# Romanian Consensus Statement for Hormone Receptor-Positive and Human Epidermal Growth Factor Receptor 2-Negative Metastatic Breast Cancer (HR+/HER2– mBC) and Triple-Negative Metastatic Breast Cancer (mTNBC)

**Authors:** Mircea Dragoș Median, Nicoleta Zenovia Antone, Simona Volovăț, Laura Mazilu, Șerban Mircea Negru, Răzvan Ovidiu Curcă, Amedeia Niță, Raluca Ileana Pătru, Andrei Ungureanu, Vlad Lupu, Cristina Marinela Oprean

PMC · DOI: 10.3390/curroncol33020120 · 2026-02-17

## TL;DR

This paper presents national treatment guidelines for two types of metastatic breast cancer in Romania, developed by oncologists and widely accepted by medical professionals.

## Contribution

The paper introduces Romania-specific consensus guidelines for HR+/HER2– and triple-negative metastatic breast cancer, adapted from international standards and validated through a survey.

## Key findings

- A modified Delphi survey of 61 oncologists showed over 90% agreement with the proposed treatment recommendations.
- Key recommendations include mandatory biopsy at metastasis and the use of modern therapies like CDK4/6 inhibitors and immunotherapies.
- The guidelines emphasize systematic toxicity monitoring and integrated supportive care.

## Abstract

Breast cancer is the most common malignant disease among Romanian women, and the number of deaths remains among the highest in Europe. This consensus document provides national standards for treating two metastatic types of breast cancer without human epidermal growth factor receptor 2 (HER2) overexpression: hormone receptor-positive/HER2-negative and triple-negative metastatic disease. A scientific board of 11 oncologists, in collaboration with the Romanian National Society for Medical Oncology, adapted international guidelines to fit Romanian realities and then assessed acceptance among medical oncologists through a survey of 61 oncologists. The recommendations include: repeating biopsy and key biomarker tests at metastasis, utilizing modern targeted and immunotherapies when appropriate, carefully monitoring and managing side effects, and providing strong supportive and palliative care. Sixty-one oncologists completed the survey, and an over 90% agreement was achieved, supporting these recommendations as the new national standard.

Breast cancer (BC) is the most common malignant disease in women in Romania, with incidence and mortality rates among the highest in Europe. This consensus statement aims to ensure equitable access to care for human epidermal growth factor receptor 2-negative metastatic BC (HR+/HER2– mBC) and triple-negative mBC (mTNBC) in Romania. Between December 2024 and June 2025, a scientific board of 11 oncologists, in collaboration with the Romanian National Society for Medical Oncology (SNOMR), developed national recommendations based on ESMO/NCCN/ABC guidelines, clinical expertise, and local conditions. A modified Delphi survey was conducted among medical oncologists to evaluate acceptance of recommendations with greatest clinical impact. Key recommendations included: mandatory biopsy at metastasis with ER/PgR/HER2 retesting, HER2-low assessment, and molecular profiling (BRCA, PIK3CA, AKT1/PTEN, ESR1, plus PD-L1 testing in mTNBC); for HR+/HER2– mBC, first-line endocrine therapy plus CDK4/6 inhibitor, followed by targeted agents, chemotherapy, or antibody–drug conjugates based on progression and visceral crisis; for mTNBC, first-line immune checkpoint inhibitor plus chemotherapy in PD-L1-positive, PARP inhibitors in BRCA-positive patients, and sacituzumab-govitecan or trastuzumab-deruxtecan later; systematic toxicity monitoring; and integrated supportive and palliative care. Sixty-one oncologists completed the survey, with >90% overall agreement, suggesting broad acceptance of recommendations as Romania’s national standard for mBC care.

## Linked entities

- **Genes:** Brca2 (BRCA2, DNA repair associated) [NCBI Gene 37916], PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207], PTEN (phosphatase and tensin homolog) [NCBI Gene 5728], ESR1 (estrogen receptor 1) [NCBI Gene 2099], CD274 (CD274 molecule) [NCBI Gene 29126]
- **Diseases:** breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, TACSTD2 (tumor associated calcium signal transducer 2) [NCBI Gene 4070] {aka EGP-1, EGP1, GA733-1, GA7331, GP50, M1S1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290] {aka CCM4, CLAPO, CLOVE, CWS5, HMH, MCAP}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, PALB2 (partner and localizer of BRCA2) [NCBI Gene 79728] {aka BROVCA5, FANCN, PNCA3}, BRCA1 (BRCA1 DNA repair associated) [NCBI Gene 672] {aka BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4}, ESR1 (estrogen receptor 1) [NCBI Gene 2099] {aka ER, ESR, ESRA, ESTRR, Era, NR3A1}, MFSD11 (major facilitator superfamily domain containing 11) [NCBI Gene 79157] {aka ET}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}, PARP1 (poly(ADP-ribose) polymerase 1) [NCBI Gene 142] {aka ADPRT, ADPRT 1, ADPRT1, ARTD1, PARP, PARP-1}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, NR4A1 (nuclear receptor subfamily 4 group A member 1) [NCBI Gene 3164] {aka GFRP1, HMR, N10, NAK-1, NGFIB, NP10}, COL11A2 (collagen type XI alpha 2 chain) [NCBI Gene 1302] {aka DFNA13, DFNB53, FBCG2, HKE5, OSMEDA, OSMEDB}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, CYP19A1 (cytochrome P450 family 19 subfamily A member 1) [NCBI Gene 1588] {aka ARO, ARO1, CPV1, CYAR, CYP19, CYPXIX}, SLC5A7 (solute carrier family 5 member 7) [NCBI Gene 60482] {aka CHT, CHT1, CMS20, DHMNVP, HMN7A, HMND7}, PTEN (phosphatase and tensin homolog) [NCBI Gene 5728] {aka 10q23del, BZS, CWS1, DEC, GLM2, MHAM}
- **Diseases:** deaths (MESH:D003643), neutropenia (MESH:D009503), metastases (MESH:D009362), Toxicity (MESH:D064420), vitamin deficiencies (MESH:D014802), bone lesions (MESH:D001847), Stomatitis (MESH:D013280), dyspareunia (MESH:D004414), colitis (MESH:D003092), endocrine disorders (MESH:D004700), HR (MESH:D002303), ILD (MESH:D017563), Peripheral neuropathy (MESH:D010523), hepatitis (MESH:D056486), BC (MESH:D001943), Mucositis (MESH:D052016), triple negative breast cancer (MESH:D064726), female (MESH:D005831), Tumor-Node-Metastasis (MESH:D008207), Cognitive Impairment (MESH:D003072), stage IV (MESH:D062706), ovarian suppression (MESH:D010049), Menopausal (MESH:D008594), sleep disorders (MESH:D012893), Pain (MESH:D010146), ET (MESH:D016751), disease (MESH:D004194), injury to (MESH:D014947), hormone-dependent disease (MESH:D009376), node (MESH:D012804), metastatic (MESH:D000092182), Dyspnea (MESH:D004417), Cancer (MESH:D009369), Hand-Foot syndrome (MESH:D060831), ADCs (MESH:D009759), Fatigue (MESH:D005221), endocrine refractory tumors (MESH:D000069279), pneumonitis (MESH:D011014), diarrhea (MESH:D003967), mood disturbances (MESH:D019964), organ failure (MESH:D009102), Nausea (MESH:D009325), Vomiting (MESH:D014839), hypoxemia (MESH:D000860), visceral crisis (MESH:D007418), 1L (MESH:C564679), 2L (MESH:C566968)
- **Chemicals:** benzodiazepines (MESH:D001569), doxorubicin (MESH:D004317), carboplatin (MESH:D016190), Everolimus (MESH:D000068338), letrozole (MESH:D000077289), epirubicin (MESH:D015251), 2L (-), cisplatin (MESH:D002945), pregabalin (MESH:D000069583), capecitabine (MESH:D000069287), Pembrolizumab (MESH:C582435), taxanes (MESH:D043823), anastrozole (MESH:D000077384), Trastuzumab deruxtecan (MESH:C000614160), Olaparib (MESH:C531550), Ribociclib (MESH:C000589651), SG (MESH:C000608132), docetaxel (MESH:D000077143), talazoparib (MESH:C586365), gemcitabine (MESH:D000093542), gabapentin (MESH:D000077206), taxane (MESH:C080625), anthracycline (MESH:D018943), oxygen (MESH:D010100), Capivasertib (MESH:C575618), exemestane (MESH:C056516), platinum (MESH:D010984), T (MESH:D014316), trastuzumab (MESH:D000068878), eribulin (MESH:C490954), Alpelisib (MESH:C585539), Palbociclib (MESH:C500026), tamoxifen (MESH:D013629), AC (MESH:D000186), duloxetine (MESH:D000068736), paclitaxel (MESH:D017239), doxorubicin/cyclophosphamide (MESH:C038334), Atezolizumab (MESH:C000594389), Abemaciclib (MESH:C000590451), pegylated liposomal doxorubicin (MESH:C506643), inavolisib (MESH:C000723546), bevacizumab (MESH:D000068258), octreotide (MESH:D015282), Elacestrant (MESH:C000626176), Fulvestrant (MESH:D000077267), vinorelbine (MESH:D000077235)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** N063H

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940007/full.md

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Source: https://tomesphere.com/paper/PMC12940007