Determining the incidence of interstitial pneumonitis and chronic kidney disease following full intensity haemopoetic stem cell transplant conditioned using a forward-planned intensity modulated total body irradiation technique. (May 2021)
- Record Type:
- Journal Article
- Title:
- Determining the incidence of interstitial pneumonitis and chronic kidney disease following full intensity haemopoetic stem cell transplant conditioned using a forward-planned intensity modulated total body irradiation technique. (May 2021)
- Main Title:
- Determining the incidence of interstitial pneumonitis and chronic kidney disease following full intensity haemopoetic stem cell transplant conditioned using a forward-planned intensity modulated total body irradiation technique
- Authors:
- Durie, Emily
Nicholson, Emma
Anthias, Chloe
Dunne, Emma M.
Potter, Mike
Ethell, Mark
Messiou, Christina
Brennan, Joy
Eagle, Sally
Talbot, James
Smyth, Gregory
Ingram, Westley
Saran, Frank
Mandeville, Henry C. - Abstract:
- Highlights: FP IMRT has a low rate of idiopathic IP with only 4% ( n = 3) CTCAE grade ≥ 3. 30% developed IP due to any cause; evidence of an underlying infective cause was identified in 73%. Only 2 long term survivors developed CKD, 1 having thrombotic microangiopathy. NRM at 4 years was 16% and no patients had evidence of primary graft failure. Abstract: Purpose/Objective: Total body irradiation (TBI) remains a key component of conditioning for allogeneic haemopoietic stem cell transplant (HSCT), with interstitial pneumonitis (IP) and chronic kidney disease (CKD) important late sequelae. We undertook a retrospective service evaluation of TBI patients treated with a forward-planned intensity modulated radiotherapy technique (FP IMRT). Material/Methods: 74 adult patients were identified; all received step and shoot FP IMRT TBI, 14.4 Gy in 8 fractions over 4 days. Mean doses to the lungs and kidneys were 12–12.5 Gy. Toxicities were defined as per CTCAE v4.0: IP as multilobar infiltrates on CT with symptoms of dyspnoea, and renal dysfunction as an Estimated Glomerular Filtration rate (eGFR) < 60 ml/min/1.73 m 2 for > 3 months. Secondary endpoints were overall survival (OS), progression free survival (PFS), cumulative incidence of non-relapse mortality (NRM), relapse risk and of acute and chronic GvHD. Results: Patients received treatment for the following diagnosis: ALL/LBL ( n = 37); AML ( n = 33), CML-BC ( n = 2) and High grade NHL ( n = 2). The rate of IP due to anyHighlights: FP IMRT has a low rate of idiopathic IP with only 4% ( n = 3) CTCAE grade ≥ 3. 30% developed IP due to any cause; evidence of an underlying infective cause was identified in 73%. Only 2 long term survivors developed CKD, 1 having thrombotic microangiopathy. NRM at 4 years was 16% and no patients had evidence of primary graft failure. Abstract: Purpose/Objective: Total body irradiation (TBI) remains a key component of conditioning for allogeneic haemopoietic stem cell transplant (HSCT), with interstitial pneumonitis (IP) and chronic kidney disease (CKD) important late sequelae. We undertook a retrospective service evaluation of TBI patients treated with a forward-planned intensity modulated radiotherapy technique (FP IMRT). Material/Methods: 74 adult patients were identified; all received step and shoot FP IMRT TBI, 14.4 Gy in 8 fractions over 4 days. Mean doses to the lungs and kidneys were 12–12.5 Gy. Toxicities were defined as per CTCAE v4.0: IP as multilobar infiltrates on CT with symptoms of dyspnoea, and renal dysfunction as an Estimated Glomerular Filtration rate (eGFR) < 60 ml/min/1.73 m 2 for > 3 months. Secondary endpoints were overall survival (OS), progression free survival (PFS), cumulative incidence of non-relapse mortality (NRM), relapse risk and of acute and chronic GvHD. Results: Patients received treatment for the following diagnosis: ALL/LBL ( n = 37); AML ( n = 33), CML-BC ( n = 2) and High grade NHL ( n = 2). The rate of IP due to any cause was 30%; positive microbiological evidence in 73% (16 /22). Idiopathic IP was seen in 8%, with only 4% ( n = 3) having IP Grade ≥ 3. Two (4%) of 52 long term survivors developed CKD, one with thrombotic microangiopathy. 4 year NRM was 16% (CI 11–32%); no treatment related deaths in matched sibling or umbilical cord blood HSCT. Conclusion: FP IMRT TBI, reducing dose to the lungs and kidneys, has lower rates of idiopathic IP and CKD compared to the literature. This technique is safe and effective conditioning for full intensity HSCT. … (more)
- Is Part Of:
- Radiotherapy and oncology. Volume 158(2021)
- Journal:
- Radiotherapy and oncology
- Issue:
- Volume 158(2021)
- Issue Display:
- Volume 158, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 158
- Issue:
- 2021
- Issue Sort Value:
- 2021-0158-2021-0000
- Page Start:
- 97
- Page End:
- 103
- Publication Date:
- 2021-05
- Subjects:
- ALL acute lymphocytic leukaemia -- AML Acute myeloid leukaemia -- ARDS acute Respiratory distress syndrome -- CKD chronic kidney disease -- CML-BC chronic myeloid leukaemia-blast crisis -- CMV cytomegalovirus -- CNI calcineurin inhibitor -- CSA cyclosporine -- CT computed tomography -- eGFR Estimated glomerular filtration rate -- FP IMRT forward-planned intensity modulated radiotherapy -- GvHD graft versus host disease -- Gy gray -- HSCT haemopoetic stem cell transplant -- IP interstitial pneumonitis -- LBL lymphoblastic lymphoma -- MMF mycophenolate mofetil -- MUD matched unrelated donor -- NHL non Hodgkins lymphoma -- NRM non-relapse mortality -- OS Overall survival -- PFS progression free survival -- SMN subsequent malignant neoplasm -- TBI total body irradiation -- TMA thrombotic microangiopathy (TMA) -- UCB umbilical cord blood
Whole-body irradiation -- Lung diseases, Interstitial -- Renal insufficiency, Chronic -- Radiotherapy, Intensity modulated -- Hematopoietic stem cell transplant -- Thrombotic microangiopathies
Oncology -- Periodicals
Radiotherapy -- Periodicals
Tumors -- Periodicals
Medical Oncology -- Periodicals
Neoplasms -- radiotherapy -- Periodicals
Radiotherapy -- Periodicals
Radiothérapie -- Périodiques
Cancérologie -- Périodiques
Tumeurs -- Périodiques
Electronic journals
616.9940642 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01678140 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01678140 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01678140 ↗
http://www.estro.org/ ↗
http://www.elsevier.com/journals ↗
http://www.journals.elsevier.com/radiotherapy-and-oncology/ ↗ - DOI:
- 10.1016/j.radonc.2021.02.020 ↗
- Languages:
- English
- ISSNs:
- 0167-8140
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 7240.790000
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