eMedicine Specialties > Hematology > Stem Cells and Disorders

Acute Lymphoblastic Leukemia: Follow-up

Author: Karen Seiter, MD, Professor, Department of Internal Medicine, Division of Oncology/Hematology, New York Medical College
Contributor Information and Disclosures

Updated: Feb 3, 2009

Follow-up

Further Inpatient Care

  • Patients with acute lymphoblastic leukemia (ALL) require admission for induction chemotherapy, and they require readmission for consolidation chemotherapy or for the treatment of toxic effects of chemotherapy.

Further Outpatient Care

  • Maintenance therapy is administered in an outpatient setting.
  • Patients come to the office to be monitored for disease status and the effects of chemotherapy.

Transfer

  • Patients with acute lymphoblastic leukemia (ALL) are best treated at a center with personnel who have significant experience in the treatment of leukemia.
  • Patients admitted to hospitals that lack appropriate blood product support facilities, leukapheresis capabilities, or physicians and nurses familiar with the treatment of patients with leukemia should be transferred to an appropriate (generally tertiary care) hospital.

Deterrence/Prevention

  • While taking chemotherapy, patients with leukemia should avoid exposure to crowds and people with contagious illnesses, especially children with viral infections.

Complications

  • Death in those with acute lymphoblastic leukemia (ALL) may occur as a result of uncontrolled infection or hemorrhage. This may occur even after the use of appropriate blood product and antibiotic support.
  • The most common complication is failure of the leukemia to respond to chemotherapy. These patients do poorly because they usually do not respond to other chemotherapy regimens.

Prognosis

  • Patients with acute lymphoblastic leukemia (ALL) are divided into the following 3 prognostic groups:
    • Good risk includes (1) no adverse cytogenetics, (2) age younger than 30 years, (3) WBC count of less than 30,000/μL, and (4) complete remission within 4 weeks.
    • Intermediate risk includes those whose condition does not meet the criteria for either good risk or poor risk.
    • Poor risk includes (1) adverse cytogenetics [(t9;22), (4;11)], (2) age older than 60 years, (3) precursor B-cell WBCs with WBC count greater than 100,000/μL, or (4) failure to achieve complete remission within 4 weeks.
      • Patients with precursor B-cell ALL have an extremely poor prognosis. Essentially, following standard chemotherapy or autologous transplantation, long-term survival is not achieved. Several reports have indicated that some patients with precursor B-cell ALL and t(4;11) may have prolonged survival following allogeneic transplantation; therefore, this is the treatment of choice.
  • The effect of immunophenotype on prognosis are as follows:
    • Czuczman et al studied 259 patients treated with several CALGB protocols for newly diagnosed acute lymphoblastic leukemia (ALL).32 B-lineage phenotype was expressed in 79% of patients; one third of these coexpressed myeloid antigens. Seventeen percent of patients demonstrated T-lineage ALL; one quarter of these coexpressed myeloid antigens. No significant difference in response rates, remission duration, or survival was observed for patients expressing myeloid antigens versus those not expressing myeloid antigens. T-lineage acute lymphoblastic leukemia (ALL) was associated with younger age, male sex, presence of a mediastinal mass, higher WBC count and hemoglobin level, longer survival, and longer disease-free survival. The number of T markers expressed also had prognostic significance. Patients expressing 6 or more markers had longer disease-free and overall survival compared with patients expressing 3 or fewer markers.
    • In a report by Preti et al, 64 of 162 patients with newly diagnosed acute lymphoblastic leukemia (ALL) coexpressed myeloid markers.33 Patients coexpressing myeloid markers were significantly older, had a higher prevalence of CD34 expression, and had a lower prevalence of common ALL antigen expression than patients without myeloid expression. A trend toward a decreased remission rate was observed for patients coexpressing myeloid markers (64%) as compared with those who did not coexpress such markers (78%) (P = 0.06). However, no significant effect on remission duration or overall survival was observed.
  • The effect of chromosome number on prognosis is displayed in Table 2.

Patient Education

  • Patients with acute lymphoblastic leukemia (ALL) should be instructed to immediately seek medical attention if they are febrile or have signs of bleeding.

Miscellaneous

Medicolegal Pitfalls

  • Patients with acute lymphoblastic leukemia (ALL) are best treated by physicians who have significant experience in the treatment of patients with acute leukemia. In addition, these patients should be treated in a setting where appropriate supportive care measures (high-level blood banking and leukapheresis) are available.
 


More on Acute Lymphoblastic Leukemia

Overview: Acute Lymphoblastic Leukemia
Differential Diagnoses & Workup: Acute Lymphoblastic Leukemia
Treatment & Medication: Acute Lymphoblastic Leukemia
Follow-up: Acute Lymphoblastic Leukemia
Multimedia: Acute Lymphoblastic Leukemia
References
Further Reading

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Further Reading

Related eMedicine Topics

Keywords

acute lymphoblastic leukemia, ALL, lymphoid precursor cells, lymphoblasts, malignant lymphoid disorder, cancer, bone marrow malignancy, bone marrow cancer, leukemia, bone marrow failure, lymphoma, bone marrow carcinoma, anemia, thrombocytopenia, neutropenia, leukemia in children,

bone pain, splenomegaly, mediastinal mass, leukostasis, dizziness, palpitations, dyspnea, disseminated intravascular coagulation, DIC, pneumonia, petechiae, ecchymoses, hepatosplenomegaly, lymphadenopathy, Philadelphia chromosome, Ph chromosome, myeloproliferative disorder

Contributor Information and Disclosures

Author

Karen Seiter, MD, Professor, Department of Internal Medicine, Division of Oncology/Hematology, New York Medical College
Karen Seiter, MD is a member of the following medical societies: American Association for Cancer Research, American College of Physicians, and American Society of Hematology
Disclosure: Novartis Honoraria Speaking and teaching; Schering Honoraria Speaking and teaching; Cephalon Honoraria Speaking and teaching

Medical Editor

Clarence Sarkodee-Adoo, MD, Consulting Staff, Department of Bone Marrow Transplantation, City of Hope Samaritan BMT Program
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Ronald A Sacher, MB, BCh, MD, FRCPC, Professor, Internal Medicine and Pathology, Director, Hoxworth Blood Center, University of Cincinnati Academic Health Center
Ronald A Sacher, MB, BCh, MD, FRCPC is a member of the following medical societies: American Society of Hematology
Disclosure: Glaxo Smith Kline Honoraria Speaking and teaching; Talecris Honoraria Board membership

CME Editor

Rajalaxmi McKenna, MD, FACP, Southwest Medical Consultants, SC, Department of Medicine, Good Samaritan Hospital, Advocate Health Systems
Rajalaxmi McKenna, MD, FACP is a member of the following medical societies: American Society of Clinical Oncology, American Society of Hematology, and International Society on Thrombosis and Haemostasis
Disclosure: Nothing to disclose.

Chief Editor

Emmanuel C Besa, MD, Professor, Department of Medicine, Division of Hematologic Malignancies, Kimmel Cancer Center, Thomas Jefferson University
Emmanuel C Besa, MD is a member of the following medical societies: American Association for Cancer Education, American College of Clinical Pharmacology, American Federation for Medical Research, American Society of Hematology, and New York Academy of Sciences
Disclosure: Nothing to disclose.

 
 
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