOMIC ORAL CYCLOPHOSPHAMIDE IN THE SALVAGE TREATMENT OF HEAVILY TREATED OVARIAN CANCER PATIENTS: A RETROSPECTIVE, MULTICENTER STUDY
    Corrado, G.
    Mascilini, F.
    Savarese, A.
    Samaritani, R.
    Salutari, V.
    Di Stefano, M.
    Malaguti, P.
    Vizza, E.
    Scambia, G.
    Ferrandina, G.
    INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2013, 23 (08)
  • [10] Metronomic oral cyclophosphamide (CTX) in patients (pts) with heavily pretreated metastatic castration-resistant prostate cancer (mCRPC)
    Fea, E.
    Vanella, P.
    Miraglio, E.
    Cauchi, C.
    Colantonio, I.
    Denaro, N.
    Di Costanzo, G.
    Garrone, O.
    Granetto, C.
    Occelli, M.
    Ricci, V.
    Vandone, A. M.
    Merlano, M. C.
    ANNALS OF ONCOLOGY, 2016, 27