Evidence map›Paper›PMID 39469157›Full record

ArticleIndian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion2024

Real World Outcomes with Treatment Free Remission in Chronic Myeloid Leukemia-Experience from a Tertiary Care Cancer Centre.

Rup Jyoti Sarma, Lakhan Kashyap, Anne Srikanth, Tanmoy Mondal, Yashwant Kashyap, Ravindra Nandhana, Suresh Kumar Bondili, Avinash Bonda, Lingaraj Nayak, Gaurav Chatterjee and 9 more

Abstract read
In one paragraph

Article in Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

19 authors.

Rup Jyoti SarmaDepartment of Medical Oncology, Tata Memorial Hospital, Homi Bhaba National Institute, Mumbai, 400012, India.ORCID 0000-0001-7223-7726
Lakhan KashyapDepartment of Medical Oncology, Dr DY Patil Medical College, Hospital and Research Centre, Dr DY Patil Vidyapeeth (Deemed to Be University), Pune, Maharashtra India.
Anne SrikanthDepartment of Medical Oncology, Tata Memorial Hospital, Homi Bhaba National Institute, Mumbai, 400012, India.
Tanmoy MondalConsultant Medical Oncologist, AMRI Hospitals, Dhakuria, West Bengal India.
Yashwant KashyapConsultant Medical Oncologist, NH MMI Hospital, Raipur, Chhattisgarh India.
Ravindra NandhanaConsultant Medical Oncologist, GEMS Medical College, Srikakulam, Andhra Pradesh India.
Suresh Kumar BondiliConsultant Medical Oncologist, Kauvery Hospital, Chennai, Tamil Nadu India.
Avinash BondaConsultant Medical and Hemato-Oncologist, Asian Institute of Gastroenterology Hospital, Hyderabad, 500032, Telangana India.
Lingaraj NayakDepartment of Medical Oncology, Tata Memorial Hospital, Homi Bhaba National Institute, Mumbai, 400012, India.
Gaurav ChatterjeeDepartment of Hematopathology, Advanced Centre for Treatment, Research and Education in Cancer, Tata Memorial Center, Homi Bhaba National Institute, Mumbai, India.
Hashmukh JainDepartment of Medical Oncology, Tata Memorial Hospital, Homi Bhaba National Institute, Mumbai, 400012, India.
Nikhil Vijay PatkarDepartment of Hematopathology, Advanced Centre for Treatment, Research and Education in Cancer, Tata Memorial Center, Homi Bhaba National Institute, Mumbai, India.
Prashant TembhareDepartment of Hematopathology, Advanced Centre for Treatment, Research and Education in Cancer, Tata Memorial Center, Homi Bhaba National Institute, Mumbai, India.
Papagudi SubramanianDepartment of Hematopathology, Advanced Centre for Treatment, Research and Education in Cancer, Tata Memorial Center, Homi Bhaba National Institute, Mumbai, India.
Sumeet GujralDepartment of Hematopathology, Tata Memorial Hospital, Homi Bhaba National Institute, Mumbai, Maharashtra India.
Manju SengarDepartment of Medical Oncology, Tata Memorial Hospital, Homi Bhaba National Institute, Mumbai, 400012, India.
Hari MenonDepartment of Hematology and Medical Oncology, St. Johns National Academy of Health Sciences, Bengaluru, India.
Reena NairDepartment of Clinical Haematology, Tata Medical Center, Kolkata, West Bengal India.
Bhausaheb BagalDepartment of Medical Oncology, Tata Memorial Hospital, Homi Bhaba National Institute, Mumbai, 400012, India.ORCID 0000-0001-9754-0182

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic myeloid leukaemia (CML) is caused by balanced translocation t(9::22)(q34;q11) resulting in formation of pathogenic BCR-ABL fusion gene. Tyrosine kinase inhibitors (TKI) have revolutionised the treatment of CML. Ongoing treatment with TKI leads to side effects and has financial impact. Teratogenic potential of TKI and growth disturbance also represent an important challenge. Thus, TKI discontinuation in form of treatment free remission (TFR) has emerged as a new and important therapeutic goal. In this retrospective study, we reviewed CML patients who were kept on TFR. Inclusion criteria was patient age ≥ 18 years diagnosed with CML in chronic phase who met the criteria for TFR and opted for same and who were in DMR but stopped TKI for any reason. We analysed the data for baseline characteristics, molecular relapse (MR), survival without molecular relapse (SWMR), TFR duration and factors affecting MR. We included 38 patients in this analysis. Thirty five (92%) patients were treated with imatinib at diagnosis. Median duration of TKI treatment was 135 months. 37 patients (97.5%) achieved DMR on TKI and median time from TKI initiation to DMR was 96 months. Median duration of DMR prior to TKI discontinuation was 41 months. TKI was discontinued after counselling for TFR in 26 patients (68%) while it was discontinued due to intolerance in 10 patients (29%). At median molecular follow up of 25 months, nine patients (23.7%) had molecular relapse. Median SWMR was not reached and 2 year estimated SWMR was 65.2% (95%CI,47.2- 83.2). Of all relapses, 5/9 (55.5%) occurred in the first six months of TFR. On univariate analysis, duration of TKI and duration of DMR were predictive of molecular relapse. On multivariate analysis, none of these factors were found to be significant. This retrospective study suggests that for CML CP patients achieving deep molecular response, discontinuing TKI therapy in real-world settings may be feasible while potentially achieving comparable outcomes.

Indexed as

Chronic Myeloid LeukemiaImatinibTreatment Free RemissionTyrosine Kinase Inhibitors

Identifiers

PMID39469157
PMCPMC11512963

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