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이 페이지는 한국어 임상 치료 설명을 새로 쓰지 않습니다. 권위 출처, 진료 전 정리 질문, 임상시험 검색어, 구축 상태를 보여주는 안전한 시작점입니다.
선택지 정리됨고형암최종 확인 2026.06
승인된 치료 너머
임상시험 및 신흥 선택지
환자가 거주하는 국가에서 아직 승인된 표준 치료가 아닌 선택지입니다 — 연구, 임상시험, 허가 외 사용, 담당 종양내과 의사가 먼저 언급하지 않을 수 있는 초기 근거입니다. 각 항목은 근거의 강도에 따라 구분됩니다. 여기에 실린 항목은 조사하고 의료진과 상의할 정보일 뿐, 효과가 입증되었거나 안전하거나 현재 이용 가능하다는 의미가 아닙니다. 임상 세부 내용은 영문이 정본입니다.
임상시험 진행 중
- Surgery; radiation therapy; chemotherapy; palliative surgery/radiation; phase I/II clinical trials of new drugs, biological therapy, or surgical techniques임상시험임상시험Reported in a clinical trialUnited States · HPV association discussed as disease biology context; no biomarker-required systemic therapy recorded from fetched source; Stage 0-IV penile cancer; stage III/IV clinical-trial context; stage IV palliative context. · NCI PDQ is an evidence summary, not a regulator/payer source. No U.S. FDA-approved penile-cancer-specific systemic therapy was verified in this cycle. Immunotherapy is recorded as a treatment type under clinical-trial/testing context, not as a penile-cancer-specific approval. Confidence/conflicts: High for U.S. treatment framework; FDA-approved systemic options remain source-pending. National Cancer Institute (NCI) — national cancer agency evidence summary
- Topical therapy; laser ablation; excisional surgery; external beam radiotherapy; brachytherapy; surgery; chemotherapy; clinical trials임상시험임상시험InvestigationalEuropean Union · No biomarker requirement stated in fetched EAU guideline page; Small/localized penile cancer local treatment; broader diagnosis/staging/treatment/follow-up guideline context. · EAU/ESMO are guideline sources, not EMA regulator approval pages. No EMA-approved penile-cancer-specific systemic therapy was verified in this cycle. Country-specific reimbursement in Germany/France remains unresolved. Confidence/conflicts: High for European guideline framework; regulator approvals and reimbursement remain active gaps. European Association of Urology (EAU) — professional guideline
- Paclitaxel + ifosfamide + cisplatin (TIP) plus toripalimab/triplizumab; albumin-paclitaxel with ifosfamide and cisplatin; becotatug vedotin plus pucotenlimab; albumin-bound paclitaxel + ifosfamide + cisplatin + nimotuzumab + triprilimab; HRYZ-T101 injection or HRYZ-T101 TCR-T cell with fludarabine + cyclophosphamide; MRG003 plus HX008; QL1706 plus lenvatinib; ivonescimab broad advanced-tumor cohort noted as a newly discovered China gap pending direct fetch임상시험 · NCT06415318임상시험Trial only (registry)China · EGFR-positive for the MRG003 + HX008 study; HPV18-positive for HRYZ-T101 studies; otherwise not biomarker-selected in the fetched registry text; Neoadjuvant locally advanced penile cancer for TIP plus toripalimab/triplizumab, becotatug vedotin plus pucotenlimab, and TIP plus nimotuzumab plus triprilimab; rare advanced tumors including penile cancer for albumin-paclitaxel/ifosfamide/cisplatin; HPV18-positive solid tumors including carcinoma of penis for HRYZ-T101; first-line EGFR-positive locally advanced or metastatic penile squamous cell carcinoma for MRG003 plus HX008; previously treated penile cancer for QL1706 plus lenvatinib. · Registry statuses vary: recruiting, not yet recruiting, completed, and unknown. Several records are basket or multi-cohort studies rather than penile-cancer-only trials. Registry text does not prove regulatory approval or access outside the named study sites. Confidence/conflicts: High that the fetched registry records support China-site investigational options in the listed settings; no NMPA approval claim is made. Ivonescimab NCT06683846 was surfaced in registry search as a China penile-cancer-relevant broad advanced-tumor study but is held as a gap until directly fetched for this disease cell. reimbursement not established in this jurisdiction trial-registry listing only — does not establish approval, reimbursement, or eligibility ClinicalTrials.gov — clinical-trial registry
- Stimotimagene copolymerplasmid plus ganciclovir임상시험 · NCT05578820임상시험Trial only (registry)Russia · Phase 1 safety, tolerability, and pharmacokinetics investigation in multiple tumor types including penile neoplasms. · The trial is completed and broad across several cancers. The registry text does not state a penile-cancer-specific cohort result, standard-of-care role, or active availability. Confidence/conflicts: Medium-high for the existence of a Russia-site broad tumor-type registry cell including penile neoplasms; low for penile-specific treatment relevance beyond investigational context. No regulator approval claim is made. reimbursement not established in this jurisdiction trial-registry listing only — does not establish approval, reimbursement, or eligibility ClinicalTrials.gov — clinical-trial registry
- Pembrolizumab; platinum-based therapy plus pembrolizumab investigational context임상시험임상시험InvestigationalMSI-H status may identify a responsive case in the fetched pembrolizumab case-series source; no broad biomarker claim made; Advanced penile SCC investigational systemic therapy context. · This is not a regulator approval, guideline recommendation, or availability claim. It should only be cataloged as an option to discuss in trial/biomarker context; no superiority or routine access implied. Confidence/conflicts: Medium; evidence is case-series/investigational and not a jurisdictional approval. Peer-reviewed literature / PMC — peer-reviewed case series
임상시험이나 초기 보고에 실렸다는 것은 해당 선택지가 연구되고 있다는 의미일 뿐, 효과가 있거나 특정 환자에게 안전하거나 현재 등록 가능하다는 뜻은 아닙니다. 어떤 선택지가 적합한지는 담당 종양내과 팀과 임상시험 팀이 함께 상의할 문제입니다. 최종 확인 2026.06.
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진료 전 정리할 정보
- What is the stage, tumor location, and nodal/metastatic status?
- Is the intent local control, organ preservation, palliation, or trial participation?
- Are clinical trials available for stage III/IV or recurrent disease?
- Is organ-preserving local treatment feasible for the tumor stage/location?