Matched and Mismatched Unrelated Donor Versus Unmanipulated Haploidentical Donors for Hematopoietic Cell Transplantation in Acute Leukemia in Remission: A Pair Matched Analysis on Behalf of the Acute Leukemia Working Party (ALWP) of the European Society for Blood and Marrow Transplantation (EBMT)

Abstract Background. The best donor source for adult patients with acute leukemia lacking an HLA-identical donor still remains to be established. The objective of this study was to compare the outcome after T-cell-replete hematopoietic stem cell transplantation from haploidentical donor (HAPLO) and transplant from Matched Unrelated Donor (MUD) or Mismatched Unrelated Donor at a single HLA-locus (MMUD) for patients with acute leukemia in remission. Methods. From January 2007 to December 2012, 313 consecutive HAPLOs were performed as first allogeneic transplants in adult patients with de novo acute leukemia in CR1 or CR2 and reported to the EBMT Registry. We were able to pair match 273 of these 313 patients with another 273 patients who received a MUD and 273 who received a MMUD transplant. The matching factors were as follow: age (+/-5y), diagnosis (myeloid or lymphoblastic leukemia), disease status at transplant (CR1 or CR2) and interval from diagnosis to transplant (+/-1mo). Results. The median follow-up was 22 months. The two-year non-relapse mortality (NRM) and relapse (RI) cumulative incidences were 28% and 30% for HAPLO, 21% and 19% for MUD, and 28% and 27% for MMUD. The two-year KM estimates of leukemia-free survival (LFS) and overall survival (OS) were 42% and 49% for HAPLO, 59% and 65% for MUD, 45% and 51% for MMUD. In multivariate analysis both NRM and RI were significantly reduced in MUD compared to HAPLO (NRM, hazard ratio (HR): 0.61, p=0.02, 95%CI: 0.40-0.91; RI, HR: 0.59, p=0.01, 95%CI: 0.39-0.89) but there was no statistical difference between HAPLO and MMUD (NRM, p=0.59; RI, p=0.52). LFS and OS were significantly higher in MUD compared to HAPLO (LFS HR: 0.61, p=0.001, 95%CI: 0.45-0.81.OS HR: 0.63, p=0.004, 95%CI: 0.46-0.86) but not statistically different between MMUD and HAPLO (LFS, p=0.45. OS, p=0.84). Of note, type of donor was neither associated with day-100 grade II-IV acute graft-versus-host disease, nor to chronic graft-versus-host disease. Conclusion. These findings suggest that LFS and OS were significantly higher in patients with acute leukemia in remission receiving a MUD compared to patients with similar characteristics receiving a HAPLO. We didn’t find significant differences between MMUD and HAPLO. In the absence of a MUD, host/donor features and urgency of transplant should drive us towards the best choice between these alternative donor sources. Disclosures No relevant conflicts of interest to declare.

Download Full-text

Impact of clostridiodes difficile infection on acute graft-versus-host disease in allogenic transplant patients.

Journal of Clinical Oncology ◽

10.1200/jco.2021.39.15_suppl.e19027 ◽

2021 ◽

Vol 39 (15_suppl) ◽

pp. e19027-e19027

Author(s):

Prasanth Lingamaneni ◽

Vatsala Katiyar ◽

Rohit Kumar ◽

Maha A.T. Elsebaie ◽

Hashim Mann ◽

...

Keyword(s):

Graft Versus Host Disease ◽

Lymphoblastic Leukemia ◽

Index Admission ◽

Unrelated Donor ◽

Cell Transplant ◽

Hematopoietic Stem ◽

Host Disease ◽

Graft Versus Host ◽

Hospitalization Costs ◽

Acute Graft

e19027 Background: Clostridiodes difficile infection (CDI) is reported to occur up to 9-fold higher in allogenic hematopoietic stem cell transplant (HSCT) recipients compared to the general population of hospitalized patients. This is attributed to disruption of gut microbiome by antibiotics, myeloablative regimens, neutropenia, prolonged hospitalization, and immunosuppressive regimens administered to prevent acute graft-versus-host disease (aGVHD). CDI by disruption of the intestinal microbiome may trigger gastrointestinal aGVHD. Previous studies from HSCT centers have reported conflicting data on the relationship between CDI and subsequent development of aGVHD. Methods: The Nationwide Readmissions Database was queried for admissions of adult allogenic HSCT patients between 2016 and 2018. Those with and without CDI during index admission were compared. Multivariable logistic regression was used to evaluate the primary outcome of risk of aGVHD in the index admission or within 100 days post-engraftment. Results: A total of 13518 allogenic HSCT patients were included in the study. Mean age was 52.4 years. 57.2% of patients were female. The most common underlying diagnoses were acute myeloid leukemia (38%), myelodysplastic syndrome (17%) and acute lymphoblastic leukemia (14%). 11.1% of the index admissions were complicated by CDI. Rates of aGVHD during the index admission or 100 days post-engraftment were similar between CDI and non-CDI groups: 13.8% vs. 12.1%, p=0.19 during index admission and 29.2% vs. 26.1%, p=0.09 during 100 days post-engraftment. Nonetheless, patients with CDI had longer length of hospital stay (34.6 vs 29.8 days, p<0.0001), higher hospitalization costs ($608K vs $506K USD) and greater rate of inpatient mortality (7.3% vs 4.6%, p<0.001). In the multivariate regression analysis, CDI during index admission was not associated with risk of development of aGVHD (Adjusted Odds Ratio 1.14, 95% Confidence Interval 0.87-1.48, p=0.34). Age and unrelated donor HSCT were predictive of risk of aGVHD. Conclusions: CDI during index admission was not predictive of aGVHD during the first 100 days post-allogenic HSCT. HSCT patients are frequency colonized with C.difficile. Diarrhea secondary to CDI may resemble gastrointestinal aGVHD. Therefore, overdiagnosis of CDI in this population is a concern. Antimicrobial stewardship and use of clinical decision support tools have been advocated recently to decrease testing of HSCT patients with C.difficile colonization. Multivariable analysis of risk factors of aGVHD.[Table: see text]

Download Full-text

Complete Resolution of Extensive Chronic Graft-Versus-Host Disease with Ibrutinib

Blood ◽

10.1182/blood.v126.23.5474.5474 ◽

2015 ◽

Vol 126 (23) ◽

pp. 5474-5474

Author(s):

Audrey Scholoff ◽

Gloria Obi ◽

Kelty R. Baker ◽

George Carrum ◽

Rammurti T Kamble

Keyword(s):

Graft Versus Host Disease ◽

Complete Resolution ◽

Conflicts Of Interest ◽

Complete Response ◽

Unrelated Donor ◽

Hematopoietic Stem ◽

Host Disease ◽

Graft Versus Host ◽

Oral Ulcers

Abstract We herein document a complete response of extensive chronic graft-versus-host disease (cGvHD) to a Bruton's tyrosine kinase (BTK) inhibitor, ibrutinib. A 41 years old female with primary refractory MCL underwent mismatched unrelated donor (MMUD) allogeneic hematopoietic stem cell transplantation in December 2011 (conditioning with CY/TBI and alemtuzumab, graft=6.6x 106/kg CD-34+ cells, tacrolimus alone for GVHD prevention). Following engraftment on day 11, she developed grade III acute GvHD involving the skin and gut on day 17 of transplantation that persisted beyond 100 days post-transplant. Her cGvHD was treated with steroids, but remained active and extensive. Despite persistent cGvHD and 100% donor chimerism she relapsed in July 2012. Treatment with radiation and bendamustine with rituximab failed. By December 2013, the patient had extensive cGvHD manifesting as scleromatous skin thickening, oral ulcers and sclerosis of the buccal mucosa, ocular dryness and diarrhea, and was started on ibrutinib1 560 mg once daily for relapsed MCL. After 8 weeks of therapy, cGvHD had begun to improve. Oral steroids were reduced and ultimately stopped after 26 weeks of ibrutinib; after 30 weeks treatment all cGvHD manifestations resolved completely. A complete remission for MCL was documented at 8 weeks of ibrutinib initiation. Currently she continues to be on 560 mg daily ibrutinib without cGvHD exacerbation or MCL relapse for 22 weeks and 52 weeks, respectively. Chronic graft versus host disease (cGvHD) is mediated donor T cells. The role of B cells in the pathogenesis of cGvHD is increasingly recognized. Two murine studies have explored the role of ibrutinib in cGVHD-like syndromes, one in which there is T cell driven sclerodermatous cGvHD and a second in which there is Ab driven multiorgan system cGvHD that includes bronchiolitis obliterans (BO). Administration of ibrutinib decreased the incidence and severity of sclerodermatous, and improved pre-existing lesions and also improved pulmonary fibrosis and reduced BO. Animals lacking BTK and ITK did not develop cGVHD, indicating that these molecules are critical to cGVHD development. Our report provides the evidence that BTK inhibition led to complete resolution of cGvHD and supports exploration of its role in future clinical trials. Disclosures No relevant conflicts of interest to declare.

Download Full-text