Successful Use of High Dose Methotrexate in Treatment of Primary CNS Lymphoma Patients Without Access to Serum Methotrexate Levels Monitoring: Challenges and Outcome.

High dose methotrexate Methotrexate toxicity Primary CNS Lymphoma Temozolomide Therapeutic drug monitoring

Journal

Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion
ISSN: 0971-4502
Titre abrégé: Indian J Hematol Blood Transfus
Pays: India
ID NLM: 9425818

Informations de publication

Date de publication:
Jan 2022
Historique:
received: 05 02 2021
accepted: 19 04 2021
entrez: 7 2 2022
pubmed: 8 2 2022
medline: 8 2 2022
Statut: ppublish

Résumé

High dose methotrexate (HDMTx) based chemotherapy forms the backbone of therapy for patients with Primary Central Nervous system Lymphoma (PCNSL). However, delivering HDMTx in resource constrained settings, especially without therapeutic drug monitoring, is difficult. We share our experience of treatment of patients with PCNSL at our center over a 10-year period with local adaptations made to deliver HDMTx. We retrospectively analysed the case records of patients diagnosed with a PCNSL over the course of 10 years from 2010 to 2020. Fifty-five patients received therapy for newly diagnosed PCNSL. Thirty-six patients received Modified De-Angelis protocol ± Rituximab with curative intent. Fourteen of these patients were unable to complete the protocol with the most common cause being development of methotrexate toxicity. Patients unable to complete the designated 5 cycles of HDMTx had a poorer PS and higher probability of having a high IELSG score at baseline. Nineteen patients were given non HDMTx based therapy either due to advanced age or poor performance status. Twenty-nine patients (52.7%) were able to achieve a complete response. The most common cause of mortality was relapse/progressive disease. The Median EFS and OS of the cohort was 29 months and 40 months respectively. All attempts should be made to have therapeutic drug level monitoring for administration of HDMTX based therapy for the patients with PCNSL, more so in patients who have poor performance status and a high IELSG score. If it is imperative to give HDMTx without access to TDM facility then a possible risk of higher toxicity should be explained to all patients, beforehand.

Identifiants

pubmed: 35125713
doi: 10.1007/s12288-021-01438-5
pii: 1438
pmc: PMC8804055
doi:

Types de publication

Journal Article

Langues

eng

Pagination

68-77

Informations de copyright

© Indian Society of Hematology and Blood Transfusion 2021.

Déclaration de conflit d'intérêts

Conflict of interestAuthors have no other interests to disclose.

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Auteurs

Charanpreet Singh (C)

Clinical Hematology and BMT Division, Department of Internal Medicine, Nehru Hospital, Postgraduate Institute of Medical Education and Research, F block, 4th Floor, Chandigarh, 160012 India.

Arihant Jain (A)

Clinical Hematology and BMT Division, Department of Internal Medicine, Nehru Hospital, Postgraduate Institute of Medical Education and Research, F block, 4th Floor, Chandigarh, 160012 India.

Aastha Takkar (A)

Department of Neurology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Aniruddha Agarwal (A)

Department of Ophthalmology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Manish Rohilla (M)

Department of Cytology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Deepesh Lad (D)

Clinical Hematology and BMT Division, Department of Internal Medicine, Nehru Hospital, Postgraduate Institute of Medical Education and Research, F block, 4th Floor, Chandigarh, 160012 India.

Alka Khadwal (A)

Clinical Hematology and BMT Division, Department of Internal Medicine, Nehru Hospital, Postgraduate Institute of Medical Education and Research, F block, 4th Floor, Chandigarh, 160012 India.

Rajender Basher (R)

Department of Nuclear Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

B D Radotra (BD)

Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Amanjit Bal (A)

Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Ashim Das (A)

Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Vishali Gupta (V)

Department of Ophthalmology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Vivek Lal (V)

Department of Neurology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Subhash Varma (S)

Clinical Hematology and BMT Division, Department of Internal Medicine, Nehru Hospital, Postgraduate Institute of Medical Education and Research, F block, 4th Floor, Chandigarh, 160012 India.

Pankaj Malhotra (P)

Clinical Hematology and BMT Division, Department of Internal Medicine, Nehru Hospital, Postgraduate Institute of Medical Education and Research, F block, 4th Floor, Chandigarh, 160012 India.

Gaurav Prakash (G)

Clinical Hematology and BMT Division, Department of Internal Medicine, Nehru Hospital, Postgraduate Institute of Medical Education and Research, F block, 4th Floor, Chandigarh, 160012 India.

Classifications MeSH