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  1. AU="Lawless, Aleigha R"
  2. AU="Mora-Ríos, Félix Gustavo"

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  1. Article ; Online: MAESTRO-Pool Enables Highly Parallel and Specific Mutation-Enrichment Sequencing for Minimal Residual Disease Detection in Cohort Studies.

    Blewett, Timothy / Rhoades, Justin / Liu, Ruolin / Xiong, Kan / Sridhar, Sainetra / Crnjac, Andjela / Cheng, Ju / Lawless, Aleigha R / Frederick, Dennie T / Flaherty, Keith T / Makrigiorgos, Gerassimos Mike / Adalsteinsson, Viktor A

    Clinical chemistry

    2023  Volume 70, Issue 2, Page(s) 434–443

    Abstract: Background: Tracing patient-specific tumor mutations in cell-free DNA (cfDNA) for minimal residual disease (MRD) detection is promising but challenging. Assaying more mutations and cfDNA stands to improve MRD detection but requires highly accurate, ... ...

    Abstract Background: Tracing patient-specific tumor mutations in cell-free DNA (cfDNA) for minimal residual disease (MRD) detection is promising but challenging. Assaying more mutations and cfDNA stands to improve MRD detection but requires highly accurate, efficient sequencing methods and proper calibration to prevent false detection with bespoke tests.
    Methods: MAESTRO (Minor Allele Enriched Sequencing Through Recognition Oligonucleotides) uses mutation-specific oligonucleotide probes to enrich cfDNA libraries for tumor mutations and enable their accurate detection with minimal sequencing. A new approach, MAESTRO-Pool, which entails pooling MAESTRO probes for all patients and applying these to all samples from all patients, was used to screen for 22 333 tumor mutations from 9 melanoma patients in 98 plasma samples. This enabled quantification of MRD detection in patient-matched samples and false detection in unmatched samples from other patients. To detect MRD, a new dynamic MRD caller was used that computes a probability for MRD detection based on the number of mutations and cfDNA molecules sequenced, thereby calibrating for variations in each bespoke test.
    Results: MAESTRO-Pool enabled sensitive detection of MRD down to 0.78 parts per million (ppm), reflecting a 10- to 100-fold improvement over existing tests. Of the 8 MRD positive samples with ultra-low tumor fractions <10 ppm, 7 were either in upward-trend preceding recurrence or downward-trend aligning with response. Of 784 patient-unmatched tests, only one was found as MRD positive (tumor fraction = 2.7 ppm), suggesting high specificity.
    Conclusions: MAESTRO-Pool enables massively parallel, tumor-informed MRD testing with concurrent benchmarking of bespoke MRD tests. Meanwhile, our new MRD caller enables more mutations and cfDNA molecules to be tested without compromising specificity. These improve the ability for detecting traces of MRD from blood.
    MeSH term(s) Humans ; Neoplasm, Residual/genetics ; High-Throughput Nucleotide Sequencing/methods ; Cohort Studies ; Cell-Free Nucleic Acids ; Mutation
    Chemical Substances Cell-Free Nucleic Acids
    Language English
    Publishing date 2023-12-08
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 80102-1
    ISSN 1530-8561 ; 0009-9147
    ISSN (online) 1530-8561
    ISSN 0009-9147
    DOI 10.1093/clinchem/hvad203
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Benefit, recurrence pattern, and toxicity to adjuvant anti-PD-1 monotherapy varies by ethnicity and melanoma subtype: An international multicenter cohort study.

    Bai, Xue / Lawless, Aleigha R / Czapla, Juliane A / Gerstberger, Stefanie C / Park, Benjamin C / Jung, Seungyeon / Johnson, Rebecca / Yamazaki, Naoya / Ogata, Dai / Umeda, Yoshiyasu / Li, Caili / Guo, Jun / Flaherty, Keith T / Nakamura, Yasuhiro / Namikawa, Kenjiro / Long, Georgina V / Menzies, Alexander M / Johnson, Douglas B / Sullivan, Ryan J /
    Boland, Genevieve M / Si, Lu

    JAAD international

    2024  Volume 15, Page(s) 105–114

    Abstract: Background: Anti-Program-Death-1 (PD-1) is a standard adjuvant therapy for patients with resected melanoma. We hypothesized that there are discrepancies in survival, recurrence pattern and toxicity to adjuvant PD-1 between different ethnicities and ... ...

    Abstract Background: Anti-Program-Death-1 (PD-1) is a standard adjuvant therapy for patients with resected melanoma. We hypothesized that there are discrepancies in survival, recurrence pattern and toxicity to adjuvant PD-1 between different ethnicities and melanoma subtypes.
    Objective: We performed a multicenter cohort study incorporating 6 independent institutions in Australia, China, Japan, and the United States. The primary outcomes were recurrence free survival (RFS) and overall survival (OS). Secondary outcomes were disease recurrence patterns and toxicities.
    Results: In total 534 patients were included. East-Asian/Hispanic/African reported significantly poorer RFS/OS. Nonacral cutaneous or melanoma of unknown primary reported the best RFS/OS, followed by acral, and mucosal was the poorest. Within the nonacral cutaneous or melanoma of unknown primary subtypes, East-Asian/Hispanic/African reported significantly poorer RFS/OS than Caucasian. In the multivariate analysis incorporating ethnicity/melanoma-subtype/age/sex/stage/lactate dehydrogenase/BRAF (v-Raf murine sarcoma viral oncogene homolog B)-mutation/adjuvant radiotherapy, East-Asian/Hispanic/African had independently significantly poorer outcomes (RFS: HR, 1.71; 95% CI, 1.19-2.44 and OS: HR, 2.34; 95% CI, 1.39-3.95), as was mucosal subtype (RFS: HR, 3.25; 95% CI, 2.04-5.17 and OS: HR, 3.20; 95% CI, 1.68-6.08). Mucosal melanoma was an independent risk factor for distant metastasis, especially liver metastasis. East-Asian/Hispanic/African had significantly lower incidence of gastrointestinal/musculoskeletal/respiratory/other-rare-type-toxicities; but higher incidences of liver toxicities.
    Limitations: A retrospective study.
    Conclusions: Ethnicity and melanoma subtype are associated with survival and recurrence pattern in melanoma patients treated with adjuvant anti-PD-1. Toxicity profile differs by ethnicity and may require a precision toxicity surveillance strategy.
    Language English
    Publishing date 2024-01-19
    Publishing country United States
    Document type Journal Article
    ISSN 2666-3287
    ISSN (online) 2666-3287
    DOI 10.1016/j.jdin.2023.11.014
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Dabrafenib plus trametinib versus anti-PD-1 monotherapy as adjuvant therapy in

    Bai, Xue / Shaheen, Ahmed / Grieco, Charlotte / d'Arienzo, Paolo D / Mina, Florentia / Czapla, Juliane A / Lawless, Aleigha R / Bongiovanni, Eleonora / Santaniello, Umberto / Zappi, Helena / Dulak, Dominika / Williamson, Andrew / Lee, Rebecca / Gupta, Avinash / Li, Caili / Si, Lu / Ubaldi, Martina / Yamazaki, Naoya / Ogata, Dai /
    Johnson, Rebecca / Park, Benjamin C / Jung, Seungyeon / Madonna, Gabriele / Hochherz, Juliane / Umeda, Yoshiyasu / Nakamura, Yasuhiro / Gebhardt, Christoffer / Festino, Lucia / Capone, Mariaelena / Ascierto, Paolo Antonio / Johnson, Douglas B / Lo, Serigne N / Long, Georgina V / Menzies, Alexander M / Namikawa, Kenjiro / Mandala, Mario / Guo, Jun / Lorigan, Paul / Najjar, Yana G / Haydon, Andrew / Quaglino, Pietro / Boland, Genevieve M / Sullivan, Ryan J / Furness, Andrew J S / Plummer, Ruth / Flaherty, Keith T

    EClinicalMedicine

    2024  Volume 71, Page(s) 102564

    Language English
    Publishing date 2024-03-27
    Publishing country England
    Document type Journal Article ; Published Erratum
    ISSN 2589-5370
    ISSN (online) 2589-5370
    DOI 10.1016/j.eclinm.2024.102564
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Disrupting CD38-driven T cell dysfunction restores sensitivity to cancer immunotherapy.

    Revach, Or-Yam / Cicerchia, Angelina M / Shorer, Ofir / Petrova, Boryana / Anderson, Seth / Park, Joshua / Chen, Lee / Mehta, Arnav / Wright, Samuel J / McNamee, Niamh / Tal-Mason, Aya / Cattaneo, Giulia / Tiwari, Payal / Xie, Hongyan / Sweere, Johanna M / Cheng, Li-Chun / Sigal, Natalia / Enrico, Elizabeth / Miljkovic, Marisa /
    Evans, Shane A / Nguyen, Ngan / Whidden, Mark E / Srinivasan, Ramji / Spitzer, Matthew H / Sun, Yi / Sharova, Tatyana / Lawless, Aleigha R / Michaud, William A / Rasmussen, Martin Q / Fang, Jacy / Palin, Claire A / Chen, Feng / Wang, Xinhui / Ferrone, Cristina R / Lawrence, Donald P / Sullivan, Ryan J / Liu, David / Sachdeva, Uma M / Sen, Debattama R / Flaherty, Keith T / Manguso, Robert T / Bod, Lloyd / Kellis, Manolis / Boland, Genevieve M / Yizhak, Keren / Yang, Jiekun / Kanarek, Naama / Sade-Feldman, Moshe / Hacohen, Nir / Jenkins, Russell W

    bioRxiv : the preprint server for biology

    2024  

    Abstract: A central problem in cancer immunotherapy with immune checkpoint blockade (ICB) is the development of resistance, which affects 50% of patients with metastatic ... ...

    Abstract A central problem in cancer immunotherapy with immune checkpoint blockade (ICB) is the development of resistance, which affects 50% of patients with metastatic melanoma
    Language English
    Publishing date 2024-03-26
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2024.02.12.579184
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Chronic Immune-Related Adverse Events Following Adjuvant Anti-PD-1 Therapy for High-risk Resected Melanoma.

    Patrinely, J Randall / Johnson, Rebecca / Lawless, Aleigha R / Bhave, Prachi / Sawyers, Amelia / Dimitrova, Maya / Yeoh, Hui Ling / Palmeri, Marisa / Ye, Fei / Fan, Run / Davis, Elizabeth J / Rapisuwon, Suthee / Long, Georgina V / Haydon, Andrew / Osman, Iman / Mehnert, Janice M / Carlino, Matteo S / Sullivan, Ryan J / Menzies, Alexander M /
    Johnson, Douglas B

    JAMA oncology

    2021  Volume 7, Issue 5, Page(s) 744–748

    Abstract: Importance: Agents targeting programmed cell death 1 (PD-1)/PD ligand 1 (PD-L1) improve long-term survival across many advanced cancers and are now used as adjuvant therapy for resected stage III and IV melanomas. The incidence and spectrum of chronic ... ...

    Abstract Importance: Agents targeting programmed cell death 1 (PD-1)/PD ligand 1 (PD-L1) improve long-term survival across many advanced cancers and are now used as adjuvant therapy for resected stage III and IV melanomas. The incidence and spectrum of chronic immune-related adverse events (irAEs) have not been well defined.
    Objective: To determine the incidence, time course, spectrum, and associations of chronic irAEs arising from adjuvant anti-PD-1 therapy.
    Design, setting, and participants: This retrospective multicenter cohort study was conducted between 2015 and 2020 across 8 academic medical centers in the United States and Australia. Patients with stage III to IV melanomas treated with anti-PD-1 in the adjuvant setting were included.
    Main outcomes and measures: Incidence, types, and time course of chronic irAEs (defined as irAEs persisting at least 12 weeks after therapy cessation).
    Results: Among 387 patients, the median (range) age was 63 (17-88) years, and 235 (60.7%) were male. Of these patients, 267 (69.0%) had any acute irAE, defined as those arising during treatment with anti-PD-1, including 52 (19.5%) with grades 3 through 5 events; 1 patient each had fatal myocarditis and neurotoxicity. Chronic irAEs, defined as those that persisted beyond 12 weeks of anti-PD-1 discontinuation, developed in 167 (43.2%) patients, of which most (n = 161; 96.4%) were mild (grade 1 or 2) and most persisted until last available follow-up (n = 143; 85.6%). Endocrinopathies (73 of 88; 83.0%), arthritis (22 of 45; 48.9%), xerostomia (9 of 17; 52.9%), neurotoxicities (11 of 15; 73.3%), and ocular events (5 of 8; 62.5%) were particularly likely to become chronic. In contrast, irAEs affecting visceral organs (liver, colon, lungs, kidneys) had much lower rates of becoming chronic irAEs; for example, colitis became chronic in 6 of 44 (13.6%) cases, of which 4 of 6 (66.7%) resolved with prolonged follow-up. Age, gender, time of onset, and need for steroids were not associated with the likelihood of chronicity of irAEs.
    Conclusion and relevance: In this multicenter cohort study, chronic irAEs associated with anti-PD-1 therapy appear to be more common than previously recognized and frequently persisted even with prolonged follow-up, although most were low grade. The risks of chronic irAEs should be integrated into treatment decision-making.
    MeSH term(s) Cohort Studies ; Humans ; Incidence ; Male ; Melanoma/drug therapy ; Melanoma/surgery ; Programmed Cell Death 1 Receptor ; Retrospective Studies
    Chemical Substances Programmed Cell Death 1 Receptor
    Language English
    Publishing date 2021-03-25
    Publishing country United States
    Document type Journal Article ; Multicenter Study ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ISSN 2374-2445
    ISSN (online) 2374-2445
    DOI 10.1001/jamaoncol.2021.0051
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Dabrafenib plus trametinib versus anti-PD-1 monotherapy as adjuvant therapy in

    Bai, Xue / Shaheen, Ahmed / Grieco, Charlotte / d'Arienzo, Paolo D / Mina, Florentia / Czapla, Juliane A / Lawless, Aleigha R / Bongiovanni, Eleonora / Santaniello, Umberto / Zappi, Helena / Dulak, Dominika / Williamson, Andrew / Lee, Rebecca / Gupta, Avinash / Li, Caili / Si, Lu / Ubaldi, Martina / Yamazaki, Naoya / Ogata, Dai /
    Johnson, Rebecca / Park, Benjamin C / Jung, Seungyeon / Madonna, Gabriele / Hochherz, Juliane / Umeda, Yoshiyasu / Nakamura, Yasuhiro / Gebhardt, Christoffer / Festino, Lucia / Capone, Mariaelena / Ascierto, Paolo Antonio / Johnson, Douglas B / Lo, Serigne N / Long, Georgina V / Menzies, Alexander M / Namikawa, Kenjiro / Mandala, Mario / Guo, Jun / Lorigan, Paul / Najjar, Yana G / Haydon, Andrew / Quaglino, Pietro / Boland, Genevieve M / Sullivan, Ryan J / Furness, Andrew J S / Plummer, Ruth / Flaherty, Keith T

    EClinicalMedicine

    2023  Volume 65, Page(s) 102290

    Abstract: Background: Both dabrafenib/trametinib (D/T) and anti-PD-1 monotherapy (PD-1) are approved adjuvant therapies for patients with stage III : Methods: This multicenter, retrospective cohort study was conducted in 15 melanoma centers in Australia, China, ...

    Abstract Background: Both dabrafenib/trametinib (D/T) and anti-PD-1 monotherapy (PD-1) are approved adjuvant therapies for patients with stage III
    Methods: This multicenter, retrospective cohort study was conducted in 15 melanoma centers in Australia, China, Germany, Italy, Japan, UK, and US. We included adult patients with resected stage III
    Findings: We included 598 patients with stage III
    Interpretation: In patients with stage III
    Funding: Dr. Xue Bai was supported by the Beijing Hospitals Authority Youth Programme (QMS20211101) for her efforts devoted to this study. Dr. Keith T. Flaherty was funded by Adelson Medical Research Foundation for the efforts devoted to this study.
    Language English
    Publishing date 2023-10-31
    Publishing country England
    Document type Journal Article
    ISSN 2589-5370
    ISSN (online) 2589-5370
    DOI 10.1016/j.eclinm.2023.102290
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Immunogenicity and Reactogenicity of SARS-CoV-2 Vaccines in Patients With Cancer: The CANVAX Cohort Study.

    Naranbhai, Vivek / Pernat, Claire A / Gavralidis, Alexander / St Denis, Kerri J / Lam, Evan C / Spring, Laura M / Isakoff, Steven J / Farmer, Jocelyn R / Zubiri, Leyre / Hobbs, Gabriela S / How, Joan / Brunner, Andrew M / Fathi, Amir T / Peterson, Jennifer L / Sakhi, Mustafa / Hambelton, Grace / Denault, Elyssa N / Mortensen, Lindsey J / Perriello, Lailoo A /
    Bruno, Marissa N / Bertaux, Brittany Y / Lawless, Aleigha R / Jackson, Monica A / Niehoff, Elizabeth / Barabell, Caroline / Nambu, Christian N / Nakajima, Erika / Reinicke, Trenton / Bowes, Cynthia / Berrios-Mairena, Cristhian J / Ofoman, Onosereme / Kirkpatrick, Grace E / Thierauf, Julia C / Reynolds, Kerry / Willers, Henning / Beltran, Wilfredo-Garcia / Dighe, Anand S / Saff, Rebecca / Blumenthal, Kimberly / Sullivan, Ryan J / Chen, Yi-Bin / Kim, Arthur / Bardia, Aditya / Balazs, Alejandro B / Iafrate, A John / Gainor, Justin F

    Journal of clinical oncology : official journal of the American Society of Clinical Oncology

    2021  Volume 40, Issue 1, Page(s) 12–23

    Abstract: Purpose: The immunogenicity and reactogenicity of SARS-CoV-2 vaccines in patients with cancer are poorly understood.: Methods: We performed a prospective cohort study of adults with solid-organ or hematologic cancers to evaluate anti-SARS-CoV-2 ... ...

    Abstract Purpose: The immunogenicity and reactogenicity of SARS-CoV-2 vaccines in patients with cancer are poorly understood.
    Methods: We performed a prospective cohort study of adults with solid-organ or hematologic cancers to evaluate anti-SARS-CoV-2 immunoglobulin A/M/G spike antibodies, neutralization, and reactogenicity ≥ 7 days following two doses of mRNA-1273, BNT162b2, or one dose of Ad26.COV2.S. We analyzed responses by multivariate regression and included data from 1,638 healthy controls, previously reported, for comparison.
    Results: Between April and July 2021, we enrolled 1,001 patients; 762 were eligible for analysis (656 had neutralization measured). mRNA-1273 was the most immunogenic (log
    Conclusion: Immune responses to SARS-CoV-2 vaccines are modestly impaired in patients with cancer. These data suggest utility of antibody testing to identify patients for whom additional vaccine doses may be effective and appropriate, although larger prospective studies are needed.
    MeSH term(s) Aged ; COVID-19 Vaccines/immunology ; COVID-19 Vaccines/therapeutic use ; Cohort Studies ; Female ; Humans ; Male ; Middle Aged ; Neoplasms/immunology ; Prospective Studies ; SARS-CoV-2/immunology
    Chemical Substances COVID-19 Vaccines
    Language English
    Publishing date 2021-11-09
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 604914-x
    ISSN 1527-7755 ; 0732-183X
    ISSN (online) 1527-7755
    ISSN 0732-183X
    DOI 10.1200/JCO.21.01891
    Database MEDical Literature Analysis and Retrieval System OnLINE

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