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Intra‐CSF topotecan in treatment of breast cancer patients with leptomeningeal metastases

BACKGROUND: There are few treatment options for patients with leptomeningeal metastases (LM). METHODS: We report a case series of patients with breast cancer and LM treated with intra‐CSF topotecan (TOPO). Outcome was assessed by clinical exam and MRI at baseline, at end of induction (4‐5 weeks), th...

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Autores principales: Jaeckle, Kurt A., Dixon, Jesse G., Anderson, Stephen Keith, Moreno‐Aspitia, Alvaro, Colon‐Otero, Gerardo, Hebenstreit, Kathy, Patel, Tejal A., Reddy, Samarth L., Perez, Edith A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643683/
https://www.ncbi.nlm.nih.gov/pubmed/32885617
http://dx.doi.org/10.1002/cam4.3422
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author Jaeckle, Kurt A.
Dixon, Jesse G.
Anderson, Stephen Keith
Moreno‐Aspitia, Alvaro
Colon‐Otero, Gerardo
Hebenstreit, Kathy
Patel, Tejal A.
Reddy, Samarth L.
Perez, Edith A.
author_facet Jaeckle, Kurt A.
Dixon, Jesse G.
Anderson, Stephen Keith
Moreno‐Aspitia, Alvaro
Colon‐Otero, Gerardo
Hebenstreit, Kathy
Patel, Tejal A.
Reddy, Samarth L.
Perez, Edith A.
author_sort Jaeckle, Kurt A.
collection PubMed
description BACKGROUND: There are few treatment options for patients with leptomeningeal metastases (LM). METHODS: We report a case series of patients with breast cancer and LM treated with intra‐CSF topotecan (TOPO). Outcome was assessed by clinical exam and MRI at baseline, at end of induction (4‐5 weeks), then every 3 months; CSF cytology was determined at baseline and with each treatment. RESULTS: Thirty‐one women [median age, 58 (37‐81); median KPS 60 (40‐100)] received treatment. At baseline, 68% had positive CSF cytology, and 90%, leptomeningeal enhancement on MRI. 84% of patients also received focal RT (not during TOPO) and 77% received concomitant systemic hormonal or chemotherapy. Median number of TOPO treatments was 14.5 (range, 3‐71); median duration of treatment, 11 weeks (1‐176); and median OS, 6.9 months (range, 0.9‐48.8). Patients remaining progression‐free during 4‐6 weeks of induction (81%) had a median OS of 11.5 months (range, 1.8‐48.8). Overall neurologic PFS at 6, 12, and 24 months was 39%, 26%, and 6%, respectively. Clearing of CSF malignant cells for >3 consecutive samples occurred in 10/21 (48%) patients with positive CSF cytology at baseline, remaining clear for a median duration of 15.9 months (range, 1.4‐34.5). Grade 3 adverse events included headache or vomiting (3pts), T2 hyperintensity surrounding the ventricular catheter (2 pts), and meningitis (2 pts). CONCLUSIONS: Intra‐CSF TOPO, with focal RT as needed for symptomatic areas of enhancement produced durable clearing of CSF malignant cells in 48% of patients positive at baseline, with promising median PFS and OS.
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spelling pubmed-76436832020-11-13 Intra‐CSF topotecan in treatment of breast cancer patients with leptomeningeal metastases Jaeckle, Kurt A. Dixon, Jesse G. Anderson, Stephen Keith Moreno‐Aspitia, Alvaro Colon‐Otero, Gerardo Hebenstreit, Kathy Patel, Tejal A. Reddy, Samarth L. Perez, Edith A. Cancer Med Clinical Cancer Research BACKGROUND: There are few treatment options for patients with leptomeningeal metastases (LM). METHODS: We report a case series of patients with breast cancer and LM treated with intra‐CSF topotecan (TOPO). Outcome was assessed by clinical exam and MRI at baseline, at end of induction (4‐5 weeks), then every 3 months; CSF cytology was determined at baseline and with each treatment. RESULTS: Thirty‐one women [median age, 58 (37‐81); median KPS 60 (40‐100)] received treatment. At baseline, 68% had positive CSF cytology, and 90%, leptomeningeal enhancement on MRI. 84% of patients also received focal RT (not during TOPO) and 77% received concomitant systemic hormonal or chemotherapy. Median number of TOPO treatments was 14.5 (range, 3‐71); median duration of treatment, 11 weeks (1‐176); and median OS, 6.9 months (range, 0.9‐48.8). Patients remaining progression‐free during 4‐6 weeks of induction (81%) had a median OS of 11.5 months (range, 1.8‐48.8). Overall neurologic PFS at 6, 12, and 24 months was 39%, 26%, and 6%, respectively. Clearing of CSF malignant cells for >3 consecutive samples occurred in 10/21 (48%) patients with positive CSF cytology at baseline, remaining clear for a median duration of 15.9 months (range, 1.4‐34.5). Grade 3 adverse events included headache or vomiting (3pts), T2 hyperintensity surrounding the ventricular catheter (2 pts), and meningitis (2 pts). CONCLUSIONS: Intra‐CSF TOPO, with focal RT as needed for symptomatic areas of enhancement produced durable clearing of CSF malignant cells in 48% of patients positive at baseline, with promising median PFS and OS. John Wiley and Sons Inc. 2020-09-03 /pmc/articles/PMC7643683/ /pubmed/32885617 http://dx.doi.org/10.1002/cam4.3422 Text en © 2020 The Authors. Cancer Medicine published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Jaeckle, Kurt A.
Dixon, Jesse G.
Anderson, Stephen Keith
Moreno‐Aspitia, Alvaro
Colon‐Otero, Gerardo
Hebenstreit, Kathy
Patel, Tejal A.
Reddy, Samarth L.
Perez, Edith A.
Intra‐CSF topotecan in treatment of breast cancer patients with leptomeningeal metastases
title Intra‐CSF topotecan in treatment of breast cancer patients with leptomeningeal metastases
title_full Intra‐CSF topotecan in treatment of breast cancer patients with leptomeningeal metastases
title_fullStr Intra‐CSF topotecan in treatment of breast cancer patients with leptomeningeal metastases
title_full_unstemmed Intra‐CSF topotecan in treatment of breast cancer patients with leptomeningeal metastases
title_short Intra‐CSF topotecan in treatment of breast cancer patients with leptomeningeal metastases
title_sort intra‐csf topotecan in treatment of breast cancer patients with leptomeningeal metastases
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643683/
https://www.ncbi.nlm.nih.gov/pubmed/32885617
http://dx.doi.org/10.1002/cam4.3422
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