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]
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]
Source links and citations
The incidence of platelet alloimmunization was similar among groups randomly assigned to receive one of the following from random donors:[22]
Source links and citations
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]
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.
Publication references
Read the original reference and check its publication notices.
- PubMed 2134613 · Original source
- PubMed 2179420 · Original source
- PubMed 3132310 · Original source
- PubMed 3314494 · Original source
- PubMed 3954967 · Original source
- PubMed 6424468 · Original source
- PubMed 6782486 · Original source
- PubMed 6994626 · Original source
- PubMed 7686404 · Original source
- PubMed 9407153 · Original source
- PubMed 9417523 · Original source
- PubMed 9716583 · Original source
Preserved source evidence · Not medical advice
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