Pembrolizumab
Vista determinista de la entidad fuente YAML. La autoridad clínica sigue con los ID de fuente citados y estado de firma del revisor.
| ID | DRUG-PEMBROLIZUMAB |
|---|---|
| Tipo | Fármaco |
| Aliaces | La clavetrudaПембролізумаб |
| Situación | reviewed 2026-04-26 | pending_clinical_signoff |
| Enfermedades | DIS-BREAST DIS-CERVICAL DIS-CHL DIS-CHOLANGIOCARCINOMA DIS-CRC DIS-ENDOMETRIAL DIS-ESOPHAGEAL DIS-HNSCC DIS-LARYNGEAL DIS-MELANOMA DIS-NSCLC DIS-PARATHYROID-CARCINOMA DIS-PENILE-SCC DIS-RCC DIS-UROTHELIAL DIS-VULVAR-VAGINAL-SCC |
| Fuentes | SRC-ESMO-BREAST-METASTATIC-2024 SRC-NCCN-BREAST-2025 |
Datos sobre drogas
| Clase | Anticuerpo monoclonal IgG4-kappa humanizado anti-PD-1 (inhibidor del punto de control inmune) |
|---|---|
| Mecanismo | Humanized IgG4 monoclonal antibody binding the programmed cell death protein 1 (PD-1) receptor on activated T cells, B cells, and NK cells. Blocks the PD-1/PD-L1 and PD-1/PD-L2 interactions, releasing the tumor-induced inhibition of cytotoxic T-cell activity and restoring anti-tumor immunity. IgG4 backbone minimizes ADCC. Activity correlates with tumor PD-L1 expression (CPS or TPS), tumor mutational burden (TMB-H ≥10 mut/Mb), microsatellite instability (MSI-H / dMMR), and inflamed tumor microenvironment phenotypes. Approved across many solid tumors and classical Hodgkin / PMBCL lymphoma. |
| Dosificación típica | Standard adult: 200 mg IV q3 weeks OR 400 mg IV q6 weeks (over 30 min). Pediatric: 2 mg/kg (up to 200 mg) IV q3w. Treatment continued until disease progression, unacceptable toxicity, or 24 months in most solid-tumor indications (35 cycles q3w). Adjuvant melanoma: 1 year (KEYNOTE-054). Neoadjuvant + adjuvant TNBC (KEYNOTE-522): 200 mg q3w × 8 cycles with chemo, then 9 cycles adjuvant. Neoadjuvant + adjuvant NSCLC (KEYNOTE-671): 200 mg q3w × 4 cycles with platinum-doublet, then 13 cycles adjuvant. Combination doses unchanged when paired with chemo, lenvatinib, axitinib, or trastuzumab. |
| Ucrania registrada | Cierto |
| NSZU reembolsado | Cierto |
| Ucrania verificada por última vez | 2026-04-27 |
Advertencias
- Reacciones adversas inmunitarias graves y fatales (cualquier órgano; puede ocurrir después de la interrupción)
Notas
Cross-disease entity. ICI-class management protocols apply uniformly: baseline TFTs, cortisol, glucose, LFTs, renal panel, troponin if combo with CTLA-4 ICI; serial labs every cycle. Grade 2 irAE — hold, start prednisone 0.5-1 mg/kg/d; Grade 3-4 — discontinue, prednisone 1-2 mg/kg/d, escalate to infliximab/MMF/IVIG/tocilizumab if refractory. Permanent discontinuation for any Grade 3-4 endocrine event NOT required if hormone replacement controls (most can resume). Endpoint predictors: PD-L1 CPS / TPS by 22C3 IHC, MSI/dMMR, TMB. PD-L1 cutoff varies by indication (TPS ≥1% NSCLC adjuvant, TPS ≥50% NSCLC 1L mono, CPS ≥1 gastric, CPS ≥10 cervical / TNBC met).
Utilizado por
Contraindications
CI-PEMBROLIZUMAB-AUTOIMMUNE- CI-PEMBROLIZUMAB-AUTOIMMUNE
Fármaco
DRUG-TORIPALIMAB- Toripalimab
Indicación
IND-HNSCC-RM-1L-PEMBRO-MONO-CPS-HIGH- IND-HNSCC-RM-1L-PEMBRO-MONO-CPS-HIGHIND-LARYNGEAL-RM-1L-PEMBRO-CHEMO- IND-LARYNGEAL-RM-1L-PEMBRO-CHEMOIND-LARYNGEAL-RM-1L-PEMBRO-MONO-CPS-HIGH- IND-LARYNGEAL-RM-1L-PEMBRO-MONO-CPS-HIGHIND-PARATHYROID-CARCINOMA-2L-PEMBROLIZUMAB-MSI- IND-PARATHYROID-CARCINOMA-2L-PEMBROLIZUMAB-MSIIND-PENILE-SCC-METASTATIC-1L-MSI-H-PEMBRO- IND-PENILE-SCC-METASTATIC-1L-MSI-H-PEMBROIND-VULVAR-VAGINAL-SCC-METASTATIC-1L-PEMBRO- IND-VULVAR-VAGINAL-SCC-METASTATIC-1L-PEMBRO
Esquema terapéutico
REG-EV-PEMBRO-UROTHELIAL- Enfortumab vedotin + pembrolizumab (metastatic urothelial, 1L)REG-LENV-PEMBRO-RCC- Lenvatinib + pembrolizumab (RCC, 1L)REG-PEMBRO-ADJUVANT-MELANOMA- Pembrolizumab adyuvante (melanoma en estadio III/IV resecado; KEYNOTE-054)REG-PEMBRO-ADJUVANT-NSCLC- Pembrolizumab adjuvant (resected NSCLC; KEYNOTE-671)REG-PEMBRO-AXI-RCC- Pembrolizumab + axitinib (RCC, riesgo total de 1L)REG-PEMBRO-CARBO-NAB-PACLITAXEL-NSCLC-SQ- Pembrolizumab + carboplatin + nab-paclitaxel (squamous NSCLC, first line)REG-PEMBRO-CARBO-PACLI-ENDOM- Pembrolizumab + carbo + paclitaxel (endometrio avanzado 1L)REG-PEMBRO-CARBO-PACLITAXEL-NSCLC-SQ- Pembrolizumab + carboplatin + paclitaxel (squamous NSCLC, first line)REG-PEMBRO-CHEMO-HNSCC-1L- Pembrolizumab + 5-FU + platino (HNSCC R/M, 1L; PD-L1 CPS ≥1)REG-PEMBRO-CHEMO-NEOADJ-NSCLC- Pembrolizumab + cisplatin-based chemo (NSCLC neoadjuvant; KEYNOTE-671)REG-PEMBRO-CHEMO-NSCLC-NONSQ- Pembrolizumab + carboplatin + pemetrexed (NSCLC non-squamous, 1L)REG-PEMBRO-CHEMO-TNBC-MET- Pembrolizumab + quimioterapia (TNBC, PD-L1+ metastásico)REG-PEMBRO-CHEMO-TNBC-NEOADJUVANT- Pembrolizumab + quimioterapia (TNBC neoadyuvante)REG-PEMBRO-CISPLATIN-5FU-ESOPH- Pembrolizumab + cisplatin + fluorouracilREG-PEMBRO-GEM-CIS-CHOLANGIO- Pembrolizumab + gemcitabine + cisplatin (KEYNOTE-966) — 1L cáncer de tracto biliar avanzadoREG-PEMBRO-LENVATINIB-ENDOM- Pembrolizumab + Lenvatinib (KEYNOTE-775) — 2L pMMR endometrialREG-PEMBRO-MONO-ESOPH-2L- Pembrolizumab en monoterapia — 2L PD-L1 CPS esófago ≥10 (KEYNOTE-181)REG-PEMBRO-MONO-HNSCC-1L- Pembrolizumab en monoterapia (HNSCC R/M, 1L; PD-L1 CPS ≥20)REG-PEMBRO-MONO-MELANOMA- Pembrolizumab en monoterapia (melanoma avanzado/metastásico, 1L; KEYNOTE-006)REG-PEMBRO-MONO-NSCLC- Pembrolizumab monotherapy (NSCLC PD-L1 ≥50%, driver-negative, 1L)REG-PEMBRO-PACLI-CARBO-BEV-CERVICAL- Pembrolizumab + paclitaxel + carboplatin ± bevacizumab (cervical cancer, 1L)REG-PEMBROLIZUMAB-CERVICAL-1L- Pembrolizumab + carboplatin + paclitaxel ± bevacizumab (persistent/recurrent/metastatic c...REG-PEMBROLIZUMAB-CHL- Pembrolizumab 200 mg IV q3w — r/r cHL post-BV (programa KEYNOTE-204)REG-PEMBROLIZUMAB-MAINTENANCE- Mantenimiento de Pembrolizumab (continuación de la quimioterapia post-inducción+pembro), q3w hasta 35 ciclosREG-PEMBROLIZUMAB-MONO- Pembrolizumab en monoterapiaREG-PEMBROLIZUMAB-MSI-MONO- Pembrolizumab en monoterapia (MSI-H mCRC 1L)