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  1. Article ; Online: The role of anti-EGFR rechallenge in metastatic colorectal cancer, from available data to future developments: A systematic review.

    Ciardiello, Davide / Mauri, Gianluca / Sartore-Bianchi, Andrea / Siena, Salvatore / Zampino, Maria Giulia / Fazio, Nicola / Cervantes, Andres

    Cancer treatment reviews

    2024  Volume 124, Page(s) 102683

    Abstract: Despite recent molecular and immunological advancements, prognosis of metastatic colorectal cancer (mCRC) patients remains poor. In this context, several retrospective and phase II studies suggested that after failure of an upfront anti-EGFR based ... ...

    Abstract Despite recent molecular and immunological advancements, prognosis of metastatic colorectal cancer (mCRC) patients remains poor. In this context, several retrospective and phase II studies suggested that after failure of an upfront anti-EGFR based regimen, a subset of patients can still benefit from further anti-EGFR blockade. Several translational studies involving circulating tumor DNA (ctDNA) analysis demonstrated that cancer clones harboring mutations driving anti-EGFR resistance, which can arise under anti-EGFR agents selective pressure, often decay after anti-EGFR discontinuation potentially restoring sensitivity to this therapeutic strategy. Accordingly, several retrospective analyses and a recent prospective trial demonstrated that ctDNA RAS and BRAF wild-type mCRC patients are those benefitting the most from anti-EGFR rechallenge. Indeed, in molecularly selected patients, anti-EGFR rechallenge strategy achieved up to 30 % response rate, with a progression free survival longer than 4 months and an overall survival longer than 1 year, which favorably compared with other standard therapeutic options available for heavily pretreated patients. Anti-EGFR is also well tolerated with no unexpected toxicities compared to the upfront setting. However, several open questions remain to be addressed towards a broader applicability of anti-EGFR strategy in the everyday clinical practice such as the identification of the best rechallenge regimen, the right placement in mCRC therapeutic algorithm, the best ctDNA screening panel. In our systematic review, we revised available data from clinical trials assessing anti-EGFR rechallenge activity in chemo-refractory mCRC patients, discussing as well potential future scenarios and development to implement this therapeutic approach. Particularly, we discussed the role of ctDNA as a safe, timely and comprehensive tool to refine patient's selection and the therapeutic index of anti-EGFR rechallenge.
    MeSH term(s) Humans ; Colorectal Neoplasms/drug therapy ; Colorectal Neoplasms/genetics ; Colorectal Neoplasms/pathology ; Retrospective Studies ; Antibodies, Monoclonal/therapeutic use ; Cetuximab ; Colonic Neoplasms/drug therapy ; Rectal Neoplasms/drug therapy ; Proto-Oncogene Proteins B-raf/genetics
    Chemical Substances Antibodies, Monoclonal ; Cetuximab (PQX0D8J21J) ; Proto-Oncogene Proteins B-raf (EC 2.7.11.1)
    Language English
    Publishing date 2024-01-12
    Publishing country Netherlands
    Document type Systematic Review ; Journal Article ; Review
    ZDB-ID 125102-8
    ISSN 1532-1967 ; 0305-7372
    ISSN (online) 1532-1967
    ISSN 0305-7372
    DOI 10.1016/j.ctrv.2024.102683
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Molecular Markers Beyond Microsatellite Instability for Assessing Prognosis in Early-Stage Colorectal Cancer: What Happens at Relapse?

    Sartore-Bianchi, Andrea

    JAMA oncology

    2016  Volume 3, Issue 4, Page(s) 481–482

    MeSH term(s) Colonic Neoplasms ; DNA Mismatch Repair ; Humans ; Microsatellite Instability ; Mutation ; Neoplasm Recurrence, Local ; Prognosis ; Proto-Oncogene Proteins B-raf ; Proto-Oncogene Proteins p21(ras) ; Randomized Controlled Trials as Topic
    Chemical Substances KRAS protein, human ; BRAF protein, human (EC 2.7.11.1) ; Proto-Oncogene Proteins B-raf (EC 2.7.11.1) ; Proto-Oncogene Proteins p21(ras) (EC 3.6.5.2)
    Language English
    Publishing date 2016-12-22
    Publishing country United States
    Document type Journal Article ; Comment
    ISSN 2374-2445
    ISSN (online) 2374-2445
    DOI 10.1001/jamaoncol.2016.5463
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Breaking Barriers in HER2+ Cancers.

    Siena, Salvatore / Marsoni, Silvia / Sartore-Bianchi, Andrea

    Cancer cell

    2020  Volume 38, Issue 3, Page(s) 317–319

    Abstract: Treatment with the immunoconjugate trastuzumab deruxtecan leads to unprecedented improvements in response and overall survival in patients with HER2-positive (HER2+) metastatic gastroesophageal carcinoma (GEA), according to a study published in the New ... ...

    Abstract Treatment with the immunoconjugate trastuzumab deruxtecan leads to unprecedented improvements in response and overall survival in patients with HER2-positive (HER2+) metastatic gastroesophageal carcinoma (GEA), according to a study published in the New England Journal of Medicine. Until now, no HER2-targeted drugs other than trastuzumab have shown significant benefit in patients with HER2+ GEA.
    MeSH term(s) Camptothecin/analogs & derivatives ; Humans ; Immunoconjugates ; Receptor, ErbB-2/genetics ; Stomach Neoplasms ; Trastuzumab/therapeutic use
    Chemical Substances Immunoconjugates ; trastuzumab deruxtecan (5384HK7574) ; Receptor, ErbB-2 (EC 2.7.10.1) ; Trastuzumab (P188ANX8CK) ; Camptothecin (XT3Z54Z28A)
    Language English
    Publishing date 2020-08-27
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 2078448-X
    ISSN 1878-3686 ; 1535-6108
    ISSN (online) 1878-3686
    ISSN 1535-6108
    DOI 10.1016/j.ccell.2020.07.012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Application of histology-agnostic treatments in metastatic colorectal cancer.

    Sartore-Bianchi, Andrea / Agostara, Alberto Giuseppe / Patelli, Giorgio / Mauri, Gianluca / Pizzutilo, Elio Gregory / Siena, Salvatore

    Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver

    2022  Volume 54, Issue 10, Page(s) 1291–1303

    Abstract: Cancer treatment is increasingly focused on targeting molecular alterations identified across different tumor histologies. While some oncogenic drivers such as microsatellite instability (MSI) and NTRK fusions are actionable with the very same approach ... ...

    Abstract Cancer treatment is increasingly focused on targeting molecular alterations identified across different tumor histologies. While some oncogenic drivers such as microsatellite instability (MSI) and NTRK fusions are actionable with the very same approach regardless of tumor type ("histology-agnostic"), others require histology-specific therapeutic adjustment ("histology-tuned") by means of adopting specific inhibitors and ad hoc combinations. Among histology-agnostic therapies, pembrolizumab or dostarlimab demonstrated comparable activity in MSI metastatic colorectal cancer (mCRC) as in other tumors with MSI status (ORR 38% vs 40% and 36% vs 39%, respectively), while entrectinib or larotrectinib proved effective in NTRK rearranged mCRC even though less dramatically than in the overall population (ORR 20% vs 57%, and 50% vs 78%, respectively). Histology-tuned approaches in mCRC are those targeting BRAF
    MeSH term(s) Antibodies, Monoclonal, Humanized ; Biomarkers, Tumor/genetics ; Colonic Neoplasms ; Colorectal Neoplasms/drug therapy ; Colorectal Neoplasms/genetics ; Colorectal Neoplasms/pathology ; Humans ; Microsatellite Instability ; Proto-Oncogene Proteins B-raf/genetics ; Rectal Neoplasms
    Chemical Substances Antibodies, Monoclonal, Humanized ; Biomarkers, Tumor ; dostarlimab ; Proto-Oncogene Proteins B-raf (EC 2.7.11.1)
    Language English
    Publishing date 2022-06-11
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 1459373-7
    ISSN 1878-3562 ; 1125-8055
    ISSN (online) 1878-3562
    ISSN 1125-8055
    DOI 10.1016/j.dld.2022.05.013
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Seroconversion after SARS-CoV-2 mRNA booster vaccine in cancer patients.

    Patelli, Giorgio / Pani, Arianna / Amatu, Alessio / Scaglione, Francesco / Sartore-Bianchi, Andrea

    European journal of cancer (Oxford, England : 1990)

    2022  Volume 167, Page(s) 175–176

    MeSH term(s) COVID-19/prevention & control ; COVID-19 Vaccines/adverse effects ; Humans ; Neoplasms ; RNA, Messenger ; SARS-CoV-2 ; Seroconversion
    Chemical Substances COVID-19 Vaccines ; RNA, Messenger
    Language English
    Publishing date 2022-03-15
    Publishing country England
    Document type Letter ; Research Support, Non-U.S. Gov't ; Comment
    ZDB-ID 82061-1
    ISSN 1879-0852 ; 0277-5379 ; 0959-8049 ; 0964-1947
    ISSN (online) 1879-0852
    ISSN 0277-5379 ; 0959-8049 ; 0964-1947
    DOI 10.1016/j.ejca.2022.02.032
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Plasticity of Resistance and Sensitivity to Anti-Epidermal Growth Factor Receptor Inhibitors in Metastatic Colorectal Cancer.

    Sartore-Bianchi, Andrea / Siena, Salvatore

    Handbook of experimental pharmacology

    2017  Volume 249, Page(s) 145–159

    Abstract: Colorectal cancer (CRC) is one of the most prevalent cancers and the second leading cause of cancer mortality worldwide. Survival in the metastatic setting has been gradually improved by the addition to cytotoxic chemotherapy of agents targeting the ... ...

    Abstract Colorectal cancer (CRC) is one of the most prevalent cancers and the second leading cause of cancer mortality worldwide. Survival in the metastatic setting has been gradually improved by the addition to cytotoxic chemotherapy of agents targeting the vascular endothelial growth factor (VEGF) and epidermal growth factor receptor (EGFR). Considerable heterogeneity exists within CRC due to the varied genetic and epigenetic mechanisms involved in differing pathways of carcinogenesis. The knowledge of molecular abnormalities underlying colorectal tumourigenesis and the progression of dysplastic precursors to invasive and ultimately metastatic lesions has advanced in recent years by comprehensive sequencing studies. From these genome-scale analyses, we know that a handful of genes are commonly affected by somatic mutations, whereas recurrent copy-number alterations and chromosomal translocations are rarer in this disease. Even though some of these molecular abnormalities make genes acting as drivers of cancer progression, translation of this recognition for therapeutic purposes is still limited, encompassing only as standard of care the exclusion of RAS-mutated cancers for better selecting patients to candidate to EGFR-targeted therapy with monoclonal antibodies. However, the effort of ameliorating molecular selection should not be considered exhausted by demonstration of RAS and BRAF-induced resistance, as the genomic landscape of response to EGFR blockade has been demonstrated to be wider and dynamically multifaceted. In this chapter we will review main molecular biomarkers of de novo (primary) and acquired (secondary) resistance to EGFR-targeted monoclonal antibodies in metastatic CRC and discuss therapeutic implications.
    MeSH term(s) Antibodies, Monoclonal/pharmacology ; Antineoplastic Agents/pharmacology ; Colorectal Neoplasms/drug therapy ; Drug Resistance, Neoplasm ; ErbB Receptors/antagonists & inhibitors ; Humans ; Mutation ; Neoplasm Metastasis ; Vascular Endothelial Growth Factor A/antagonists & inhibitors
    Chemical Substances Antibodies, Monoclonal ; Antineoplastic Agents ; Vascular Endothelial Growth Factor A ; ErbB Receptors (EC 2.7.10.1)
    Language English
    Publishing date 2017-04-25
    Publishing country Germany
    Document type Journal Article
    ISSN 0171-2004
    ISSN 0171-2004
    DOI 10.1007/164_2017_19
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Targeting HER2 heterogeneity in breast and gastrointestinal cancers.

    Valenza, Carmine / Guidi, Lorenzo / Battaiotto, Elena / Trapani, Dario / Sartore Bianchi, Andrea / Siena, Salvatore / Curigliano, Giuseppe

    Trends in cancer

    2023  Volume 10, Issue 2, Page(s) 113–123

    Abstract: About 20% of breast and gastric cancers and 3% of colorectal carcinomas overexpress the human epidermal growth factor receptor 2 (HER2) and are sensitive to HER2-directed agents. The expression of HER2 may differ within the same tumoral lesion (spatial ... ...

    Abstract About 20% of breast and gastric cancers and 3% of colorectal carcinomas overexpress the human epidermal growth factor receptor 2 (HER2) and are sensitive to HER2-directed agents. The expression of HER2 may differ within the same tumoral lesion (spatial intralesional heterogeneity), from different tumor locations (spatial interlesional heterogeneity), and throughout treatments (temporal heterogeneity). Spatial and temporal heterogeneity may impact on response and resistance to HER2-targeting agents and its prevalence and predictive role changes across HER2-overexpressing solid tumors. Therefore, the definition and the characterization of HER2 heterogeneity pose many challenges and its implementation as a reproducible predictive biomarker would help in guiding treatment modulation.
    MeSH term(s) Humans ; Gastrointestinal Neoplasms/drug therapy ; Gastrointestinal Neoplasms/genetics ; Breast/pathology ; Antineoplastic Agents ; Stomach Neoplasms/drug therapy ; Stomach Neoplasms/genetics
    Chemical Substances Antineoplastic Agents
    Language English
    Publishing date 2023-11-25
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2852626-0
    ISSN 2405-8025 ; 2405-8033 ; 2405-8033
    ISSN (online) 2405-8025 ; 2405-8033
    ISSN 2405-8033
    DOI 10.1016/j.trecan.2023.11.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: The Amount of Evidence Needed to Support ERBB2 as a Biomarker for Resistance to EGFR Inhibitors in Metastatic Colorectal Cancer.

    Sartore-Bianchi, Andrea / Marsoni, Silvia / Siena, Salvatore

    JAMA oncology

    2019  Volume 5, Issue 10, Page(s) 1510–1511

    Language English
    Publishing date 2019-08-09
    Publishing country United States
    Document type Journal Article
    ISSN 2374-2445
    ISSN (online) 2374-2445
    DOI 10.1001/jamaoncol.2019.2982
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Young-onset colorectal cancer: treatment-related nausea, vomiting and diarrhoea.

    Mauri, Gianluca / Pedrani, Martino / Ghezzi, Silvia / Bencardino, Katia / Mariano, Sara / Bonazzina, Erica / Serra, Francesco / Pedrazzoli, Paolo / Caccialanza, Riccardo / Cavestro, Giulia Martina / Siena, Salvatore / Artale, Salvatore / Sartore-Bianchi, Andrea

    BMJ supportive & palliative care

    2024  Volume 13, Issue e3, Page(s) e885–e889

    Abstract: Objectives: Early-onset colorectal cancer (EO-CRC) incidence is increasing, raising a clinical challenge. Clinicians tend to treat EO-CRC patients with more intensive regimens despite the lack of survival benefits, based on an age-related bias. Limited ... ...

    Abstract Objectives: Early-onset colorectal cancer (EO-CRC) incidence is increasing, raising a clinical challenge. Clinicians tend to treat EO-CRC patients with more intensive regimens despite the lack of survival benefits, based on an age-related bias. Limited evidence is available regarding treatment-related toxicities in this peculiar subset of patients.
    Methods: We performed a literature search in MEDLINE/PubMed, EMBASE and Scopus, looking for reporting of nausea, vomiting and diarrhoea occurring in patients with EO-CRC, defined by age lower than 50 years old at initial diagnosis, while receiving anticancer treatment.
    Results: 2318 records were screened and 9 full-text articles were considered eligible for inclusion for a total of 59 783 patients (of whom 8681 EO-CRC patients). We found nausea and vomiting occurring at higher incidence among EO-CRC compared with older patients, while no difference was reported as for diarrhoea. Peritoneal involvement, age younger than 40, female gender, suboptimal adherence to guidelines and oxaliplatin might represent potential risk factors for increased nausea and vomiting in patients with EO-CRC.
    Conclusion: EO-CRC patients experience more nausea and vomiting but equal or less diarrhoea compared with older patients. Adherence to clinical guidelines is recommended, and more data are warranted to assess if an enhanced antiemetic approach might be required, particularly in case of specific risk factors.
    MeSH term(s) Humans ; Female ; Middle Aged ; Vomiting/chemically induced ; Nausea/epidemiology ; Nausea/chemically induced ; Antiemetics/therapeutic use ; Oxaliplatin/therapeutic use ; Colorectal Neoplasms/complications ; Colorectal Neoplasms/drug therapy ; Colorectal Neoplasms/epidemiology
    Chemical Substances Antiemetics ; Oxaliplatin (04ZR38536J)
    Language English
    Publishing date 2024-01-08
    Publishing country England
    Document type Journal Article
    ISSN 2045-4368
    ISSN (online) 2045-4368
    DOI 10.1136/spcare-2023-004203
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Ongoing Clinical Trials and Future Research Scenarios of Circulating Tumor DNA for the Treatment of Metastatic Colorectal Cancer.

    Roazzi, Laura / Patelli, Giorgio / Bencardino, Katia Bruna / Amatu, Alessio / Bonazzina, Erica / Tosi, Federica / Amoruso, Brunella / Bombelli, Anna / Mariano, Sara / Stabile, Stefano / Porta, Camillo / Siena, Salvatore / Sartore-Bianchi, Andrea

    Clinical colorectal cancer

    2024  

    Abstract: Liquid biopsy using circulating tumor DNA (ctDNA) has emerged as a minimally invasive, timely approach to provide molecular diagnosis and monitor tumor evolution in patients with cancer. Since the molecular landscape of metastatic colorectal cancer (mCRC) ...

    Abstract Liquid biopsy using circulating tumor DNA (ctDNA) has emerged as a minimally invasive, timely approach to provide molecular diagnosis and monitor tumor evolution in patients with cancer. Since the molecular landscape of metastatic colorectal cancer (mCRC) is substantially heterogeneous and dynamic over space and time, ctDNA holds significant advantages as a biomarker for this disease. Numerous studies have demonstrated that ctDNA broadly recapitulates the molecular profile of the primary tumor and metastases, and have mainly focused on the genotyping of RAS and BRAF, that is propaedeutic for anti-EGFR treatment selection. However, ctDNA soon broadened its scope towards the assessment of early tumor response, as well as the identification of drug resistance biomarkers to drive potential molecular actionability. In this review article, we provide an overview of the current state-of-the-art of this methodology and its applications, focusing on ongoing clinical trials that employ ctDNA to prospectively guide treatment in patients with mCRC.
    Language English
    Publishing date 2024-02-16
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2112638-0
    ISSN 1938-0674 ; 1533-0028
    ISSN (online) 1938-0674
    ISSN 1533-0028
    DOI 10.1016/j.clcc.2024.02.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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