Nos EUA, a taxa estimada de sobrevida relativa em 5 anos para a LLA é 72.0%. (dados de 2014-2020).[10]National Cancer Institute. SEER Explorer: All cancer sites combined. Recent trends in SEER age-adjusted incidence rates, 2000-2020. 2023 [internet publication].
https://seer.cancer.gov/statistics-network/explorer/application.html?site=1&data_type=1&graph_type=2&compareBy=sex&chk_sex_3=3&chk_sex_2=2&rate_type=2&race=1&age_range=1&hdn_stage=101&advopt_precision=1&advopt_show_ci=on&hdn_view=0&advopt_show_apc=on&advopt_display=2#resultsRegion0
O desfecho nos pacientes adultos depende da idade. A taxa de sobrevida relativa em 5 anos estimada (dados de 2014-2020) é:[10]National Cancer Institute. SEER Explorer: All cancer sites combined. Recent trends in SEER age-adjusted incidence rates, 2000-2020. 2023 [internet publication].
https://seer.cancer.gov/statistics-network/explorer/application.html?site=1&data_type=1&graph_type=2&compareBy=sex&chk_sex_3=3&chk_sex_2=2&rate_type=2&race=1&age_range=1&hdn_stage=101&advopt_precision=1&advopt_show_ci=on&hdn_view=0&advopt_show_apc=on&advopt_display=2#resultsRegion0
81.6% para pacientes com idade <50 anos
41.7% para pacientes com idade entre 50-64 anos
25.3% para pacientes com idade de 65 anos ou mais
Fatores de prognóstico
As características de prognóstico desfavorável incluem idade avançada, contagem elevada de leucócitos à apresentação, falha em atingir a remissão completa (RC) e anormalidades citogenéticas adversas.
Pacientes mais jovens com leucócitos inferiores a 30 x 10⁹/L (30,000/microlitro) que respondem ao tratamento em 4 semanas têm melhor prognóstico.[1]Pui CH, Relling MV, Downing JR. Acute lymphoblastic leukemia. N Engl J Med. 2004 Apr 8;350(15):1535-48.
http://www.ncbi.nlm.nih.gov/pubmed/15071128?tool=bestpractice.com
[87]Pui CH, Evans WH. Treatment of acute lymphoblastic leukemia. N Engl J Med. 2006 Jan 12;354(2):166-78.
http://www.ncbi.nlm.nih.gov/pubmed/16407512?tool=bestpractice.com
[169]Thomas X, Le QH. Current therapeutic strategies in acute lymphoblastic leukemia in the adult. Bull Cancer. 2003 Oct;90(10):833-50.
http://www.ncbi.nlm.nih.gov/pubmed/14706913?tool=bestpractice.com
[170]Thomas X, Le QH. Prognostic factors in adult acute lymphoblastic leukemia. Hematology. 2003 Aug;8(4):233-42.
http://www.ncbi.nlm.nih.gov/pubmed/12911941?tool=bestpractice.com
[171]Pui CH, Carroll WL, Meshinchi S, et al. Biology, risk stratification, and therapy of pediatric acute leukemias: an update. J Clin Oncol. 2011 Feb 10;29(5):551-65.
http://www.ncbi.nlm.nih.gov/pubmed/21220611?tool=bestpractice.com
[172]Rowe JM. Prognostic factors in adult acute lymphoblastic leukaemia. Br J Haematol. 2010 Aug;150(4):389-405.
http://www.ncbi.nlm.nih.gov/pubmed/20573154?tool=bestpractice.com
O risco individual depende de diversos fatores clínicos e biológicos, incluindo:
No entanto, entre as crianças, aquelas com <1 ano de idade são consideradas de risco muito alto, aquelas com idade ≥10 anos são consideradas de risco alto e aquelas com idade de 1-9 anos são consideradas de risco padrão.[74]Hunger SP, Loh ML, Whitlock JA, et al. Children's Oncology Group's 2013 blueprint for research: acute lymphoblastic leukemia. Pediatr Blood Cancer. 2013 Jun;60(6):957-63.
http://www.ncbi.nlm.nih.gov/pubmed/23255467?tool=bestpractice.com
[173]Smith M, Arthur D, Camitta B, et al. Uniform approach to risk classification and treatment assignment for children with acute lymphoblastic leukemia. J Clin Oncol. 1996 Jan;14(1):18-24.
http://www.ncbi.nlm.nih.gov/pubmed/8558195?tool=bestpractice.com
Os adultos com >35 anos de idade são considerados de alto risco, embora o impacto da idade seja uma variável contínua.[75]Rowe JM, Buck G, Burnett AK, et al. Induction therapy for adults with acute lymphoblastic leukemia: results of more than 1500 patients from the international ALL trial: MRC UKALL XII/ECOG E2993. Blood. 2005 Dec 1;106(12):3760-7.
https://ashpublications.org/blood/article/106/12/3760/109755/Induction-therapy-for-adults-with-acute
http://www.ncbi.nlm.nih.gov/pubmed/16105981?tool=bestpractice.com
[76]Goldstone AH, Richards SM, Lazarus HM, et al. In adults with standard-risk acute lymphoblastic leukemia, the greatest benefit is achieved from a matched sibling allogeneic transplantation in first complete remission, and an autologous transplantation is less effective than conventional consolidation/maintenance chemotherapy in all patients: final results of the International ALL Trial (MRC UKALL XII/ECOG E2993). Blood. 2008 Feb 15;111(4):1827-33.
https://ashpublications.org/blood/article/111/4/1827/133215/In-adults-with-standard-risk-acute-lymphoblastic
http://www.ncbi.nlm.nih.gov/pubmed/18048644?tool=bestpractice.com
Contagem leucocitária na apresentação: uma variável contínua, >30 × 10⁹/L (>30,000/microlitro) para LLA-B e >100 × 10⁹/L (>100,000/microlitro) para LLA-T são considerados de alto risco para adultos e >50 × 10⁹/L (>50,000/microlitro) para LLA-B é considerado de alto risco para crianças.[74]Hunger SP, Loh ML, Whitlock JA, et al. Children's Oncology Group's 2013 blueprint for research: acute lymphoblastic leukemia. Pediatr Blood Cancer. 2013 Jun;60(6):957-63.
http://www.ncbi.nlm.nih.gov/pubmed/23255467?tool=bestpractice.com
Anormalidades citogenéticas e moleculares. Consulte Critérios diagnósticos.
Subtipo imunofenotípico: A expressão de CD20 está associada a um prognóstico desfavorável.[77]Jeha S, Behm F, Pei D, et al. Prognostic significance of CD20 expression in childhood B-cell precursor acute lymphoblastic leukemia. Blood. 2006 Nov 15;108(10):3302-4.
https://ashpublications.org/blood/article/108/10/3302/22786/Prognostic-significance-of-CD20-expression-in
http://www.ncbi.nlm.nih.gov/pubmed/16896151?tool=bestpractice.com
Resposta à terapia de indução: pacientes que recebem terapia de indução que não atingem RC ou que respondem mal são considerados de alto risco.
Presença de doença residual mensurável (DRM; por exemplo, ≥0.01%) após a terapia de indução: a DRM persistente após a indução está associada desfechos desfavoráveis.[78]Dekker SE, Rea D, Cayuela JM, et al. Using measurable residual disease to optimize management of AML, ALL, and chronic myeloid leukemia. Am Soc Clin Oncol Educ Book. 2023 Jun;43:e390010.
https://ascopubs.org/doi/10.1200/EDBK_390010?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%20%200pubmed
http://www.ncbi.nlm.nih.gov/pubmed/37311155?tool=bestpractice.com
Comprometimento do sistema nervoso central (SNC)
O envolvimento do SNC é uma das principais complicações da LLA, ocorrendo em 5% a 7% dos pacientes no momento do diagnóstico; a incidência é maior nos pacientes com LLA-T (8%) e LLA-B madura (linfoma de Burkitt/leucemia, 13%).[50]Reman O, Pigneux A, Huguet F, et al. Central nervous system involvement in adult acute lymphoblastic leukemia at diagnosis and/or at first relapse: results from the GET-LALA group. Leuk Res. 2008 Nov;32(11):1741-50.
http://www.ncbi.nlm.nih.gov/pubmed/18508120?tool=bestpractice.com
[51]Lazarus HM, Richards SM, Chopra R, et al. Central nervous system involvement in adult acute lymphoblastic leukemia at diagnosis: results from the international ALL trial MRC UKALL XII/ECOG E2993. Blood. 2006 Jul 15;108(2):465-72.
https://ashpublications.org/blood/article/108/2/465/109893/Central-nervous-system-involvement-in-adult-acute
http://www.ncbi.nlm.nih.gov/pubmed/16556888?tool=bestpractice.com
[52]Pui CH. Central nervous system disease in acute lymphoblastic leukemia: prophylaxis and treatment. Hematology Am Soc Hematol Educ Program. 2006 Jan;(1):142-6.
https://ashpublications.org/hematology/article/2006/1/142/19688/Central-Nervous-System-Disease-in-Acute
http://www.ncbi.nlm.nih.gov/pubmed/17124053?tool=bestpractice.com
[53]Lamanna N, Weiss M. Treatment options for newly diagnosed patients with adult acute lymphoblastic leukemia. Curr Hematol Rep. 2004 Jan;3(1):40-6.
http://www.ncbi.nlm.nih.gov/pubmed/14695849?tool=bestpractice.com
[54]Richards S, Pui CH, Gayon P, et al. Systematic review and meta-analysis of randomized trials of central nervous system directed therapy for childhood acute lymphoblastic leukemia. Pediatr Blood Cancer. 2013 Feb;60(2):185-95.
https://onlinelibrary.wiley.com/doi/10.1002/pbc.24228
http://www.ncbi.nlm.nih.gov/pubmed/22693038?tool=bestpractice.com
O envolvimento do SNC pode levar a morbidade neurológica grave (ou seja, paralisias de nervos cranianos), sendo um grande obstáculo à cura, representando até 40% das recaídas iniciais em ensaios clínicos.[79]Krishnan S, Wade R, Moorman AV, et al. Temporal changes in the incidence and pattern of central nervous system relapses in children with acute lymphoblastic leukaemia treated on four consecutive Medical Research Council trials, 1985-2001. Leukemia. 2010 Feb;24(2):450-9.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2820451
http://www.ncbi.nlm.nih.gov/pubmed/20016529?tool=bestpractice.com
[80]Laningham FH, Kun LE, Reddick WE, et al. Childhood central nervous system leukemia: historical perspectives, current therapy, and acute neurological sequelae. Neuroradiology. 2007 Nov;49(11):873-88.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386669
http://www.ncbi.nlm.nih.gov/pubmed/17924103?tool=bestpractice.com
[81]Pui CH, Howard SC. Current management and challenges of malignant disease in the CNS in paediatric leukaemia. Lancet Oncol. 2008 Mar;9(3):257-68.
http://www.ncbi.nlm.nih.gov/pubmed/18308251?tool=bestpractice.com
Estudos mostraram que o uso de esquemas intensivos em pacientes com envolvimento do SNC ao diagnóstico resulta em desfechos semelhantes (ou seja, RC, sobrevida livre de doença e sobrevida global) aos de pacientes sem envolvimento do SNC ao diagnóstico, particularmente entre os adultos.[50]Reman O, Pigneux A, Huguet F, et al. Central nervous system involvement in adult acute lymphoblastic leukemia at diagnosis and/or at first relapse: results from the GET-LALA group. Leuk Res. 2008 Nov;32(11):1741-50.
http://www.ncbi.nlm.nih.gov/pubmed/18508120?tool=bestpractice.com
[51]Lazarus HM, Richards SM, Chopra R, et al. Central nervous system involvement in adult acute lymphoblastic leukemia at diagnosis: results from the international ALL trial MRC UKALL XII/ECOG E2993. Blood. 2006 Jul 15;108(2):465-72.
https://ashpublications.org/blood/article/108/2/465/109893/Central-nervous-system-involvement-in-adult-acute
http://www.ncbi.nlm.nih.gov/pubmed/16556888?tool=bestpractice.com
[82]Thomas X, Boiron JM, Huguet F, et al. Outcome of treatment in adults with acute lymphoblastic leukemia: analysis of the LALA-94 trial. J Clin Oncol. 2004 Oct 15;22(20):4075-86.
https://ascopubs.org/doi/10.1200/JCO.2004.10.050
http://www.ncbi.nlm.nih.gov/pubmed/15353542?tool=bestpractice.com
[83]Petersdorf SH, Kopecky KJ, Head DR, et al. Comparison of the L10M consolidation regimen to an alternative regimen including escalating methotrexate/L-asparaginase for adult acute lymphoblastic leukemia: a Southwest Oncology Group Study. Leukemia. 2001 Feb;15(2):208-16.
http://www.ncbi.nlm.nih.gov/pubmed/11236936?tool=bestpractice.com
[84]Kantarjian HM, O'Brien S, Smith TL, et al. Results of treatment with hyper-CVAD, a dose-intensive regimen, in adult acute lymphocytic leukemia. J Clin Oncol. 2000 Feb;18(3):547-61.
http://www.ncbi.nlm.nih.gov/pubmed/10653870?tool=bestpractice.com
[85]Hoelzer D, Thiel E, Löffler H, et al. Prognostic factors in a multicenter study for treatment of acute lymphoblastic leukemia in adults. Blood. 1988 Jan;71(1):123-31.
https://www.sciencedirect.com/science/article/pii/S0006497120782339
http://www.ncbi.nlm.nih.gov/pubmed/3422030?tool=bestpractice.com
No entanto, os desfechos costumam ser desaforáveis nos pacientes com recidiva no SNC (sobrevida global mediana <1 ano).[86]Surapaneni UR, Cortes JE, Thomas D, et al. Central nervous system relapse in adults with acute lymphoblastic leukemia. Cancer. 2002 Feb 1;94(3):773-9.
https://acsjournals.onlinelibrary.wiley.com/doi/full/10.1002/cncr.10265?sid=nlm%3Apubmed
http://www.ncbi.nlm.nih.gov/pubmed/11857312?tool=bestpractice.com
Os pacientes com envolvimento do SNC (particularmente recidiva no SNC) geralmente justificam a consideração de um transplante alogênico de células-tronco (TCT) pós-remissão.[59]Hoelzer D, Bassan R, Dombret H, et al. Acute lymphoblastic leukaemia in adult patients: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2016 Sep;27(suppl 5):v69-82.
https://www.annalsofoncology.org/article/S0923-7534(19)31639-4/fulltext
http://www.ncbi.nlm.nih.gov/pubmed/27056999?tool=bestpractice.com
[69]Kopmar NE, Cassaday RD. How I prevent and treat central nervous system disease in adults with acute lymphoblastic leukemia. Blood. 2023 Mar 23;141(12):1379-88.
https://ashpublications.org/blood/article/141/12/1379/493851/How-I-prevent-and-treat-central-nervous-system
http://www.ncbi.nlm.nih.gov/pubmed/36548957?tool=bestpractice.com
Doença recidivante/refratária
Geralmente, o prognóstico é desfavorável na doença refratária ou recidivante. A sobrevida mediana é inferior a 1 ano, e menos de 25% dos pacientes sobrevive em longo prazo.[138]Oriol A, Vives S, Hernández-Rivas JM, et al; Programa Español de Tratamiento en Hematologia Group. Outcome after relapse of acute lymphoblastic leukemia in adult patients included in four consecutive risk-adapted trials by the PETHEMA Study Group. Haematologica. 2010 Apr;95(4):589-96.
https://haematologica.org/article/view/5555
http://www.ncbi.nlm.nih.gov/pubmed/20145276?tool=bestpractice.com
A sobrevida em longo prazo depende da obtenção de remissão completa (RC) com transplante alogênico de células-tronco hematopoéticas (HCT) subsequente.
O risco de um indivíduo depende de diversos fatores clínicos e biológicos, tais como:[174]Teachey DT, Hunger SP. Predicting relapse risk in childhood acute lymphoblastic leukaemia. Br J Haematol. 2013 Sep;162(5):606-20.
https://onlinelibrary.wiley.com/doi/10.1111/bjh.12442
http://www.ncbi.nlm.nih.gov/pubmed/23808872?tool=bestpractice.com
[175]Kebriaei P, Poon LM. The role of allogeneic hematopoietic stem cell transplantation in the therapy of patients with acute lymphoblastic leukemia. Curr Hematol Malig Rep. 2012 Jun;7(2):144-52.
http://www.ncbi.nlm.nih.gov/pubmed/22410763?tool=bestpractice.com
[176]Cassaday RD, Alan Potts D Jr, Stevenson PA, et al. Evaluation of allogeneic transplantation in first or later minimal residual disease - negative remission following adult-inspired therapy for acute lymphoblastic leukemia. Leuk Lymphoma. 2016 Sep;57(9):2109-18.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5010422
http://www.ncbi.nlm.nih.gov/pubmed/27002921?tool=bestpractice.com
Idade: pacientes mais jovens são mais propensos a atingir RC e têm melhor sobrevida.
Longa duração da primeira RC: a sobrevida é melhor para indivíduos cuja duração da primeira remissão é superior a 2 anos.
Local da recidiva: se houver envolvimento de locais adicionais.
Status da doença no TCT: pacientes submetidos a TCT em RC após o resgate tiveram melhor resultado que aqueles que não estavam em RC no momento do TCT. Pacientes que obtêm remissão negativa para DRM com terapia de resgate antes do TCT podem também apresentar desfechos melhores, mas isso não tenha sido definitivamente estabelecido em nenhum ensaio prospectivo.