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← Acute Lymphoblastic Leukemia

HEALTH PROFESSIONAL · SOURCE READING

Supportive care

Source: Acute Lymphoblastic Leukemia Treatment (PDQ®)–Health Professional Version, National Cancer Institute.

Source updated: March 17, 2025 · Captured 2026-09-09.

Selected source text with whitespace normalised. This Triangle page is not an NCI PDQ summary.

Context: Treatment of Untreated ALL / Treatment Options for Untreated ALL / Remission induction therapy

Since myelosuppression is an anticipated consequence of both leukemia and its treatment with chemotherapy, patients must be closely monitored during remission induction treatment. Facilities must be available for hematologic support and for the treatment of infectious complications.

Supportive care during remission induction treatment should routinely include red blood cell and platelet transfusions, when appropriate.[19,20]

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Evidence (supportive care):

Randomized clinical trials have shown similar outcomes for patients who received prophylactic platelet transfusions at a level of 10,000/mm3 rather than at a level of 20,000/mm3.[21]

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The incidence of platelet alloimmunization was similar among groups randomly assigned to receive one of the following from random donors:[22]

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The incidence of platelet alloimmunization was similar among groups randomly assigned to receive one of the following from random donors:[22]

Pooled platelet concentrates.

The incidence of platelet alloimmunization was similar among groups randomly assigned to receive one of the following from random donors:[22]

Filtered, pooled platelet concentrates.

The incidence of platelet alloimmunization was similar among groups randomly assigned to receive one of the following from random donors:[22]

Ultraviolet B-irradiated, pooled platelet concentrates.

The incidence of platelet alloimmunization was similar among groups randomly assigned to receive one of the following from random donors:[22]

Filtered platelets obtained by apheresis.

Empiric broad-spectrum antimicrobial therapy is an absolute necessity for febrile patients who are profoundly neutropenic.[23,24] Careful instruction in personal hygiene and dental care and in recognizing early signs of infection are appropriate for all patients. Elaborate isolation facilities, including filtered air, sterile food, and gut flora sterilization, are not routinely indicated but may benefit patients undergoing transplants.[25,26]

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Rapid marrow ablation with consequent earlier marrow regeneration decreases morbidity and mortality. White blood cell transfusions can be beneficial in selected patients with aplastic marrow and serious infections that are not responding to antibiotics.[27] Prophylactic oral antibiotics may be appropriate in patients with expected prolonged, profound granulocytopenia (<100/mm3 for 2 weeks), although further studies are necessary.[28] Serial surveillance cultures may be helpful in detecting the presence or acquisition of resistant organisms in these patients.

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As suggested in a CALGB study (CLB-9111), the use of myeloid growth factors during remission-induction therapy appears to decrease the time to hematopoietic reconstitution.[29,30]

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Publication references

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Preserved source evidence · Not medical advice