Publications by authors named "Vaskar Saha"

Article Synopsis
  • During the maintenance treatment phase for acute lymphoblastic leukemia (ALL), personalized dosing of oral antimetabolite drugs is essential, but challenging, leading to a higher relapse risk if not done correctly.
  • An open-source R-based analytical toolkit, including the allMT R package and the VIATAMIN application, has been developed to assist in evaluating and improving drug titration during treatment.
  • The toolkit provides visual analyses of drug dosing patterns, assesses prescriber compliance, and intends to integrate into a clinical support system for real-time adjustments, with future updates planned to include more factors affecting drug titration.
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Article Synopsis
  • Acute lymphoblastic leukemia (ALL) treatment for children includes a 2-year outpatient maintenance therapy (MT), which transitioned from entirely outpatient to a hybrid e-clinic/outpatient model over 8 years.
  • The study analyzed data from 478 children on MT, finding that the hybrid model reduced outpatient visits by about two-thirds while maintaining treatment effectiveness and increasing dose intensity.
  • Families reported significant satisfaction with the hybrid service, which also cut maintenance treatment costs by roughly 50%, demonstrating it as an effective and less burdensome approach for patients.
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Background: Research is essential for the advancement of science, technology and development. Research requires funding and resource allocation. And funding requires the ability to write research grant application.

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Cure rates in pediatric acute lymphoblastic leukemia (ALL) currently approach 90% in the developed world. Treatment involves 6-8 mo of intensive multi-drug chemotherapy followed by 24 mo of maintenance treatment (ALL-MT). The cornerstone of ALL-MT is the daily administration of oral 6-mercaptopurine (6MP), a purine analogue.

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Purpose: In the absence of a standardized tool to assess the quality of pediatric hematology/oncology training programs, the Education Program Assessment Tool (EPAT) was conceptualized as a user-friendly and adaptable tool to evaluate and identify areas of opportunity, pinpoint needed modifications, and monitor progress for training programs around the world.

Methods: The development of EPAT consisted of three main phases: operationalization, consensus, and piloting. After each phase, the tool was iteratively modified based on feedback to improve its relevance, usability, and clarity.

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Background: The outcome of children with Philadelphia chromosome-positive (Ph-positive) acute lymphoblastic leukaemia significantly improved with the combination of imatinib and intensive chemotherapy. We aimed to investigate the efficacy of dasatinib, a second-generation ABL-class inhibitor, with intensive chemotherapy in children with newly diagnosed Ph-positive acute lymphoblastic leukaemia.

Methods: CA180-372/COG AALL1122 was a joint Children's Oncology Group (COG) and European intergroup study of post-induction treatment of Ph-positive acute lymphoblastic leukaemia (EsPhALL) open-label, single-arm, phase 2 study.

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Outcomes for children with acute lymphoblastic leukemia (ALL) have improved worldwide to >85%. For those who relapse, outcomes have remained static at ~50% making relapsed acute lymphoblastic leukemia one of the leading causes of death in childhood cancers. Those relapsing within 18 mo in the bone marrow have a particularly dismal outcome.

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Background: To evaluate the treatment cost and cost effectiveness of a risk-stratified therapy to treat pediatric acute lymphoblastic leukemia (ALL) in India.

Methods: The cost of total treatment duration was calculated for a retrospective cohort of ALL children treated at a tertiary care facility. Children were risk stratified into standard (SR), intermediate (IR) and high (HR) for B-cell precursor ALL, and T-ALL.

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Purpose: Formal training in clinical research methodologies is limited in limited-resource countries. Through collaboration among high- and middle-resource settings and in response to an identified need verbalized by regional pediatric oncology practitioners, Pediatric Oncology East & Mediterranean Group and St Jude Global developed a workshop focused on capacity building in research skills. Here, we describe its structure, implementation, and early results.

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Background: The north and north-eastern regions of India have among the highest incidence of gallbladder cancer (GBC) in the world. We report the clinicopathological charateristics and outcome of GBC patients in India.

Methods: Electronic medical records of patients diagnosed with GBC at Tata Medical Center, Kolkata between 2017 and 2019 were analyzed.

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In successive UK clinical trials (UKALL 2003, UKALL 2011) for paediatric acute lymphoblastic leukaemia (ALL), polyethylene glycol-conjugated E. coli L-asparaginase (PEG-EcASNase) 1000 iu/m was administered intramuscularly with risk-stratified treatment. In induction, patients received two PEG-EcASNase doses, 14 days apart.

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Background: In the west, survival following treatment of childhood acute lymphoblastic leukaemia (ALL) approaches 90%. Outcomes in India do not exceed 70%. To address this disparity, the Indian Collaborative Childhood Leukaemia group (ICiCLe) developed in 2013 a contemporary treatment protocol for uniform risk-stratified management of first presentation ALL based on cytogenetics and minimal residual disease levels (MRD).

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Article Synopsis
  • The study analyzed the outcomes of 393 children with high-risk relapsed acute lymphoblastic leukaemia (ALL) from two clinical trials, focusing on the impact of minimal residual disease (MRD) and genetic factors on survival.
  • Results indicated that the event-free survival rates for B-cell precursor (BCP) and T-cell ALL were similar, but better MRD responses led to significantly improved disease-free and overall survival rates.
  • The conclusion suggests that new therapeutic strategies are necessary to enhance remission rates and maintain long-term survival after stem cell transplantation in high-risk ALL patients.
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Background: The biotherapeutic asparaginase is a cornerstone of therapy in acute lymphoblastic leukaemia (ALL). With limited access to the original native Escherichia coli-derived asparaginase (EcASNase), a variety of EcASNase biogenerics are used in low-middle-income countries (LMICs). The variable quality of these biogenerics potentially influences clinical outcomes.

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Importance: Blinatumomab is a CD3/CD19-directed bispecific T-cell engager molecule with efficacy in children with relapsed or refractory B-cell acute lymphoblastic leukemia (B-ALL).

Objective: To evaluate event-free survival in children with high-risk first-relapse B-ALL after a third consolidation course with blinatumomab vs consolidation chemotherapy before allogeneic hematopoietic stem cell transplant.

Design, Setting, And Participants: In this randomized phase 3 clinical trial, patients were enrolled November 2015 to July 2019 (data cutoff, July 17, 2019).

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Background: L-asparaginase is a key component of treatment for patients with acute lymphoblastic leukaemia (ALL) in the UK. Commonly used forms of asparaginase are native E. coli-derived asparaginase (native asparaginase) and pegaspargase in first-line combination therapy, and native Erwinia chrysanthemi-derived asparaginase (Erwinia asparaginase) as second-line treatment.

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Article Synopsis
  • The UKALL 2011 trial evaluated the effects of different dosing regimens of dexamethasone in treating acute lymphoblastic leukaemia, focusing on a short (10 mg/m/d for 14 days) versus a standard (6 mg/m/d for 28 days) approach to see which would be more effective and have fewer toxicities.
  • Blood samples from 174 children were analyzed to study how dexamethasone levels varied, finding significant differences in drug exposure amongst patients and a higher cumulative exposure with the longer dosing regimen.
  • The findings suggest that the duration of dexamethasone therapy and the overall drug exposure may have a greater impact on treatment response than the actual dose taken, with no
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  • A study in India assessed bortezomib (BZB) and reduced doses of cytarabine in treating children with relapsed acute lymphoblastic leukemia (rALL), involving 55 participants.
  • Out of those treated, 88% achieved second remission and a significant number showed low minimal residual disease after induction therapy.
  • The results showed promising one-year survival rates, with 74.7% event-free survival and 79.6% overall survival in the group receiving treatment.
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