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OncoMatch/Clinical Trials/Testicular / Germ Cell Cancer

Testicular / Germ Cell Cancer Clinical Trials

Recruiting trials·Updated daily from ClinicalTrials.gov

OncoMatch filters Testicular / Germ Cell Cancer trials by the molecular markers that determine eligibility — KIT, KRAS, and more. Enter your biomarker results to see only the trials you may qualify for.

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Trial context

About Testicular / Germ Cell Cancer trials

Testicular cancer (germ cell tumors / GCT) is one of the most curable solid cancers, with stage I-II 5-year survival above 95%. KIT alterations occur in a subset of seminomas and may appear in molecularly selected exploratory trials, but tumor markers and IGCCCG risk classification drive eligibility far more often than sequencing results. KRAS mutations are less common and primarily relevant in non-seminoma cohorts. Tumor markers (AFP, β-hCG, LDH) are central to GCT clinical management and drive IGCCCG risk classification more than mutation status in most cases. These markers are tracked in blood rather than via tumor sequencing.

Testicular cancer trial activity centers on stage, IGCCCG risk classification, and prior chemotherapy. Front-line trials test variations on the BEP regimen (bleomycin, etoposide, cisplatin), de-escalation strategies for early-stage disease (single-cycle adjuvant carboplatin for stage I seminoma vs surveillance), and intensification for poor-risk patients. Salvage trials test TIP (paclitaxel, ifosfamide, cisplatin) and high-dose chemotherapy with autologous stem cell transplant for platinum-refractory or relapsed disease. Mediastinal germ cell tumor trials are typically separate because of worse prognosis. Late-effects and survivorship trials are an active area given the high cure rates and long survival in this young patient population, focused on reducing cardiovascular toxicity (post-bleomycin and post-cisplatin), second malignancy risk, and fertility preservation.

Testicular cancer trial intake usually checks histology, IGCCCG risk classification, and prior chemotherapy. Histology (seminoma vs non-seminoma vs mixed) gates which trial set applies. IGCCCG risk classification (good, intermediate, poor) by tumor markers, primary site, and metastatic distribution determines trial eligibility for risk-stratified studies. Prior BEP / EP exposure for line-specific trials. Prior salvage chemotherapy (TIP) and prior high-dose chemotherapy + autoSCT for refractory trials. Pulmonary function status, particularly post-bleomycin (DLCO), gates trials testing further bleomycin or pulmonary-toxic agents. Performance status, with most trials accepting ECOG 0-1. Fertility preservation considerations, where many trials include sperm banking discussions and accept patients who have completed banking.

Biomarker panel

Biomarkers tested in Testicular / Germ Cell Cancer trials

These are the molecular markers most commonly required or evaluated in Testicular / Germ Cell Cancer eligibility criteria. OncoMatch extracts them from each trial's protocol and matches them against your test results.

KITKRAS

How OncoMatch finds Testicular / Germ Cell Cancer trials for you

01

AI reads the protocol

Every Testicular / Germ Cell Cancer trial on ClinicalTrials.gov has eligibility criteria written for regulators. OncoMatch uses large language models to extract the structured requirements — biomarkers, stage, prior therapy, and more — from that text.

02

You enter your results

Select Testicular / Germ Cell Cancer and mark your biomarker results — KIT, KRAS — as positive, negative, or not tested. Your data never leaves your device.

03

See only relevant trials

Results filter instantly. Each trial shows exactly which criteria you meet, which you don't, and which need more information. Bring the list to your oncologist.

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