| Literature DB >> 32715776 |
Hagar Elghazawy1, Joaira Bakkach2, Mohamed S Zaghloul3, Atlal Abusanad4, Mariam Mohamed Hussein1, Mohamed Alorabi1, Nermean Bahie Eldin1, Thanaa Helal5, Tarek M Zaghloul6, Bhanu Prasad Venkatesulu7, Hesham Elghazaly1, Sana Al-Sukhun8.
Abstract
Breast cancer is the most common malignancy among women worldwide. The current COVID-19 pandemic represents an unprecedented challenge leading to care disruption, which is more severe in low- and middle-income countries (LMIC) due to existing economic obstacles. This review presents the global perspective and preparedness plans for breast cancer continuum of care amid the COVID-19 outbreak and discusses challenges faced by LMIC in implementing these strategies. Prioritization and triage of breast cancer patients in a multidisciplinary team setting are of paramount importance. Deescalation of systemic and radiation therapy can be utilized safely in selected clinical scenarios. The presence of a framework and resource-adapted recommendations exploiting available evidence-based data with judicious personalized use of current resources is essential for breast cancer care in LMIC during the COVID-19 pandemic.Entities:
Keywords: COVID-19; SARS-CoV-2; breast cancer; coronavirus; low- and middle-income countries; pandemic
Year: 2020 PMID: 32715776 PMCID: PMC7386379 DOI: 10.2217/fon-2020-0574
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404
Tailored recommendations for systemic therapy in breast cancer patients during the COVID-19 pandemic according to treatment setting.
| Treatment setting | Recommendations | Notes | Ref. |
|---|---|---|---|
| Neo/adjuvant setting | Chemotherapy should be administered for 12–24 weeks (four–eight cycles) | Phase III trial showed that 5-FU fails to improve the efficacy of ANT-based regimens and increases toxicity | [ |
| Metastatic setting | Consider modification of chemotherapy schedules to reduce clinical visits (3 weeks dosing instead of weekly when appropriate) | [ |
AC: Adriamycin and cyclophosphamide; ANT: Anthracyclines; BC: Breast cancer; CMF: Cyclophosphamide, methotrexate, fluorouracil; DCIS: Ductal carcinoma in situ; DM1: Ado-trastuzumab emtansine; EC: Epirubicin, cyclophosphamide; ER: Estrogen receptor; LCIS: Lobular carcinoma in situ; LHRH: Luteinizing-hormone releasing hormone; PD-L1: Programmed death-ligand 1; TNBC: Triple-negative breast cancer; 5-FU: 5-fluorouracil.
Tailored recommendations for systemic therapy in breast cancer patients during the COVID-19 pandemic according to tumor biology.
| Breast cancer biology | Recommendations | Notes | Ref. |
|---|---|---|---|
| Atypical hyperplasia− | Effectively treated with either tamoxifen or aromatase inhibitors | [ | |
| Low-risk luminal BC (stage I–II, ER+/HER2−, low-grade, lobular BC, oncotype score <25, luminal A signature) | Consider neoadjuvant endocrinal treatment for 6–12 months or till maximum response | These low-risk patients do not usually benefit from chemotherapy | [ |
| Premenopausal BC patients who are planned for LHRH agonists | Consider applying /3 months dosing, to reduce patient visits | [ | |
| Non-metastatic HER2+ BC | Should be treated with chemotherapy and anti-HER2 therapy | Anti-HER2 agents (trastuzumab and pertuzumab) should be safe to use; they are unlikely to affect immune function | [ |
| TNBC | Platinum should not be used routinely in the adjuvant setting | Close monitoring for specific symptoms of infection or pneumonitis | [ |
| Metastatic HER2+ BC patients | Consider early introduction of anti-HER2 agents (e.g., pertuzumab/trastuzumab) | This is more likely to improve outcomes without impact | [ |
| Metastatic ER+HER2− BC patients | Consider delaying adding CDK4/6, mTOR, or PIK3CA inhibitors to endocrine therapy, especially in elderly patients with comorbidities, in the following situations: | Use of these agents must be weighed against the increased risk of adverse events (e.g., neutropenia, pneumonitis) | [ |
AC: Adriamycin and cyclophosphamide; ANT: Anthracyclines; BC: Breast cancer; CMF: Cyclophosphamide, methotrexate, fluorouracil; DCIS: Ductal carcinoma in situ; DM1: Ado-trastuzumab emtansine; EC: Epirubicin, cyclophosphamide; ER: Estrogen receptor; LCIS: Lobular carcinoma in situ; LHRH: Luteinizing-hormone releasing hormone; PD-L1: Programmed death-ligand 1; TNBC: Triple-negative breast cancer; 5-FU: 5-fluorouracil.
Tailored recommendations for radiation therapy techniques in breast cancer patients during the COVID-19 pandemic.
| Breast cancer population/setting | Recommendations | Notes | Ref. |
|---|---|---|---|
| Partial breast irradiation (EBRT) | For appropriate patients (ASTRO criteria) | High-level evidence supports equal or superior survival versus WBRT | [ |
| Partial breast irradiation (IORT) | For appropriate patients (ASTRO criteria) | [ | |
| WBRT +/- regional lymph nodes | • Hypofractionation: | High level evidence supports long-term efficacy and safety | [ |
| Chest wall +/- regional lymph nodes | 2.67 Gy/15 Fr, daily, 3DCRT | No difference in efficacy or toxicity versus conventional RT | [ |
| Deep inspiratory breath hold techniques | Avoid active breathing control due to risk of aerosol contamination | [ | |
| Brain metastasis | SRS (15 Gy/1 Fr) for 1–3 metastases, good KPS, no extracranial disease. | No confirmed survival benefit versus observation | [ |
| Bone metastasis | With or without cord compression: 8 Gy/1 Fr | No survival difference between different fractionations; controversy in pain flare | [ |
BID: Twice a day; EBRT: External beam radiotherapy; Fr: Fraction; IMRT: Intensity modulated radiotherapy; IORT: Intraoperative radiotherapy; KPS: Karnofsky Performance Status; RT: Radiotherapy; SRS: Stereotactic radiosurgery; WBRT: Whole breast radiotherapy; 3DCRT: 3D conformal radiotherapy.