| Literature DB >> 35312952 |
Diogo Alpuim Costa1,2, José Guilherme Gonçalves Nobre3, João Paulo Fernandes4, Marta Vaz Batista5, Ana Simas6, Carolina Sales7, Helena Gouveia8, Leonor Abreu Ribeiro4,9, Andreia Coelho10, Margarida Brito11,12, Mariana Inácio13, André Cruz14, Mónica Mariano15, Joana Savva-Bordalo16, Ricardo Fernandes17, André Oliveira18, Andreia Chaves4,5, Mário Fontes-Sousa4,12,19, Mafalda Sampaio-Alves20,21, Diogo Martins-Branco22, Noémia Afonso23.
Abstract
INTRODUCTION: Cancer care providers have faced many challenges in delivering safe care for patients during the COVID-19 pandemic. This cross-sectional survey-based study investigated the impact of the pandemic on clinical practices of Portuguese medical oncologists caring for patients with breast cancer.Entities:
Keywords: Breast cancer; COVID-19; Clinical practice; Patient management
Year: 2022 PMID: 35312952 PMCID: PMC8935098 DOI: 10.1007/s40487-022-00191-7
Source DB: PubMed Journal: Oncol Ther ISSN: 2366-1089
Demographics of respondents
| Parameter | |
|---|---|
| Age, years, | |
| < 40 | 74 (57.4) |
| 40–50 | 26 (20.2) |
| > 50 | 29 (22.5) |
| Sex, | |
| Male | 45 (34.9) |
| Female | 84 (65.1) |
| Regional health administration, | |
| Lisbon and Tagus Valley | 62 (48.1) |
| North | 33 (25.6) |
| Central | 9 (7.0) |
| Azores | 8 (6.2) |
| Algarve | 7 (5.4) |
| Alentejo | 6 (4.7) |
| Madeira | 4 (3.1) |
| Median duration of clinical practice (range), years | 5 (0–37) |
| Institution, | |
| Multidisciplinary team dedicated exclusively to breast cancer | 100 (77.5) |
| Multidisciplinary tumor board in breast cancer care | 127 (98.4) |
| Type of practice, | |
| Exclusively public | 84 (65.1) |
| Exclusively private | 21 (16.3) |
| Public and private | 24 (18.6) |
| Annual breast cancer cases, | |
| > 200 | 62 (48.1) |
| 100–200 | 44 (34.1) |
| 50–100 | 15 (11.6) |
| < 50 | 8 (6.2) |
| Multidisciplinary tumor board in breast cancer care | 127 (98.4) |
| Type of practice, | |
| Exclusively public | 84 (65.1) |
| Exclusively private | 21 (16.3) |
| Public and private | 24 (18.6) |
| Annual breast cancer cases, | |
| > 200 | 62 (48.1) |
| 100–200 | 44 (34.1) |
| 50–100 | 15 (11.6) |
| < 50 | 8 (6.2) |
aInstitutions could have both a multidisciplinary team dedicated exclusively to breast cancer and a multidisciplinary tumor board in breast cancer care
Impact of COVID-19 pandemic on (neo)adjuvant treatment of breast cancer
| Disease or treatment type | |
|---|---|
| Breast cancer ≥ 2 cm and/or node positive disease,a
| |
| Maintained neoadjuvant therapy | 129 (100.0) |
| Operable locally advanced breast cancer,b
| |
| Maintained neoadjuvant therapy | 82 (63.6) |
| Maintained adjuvant therapy | 28 (21.7) |
| Changed to adjuvant therapy | 12 (9.3) |
| Changed to neoadjuvant therapy | 7 (5.4) |
| Neoadjuvant hormone therapy or chemotherapyc due to the potentially more difficult access to surgery during the pandemic, | |
| Yes, with lower frequency | 1 (0.8) |
| Yes, with the same frequency | 17 (13.1) |
| Yes, with greater frequency | 54 (41.9) |
| No | 57 (44.2) |
| Preference for adjuvant short-term chemotherapy regimens,d
| |
| Maintained preference for chemotherapy without anthracyclines | 55 (42.6) |
| Changed preference to chemotherapy with anthracyclines | 1 (0.8) |
| Maintained preference for chemotherapy with anthracyclines | 59 (45.7) |
| Changed preference to chemotherapy without anthracyclines | 6 (4.7) |
| Do not generally prescribe short-term chemotherapy regimens | 8 (6.2) |
| Preferred taxanes regimen in the sequential scheme of chemotherapy, | |
| Maintained preference for weekly paclitaxel | 72 (55.8) |
| Changed preference to docetaxel q3w | 28 (21.7) |
| Maintained preference for docetaxel q3w | 15 (11.6) |
| Changed preference to weekly paclitaxel | 4 (3.1) |
| Other | 7 (7.8) |
| Maintained/changed preference to dose-dense paclitaxel | 5 (3.9) |
| Maintained/changed preference to paclitaxel q3w | 2 (1.6) |
| Preferred taxanes regimen associated with (dual) anti-HER2 blockade, | |
| Maintained preference for weekly paclitaxel | 72 (55.8) |
| Changed preference to docetaxel q3w | 21 (16.3) |
| Maintained preference for docetaxel q3w | 33 (25.6) |
| Changed preference to weekly docetaxel | 3 (2.3) |
| (Neo)adjuvant chemotherapy with anthracyclines (standard versus dose-dense),e
| |
| Maintained preference for standard regimen | 24 (18.6) |
| Changed preference to dose-dense regimen | 2 (1.6) |
| Maintained preference for dose-dense regimen | 89 (69.0) |
| Changed preference to standard regimen | 14 (10.8) |
| Neoadjuvant carboplatin,f
| |
| Yes, with lower frequency | 16 (12.4) |
| Yes, with the same frequency | 93 (72.1) |
| Yes, with greater frequency | 2 (1.5) |
| No | 18 (14.0) |
| Adjuvant capecitabine,f
| |
| Yes, with lower frequency | 6 (4.65) |
| Yes, with the same frequency | 106 (82.2) |
| Yes, with greater frequency | 6 (4.65) |
| No | 11 (8.5) |
HER2 human epidermal growth factor receptor 2, q3w every 3 weeks
aTriple-negative or HER2-positive disease
bLuminal B-like/HER2-negative disease
cNeoadjuvant in certain contexts (e.g., luminal A-like)
dIn patients with no relevant comorbidities
eTriple-negative and/or lymphatic disease-positive breast cancer
fTriple-negative disease
Impact of COVID-19 pandemic on treatment of metastatic breast cancer
| Disease or treatment type | |
|---|---|
| Triple-negative disease without visceral crisis, | |
| Maintained preference for single-agent chemotherapy | 91 (70.5) |
| Changed preference to combined regimen (i.e., polychemotherapy or chemoimmunotherapya) | 3 (2.3) |
| Maintained preference for combined regimen (i.e., polychemotherapy or chemoimmunotherapya) | 30 (23.3) |
| Changed preference to single-agent chemotherapy | 5 (3.9) |
| Triple-negative disease with visceral crisis, | |
| Maintained preference for single-agent chemotherapy | 44 (34.1) |
| Changed preference to combined regimen (i.e., polychemotherapy or chemoimmunotherapya) | 7 (5.4) |
| Maintained preference for combined regimen (i.e., polychemotherapy or chemoimmunotherapya) | 75 (58) |
| Changed preference to single-agent chemotherapy | 3 (2.3) |
| Oral versus IV chemotherapy (for the same agent), | |
| Maintained preference for oral administration | 69 (53.5) |
| Changed preference to IV administration | 2 (1.5) |
| Maintained preference for IV administration | 10 (7.8) |
| Changed preference to oral administration | 48 (37.2) |
| Metronomic chemotherapy,b
| |
| Yes, with lower frequency | 3 (2.3) |
| Yes, with the same frequency | 67 (51.9) |
| Yes, with greater frequency | 30 (23.3) |
| No | 29 (22.5) |
| Hormone receptor-positive disease, less aggressive,c
| |
| Maintained preference for hormone therapy alone | 43 (33.3) |
| Changed preference to hormone therapy combined with cyclin inhibitors | 4 (3.1) |
| Maintained preference for hormone therapy combined with cyclin inhibitors | 68 (52.7) |
| Changed preference to hormone therapy alone | 14 (10.9) |
| Hormone receptor-positive disease, more aggressive,d
| |
| Maintained preference for hormone therapy alone | 4 (3.1) |
| Changed preference to hormone therapy combined with cyclin inhibitors | 8 (6.2) |
| Maintained preference for hormone therapy combined with cyclin inhibitors | 117 (90.7) |
| Changed preference to hormone therapy alone | 0 (0) |
| Usual scheme of monitoring response and AEs in patients receiving cyclin inhibitors, | |
| Twice in 2 weeks for two cycles, then monthly | 92 (71.3) |
| Monthly | 35 (27.1) |
| Other | 2 (1.6) |
AEs adverse events, IV intravenous
aIf programmed death-ligand 1 ≥ 1%
bIn selected cases
cLess aggressive disease (e.g., older patients or patients with bone-only disease)
dMore aggressive disease (e.g., visceral disease)
Impact of COVID-19 pandemic on other aspects of breast cancer management
| Parameter | |
|---|---|
| Ovarian suppression, | |
| Prefer chemical over surgical | 68 (52.7) |
| Prefer replacement of monthly with a quarterly scheme | 65 (50.4) |
| Bisphosphonates (adjuvant treatment), | |
| Maintained preference for oral administration | 17 (13.2) |
| Changed preference to IV administration | 1 (0.8) |
| Maintained preference for IV administration | 81 (62.8) |
| Changed preference to oral administration | 21 (16.2) |
| Do not prescribe this type of drug in adjuvant treatment | 9 (7.0) |
| Bisphosphonates (metastatic treatment), | |
| Maintained preference for monthly scheme | 39 (30.2) |
| Changed preference to quarterly scheme | 53 (41.1) |
| Maintained preference for quarterly scheme | 37 (28.7) |
| Increased use of G-CSF/GM-CSF, | 68 (52.7) |
| Reduced use of corticosteroids, | 12 (9.3) |
| Early referral to palliative care, | |
| Yes, with lower frequency | 4 (3.1) |
| Yes, with the same preference | 95 (73.6) |
| Yes, with greater frequency | 14 (10.9) |
| No | 16 (12.4) |
| Reduced referral/inclusion in clinical trials, | 68 (52.7) |
| First-/second-generation platforms/signaturesa, | |
| Yes, with lower frequency | 2 (1.5) |
| Yes, with the same frequency | 101 (78.2) |
| Yes, with greater frequency | 15 (11.6) |
| No | 11 (8.5) |
| Genomic profiling of breast cancer, | |
| Yes, with lower frequency | 3 (2.3) |
| Yes, with the same frequency | 76 (58.9) |
| Yes, with greater frequency | 4 (3.1) |
| No | 46 (35.7) |
| Implementation of telemedicineb pre-COVID-19, | 12 (9.3) |
| Types of response/surveillance assessment appointments, | |
| Same frequency of face-to-face appointments | 17 (13.2) |
| Reduced use of face-to-face appointments and promotion of telemedicine | 102 (79.1) |
| Almost exclusively telemedicine | 8 (6.2) |
| Other | 2 (1.5) |
G-CSF granulocyte colony-stimulating factor, GM-CSF granulocyte–macrophage colony-stimulating factor, IV intravenous
aMammaPrint, Oncotype Dx, EndoPredict, Prosigna or Breast Cancer Index
bIn selected cases
| We wanted to investigate how clinical practices for breast cancer had changed in Portugal in response to the COVID-19 pandemic. |
| We performed this via an anonymous peer-reviewed online survey that was answered by 129 medical oncologists in Portugal. |
| Compared with pre-pandemic clinical practice, respondents reported a reduction in visits for new breast cancer diagnoses; increased use of telemedicine, oral formulations and metronomic regimens; and reduced use of dose-dense regimens. |
| Decision-making in the most aggressive forms of breast cancer, such as triple-negative disease, was largely unchanged by the pandemic. |
| It is not known whether changes in practice have affected breast cancer outcomes in Portugal. |