| Literature DB >> 34988767 |
Annie Tang1, Elad Neeman2, Brooke Vuong3, Vignesh A Arasu4, Raymond Liu2,5, Gillian E Kuehner6, Alison C Savitz7, Liisa L Lyon5, Prachi Anshu8, Samantha A Seaward9, Milan D Patel10, Laurel A Habel5, Lawrence H Kushi5, Margaret Mentakis3, Eva S Thomas11, Tatjana Kolevska12, Sharon B Chang13.
Abstract
PURPOSES: To delineate operational changes in Kaiser Permanente Northern California breast care and evaluate the impact of these changes during the initial COVID-19 Shelter-in-Place period (SiP, 3/17/20-5/17/20).Entities:
Keywords: Breast; COVID-19; Presentation; Telehealth; Treatment times
Mesh:
Year: 2022 PMID: 34988767 PMCID: PMC8731186 DOI: 10.1007/s10549-021-06468-1
Source DB: PubMed Journal: Breast Cancer Res Treat ISSN: 0167-6806 Impact factor: 4.624
Study Design
| Study design | Retrospective cohort |
|---|---|
| Participants | Patients newly diagnosed with breast cancer March 17-May 17, 2019 and March 17-May 17, 2020 |
| Data sources | • Institutional breast cancer tracking database • Electronic health records |
| Data collection | • Database queries • Chart review |
| Outcomes | • Patient characteristics • Tumor characteristics • Consultation type, timing • Treatment type, timing |
Retrospective cohort study comparing patients newly diagnosed with breast cancer March 17, 2019 – May 17, 2019 to patients diagnosed March 17, 2020 – May 17, 2020
KPNC Surgical and Medical Oncology Treatment Guidelines March 17, 2020 – May 17, 2020
| Specialty | Category | Patient/Cancer Characteristics | Recommendation |
|---|---|---|---|
| Surgical Oncology | High Priority Case – Delay may be associated with significant impact on patient outcomes | • Invasive Cancer – particularly if node-positive, triple-negative, HER2 + , locally advanced, recurrence, or lobular • Recent completion of neoadjuvant chemotherapy | Proceed with surgery |
| Intermediate Priority Case – Delay may be associated with minimal-moderate impact on patient outcomes | • Age ≥ 65 years, patients with comorbidities, low or intermediate-grade, T1, strongly ER + and Her2- invasive cancers • DCIS • Discordant breast biopsies or core biopsy showing ADH/atypical papilloma/radial scar/pleomorphic LCIS- weighing patient’s risk factors, imaging characteristics, and patient preference • Intraoperative radiotherapy cases | Consider postponing • Prior to postponing any invasive cancer, consider axillary ultrasound to document normal axillary lymph nodes • Consider proceeding with DCIS surgery if palpable DCIS and/or extensive breast involvement on imaging, high grade, ER-, or any concerns for undiagnosed invasive component • Consider discussing with medical oncology if there is a benefit to starting endocrine therapy | |
| Low Priority Case – Delay associated with low impact on patient outcome | • Benign breast lumps (Fibroadenoma, phyllodes, papilloma) • Nipple discharge • Prophylactic mastectomy | Cancel surgery | |
| Medical Oncology | General suggestions: •To reduce immunosuppressing patients and hospital visits overall (labs, infusions. etc.): avoid neoadjuvant therapy for patients with operable cancers •For premenopausal patients on monthly Lupron (to facilitate aromatase inhibitor use), would continue monthly (rather than every 3 months) or consider switching to tamoxifen without Lupron •For patients whose coverage requires coming in for GCSF injections, switch to Fulphilia (biosimilar for Neulasta). For those who self-administer, continue with Zarxio at home •Port flushes can be done every 3 months, rather than monthly •Zometa (adjuvant or metastatic) can be delayed 2 + months •Multigated acquisition (MUGA) scans that have been stable while on HER2 antibodies can be delayed several months. Important to do first MUGA after starting HER2 antibodies to ensure ejection fraction has not decreased. MUGAs should be kept on schedule for those with marginal ejection fractions | ||
| Adjuvant | ER + /HER2- | • Can start adjuvant endocrine therapy after surgery regardless of timing of radiation (i.e., can start prior to start of radiation treatment) • If surgery must be delayed, consider neoadjuvant endocrine therapy for selected patients • Carefully weigh pros/cons of chemotherapy for those for whom you would normally recommend it (e.g., node-positive, borderline or high Oncotype Dx scores) • Consider Oncotype Dx in all patients with 1–3 positive lymph nodes (carefully discussing lack of data in premenopausal patients) | |
| HER2 + | • Use HER2 antibodies/chemo after weighing risks/benefit • Consider adjuvant TDM-1 instead of weekly Herceptin/Taxol to reduce visits | ||
| Triple-negative | • Use chemotherapy after weighing risks/benefits • Can consider Taxol every 2 weeks instead of weekly to reduce visits, but would require GCSF, associated with more neuropathy, and weekly associated with much less immunosuppression | ||
| Metastatic | If asymptomatic, please consider delaying initiation of chemo | ||
| ER + /HER2- | • Consider endocrine therapy alone (not adding palbociclib) to avoid labs, visits, and neutropenia | ||
| HER2 + | • Consider HER2 antibodies alone (+ endocrine therapy if ER +) | ||
| Triple-negative | • Weigh risks/benefit of chemo | ||
HER2: human epidermal growth factor receptor 2; ER: estrogen receptor; ADH: atypical ductal hyperplasia; DCIS: ductal carcinoma in situ; LCIS: lobular carcinoma in situ; MUGA: multigated acquisition; GCSF: granulocyte colony-stimulating factor
Demographic and Clinical Characteristics of Patients Diagnosed with Breast Cancer March 17 – May 17, 2019 vs. March 17 – May 17, 2020
| Characteristic | 2019 ( | 2020 ( | |
|---|---|---|---|
| No (%) | No (%) | ||
| Age, years | 0.04 | ||
| < 40 | 25 (4) | 14 (6) | |
| 40–64 | 373 (53) | 147 (60) | |
| ≥ 65 | 305 (43) | 86 (35) | |
| Race | 0.37 | ||
| White | 386 (55) | 143 (58) | |
| Asian | 143 (20) | 41 (17) | |
| Hispanic | 100 (14) | 29 (12) | |
| Black | 44 (6) | 19 (8) | |
| Other/Unknown | 30 (4) | 15 (6) | |
| BMI, | 0.63 | ||
| Obese (BMI ≥ 30) | 268 (38) | 90 (36) | |
| Charlson Comorbidity Index | 0.73 | ||
| Greater than 3 | 88 (12) | 33 (13) | |
| Genetic Mutation | 24 (3) | 15 (6) | 0.07 |
| Detection Method | < 0.001 | ||
| Screening Mammogram | 440 (63) | 54 (22) | |
| Symptomatic | 263 (37) | 193 (78) | |
| Histology | 0.16 | ||
| DCIS | 95 (14) | 21 (9) | |
| IDC | 489 (70) | 184 (75) | |
| ILC | 64 (9) | 26 (11) | |
| Other | 55 (8) | 16 (7) | |
| T Stage | 0.02 | ||
| Tis | 95 (14) | 21 (9) | |
| T1mi | 16 (2) | 6 (2) | |
| T1a | 46 (7) | 7 (3) | |
| T1b | 90 (13) | 19 (8) | |
| T1c | 177 (25) | 66 (27) | |
| T2 | 217 (31) | 98 (40) | |
| T3 | 37 (5) | 18 (7) | |
| T4 | 21 (3) | 10 (4) | |
| Tx/T0 | 4 (0) | 2 (1) | |
| ≥ T1c | 452 (64) | 192 (78) | < 0.001 |
| N Stageb | 0.88 | ||
| N1 | 125 (69) | 60 (68) | |
| N1m | 20 (11) | 8 (9) | |
| N2 | 14 (8) | 9 (10) | |
| N3 | 21 (12) | 11 (13) | |
| M Stage | 0.001 | ||
| M0 | 685 (97) | 227 (92) | |
| M1 | 17 (2) | 18 (7) | |
| Mx | 1 (0) | 2 (1) | |
| Invasive Cancer | 608 (87) | 229 (91) | 0.03 |
| Grade | 0.004 | ||
| 1 | 166 (27) | 44 (20) | |
| 2 | 277 (46) | 95 (42) | |
| 3 | 149 (25) | 83 (37) | |
| Unknown | 16 (3) | 4 (2) | |
| Receptor Status | 0.04 | ||
| HR + /HER2- | 460 (76) | 150 (67) | |
| HR + /HER2 + | 55 (9) | 29 (13) | |
| HR-/HER2 + | 28 (5) | 9 (4) | |
| HR-/HER2- | 59 (10) | 35 (16) | |
| Unknown | 4 (1) | 2 (1) |
BMI: Body Mass Index; DCIS: Ductal Carcinoma In Situ; IDC: Invasive Ductal Carcinoma; ILC: Invasive Lobular Carcinoma; HR: Hormone Receptor; HER2: Herceptin Epidermal Growth Factor Receptor 2
aChi-square or Fisher’s exact test
bTotal n = 268
Initial New Physician Consultation Types and Timing by Specialty, for Patients Diagnosed with Breast Cancer March 17 – May 17, 2019 vs. March 17 – May 17, 2020
| Type of Visit | Total Visits, No. (%) | Median Days to Consultation (IQR) | ||||
|---|---|---|---|---|---|---|
| 2019 | 2020 | 2019 | 2020 | |||
| All Patients | < 0.001 | N/A | ||||
| Office Visits | 822 (99.2%) | 92 (29.6%) | N/A | N/A | ||
| Telehealth Visits | 7 (0.8%) | 219 (70.4%) | N/A | N/A | ||
| Video Visits | 1 (0.1%) | 130 (41.8%) | N/A | N/A | ||
| Telephone Visits | 6 (0.7%) | 88 (28.3) | N/A | N/A | ||
| Surgical Oncology Firstb | < 0.001 | 11 (8–13) | 7(6–11) | < 0.001 | ||
| Office Visits | 553 (100%) | 71 (42.0%) | 11 (8–13) | 9 (7–12) | 0.12 | |
| Telehealth Visits | 0 (0%) | 98 (58.0%) | N/A | 7 (5–9.25) | N/A | |
| Video Visits | 0 (0%) | 57 (33.7%) | N/A | 7 (5.5–10) | N/A | |
| Telephone Visits | 0 (0%) | 41 (24.3%) | N/A | 7 (4–9) | N/A | |
| All Medical Oncologyc | < 0.001 | N/A | ||||
| Office Visits | 269 (97.5%) | 21 (14.9%) | N/A | N/A | ||
| Telehealth Visits | 7 (2.5%) | 120 (85.1%) | N/A | N/A | ||
| Video Visits | 1 (0.4%) | 73 (51.8%) | N/A | N/A | ||
| Telephone Visits | 6 (2.2%) | 47 (33.3%) | N/A | N/A | ||
| Neoadjuvant Medical Oncologyd | < 0.001 | 13.5 (10.5–21) | 12 (7–15) | 0.19 | ||
| Office Visits | 93 (98.9%) | 18 (28.6%) | 14 (11–21) | 9.5 (6.75–14.0) | 0.28 | |
| Telehealth Visits | 1 (1%) | 45 (71.4%) | N/A | 12 (8–17) | N/A | |
| Video Visits | 1 (1%) | 23 (35.9%) | N/A | 10 (7–13) | N/A | |
| Telephone Visits | 0 (0%) | 22 (34.4%) | N/A | 15 (10–20.5) | N/A | |
| Adjuvant Medical Oncologye | < 0.001 | 15 (10–21) | 13 (8–19) | 0.01 | ||
| Office Visits | 176 (96.7%) | 3 (3.8%) | 15 (10.25–21) | 13 (13–16) | 0.95 | |
| Telehealth Visits | 6 (3.3%) | 75 (96.2%) | 12.5 (7.75–21.5) | 13 (8–19) | 0.89 | |
| Video Visits | 0 (0%) | 50 (64.1%) | N/A | 14 (9–21) | N/A | |
| Telephone Visits | 6 (3.3%) | 25 (32.1%) | 12.5 (7.75–21.5) | 11 (7–14) | 0.71 | |
N/A: not applicable
aChi-square or Fisher’s exact test for categorical variables, Wilcoxon rank-sum test for continuous variables
bPatients who had surgery first including those who had adjuvant chemotherapy and excluding those who were previously followed by surgery prior to cancer diagnosis, Total n = 722
cTotal = 417
dPatients who had either chemotherapy or endocrine therapy first, Total n = 157
eTotal n = 261
First Treatment Type and Treatment Timing for Patients Diagnosed with Breast Cancer March 17 – May 17, 2019 vs. March 17 – May 17, 2020
| 2019 ( | 2020 ( | ||
|---|---|---|---|
| No. (%) | No. (%) | ||
| First treatment type | < 0.001 | ||
| Surgery | 583 (83) | 176 (71) | |
| Neoadjuvant Chemotherapy | 75 (11) | 40 (16) | |
| Neoadjuvant HT | 3 (0) | 14 (6) | |
| Palliative Endocrine | 20 (3) | 10 (4) | |
| No treatment | 22 (3) | 7 (3) | |
| Breast operationsb | 0.02 | ||
| Partial Mastectomy | 441 (76) | 117 (67) | |
| Mastectomy | 139 (24) | 57 (33) | |
| Lymph node operationsc | 0.69 | ||
| ALND | 123 (23) | 39 (24) | |
| SLNB | 422 (77) | 123 (76) | |
| First treatment timing | |||
| Time to Surgeryd: median days (IQR) | 26 (20 – 36) | 19 (14 – 27) | < 0.001 |
| Time to Neoadjuvant Chemotherapye: median days (IQR) | 28 (21 – 32) | 23 (18 – 28) | 0.03 |
| Time to Adjuvant Chemotherapyf: median days (IQR) | 37 (30 – 48) | 34 (29 – 44) | 0.10 |
HT: Hormone therapy; ALND: Axillary Lymph Node Dissection; SLNB: Sentinel Lymph Node Biopsy; IQR: Interquartile range
aChi-square or Wilcoxon rank-sum tests
bTotal n = 754; cTotal n = 707
dTotal n = 759
eTotal n = 103
fTotal n = 261
Fig. 1Summary of KPNC Breast Care Operational Changes During the Initial SiP Period (March 17, 2020 – May 17, 2020) and Clinical Impact. Abbreviations: KPNC: Kaiser Permanente Northern California; SiP: Shelter in Place