Exceptional Response to Lu-177 FAP 2286 Radioisotope Therapy in CNS Hemangiopericytoma: A Novel Therapeutic Breakthrough

Hemangiopericytoma, now reclassified as solitary fibrous tumour, of the central nervous system (CNS), constitutes an exceedingly rare mesenchymal neoplasm originating from the pericytes of meningeal capillaries. These neoplasms typically exhibit a slow growth pattern, with the level of aggressiveness escalating in correlation with higher grades. Minor subsets of this population experience recurrence, and the optimal therapeutic strategy in such circumstances remains ambiguous. Therefore, there exists a continual opportunity for the introduction of innovative treatment modalities. Fibroblast Activation Protein is significantly overexpressed in these tumours, rendering it a promising target for both diagnostic purposes and radioisotope therapy (RIT). We present an unusual case of hemangiopericytoma of the CNS, classified as WHO Grade 3, which manifested recurrence following subtotal resection and adjuvant radiotherapy. The patient subsequently underwent two sessions of Lutetium-177 FAP 2286 (Lu177 FAP2286) radionuclide therapy and exhibited a remarkable response to the FAP-targeted treatment.

Authors

Institutions

Publication Details

Journal
Indian Journal of Nuclear Medicine
Published
2026-05-21
DOI
https://doi.org/10.25259/ijnm_53_2026
Primary Topic
Soft tissue tumor case studies
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Exceptional Response to Lu-177 FAP 2286 Radioisotope Therapy in CNS Hemangiopericytoma: A Novel Therapeutic Breakthrough

Pramukh Kulkarni, Indraja D. Dev, A. Puranik, Tejpal Gupta et al.
Indian Journal of Nuclear Medicine
Soft tissue tumor case studies
article

Exceptional Response to Lu-177 FAP 2286 Radioisotope Therapy in CNS Hemangiopericytoma: A Novel Therapeutic Breakthrough

Pramukh Kulkarni, Indraja D. Dev, A. Puranik, Tejpal Gupta, Archi Agrawal
article en

Abstract

Hemangiopericytoma, now reclassified as solitary fibrous tumour, of the central nervous system (CNS), constitutes an exceedingly rare mesenchymal neoplasm originating from the pericytes of meningeal capillaries. These neoplasms typically exhibit a slow growth pattern, with the level of aggressiveness escalating in correlation with higher grades. Minor subsets of this population experience recurrence, and the optimal therapeutic strategy in such circumstances remains ambiguous. Therefore, there exists a continual opportunity for the introduction of innovative treatment modalities. Fibroblast Activation Protein is significantly overexpressed in these tumours, rendering it a promising target for both diagnostic purposes and radioisotope therapy (RIT). We present an unusual case of hemangiopericytoma of the CNS, classified as WHO Grade 3, which manifested recurrence following subtotal resection and adjuvant radiotherapy. The patient subsequently underwent two sessions of Lutetium-177 FAP 2286 (Lu177 FAP2286) radionuclide therapy and exhibited a remarkable response to the FAP-targeted treatment.

Indian Journal of Nuclear MedicineVol. 0
Homi Bhabha National Institute (IN)
Good health and well-being
Openalex Percentile: Top 5%
Soft tissue tumor case studies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.