Management of Recurrent or Residual Cervical Cancer with Cisplatin and Topotecan Combination Therapy in a Palliative Setting: A Prospective Study

被引:0
|
作者
Taba T. [1 ,2 ]
Barmon D. [1 ,2 ]
Begum D. [1 ,2 ,3 ]
Kataki A.C. [2 ]
Kamei H. [1 ,2 ]
机构
[1] Department of Gynaecologic Oncology, Dr. B. Borooah Cancer Institute, Guwahati, Assam
[2] Dr. B. Borooah Cancer Institute, Guwahati, Assam
[3] C/O Mukut Ali House No 23 D Near Darandha Maszid Panjabari Road Sixmile Khanapara, Guwahati, 781022, Assam
关键词
Cisplatin; Palliative chemotherapy; Residual or recurrent cervical cancer; Topotecan;
D O I
10.1007/s40944-018-0239-0
中图分类号
学科分类号
摘要
Context: Treatment options for patients with recurrent or residual cervical tumour are limited. Several new cytotoxic drugs have been recently investigated, comparing single agent with multiple drugs combination. The uses of chemotherapy in these cases are considered palliative because of low response rates and a negligible impact on long-term survival. Aims and Objectives: To evaluate the efficacy and side effects of cisplatin plus topotecan combined chemotherapy in persistent or recurrent cervical cancer not amenable to curative treatment by surgery and/or radiation and to evaluate the median progression-free interval and overall survival after the completion of treatment. Materials and Methods: In total, 17 patients with residual or recurrent cervical cancer were enrolled in this trial. They were given a standard dose of chemotherapy according to their body surface area, i.e. topotecan 0.75 mg/m2 intravenously on day 1, 2 and 3, and cisplatin 50 mg/m2 intravenously on day 1. Treatments were repeated every 21 days for 6 cycles or until disease progression or unacceptable toxicities and then followed up 3 months for 1 year. OS and PFS rates were estimated by means of the Kaplan–Meier method. Toxicities analysis was also done. Results: Topotecan and cisplatin combined chemotherapy was well tolerated by all the patients with grade 2 neutropenia, leukopenia and thrombocytopenia occurring in 5.8%, anaemia in 53% and mild nausea in 11.8%. There were complete remission in 2 patients (11.8%) and partial remission in another 3 patients (17.6%) at the end of study with overall response of 29.4%. There were 3 patients (17.6%) with stable disease. The median OS was 10 months, and the median PFS was 4 months. Conclusion: Topotecan and cisplatin combination was found to be effective, safe and well tolerated in patients with persistent or recurrent cervical cancer. © 2018, Association of Gynecologic Oncologists of India.
引用
收藏
相关论文
共 50 条
  • [1] Topotecan with in combination cisplatin for the treatment of stage IVB, recurrent, or persistent cervical cancer
    Brave, Michael
    Dagher, Ramzi
    Farrell, Ann
    Abraham, Sophia
    Ramchandani, Roshni
    Gobburu, Jogarao
    Booth, Brian
    Jiang, Xiaoping
    Sridhara, Rajeshwari
    Justice, Robert
    Pazdur, Richard
    ONCOLOGY-NEW YORK, 2006, 20 (11): : 1401 - +
  • [2] TOPOTECAN IN COMBINATION WITH CISPLATIN FOR THE TREATMENT OF ADVANCE/RECURRENT CERVICAL CANCER, EXPERIENCE IN A SINGLE CENTER
    Camacho, C.
    Luis, M.
    Abreu, M.
    Faustino, C.
    Afonso, N.
    Ribas, P.
    Pereira, D.
    INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2013, 23 (08)
  • [3] Treatment of advanced cervical cancer with Topotecan in combination with Cisplatin
    Rudesheim, Sabine M.
    GEBURTSHILFE UND FRAUENHEILKUNDE, 2007, 67 (06) : 39 - 39
  • [4] Feasibility study on combination chemotherapy using nogitecan hydrochloride (topotecan) and cisplatin for patients with metastatic, persistent, or recurrent uterine cervical cancer
    Muneaki Shimada
    Shinya Sato
    Tetsuro Oishi
    Hiroaki Itamochi
    Junzo Kigawa
    Nobuhiro Takeshima
    Daisuke Aoki
    Yoichi Aoki
    Yoshihiro Nambu
    Kazunori Ochiai
    International Journal of Clinical Oncology, 2016, 21 : 969 - 974
  • [5] Feasibility study on combination chemotherapy using nogitecan hydrochloride (topotecan) and cisplatin for patients with metastatic, persistent, or recurrent uterine cervical cancer
    Shimada, Muneaki
    Sato, Shinya
    Oishi, Tetsuro
    Itamochi, Hiroaki
    Kigawa, Junzo
    Takeshima, Nobuhiro
    Aoki, Daisuke
    Aoki, Yoichi
    Nambu, Yoshihiro
    Ochiai, Kazunori
    INTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY, 2016, 21 (05) : 969 - 974
  • [6] Phase II trial of topotecan, cisplatin, and bevacizurnab for recurrent or persistent cervical cancer
    Zighelboim, I.
    Wright, J. D.
    Powell, M. A.
    Case, A. S.
    Eisenhauer, E. L.
    Cohn, D. E.
    Valea, F. A.
    Secord, A. A.
    Lippmann, L. T.
    Rader, J. S.
    JOURNAL OF CLINICAL ONCOLOGY, 2010, 28 (15)
  • [7] Phase I study of topotecan continuous infusion and weekly cisplatin with radiation therapy for locally advanced/recurrent cervical cancer.
    Padilla, LA
    Mitchell, SK
    Carson, LF
    JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (16) : 486S - 486S
  • [8] Phase II trial of topotecan, cisplatin, and bevacizumab for recurrent or persistent cervical cancer
    Zighelboim, Israel
    Wright, Jason D.
    Gao, Feng
    Case, Ashley Stephens
    Massad, L. Stewart
    Mutch, David Gardner
    Powell, Matthew A.
    Thaker, Premal H.
    Eisenhauer, Eric Lawernce
    Cohn, David E.
    Valea, Fidel A.
    Secord, Angeles Alvarez
    Lippmann, Lynne T.
    Rader, Janet Sue
    JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (15)
  • [9] Randomized study to compare Paclitaxel/Topotecan vs. Cisplatin/Topotecan in patients with recurrent cervical cancer - AGO-Cervix-1 study
    Thiel, F. C.
    Hilpert, F.
    Rein, D.
    Liebrich, C.
    Fasching, P. A.
    Beckmann, M. W.
    GEBURTSHILFE UND FRAUENHEILKUNDE, 2008, 68 : S28 - S28
  • [10] AGO-Cervix-1 study: A prospective, randomized phase III study to compare the effects of clitaxel and Topotecan to those of Cisplatin and Topotecan for treatment of patients with recurrent or persistent cervical cancer
    Thiel, F.
    Rein, D. T.
    Runnebaum, I. B.
    Petry, K. U.
    Fasching, P. A.
    Beckmann, M. W.
    GEBURTSHILFE UND FRAUENHEILKUNDE, 2008, 68 (05) : 553 - 553