Skip to main content

Table 2 Summary of the recommendations

From: Evidence-based expert consensus on the management of primary central nervous system lymphoma in China

Management

Recommendations

Biopsy and diagnosis

We suggest the histopathological specimens of PCNSL patients should be obtained as safely and comprehensively as possible by multimodal tomography-guided biopsy or minimally invasive surgery (2C)

We recommend that corticosteroids should be withdrawn from, or not be administered to, patients with suspected PCNSL before biopsy, if the patient’s status so permits (1C)

We suggest that corticosteroids should be withdrawn from patients with suspected PVRL at least 2 weeks before biopsy, if the patient’s status permits (2D)

Staging and following-up evaluation

We recommend MRI (enhanced and DWI) for the diagnosis and evaluation of PCNSL patients (1B)

We suggest that whole-body PET-CT be used to evaluate PCNSL patients at certain time points, such as the time of initial diagnosis or at relapse (2B)

We suggest that MMSE be used to assess cognitive function in the management of PCNSL patients (2B)

Induction therapy

We recommend that newly diagnosed PCNSL patients should be treated with a combined HD-MTX-based regimen, if the patient is fit for chemotherapy (1B). The combined therapeutics can be rituximab (2C), cytarabine (2B), temozolomide (2C) or other drugs which can cross the BBB (2C)

We suggest that newly diagnosed PCNS-DLBCL patients can be treated with a rituximab-inclusive regimen at induction therapy (2C)

Consolidation therapy

Compared with non-reduced dose WBRT, we suggest that ASCT can be used as consolidation therapy for PCNSL patients who are fit for conditioning chemotherapy (2C)

Refractory/relapsed

We suggest that refractory or relapsed PCNSL patients can be treated with ibrutinib with or without high-dose chemotherapy as re-induction therapy (2C)

We suggest that stereotactic radiosurgery can be used for PCNSL patients with a limited recurrent lesion who were refractory to chemotherapy and have previously received WBRT (2D)

Intraocular involvement

We suggest that patients with suspected of PVRL should be diagnosed by vitreous biopsy (2D)

We suggest that PVRL patients or PCNSL patients with concurrent VRL can be treated with combined systemic and local therapy (2C)