A successful compartmental approach for the treatment of breast cancer brain metastases.


Journal

Cancer chemotherapy and pharmacology
ISSN: 1432-0843
Titre abrégé: Cancer Chemother Pharmacol
Pays: Germany
ID NLM: 7806519

Informations de publication

Date de publication:
03 2019
Historique:
received: 07 10 2018
accepted: 04 12 2018
pubmed: 6 1 2019
medline: 1 1 2020
entrez: 6 1 2019
Statut: ppublish

Résumé

Brain metastases are challenging daily practice in oncology and remain a compartmental problem since most anti-cancer drugs do not cross the blood-brain barrier at relevant pharmacological concentrations. In a young woman with HER2-overexpressing breast cancer resistant to standard treatments, at the time of brain metastases progression, a ventricular reservoir was implanted for intrathecal drug injections and detailed pharmacokinetic studies. A first association of intrathecal trastuzumab with intravenous cisplatin was offered to the patient. For trastuzumab, the mean cerebrospinal fluid trough concentration of 53.4 mg/L reached relevant levels, enabling the stabilization of the metastases. Adding intravenous cisplatin was not beneficial, since the cerebrospinal fluid exposure was almost undetectable under 0.08 mg/L. We then offered the patient an intrathecal combination of trastuzumab and methotrexate, because of their in vitro synergic cytotoxicity. The cerebrospinal fluid peak of methotrexate was 1037 µmol/L at 2 h, and the concentrations remained above the theoretical therapeutic concentration. After 2 months of this drug combination, we obtained an excellent response on the brain metastases. Our preliminary study supports the interest of a compartmental approach through a direct administration of drugs into the cerebrospinal fluid for the treatment of breast cancer brain metastases.

Sections du résumé

BACKGROUND
Brain metastases are challenging daily practice in oncology and remain a compartmental problem since most anti-cancer drugs do not cross the blood-brain barrier at relevant pharmacological concentrations.
METHODS
In a young woman with HER2-overexpressing breast cancer resistant to standard treatments, at the time of brain metastases progression, a ventricular reservoir was implanted for intrathecal drug injections and detailed pharmacokinetic studies.
RESULTS
A first association of intrathecal trastuzumab with intravenous cisplatin was offered to the patient. For trastuzumab, the mean cerebrospinal fluid trough concentration of 53.4 mg/L reached relevant levels, enabling the stabilization of the metastases. Adding intravenous cisplatin was not beneficial, since the cerebrospinal fluid exposure was almost undetectable under 0.08 mg/L. We then offered the patient an intrathecal combination of trastuzumab and methotrexate, because of their in vitro synergic cytotoxicity. The cerebrospinal fluid peak of methotrexate was 1037 µmol/L at 2 h, and the concentrations remained above the theoretical therapeutic concentration. After 2 months of this drug combination, we obtained an excellent response on the brain metastases.
CONCLUSION
Our preliminary study supports the interest of a compartmental approach through a direct administration of drugs into the cerebrospinal fluid for the treatment of breast cancer brain metastases.

Identifiants

pubmed: 30610367
doi: 10.1007/s00280-018-3752-z
pii: 10.1007/s00280-018-3752-z
doi:

Substances chimiques

ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1
Trastuzumab P188ANX8CK
Cisplatin Q20Q21Q62J

Types de publication

Case Reports Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

573-580

Auteurs

Thuy T Nguyen (TT)

U1165, Université Paris 7, INSERM, Hôpital Saint-Louis, 1 Avenue Claude Vellefaux, 75010, Paris, France.
AP-HP Hôpital Avicenne, Service d'Oncologie Médicale, 93000, Bobigny, France.
Medical Oncology Department A, National Cancer Hospital, Ha Noi, Viet Nam.

Eurydice Angeli (E)

U1165, Université Paris 7, INSERM, Hôpital Saint-Louis, 1 Avenue Claude Vellefaux, 75010, Paris, France.

François Darrouzain (F)

Université François-Rabelais de Tours, CNRS, GICC UMR 7292, 37000, Tours, France.
CHRU de Tours, Pharmacologie-Toxicologie, 37000, Tours, France.

Quang T Nguyen (QT)

Medical Oncology Department A, National Cancer Hospital, Ha Noi, Viet Nam.

Céline Desvignes (C)

CHRU de Tours, Pharmacologie-Toxicologie, 37000, Tours, France.

Marthe Rigal (M)

AP-HP Hôpital Avicenne, Pharmacie, 93000, Bobigny, France.

Osman Nevine (O)

AP-HP Hôpital Avicenne, Pharmacie, 93000, Bobigny, France.

Patrick Nicolas (P)

AP-HP Hôpital Avicenne, Service de Biochimie, 93000, Bobigny, France.

Quang V Le (QV)

Surgery Department A, National Cancer Hospital, Ha Noi, Viet Nam.

Sabine Winterman (S)

AP-HP Hôpital Avicenne, Service d'Oncologie Médicale, 93000, Bobigny, France.

Marie-Christine Pailler (MC)

AP-HP Hôpital Avicenne, Service d'Oncologie Médicale, 93000, Bobigny, France.

Laurent Zelek (L)

AP-HP Hôpital Avicenne, Service d'Oncologie Médicale, 93000, Bobigny, France.
Université Paris 13, 93430, Villetaneuse, France.

Gilles Paintaud (G)

Université François-Rabelais de Tours, CNRS, GICC UMR 7292, 37000, Tours, France.
CHRU de Tours, Pharmacologie-Toxicologie, 37000, Tours, France.

Anne Janin (A)

U1165, Université Paris 7, INSERM, Hôpital Saint-Louis, 1 Avenue Claude Vellefaux, 75010, Paris, France. anne.janin1165@gmail.com.
AP-HP Hôpital Saint-Louis, Laboratoire de Pathologie, 75010, Paris, France. anne.janin1165@gmail.com.
Université Paris Diderot, Sorbonne Paris Cité, UMR-S 1165, 75010, Paris, France. anne.janin1165@gmail.com.

Guilhem Bousquet (G)

U1165, Université Paris 7, INSERM, Hôpital Saint-Louis, 1 Avenue Claude Vellefaux, 75010, Paris, France. guilhem.bousquet@aphp.fr.
AP-HP Hôpital Avicenne, Service d'Oncologie Médicale, 93000, Bobigny, France. guilhem.bousquet@aphp.fr.
Université Paris 13, 93430, Villetaneuse, France. guilhem.bousquet@aphp.fr.
Université Paris Diderot, Sorbonne Paris Cité, UMR-S 1165, 75010, Paris, France. guilhem.bousquet@aphp.fr.

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Classifications MeSH