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      Efficacy of Slow Rate Ventriculolumbar Perfusion Chemotherapy for Leptomeningeal Carcinomatosis: Interim Result of a Phase II Study = Efficacy of Slow Rate Ventriculolumbar Perfusion Chemotherapy for Leptomeningeal Carcinomatosis: Interim Result of a Phase II Study

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      https://www.riss.kr/link?id=A106436571

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      다국어 초록 (Multilingual Abstract)

      Background To evaluate the efficacy of modified ventriculolumbar perfusion (VLP) chemotherapy with methotrexate on leptomeningeal carcinomatosis in terms of symptomatic response and side effects.
      Methods Previous infusion rate of 20 mL/h was reduced to 15 mL/h for the purpose of decreasing constitutional side effects of VLP such as nausea/vomiting, insomnia and confusion. The primary outcome was the response rate of increased intracranial pressure (ICP), and the secondary outcome was the occurrence of side effects compared to previous 20 mL/h trial. This interim analysis to validate the reduced infusion rate is not to affect the original effect of VLP chemotherapy.
      Results All forty-seven patients were enrolled including 22 patients with increased ICP. Thirteen patients out of these (59%) got normalized ICP after VLP chemotherapy. Moderate to severe (grade 2-3) confusion was observed in 3 patients (6%) and it was significantly reduced compared to those (23%) in the VLP 20 mL/h (p=0.017). Grade 2-3 nausea/vomiting was also reduced from 64% to 45% but failed to reach statistical significance (p=0.08). Median overall survival (OS) was 5.3 months (95% confidence interval, 3.55-7.05) and patients OS, who received maintenance VLP was significantly prolonged compared to patients who underwent induction VLP only (5.8 vs. 3.4 months, p=0.025).
      Conclusion VLP of reduced perfusion rate (15 mL/h) showed compatible control rate of increased ICP at this interim analysis. Decreased moderate to severe side effects and prolonged OS in patients received maintenance VLP encourage us to evaluate the effectiveness of this trial further.
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      Background To evaluate the efficacy of modified ventriculolumbar perfusion (VLP) chemotherapy with methotrexate on leptomeningeal carcinomatosis in terms of symptomatic response and side effects. Methods Previous infusion rate of 20 mL/h was reduced t...

      Background To evaluate the efficacy of modified ventriculolumbar perfusion (VLP) chemotherapy with methotrexate on leptomeningeal carcinomatosis in terms of symptomatic response and side effects.
      Methods Previous infusion rate of 20 mL/h was reduced to 15 mL/h for the purpose of decreasing constitutional side effects of VLP such as nausea/vomiting, insomnia and confusion. The primary outcome was the response rate of increased intracranial pressure (ICP), and the secondary outcome was the occurrence of side effects compared to previous 20 mL/h trial. This interim analysis to validate the reduced infusion rate is not to affect the original effect of VLP chemotherapy.
      Results All forty-seven patients were enrolled including 22 patients with increased ICP. Thirteen patients out of these (59%) got normalized ICP after VLP chemotherapy. Moderate to severe (grade 2-3) confusion was observed in 3 patients (6%) and it was significantly reduced compared to those (23%) in the VLP 20 mL/h (p=0.017). Grade 2-3 nausea/vomiting was also reduced from 64% to 45% but failed to reach statistical significance (p=0.08). Median overall survival (OS) was 5.3 months (95% confidence interval, 3.55-7.05) and patients OS, who received maintenance VLP was significantly prolonged compared to patients who underwent induction VLP only (5.8 vs. 3.4 months, p=0.025).
      Conclusion VLP of reduced perfusion rate (15 mL/h) showed compatible control rate of increased ICP at this interim analysis. Decreased moderate to severe side effects and prolonged OS in patients received maintenance VLP encourage us to evaluate the effectiveness of this trial further.

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      참고문헌 (Reference)

      1 Bleyer WA, "“Concentration x time” methotrexate via a subcutaneous reservoir: a less toxic regimen for intraventricular chemotherapy of central nervous system neoplasms" 51 : 835-842, 1978

      2 Gwak HS, "Ventriculolumbar perfusion chemotherapy with methotrexate for treating leptomeningeal carcinomatosis:a Phase II Study" 19 : 1044-1045, 2014

      3 Nakagawa H, "Ventriculolumbar perfusion chemotherapy with methotrexate and cytosine arabinoside for meningeal carcinomatosis: a pilot study in 13 patients" 45 : 256-264, 1996

      4 Gwak HS, "Ventriculolumbar perfusion chemotherapy for the treatment of leptomeningeal carcinomatosis: a phase I study with pharmacokinetic data" 36 : 491-499, 2013

      5 Price RA, "The central nervous system in childhood leukemia. II. Subacute leukoencephalopathy" 35 : 306-318, 1975

      6 Debus OM, "Spontaneous central melatonin secretion and resorption kinetics of exogenous melatonin: a ventricular CSF study" 33 : 213-217, 2002

      7 Chamberlain MC, "Radioisotope CSF flow studies in leptomeningeal metastases" 38 : 135-140, 1998

      8 Chamberlain MC, "Prognostic significance of 111indium-DTPA CSF flow studies in leptomeningeal metastases" 46 : 1674-1677, 1996

      9 Fleischhack G, "Pharmacokinetics following intraventricular administration of chemotherapy in patients with neoplastic meningitis" 44 : 1-31, 2005

      10 Simon R, "Optimal two-stage designs for phase II clinical trials" 10 : 1-10, 1989

      1 Bleyer WA, "“Concentration x time” methotrexate via a subcutaneous reservoir: a less toxic regimen for intraventricular chemotherapy of central nervous system neoplasms" 51 : 835-842, 1978

      2 Gwak HS, "Ventriculolumbar perfusion chemotherapy with methotrexate for treating leptomeningeal carcinomatosis:a Phase II Study" 19 : 1044-1045, 2014

      3 Nakagawa H, "Ventriculolumbar perfusion chemotherapy with methotrexate and cytosine arabinoside for meningeal carcinomatosis: a pilot study in 13 patients" 45 : 256-264, 1996

      4 Gwak HS, "Ventriculolumbar perfusion chemotherapy for the treatment of leptomeningeal carcinomatosis: a phase I study with pharmacokinetic data" 36 : 491-499, 2013

      5 Price RA, "The central nervous system in childhood leukemia. II. Subacute leukoencephalopathy" 35 : 306-318, 1975

      6 Debus OM, "Spontaneous central melatonin secretion and resorption kinetics of exogenous melatonin: a ventricular CSF study" 33 : 213-217, 2002

      7 Chamberlain MC, "Radioisotope CSF flow studies in leptomeningeal metastases" 38 : 135-140, 1998

      8 Chamberlain MC, "Prognostic significance of 111indium-DTPA CSF flow studies in leptomeningeal metastases" 46 : 1674-1677, 1996

      9 Fleischhack G, "Pharmacokinetics following intraventricular administration of chemotherapy in patients with neoplastic meningitis" 44 : 1-31, 2005

      10 Simon R, "Optimal two-stage designs for phase II clinical trials" 10 : 1-10, 1989

      11 Sandberg DI, "Ommaya reservoirs for the treatment of leptomeningeal metastases" 47 : 49-54, 2000

      12 Freilich RJ, "Neuroimaging and cerebrospinal fluid cytology in the diagnosis of leptomeningeal metastasis" 38 : 51-57, 1995

      13 Shapiro WR, "Methotrexate: distribution in cerebrospinal fluid after intravenous, ventricular and lumbar injections" 293 : 161-166, 1975

      14 Balis FM, "Methotrexate distribution within the subarachnoid space after intraventricular and intravenous administration" 45 : 259-264, 2000

      15 Chamberlain MC, "Leptomeningeal metastases: a review of evaluation and treatment" 37 : 271-284, 1998

      16 Taillibert S, "Leptomeningeal metastases from solid malignancy:a review" 75 : 85-99, 2005

      17 Bruna J, "Leptomeningeal carcinomatosis: prognostic implications of clinical and cerebrospinal fluid features" 115 : 381-389, 2009

      18 Blasberg RG, "Distribution of methotrexate in the cerebrospinal fluid and brain after intraventricular administration" 61 : 633-641, 1977

      19 Wasserstrom WR, "Diagnosis and treatment of leptomeningeal metastases from solid tumors: experience with 90 patients" 49 : 759-772, 1982

      20 Park JH, "Clinical outcomes of leptomeningeal metastasis in patients with non-small cell lung cancer in the modern chemotherapy era" 76 : 387-392, 2012

      21 Gwak HS, "Chemoport with a non-collapsible chamber as a replacement for an Ommaya reservoir in the treatment of leptomeningeal carcinomatosis" 153 : 1971-1978, 2011

      22 Rubin RC, "Cerebrospinal fluid perfusion for central nervous system neoplasms" 16 : 680-692, 1966

      23 Grossman SA, "Cerebrospinal fluid flow abnormalities in patients with neoplastic meningitis. An evaluation using 111indium-DTPA ventriculography" 73 : 641-647, 1982

      24 Chamberlain MC, "Carcinoma meningitis secondary to non-small cell lung cancer: combined modality therapy" 55 : 506-512, 1998

      25 Trotti A, "CTCAE v3.0: development of a comprehensive grading system for the adverse effects of cancer treatment" 13 : 176-181, 2003

      26 Gwak HS, "Analysis of treatment outcomes of intraventricular chemotherapy in 105 patients for leptomeningeal carcinomatosis from non-small-cell lung cancer" 8 : 599-605, 2013

      27 Yoon Hwan Byun, "A Novel Implantable Cerebrospinal Fluid Reservoir : A Pilot Study" 대한신경외과학회 61 (61): 640-644, 2018

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2022 평가예정 계속평가 신청대상 (계속평가)
      2021-12-01 평가 등재후보로 하락 (재인증) KCI등재후보
      2018-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2016-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.02 0.02 0.05
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0 0 0.212 0.03
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