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LetterLETTERS TO THE EDITOR
Open Access

Comment on “Pneumocystis jirovecii Pneumonia in Patients Treated for Solid Organ Malignancy”

Saad Khan and Bilal Ahmad
Ochsner Journal September 2024, 24 (3) 167; DOI: https://doi.org/10.31486/toj.24.0088
Saad Khan
Saidu Medical College, Saidu Sharif, Swat District, Khyber Pakhtunkhwa, Pakistan
MBBS
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Bilal Ahmad
Saidu Medical College, Saidu Sharif, Swat District, Khyber Pakhtunkhwa, Pakistan
MBBS
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TO THE EDITOR

We recently came across the case series published in the Ochsner Journal by Jackson and colleagues,1 and the paper really struck a chord with us. This work shines a light on a critical clinical challenge that we think deserves a lot more attention—the management of Pneumocystis jirovecii pneumonia (PJP) in patients receiving dose-dense chemotherapy for solid organ malignancies.

As the authors point out, using these intense chemotherapy regimens, such as doxorubicin and cyclophosphamide, has become standard practice for treating early-stage breast cancer. But the downside is that dose-dense chemotherapy seems to be considerably increasing the risk of opportunistic infections such as PJP in these vulnerable patients. And based on the 2 case reports presented by Jackson et al, the consequences can be critical.

The mechanical ventilation and intensive supportive care that these patients required really drives home just how serious PJP can be in this context. Even more concerning is the authors' observation that clear guidelines on PJP prophylaxis are lacking. Current recommendations suggest prophylaxis for groups with a risk >3.5%,2 but the 0.6% incidence rate reported by Waks et al suggests that the >3.5% threshold may not be appropriate.3

In our view, the existing evidence3-6 calls for us to take a hard look at the current guidelines and become much more proactive about PJP prevention in patients on dose-dense chemotherapy. Here are 3 issues we need to focus on:

Better Data Through Prospective Studies

We need to conduct prospective studies to determine the true incidence of PJP in this patient population, including the impact of concurrent steroid use. Incidence data are crucial for informing new guidelines.

Tailored Prophylaxis Guidelines

Based on the findings from those studies, we should develop evidence-based guidelines for PJP prophylaxis that are specifically tailored to patients receiving dose-dense chemotherapy. The risk threshold for starting prophylaxis may need to be lowered.

Raising Clinician Awareness

Oncologists and infectious disease specialists need to be made much more aware of the heightened PJP risk in these patients. Emphasizing early recognition and treatment could make a big difference.

Addressing these issues is vital for improving outcomes in patients with solid organ malignancies who are receiving dose-dense chemotherapy. We commend Jackson et al for reporting on this important topic and hope their case series spurs further research and clinical guidance in this area.

  • ©2024 by the author(s); Creative Commons Attribution License (CC BY)

©2024 by the author(s); licensee Ochsner Journal, Ochsner Clinic Foundation, New Orleans, LA. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (creativecommons.org/licenses/by/4.0/legalcode) that permits unrestricted use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

REFERENCES

  1. 1.↵
    1. Jackson I,
    2. Isern R,
    3. Jesina S,
    4. Velagapudi M,
    5. Pruett W
    . Pneumocystis jirovecii pneumonia in patients treated for solid organ malignancy. Ochsner J. 2024;24(3). doi: 10.31486/toj.24.0024
    OpenUrlAbstract/FREE Full Text
  2. 2.↵
    1. Taplitz RA,
    2. Kennedy EB,
    3. Bow EJ,
    4. et al.
    Antimicrobial prophylaxis for adult patients with cancer-related immunosuppression: ASCO and IDSA clinical practice guideline update. J Clin Oncol. 2018;36(30):3043-3054. doi: 10.1200/JCO.18.00374
    OpenUrlCrossRefPubMed
  3. 3.↵
    1. Waks AG,
    2. Tolaney SM,
    3. Galar A,
    4. et al.
    Pneumocystis jiroveci pneumonia (PCP) in patients receiving neoadjuvant and adjuvant anthracycline-based chemotherapy for breast cancer: incidence and risk factors. Breast Cancer Res Treat. 2015;154(2):359-367. doi: 10.1007/s10549-015-3573-2
    OpenUrlCrossRefPubMed
  4. 4.
    1. Thomas CF Jr.,
    2. Limper AH
    . Current insights into the biology and pathogenesis of Pneumocystis pneumonia. Nat Rev Microbiol. 2007;5(4):298-308. doi: 10.1038/nrmicro1621
    OpenUrlCrossRefPubMed
  5. 5.
    1. Stern A,
    2. Green H,
    3. Paul M,
    4. Vidal L,
    5. Leibovici L
    . Prophylaxis for Pneumocystis pneumonia (PCP) in non-HIV immunocompromised patients. Cochrane Database Syst Rev. 2014;2014(10):CD005590. doi: 10.1002/14651858.CD005590.pub3
    OpenUrlCrossRef
  6. 6.↵
    1. Jeon CH,
    2. Kim SH,
    3. Kim S,
    4. Bae M,
    5. Lee SJ,
    6. Lim S
    . Pneumocystis jirovecii pneumonia in patients with solid malignancies: a retrospective study in two hospitals. Pathogens. 2022;11(10):1169. doi: 10.3390/pathogens11101169
    OpenUrlCrossRef
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Comment on “Pneumocystis jirovecii Pneumonia in Patients Treated for Solid Organ Malignancy”
Saad Khan, Bilal Ahmad
Ochsner Journal Sep 2024, 24 (3) 167; DOI: 10.31486/toj.24.0088

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Comment on “Pneumocystis jirovecii Pneumonia in Patients Treated for Solid Organ Malignancy”
Saad Khan, Bilal Ahmad
Ochsner Journal Sep 2024, 24 (3) 167; DOI: 10.31486/toj.24.0088
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