A systematic review of post-transplant lymphoproliferative disorder after lung transplant.

Authors

null

Mobeen Zaka Haider

King Edward Medical University, Lahore, Pakistan

Mobeen Zaka Haider , Zarlakhta Zamani , Fnu Kiran , Hasan Mehmood Mirza , Muhammad Taqi , Hafsa Shahid , Deepak Kumar , Karun Neupane , Yousra Khalid , Mohsin Sheraz Mughal , Muhammad Salman Faisal , Muhammad Umair Mushtaq , Faiz Anwer

Organizations

King Edward Medical University, Lahore, Pakistan, Department of Pathology, Sindh Institute of Urology and Transplantation, Karachi, Pakistan, Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA, Mayo Hospital, Lahore, Pakistan, Jinnah Postgraduate Medical Center, Karachi, Pakistan, Manipal College of Medical Sciences, Pokhara, Nepal, Rutger/RWJ/Monmouth Medical Center, Long Branch, NJ, Department of Hematology, BMT, Ohio State University, Columbus, OH, Division of Hematologic Malignancies and Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS, Cleveland Clinic Taussig Cancer Institute, Cleveland, OH

Research Funding

No funding received
None

Background: Post-transplant lymphoproliferative disorder (PTLD) is a serious complication after solid organ transplantation. This study aims to explore the association of PTLD diagnosed after lung transplant with infectious agents and immunosuppression regimen, explore types of PTLD, and their outcome. Methods: Following the PRISMA guideline, we searched the literature on PubMed, Cochrane, Embase, and clinicaltrials.gov. 1741 articles were screened and included five studies. Results: We analyzed data from five studies, n=13,643 transplant recipients with n=287 (2.10%) developed PTLD. Four studies showed that 32/63 (51%) PTLD patients were male and 31 (49%) were female. Three studies reported 53/55 (96.4%) patients were EBV positive at PTLD diagnosis. Courtwright. et al, reported that 217/224 (97%) PTLD was associated with either EBV positive donor or recipient. Four studies showed that the monomorphic B cell type 48/63 (76%) was the most common histological type of PTLD diagnosed with DLBCL the most common subtype 31/48 (64.6%). Data from 3 studies showed that the onset of PTLD following lung transplant varies with a median duration of 18.3 months (45 days to 20.2 years). Three studies showed that 26/55 (47.3%) patients had early-onset (≤ 1 yr of Tx) and 29/55 (52.7%) patients had late-onset PTLD (> 1 yr of Tx). Management of PTLD included a reduction in immunosuppression including corticosteroids, CNI, purine synthesis inhibitors, Rituximab, and chemotherapeutic agents. Three studies showed a mortality rate of 30/45 (66.7%) and 13/30 (43.3%) deaths were PTLD related. Conclusions: Our review concludes that PTLD is a serious complication, only 2% of lung transplant recipients developed PTLD. EBV seropositivity is the most factor associated with PTLD diagnosis. Monomorphic PTLD was reported as the most common type in the adult population and no association between gender and PTLD was found. The analysis shows that there is a slightly lower incidence of early (≤ 1 yr of Tx) than late-onset (> 1 yr of Tx) PTLD. Table 1 PTLD after a Lung transplant in adults - a review.

Study
PTLD /Total pts
Sex

M/F
EBV Status
Type of PTLD
Management
Mortality rate

Survival(srv)


Baldanti
5/111

4.5%
4/1
PostTx + : 5/5
HL : 1/5

DLBCL: 3/5

Neoplastic nodule: 1/5
RIS

MMF CyA
4/5
Courtwright
224/11643 1.9%

+ :217/224



Jaksch
18/1157 1.6%
10/8
PostTx + : 18/18


Mono B : 9/18

Poly B: 9/18
IS: CyA; Tac

AZA; MMF; CS
1 y srv 50%

3 y srv 38%




Saueressig
8/93

8.6%
2/6
PreTx -: ⅞

+: ⅛


mono B 4/8

Poly B ⅜

Plasmacytic hyperplasia 1/8
RIS; Rituximab ChemoRx with CHOP; Anti IL 6 monoclonal antibody
2/8



1 y srv 87.5%

5 y srv 73%
Wudhikarn
32/639

5%
16/16
PreTx +: 24/32

- : 8/32

Post-Tx +: 30/32


Mono DLBCL: 28/32

other 4
RIS

IS with AZA

MMF CyA; CS
24/32



Med srv 10m

AZA: Azathioprine; CS: corticosteroid; CyA: Cyclosporine; DLBCL: diffuse large B-cell lymphoma; Tx: Transplant MMF: Mycophenolate mofetil; Mono: Monomorphic; RIS: reduction in immunosuppression Tac: Tacrolimus; y: years

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Abstract Details

Meeting

2021 ASCO Annual Meeting

Session Type

Publication Only

Session Title

Publication Only: Hematologic Malignancies—Leukemia, Myelodysplastic Syndromes, and Allotransplant

Track

Hematologic Malignancies

Sub Track

Other Leukemia, Myelodysplastic Syndromes, and Allotransplant

Citation

J Clin Oncol 39, 2021 (suppl 15; abstr e19046)

DOI

10.1200/JCO.2021.39.15_suppl.e19046

Abstract #

e19046

Abstract Disclosures

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