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Non-seminomatous germ cell tumour: lines of therapy

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5 standard-of-care settings across 3 lines and 2 biomarker subgroups. Rows come from the cancer page's standard of care; the grid places each on its line and subgroup.

LineAll comersIMDC risk
Early / localised1·
Advanced, first line11
Second line2·

Early / localised

SubgroupSettingApproachProducts and trialsEvidence
All comersStage IOrchidectomy then surveillance; one cycle of adjuvant BEP for men with lymphovascular invasion who choose it; nerve-sparing retroperitoneal dissection in selected cases.81

Advanced, first line

SubgroupSettingApproachProducts and trialsEvidence
All comersMetastatic, good riskThree cycles of BEP (or four of EP if bleomycin is contraindicated).81
IMDC riskMetastatic, intermediate and poor riskFour cycles of BEP, or VIP; poor-risk patients with slow marker decline are switched to intensified therapy (GETUG 13); treatment in high-volume centres.81

Second line

SubgroupSettingApproachProducts and trialsEvidence
All comersResidual masses after chemotherapyRetroperitoneal lymph node dissection and resection of other residual masses when markers have normalised.-
All comersRelapseConventional (TIP) or high-dose chemotherapy with stem cell support, as compared in the TIGER trial; late relapse treated surgically where possible.87

Lines and subgroups are parsed from the setting text of each standard-of-care row and can misclassify an unusual phrasing; the row’s own setting is always shown. Guideline chips reflect the NCCN category and ESMO-MCBS grade recorded on the cancer page, checked on its stated date. Not medical advice.