A refractory case of CDK4-amplified spinal astrocytoma achieving complete response upon treatment with a Palbociclib-based regimen:a case report

BMC Cancer. 2020 Jul 8;20(1):630. doi: 10.1186/s12885-020-07061-3.

Abstract

Background: Spinal cord astrocytoma is a rare neoplasm, and patients usually recur within months after surgery. There is currently a lack of consensus regarding post-operative treatment. Clinical data on the activity of systemic treatment like chemoradiotherapy and anti-angiogenic agents also remained scant. Next-generation sequencing (NGS) -based genomic profiling thus may help identify potential treatment options for a subset of patients that harbor actionable genetic alterations.

Case presentation: We reported for the first time a refractory case of grade III spinal cord astrocytoma that underwent two surgeries but eventually progressed following post-operative chemoradiotherapy plus bevacizumab. Hybridization capture-based NGS using a 381-gene panel disclosed cyclin dependent kinase 4 (CDK4) amplification and after receiving a triplet regimen containg palbociclib for 15 months, the patient achieved complete response.

Conclusions: This case demonstrated the importance of genetic profiling and the benefit of a multi-modality treatment strategy in cancer management.

Keywords: Palbociclib; Spinal astrocytoma; Targeted therapy; next-generation sequencing.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Antineoplastic Combined Chemotherapy Protocols / pharmacology
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Astrocytoma / genetics
  • Astrocytoma / pathology
  • Astrocytoma / therapy*
  • Bevacizumab / pharmacology
  • Bevacizumab / therapeutic use
  • Chemoradiotherapy, Adjuvant / methods
  • Chemotherapy, Adjuvant / methods
  • Cyclin-Dependent Kinase 4 / antagonists & inhibitors*
  • Cyclin-Dependent Kinase 4 / genetics
  • Disease Progression
  • Drug Resistance, Neoplasm / drug effects
  • Drug Resistance, Neoplasm / genetics
  • Gene Amplification
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Male
  • Molecular Targeted Therapy / methods
  • Piperazines / pharmacology
  • Piperazines / therapeutic use*
  • Pyridines / pharmacology
  • Pyridines / therapeutic use*
  • Spinal Cord / pathology
  • Spinal Cord / surgery
  • Spinal Cord Neoplasms / genetics
  • Spinal Cord Neoplasms / pathology
  • Spinal Cord Neoplasms / therapy*
  • Treatment Outcome

Substances

  • Piperazines
  • Pyridines
  • Bevacizumab
  • CDK4 protein, human
  • Cyclin-Dependent Kinase 4
  • palbociclib