Publications by authors named "Rege-Cambrin G"

TKIs long-term treatment in CML may lead to persistent adverse events (AEs) that can promote relevant morbidity and mortality. Consequently, TKIs dose reduction is often used to prevent AEs. However, data on its impact on successful treatment-free remission (TFR) are quite scarce.

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We report the final analysis, with a 10-year follow-up, of the phase II study GIMEMA CML 0307 (NCT00481052), which enrolled 73 adult patients (median age 51 years; range, 18-83) with newly diagnosed chronic-phase chronic myeloid leukemia to investigate the efficacy and the toxicity of front-line treatment with nilotinib. The initial dose was 400 mg twice daily; the dose was reduced to 300 mg twice daily as soon as this dose was approved and registered. The 10-year overall survival and progression- free survival were 94.

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Treatment-free remission (TFR) has become a primary therapeutic goal in CML and is also considered feasible by international guidelines. TKIs dose reduction is often used in real-life practice to reduce adverse events, although its impact on TFR is still a matter of debate. This study aimed to explore the attitude of Italian hematologists towards prescribing TKIs at reduced doses and its impact on TFR.

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mRNA levels represent the key molecular marker for the evaluation of minimal residual disease (MRD) in chronic myeloid leukemia (CML) patients and real-time quantitative PCR (RT-qPCR) is currently the standard method to monitor it. In the era of tyrosine kinase inhibitors (TKIs) discontinuation, droplet digital PCR (ddPCR) has emerged to provide a more precise detection of MRD. To hypothesize the use of ddPCR in clinical practice, we designed a multicentric study to evaluate the potential value of ddPCR in the diagnostic routine.

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Limited information is available on the impact of the COVID-19 pandemic on the management of chronic myeloid leukaemia (CML). The Campus CML network collected retrospective information on 8 665 CML patients followed at 46 centres throughout Italy during the pandemic between February 2020 and January 2021. Within this cohort, we recorded 217 SARS-CoV-2-positive patients (2·5%).

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An observational prospective study was conducted by the CML Italian network to analyze the role of baseline patient characteristics and first line treatments on overall survival and CML-related mortality in 1206 newly diagnosed CML patients, 608 treated with imatinib (IMA) and 598 with 2 generation tyrosine kinase inhibitors (2GTKI). IMA-treated patients were much older (median age 69 years, IQR 58-77) than the 2GTKI group (52, IQR 41-63) and had more comorbidities. Estimated 4-year overall survival of the entire cohort was 89% (95%CI 85.

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In recent years, the digital polymerase chain reaction has received increasing interest as it has emerged as a tool to provide more sensitive and accurate detection of minimal residual disease. In order to start the process of data alignment, we assessed the consistency of the BCR-ABL1 quantification results of the analysis of 16 RNA samples at different levels of disease. The results were obtained by two different laboratories that relied on The Qx100/Qx200 Droplet Digital PCR System (Bio-Rad) and Quant Studio 3D dPCR System (Thermofisher) platforms.

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Article Synopsis
  • Intermittent treatment with TKIs is a viable option for 70%-80% of CML patients who can't achieve a stable deep molecular response and need a break from continuous therapy.
  • The OPTkIMA study, launched in 2015, aimed to assess if a month-on/month-off dosing schedule for TKIs could maintain molecular response and enhance health-related quality of life.
  • Results showed that 81% of patients maintained their molecular response, and although quality of life worsened initially, it returned to baseline by the end of the year, highlighting the potential benefits of de-escalated TKI regimens for elderly CML patients.
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Chronic myeloid leukemia is a myeloproliferative neoplasm characterized by the presence of the Philadelphia chromosome that originates from the reciprocal translocation t(9;22)(q34;q11.2) and encodes for the constitutively active tyrosine kinase protein BCR-ABL1 from the () sequence and the () gene. Despite BCR-ABL1 being one of the most studied oncogenic proteins, some molecular mechanisms remain enigmatic, and several of the proteins, acting either as positive or negative BCR-ABL1 regulators, are still unknown.

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Article Synopsis
  • Successful discontinuation of tyrosine kinase inhibitors (TKIs) in chronic-phase chronic myeloid leukemia (CML) patients has been achieved, highlighting the importance of careful molecular monitoring during and after treatment.
  • A study of 281 CML patients in Italy showed that a significant number (75.6%) who lost major molecular response (MMR) did so within the first six months after stopping TKI treatment, emphasizing the need for timely monitoring.
  • Adopting a less frequent monitoring schedule after the initial six months does not seem to negatively impact treatment-free remission (TFR) success, suggesting that patients can be safely monitored with reduced intensity over time.
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  • A study found that 2% of chronic myeloid leukemia (CML) patients have atypical RNA transcripts that are hard to measure using standard techniques like real-time PCR and NESTED PCR, making it difficult to monitor their treatment responses.
  • * The research introduced a highly sensitive method called droplet digital PCR (ddPCR) that can accurately quantify these atypical transcripts, even at very low levels (as low as 0.001%).
  • * The findings suggest that ddPCR could help identify patients with a deep molecular response, potentially qualifying them for treatment-free remission options that were previously inaccessible due to unreliable testing.
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  • There is a strong connection between thymoma (a type of tumor) and pure red cell aplasia, which is well-established in research.
  • Acquired amegakaryocytic thrombocytopenia, a condition that affects platelet production, is less commonly reported in relation to thymoma.
  • In this case, adding eltrombopag (a medication that stimulates platelet production) to standard immunosuppressive treatment did not help the patient, likely because the tumor was not surgically removed.
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Several papers authored by international experts have proposed recommendations on the management of BCR-ABL1+ chronic myeloid leukemia (CML). Following these recommendations, survival of CML patients has become very close to normal. The next, ambitious, step is to bring as many patients as possible into a condition of treatment-free remission (TFR).

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Article Synopsis
  • Philadelphia positive lymphoblastic lymphoma (LBL) is less understood than Philadelphia positive acute lymphoblastic leukemia, with only two documented cases reported in literature, both resulting in death during treatment.
  • A patient treated with a unique, chemo-free regimen using dasatinib, steroids, and local radiotherapy has survived 3 years post-diagnosis, indicating a potential alternative approach.
  • The diagnosis and treatment of Philadelphia positive LBL are particularly challenging due to its rarity and complexity.
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Very elderly (> 75 years) chronic myeloid leukaemia (CML) patients at diagnosis are sometimes treated with different doses of imatinib (IM) based on concomitant diseases and physicians' judgement. However, data on long-term follow-up of these patients are still lacking. To investigate treatment response and outcome, we retrospectively revised an Italian database of 263 very elderly CML patients receiving IM from the time of diagnosis.

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The main objective of this study is to gain further insights on how chronic myeloid leukemia (CML) patients involved in an interventional clinical trial with the purpose of reaching treatment free remission (TFR) phase, perceived and experienced TFR failure. TFR failure was defined for the individual patient as either not being eligible for drug discontinuation or as having relapse in the TFR phase with reintroduction of nilotinib treatment. Using a qualitative approach, out of 25 patients with CML who experienced TFR failure 14 were interviewed.

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Article Synopsis
  • A study involving 293 Italian patients with chronic myeloid leukemia (CML) showed that discontinuing tyrosine kinase inhibitors (TKI) after reaching a deep molecular response is generally safe, with an overall estimated treatment-free remission (TFR) rate of 62% after a median follow-up of 34 months.
  • The majority of patients were using imatinib (72%), with fewer on second-generation TKIs (28%); those on second-generation TKIs had shorter treatment durations compared to imatinib.
  • Most patients (88%) stopped treatment based on clinical practice, primarily due to shared decisions or toxicity, with no relapses reported during the study period.
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Pleural effusion (PE) represents the leading cause of dasatinib (DAS) discontinuation. However, the pathogenic mechanism of this adverse event (AE) is unknown and its management unclear. We investigated if a DAS dose reduction after the first PE would prevent the recurrence of this AE.

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Current diagnostic criteria for Philadelphia-negative myeloproliferative neoplasia (MPN) have been redefined by the discovery of Janus kinase 2 (JAK2), myeloproliferative leukemia (MPL) and calreticulin (CALR) genetic alterations. Only few cases of coexistence of CALR-mutated MPN and Philadelphia-positive chronic myeloid leukemia (CML) have been described so far. Here we report the case of a patient with CML diagnosed in 2001, treated with imatinib and pegylated interferon (IFN) frontline.

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Background: About 40% of all patients with chronic myeloid leukemia are currently old or very old. They are effectively treated with imatinib, even though underrepresented in clinical studies. Furthermore, as it happens in the general population, they often receive multiple drugs for associated chronic illnesses.

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