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  • Medicine  (5)
  • XA 52760  (5)
  • 1
    Online Resource
    Online Resource
    American Society of Clinical Oncology (ASCO) ; 2021
    In:  Journal of Clinical Oncology Vol. 39, No. 15_suppl ( 2021-05-20), p. e21571-e21571
    In: Journal of Clinical Oncology, American Society of Clinical Oncology (ASCO), Vol. 39, No. 15_suppl ( 2021-05-20), p. e21571-e21571
    Abstract: e21571 Background: Delay in surgical resection has been found to be associated with poorer overall survival (OS) in patients with stage 1 cutaneous melanoma. However, the impact of surgical timing on survival in stage 3 cutaneous melanoma remains unknown, especially in the era of immunotherapy. We sought to evaluate to the effect of time to definitive surgical intervention on OS in stage 3 cutaneous melanoma at Commission on Cancer accredited institutions. Methods: The National Cancer Database (2012-2016) was used to identify patients who underwent biopsy and definitive surgical intervention of cutaneous melanoma. Time to intervention (TTI) was analyzed from the time of initial biopsy to definitive surgical resection and classified into quartiles, (Q1≤22 days; Q2 = 23-33 days; Q3 = 34-49 days; Q4≥50 days) using χ2 and multivariable logistic regression. Survival was analyzed using Kaplan-Meier and Cox proportional hazard models. Results: We analyzed 4560 patients with a median age of 61 years (18-90) and most patients being non-Hispanic white and male (91.6% and 63%, respectively). Median Breslow thickness was 2.8 mm (0-9.8 mm). Median TTI was 33 days (0-352 days) with a mean OS of 52, 49.8, 48.4, 48.3 months for Q1 to Q4 respectively (p = 0.008). Age ≤50 years, treatment at a comprehensive community cancer center and only 1 positive lymph node (LN) were all associated with Q1 TTI (p = 0.002, p 〈 0.001 and p 〈 0.001, respectively). Black race, treatment at an academic facility, 〉 4 LN positive, 〉 4 mm thickness, and no administration of immunotherapy were all associated with Q4 TTI (p = 0.002, p 〈 0.0001, p 〈 0.0001, p 〈 0.0001 and p 〈 0.0001 respectively) on univariate analysis. Patients in Q4 TTI were more likely to be older (OR 1.01, 95% CI 1.00-1.02, p = 0.01), have T2-T4 tumors (OR 1.6, 95% CI 1.2-2.2, p 〈 0.001), and be treated at an academic facility (OR 2.4, 95% CI 1.8-3.5, p 〈 0.001) on multivariable analysis. In the survival analysis, multiple positive LNs (2, 3-4, 〉 4 LNs; HR 1.4, 1.6 and 2.9, p 〈 0.001), lymphovascular invasion (HR 1.4, p 〈 0.001), Breslow thickness 〉 4 mm (HR 1.7, p 〈 0.001), Charlson-Deyo score ≥2 (HR 1.5, p 〈 0.001), increasing age (HR 1.03, p 〈 0.001), and longer TTI (Q3-Q4) (HR 1.2, p = 0.001) were all associated with worse OS. There was no difference in survival based on TTI in patients who had received adjuvant immunotherapy in Q1-Q2 vs Q3-Q4 (p = 0.3). Conclusions: In stage 3 cutaneous melanoma, longer TTI ( 〉 33 days) was associated with worse OS but may be due to older age, higher T stage, and barriers to access. However, adjuvant immunotherapy may offer protection from delays in definitive surgery.
    Type of Medium: Online Resource
    ISSN: 0732-183X , 1527-7755
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Clinical Oncology (ASCO)
    Publication Date: 2021
    detail.hit.zdb_id: 2005181-5
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  • 2
    In: Journal of Clinical Oncology, American Society of Clinical Oncology (ASCO), Vol. 32, No. 15_suppl ( 2014-05-20), p. e19098-e19098
    Type of Medium: Online Resource
    ISSN: 0732-183X , 1527-7755
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Clinical Oncology (ASCO)
    Publication Date: 2014
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  • 3
    In: Journal of Clinical Oncology, American Society of Clinical Oncology (ASCO), Vol. 39, No. 1 ( 2021-01-01), p. 66-78
    Abstract: As cancer surgery restarts after the first COVID-19 wave, health care providers urgently require data to determine where elective surgery is best performed. This study aimed to determine whether COVID-19–free surgical pathways were associated with lower postoperative pulmonary complication rates compared with hospitals with no defined pathway. PATIENTS AND METHODS This international, multicenter cohort study included patients who underwent elective surgery for 10 solid cancer types without preoperative suspicion of SARS-CoV-2. Participating hospitals included patients from local emergence of SARS-CoV-2 until April 19, 2020. At the time of surgery, hospitals were defined as having a COVID-19–free surgical pathway (complete segregation of the operating theater, critical care, and inpatient ward areas) or no defined pathway (incomplete or no segregation, areas shared with patients with COVID-19). The primary outcome was 30-day postoperative pulmonary complications (pneumonia, acute respiratory distress syndrome, unexpected ventilation). RESULTS Of 9,171 patients from 447 hospitals in 55 countries, 2,481 were operated on in COVID-19–free surgical pathways. Patients who underwent surgery within COVID-19–free surgical pathways were younger with fewer comorbidities than those in hospitals with no defined pathway but with similar proportions of major surgery. After adjustment, pulmonary complication rates were lower with COVID-19–free surgical pathways (2.2% v 4.9%; adjusted odds ratio [aOR], 0.62; 95% CI, 0.44 to 0.86). This was consistent in sensitivity analyses for low-risk patients (American Society of Anesthesiologists grade 1/2), propensity score–matched models, and patients with negative SARS-CoV-2 preoperative tests. The postoperative SARS-CoV-2 infection rate was also lower in COVID-19–free surgical pathways (2.1% v 3.6%; aOR, 0.53; 95% CI, 0.36 to 0.76). CONCLUSION Within available resources, dedicated COVID-19–free surgical pathways should be established to provide safe elective cancer surgery during current and before future SARS-CoV-2 outbreaks.
    Type of Medium: Online Resource
    ISSN: 0732-183X , 1527-7755
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Clinical Oncology (ASCO)
    Publication Date: 2021
    detail.hit.zdb_id: 2005181-5
    Location Call Number Limitation Availability
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  • 4
    In: Journal of Clinical Oncology, American Society of Clinical Oncology (ASCO)
    Abstract: Patients with isolated distal deep vein thrombosis (DVT) have lower rates of adverse outcomes (death, venous thromboembolism [VTE] recurrence or major bleeding) than those with proximal DVT. It is uncertain if such findings are also observed in patients with cancer. METHODS Using data from the international Registro Informatizado de la Enfermedad TromboEmbolica venosa registry, we compared the risks of adverse outcomes at 90 days (adjusted odds ratio [aOR]; 95% CI) and 1 year (adjusted hazard ratio [aHR; 95% CI] ) in 886 patients with cancer-associated distal DVT versus 5,196 patients with cancer-associated proximal DVT and 5,974 patients with non–cancer-associated distal DVT. RESULTS More than 90% of patients in each group were treated with anticoagulants for at least 90 days. At 90 days, the adjusted risks of death, VTE recurrence, or major bleeding were lower in patients with non–cancer-associated distal DVT than in patients with cancer-associated distal DVT (reference): aOR = 0.16 (0.11-0.22), aOR = 0.34 (0.22-0.54), and aOR = 0.47 (0.27-0.80), respectively. The results were similar at 1-year follow-up: aHR = 0.12 (0.09-0.15), aHR = 0.39 (0.28-0.55), and aHR = 0.51 (0.32-0.82), respectively. Risks of death, VTE recurrence, and major bleeding were not statistically different between patients with cancer-associated proximal versus distal DVT, both at 90 days: aOR = 1.11 (0.91-1.36), aOR = 1.10 (0.76-1.62), and aOR = 1.18 (0.76-1.83), respectively, and 1 year: aHR = 1.01 (0.89-1.15), aHR = 1.02 (0.76-1.35), and aHR = 1.10 (0.76-1.61), respectively. However, more patients with cancer-associated proximal DVT, compared with cancer-associated distal DVT, developed fatal pulmonary embolism (PE) during follow-up: The risk difference was 0.40% (95% CI, 0.23 to 0.58). CONCLUSION Cancer-associated distal DVT has serious and relatively comparable outcomes compared with cancer-associated proximal DVT. The lower risk of fatal PE from cancer-associated distal DVT needs further investigation.
    Type of Medium: Online Resource
    ISSN: 0732-183X , 1527-7755
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Clinical Oncology (ASCO)
    Publication Date: 2023
    detail.hit.zdb_id: 2005181-5
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  • 5
    In: Journal of Clinical Oncology, American Society of Clinical Oncology (ASCO), Vol. 41, No. 16_suppl ( 2023-06-01), p. 7010-7010
    Abstract: 7010 Background: Clonal hematopoiesis (CH) of indeterminate potential (CHIP) is found in healthy populations as well as cancer patients (pts) and is associated with (w/) cardiovascular disease (CVD), risk of hematologic neoplasms (HN), and all-cause mortality. Germline variants (var) predispose to CHIP. However, described var are nonspecific to solid tumor pts. Identifying CHIP risk factors and mitigation strategies is paramount for improving outcomes. Methods: Pts in breast (BC) and head & neck cancer (HNC) survivorship (2020-2023) following curative treatment (tx) were eligible for our 10 year (yr) prospective study of annual next generation sequencing (NGS) and complete blood count (CBC) to identify CHIP. Mutations (mt) were classified as clinically significant (CS) or var of unknown significance (VUS), and as CH (med. VAF 4.7%) or potentially germline (PG; med. VAF 50%). Pts w/ CHIP were managed in both CHIP Clinic (CC) and Preventive Cardiology (PC) for monitoring and CVD reduction. Fisher’s exact and ANOVA tests were used for analyses. Results: Of 168 pts enrolled (117 BC, 51 HNC), 158 had NGS: 73 yr 1, 85 through yr 2 or 3; 22 pts received chemotherapy (CT), 49 radiation therapy (RT), 72 CT & RT (CRT). Sixty-eight pts (43%) had a mt; 21 (13%) had CHIP (6 w/ PG VUS). CHIP was found to be associated w/ older age (69 vs. 58, p= 0.0002). The most common CHIP mt were DNMT3A (n = 11), PPM1D (6), TET2 (6), JAK2 a nd TP53 (2). Two pts without yr 1 mt developed CHIP in yr 2. For PPM1D, 2 PG VUS were point mt from DNA transitions while 6 CHIP were truncating from transversions and deletions. All pts w/ PPM1D had RT (7/8 CRT), suggesting a molecular signature which varies from transition-driven aging. Six pts had thrombocytopenia (TP), 3 w/ PPM1D CHIP. TP was more common in CHIP (OR 11, p= 0.0356) and PPM1D (OR 29, p= 0.0016). In this cohort, anemia was not seen in pts w/ CHIP ( p= 0.048). Normal CBC was 6x less common in pts w/ CRT ( p= 2.3x10 -7 ). Seven CHIP pts were seen by PC; 4 had yr 2 NGS following PC visit. All pts had addition of new/dose escalation of current CVD medication. Two CHIP pts had stable NGS; 2 CHIP & PG VUS pts had clonal changes including mt disappearance and acquisition. Of note, the PG VUS’s were assessed for institutional incidence in 3,918 HN pts w/ NGS data and in Mastermind (MM) for frequency of occurrence in published literature. Sixteen PG VUS (40%) occurred at our institution (13 found in MM, 7 classified as rare (avg gnomAD MAF 6x10 -4 )) and associated w/ HN, notably TET2 (n = 3). Conclusions: This ongoing prospective study is one of the largest to report characteristics and outcomes of CHIP pts in CC/PC and is expected to accrue more in expansion. We anticipate highlighting risk factors for CHIP progression and report novel PG VUS, which may portend health risks based on their prevalence in HN. Furthermore, it appears that a strategy for CVD prevention may promote clonal stability in survivorship pts.
    Type of Medium: Online Resource
    ISSN: 0732-183X , 1527-7755
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Clinical Oncology (ASCO)
    Publication Date: 2023
    detail.hit.zdb_id: 2005181-5
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