Progressive reduction in treatment-related deaths in Medical Research Council childhood lymphoblastic leukaemia trials from 1980 to 1997 (UKALL VIII, X and XI)

被引:61
作者
Hargrave, DR
Hann, IM
Richards, SM
Hill, FG
Lilleyman, JS
Kinsey, S
Bailey, CC
Chessells, JM
Mitchell, C
Eden, OB
机构
[1] Royal Marsden Hosp, Dept Paediat Oncol, Sutton SM2 5PT, Surrey, England
[2] Great Ormond St Hosp Sick Children, Dept Paediat Haematol & Oncol, London WC1N 3JH, England
[3] Radcliffe Infirm, Clin Trial Serv Unit, Oxford OX2 6HE, England
[4] Childrens Hosp, Dept Haematol, Birmingham B16 8ET, W Midlands, England
[5] Royal London Hosp, Dept Paediat Oncol, London E1 1BB, England
[6] St James Hosp, Childrens Day Hosp, Leeds LS9 7TF, W Yorkshire, England
[7] John Radcliffe Infirm, Paediat Oncol Unit, Oxford, England
[8] Manchester Childrens Hosp Trust, Acad Unit Paediat Oncol, Manchester, Lancs, England
[9] Christie Hosp Trust, Acad Unit Paediat Oncol, Manchester, Lancs, England
关键词
acute lymphoblastic leukaemia; induction; first remission; treatment-related death;
D O I
10.1046/j.1365-2141.2001.02543.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the last 20 years, the survival rate for children with acute lymphoblastic leukaemia (ALL) has markedly improved, largely owing to a decrease in relapses. However, children still die from complications of treatment and these are potentially preventable. We have analysed data from three large consecutive national protocols for ALL from 1980 to 1997 [Medical Research Council United Kingdom ALL (MRC UKALL) trials VIII, X and XI] to compare the incidence and causes of treatment-related deaths (TRD). The percentage of TRD has fallen from 9% to 2% (UKALL VIII to XI), largely as a result of a decrease in fatal infections. Deaths during induction have fallen from 3% to 1%, the main causes of death being bacterial, followed by fungal infection, while other causes, chiefly haemorrhage, have not declined. Remission deaths also decreased from 6% to 1%, particularly those deaths due to measles and pneumocystis carinii. More guidelines for surveillance and treatment of infections have been included within progressively more intensive protocols. Risk factor analysis showed increased TRD in patients with Down's syndrome, high leucocyte count and older age in UKALL XI. In contrast, the introduction of blocks of intensification was not associated with an increased death rate. While improved supportive care has reduced the incidence of TRD, there is still scope for further reduction by prompt treatment of suspected infection. Maintenance of herd immunity remains of vital importance in avoiding deaths from measles.
引用
收藏
页码:293 / 299
页数:7
相关论文
共 22 条
  • [1] ANNEREN G, 1992, ARCH DIS CHILD, V67, P1052
  • [2] REMISSION DEATH IN ACUTE LYMPHOBLASTIC-LEUKEMIA - A CHANGING PATTERN
    ATRA, A
    RICHARDS, SM
    CHESSELLS, JM
    [J]. ARCHIVES OF DISEASE IN CHILDHOOD, 1993, 69 (05) : 550 - 554
  • [3] DIFFERING COMPLICATIONS OF HYPERLEUKOCYTOSIS IN CHILDREN WITH ACUTE LYMPHOBLASTIC OR ACUTE NONLYMPHOBLASTIC LEUKEMIA
    BUNIN, NJ
    PUI, CH
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1985, 3 (12) : 1590 - 1595
  • [4] HEPATOSPLENIC CANDIDIASIS IN CHILDREN WITH CANCER - 3 CASES IN LEUKEMIC CHILDREN AND A LITERATURE-REVIEW
    CARSTENSEN, H
    WIDDING, E
    STORM, K
    OSTERGAARD, E
    HERLIN, T
    [J]. PEDIATRIC HEMATOLOGY AND ONCOLOGY, 1990, 7 (01) : 3 - 12
  • [5] INTENSIFICATION OF TREATMENT AND SURVIVAL IN ALL CHILDREN WITH LYMPHOBLASTIC-LEUKEMIA - RESULTS OF UK MEDICAL-RESEARCH-COUNCIL TRIAL UKALL-X
    CHESSELLS, JM
    BAILEY, C
    RICHARDS, SM
    EDEN, OB
    BARBOR, PRH
    BARRETT, A
    BARTON, C
    BROADBENT, V
    DEMPSEY, SI
    DURRANT, J
    EMERSON, P
    EVANS, DIK
    FENNELLY, JJ
    GALTON, DAG
    GIBSON, B
    GRAY, R
    HANN, IM
    HARDISTY, RM
    HILL, FGH
    KERNAHAN, J
    KING, DJ
    LILLEYMAN, JS
    MANN, J
    MARTIN, J
    MCELWAIN, TJ
    MELLOR, ST
    JONES, PHM
    OAKHILL, A
    PETO, J
    RADFORD, M
    REES, JKH
    STEVENS, RF
    SUMMERFIELD, GP
    THOMPSON, EN
    [J]. LANCET, 1995, 345 (8943) : 143 - 148
  • [6] PNEUMONITIS IN LYMPHOBLASTIC-LEUKEMIA OF CHILDHOOD
    DARBYSHIRE, P
    EDEN, T
    JAMESON, B
    KAY, H
    LILLEYMAN, J
    RANKIN, A
    [J]. EUROPEAN PAEDIATRIC HAEMATOLOGY AND ONCOLOGY, 1985, 2 (03): : 141 - 147
  • [7] DeStefano F, 2000, J Pediatr, V136, P125
  • [8] Down's syndrome in childhood acute lymphoblastic leukemia:: clinical characteristics and treatment outcome in four consecutive BFM trials
    Dördelmann, M
    Schrappe, M
    Reiter, A
    Zimmermann, M
    Graf, N
    Schott, G
    Lampert, F
    Harbott, J
    Niemeyer, C
    Ritter, J
    Dörffel, W
    Nessler, G
    Kühl, J
    Riehm, H
    [J]. LEUKEMIA, 1998, 12 (05) : 645 - 651
  • [9] RESULTS OF MEDICAL-RESEARCH-COUNCIL CHILDHOOD LEUKEMIA TRIAL UKALL-VIII (REPORT TO THE MEDICAL-RESEARCH-COUNCIL ON BEHALF OF THE WORKING PARTY ON LEUKEMIA IN CHILDHOOD)
    EDEN, OB
    LILLEYMAN, JS
    RICHARDS, S
    SHAW, MP
    PETO, J
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1991, 78 (02) : 187 - 196
  • [10] EORTC International Antimicrobial Therapy Cooperative Group, 1990, Eur J Cancer, V26, P569