The Hematopoietic Stem Cell Transplant Comorbidity Index (HCT-CI) Can Predict for Readmission Following Autologous Stem Cell Transplant for Lymphoma and Multiple Myeloma

Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 4286-4286
Author(s):  
Samantha M. Jaglowski ◽  
Craig C. Hofmeister ◽  
Patrick Elder ◽  
Sam Penza ◽  
Yvonne A Efebera ◽  
...  

Abstract Abstract 4286 Introduction: Patients (pts) who undergo autologous stem cell transplant (ASCT) for lymphoma and multiple myeloma (MM) are often older and frequently have multiple comorbidities, as well as diminished performance status (PS). The presence of comorbidities has been shown to influence overall survival (OS) following ASCT for non-Hodgkin's lymphoma, but not for MM, and comorbidity indices can predict readmission in multiple settings. The hematopoietic cell transplantation-specific comorbidity index (HCT-CI) can predict risk of readmission following allo-SCT, but this has not been evaluated for ASCT. Methods: We conducted an analysis of 688 consecutive pts who received ASCT at the Ohio State University from 2000–2010 for lymphoma or MM in order to identify pre-transplant factors associated with readmission and early mortality. Univariate and multivariate logistic regression were used to predict the odds of readmission within the first 100 days following ASCT or the odds of death within the first 100 days. Cox regression was used to evaluate OS. Results: 408 (59%) of pts were male, 46 (7%) were age ≥70, 367 (53%) had MM and 322 (47%) had lymphoma (110 Hodgkin's lymphoma, 125 diffuse large B cell lymphoma (DLBCL), 17 follicular lymphoma, 51 mantle cell lymphoma, 17 peripheral T cell lymphoma, 2 gray zone). The most common conditioning regimens were melphalan (327), BEAM (167), and BuCyVP (110). Sixty five percent had a Karnofsky PS (KPS) of ≥90. HCT-CI score was available in 431 patients and was 0 in 99 (23%), 1–2 in 169 (39%), and ≥3 in 163 (38%). 14% were readmitted within 100 days of transplant, and 4% died within the first 100 days. On univariate analysis, increased odds of readmission were significantly associated with conditioning with BuCyVP relative to melphalan, KPS≤80, and HCT-CI≥3 (Table 1). In transplants after 2006 when HCT-CI was incorporated as standard of care, HCT-CI≥3 remained statistically significant for readmission (OR 2.54, 95% CI 1.15–5.56). Mortality within 100 days was associated with readmission, gender, DLBCL vs MM, KPS≤80, and use of plerixafor for mobilization on univariate analysis. Early mortality was significantly associated with female sex (OR 0.16, 95% CI 0.03–0.66) and readmission within 100 days (OR 3.90, 95% CI 1.3–11.6) on multivariate analysis. After excluding patients who died within the first 30 days and who relapsed within the first 100 days, readmission within 100 days of transplant (HR 1.75, 95% CI 1.21–2.56, p=0.003) (Figure 1), and KPS≤80 (HR 1.41, 95% CI 1.05–1.87, p=0.02) are associated with inferior OS, but HCT-CI was not. Conclusion: While an HCT-CI score ≥3 was associated with readmission, it was not associated with early mortality or OS in pts with MM or lymphoma. Readmission within 100 days and KPS≤80 were significantly associated with inferior OS, and readmission was significantly associated with early mortality. Evaluation of other assessment tools, including frailty assessments, may identify patients who could benefit from earlier rehabilitative interventions, either prior to or following ASCT. Disclosures: No relevant conflicts of interest to declare.

Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 1170-1170
Author(s):  
Rebecca L. Olin ◽  
David L. Porter ◽  
Selina M. Luger ◽  
Stephen J. Schuster ◽  
Donald Tsai ◽  
...  

Abstract Introduction: Autologous stem cell transplant (ASCT) as part of initial therapy has been shown to prolong survival of patients with multiple myeloma, with some achieving durable complete remission. However, the majority of patients ultimately relapse after ASCT and require salvage treatment. Options for the treatment of such patients have increased significantly over recent years, including not only novel chemotherapeutic and biological agents but also additional ASCTs. We performed a retrospective analysis of our experience with salvage ASCT for multiple myeloma to determine which clinical variables influence outcome. Methods: Between October 1992 and February 2005, we performed 342 ASCTs for multiple myeloma. Twenty-six of these were salvage transplants for relapsed disease after prior ASCT, and all were included in the analysis. Patients who received two planned (tandem) ASCTs were not included. Results: The median age at diagnosis was 47 (range 25–66), and median ISS and DS stages at diagnosis were 1 and 2, respectively. The initial ASCT was melphalan-based in 21/26; six (23%) achieved a complete response (CR) to the initial transplant, and fifteen (58%) achieved a partial response (PR). The median event-free survival (EFS) after the initial transplant was 19.5 months (range 2–60). The median time between initial and salvage ASCT was 2.6 years (range 0.3–7.6). Twenty-two patients (85%) received non-transplant therapy between ASCTs, and the median number of lines of therapy prior to salvage ASCT was 3. At the time of salvage ASCT, the median age was 52.5 (range 28–69). Fourteen patients received melphalan alone, eight received melphalan/TBI, and four received other regimens. Eleven patients (42%) achieved a response to therapy (1 CR, 10 PR). One patient (4%) died of transplant-related toxicity. The median follow-up after salvage ASCT is 12 months (range 0.2–58). Median EFS is 9 months, and median overall survival (OS) is 36 months. The 2-year EFS is 14%, and 2-year OS is 52%. On univariate analysis, both response to and EFS after initial transplant significantly predict improved EFS after salvage transplant (p=0.0008 and p=0.0065 respectively). Both also predict improved OS (p=0.03 and 0.0005 respectively). A greater than 12 month interval between first and second transplant also correlated with OS (p=0.04). There was no significant difference in EFS or OS by preparative regimen. Interestingly, type of response to the salvage transplant (CR/PR or less than PR) did not predict improved EFS or OS. Conclusion: This study suggests that salvage ASCT after relapse from initial ASCT is a feasible therapy for patients with heavily treated multiple myeloma, particularly those with a prolonged response to the first transplant.


eJHaem ◽  
2021 ◽  
Author(s):  
Noa Biran ◽  
Wanting Zhai ◽  
Roxanne E. Jensen ◽  
Jeanne Mandelblatt ◽  
Susan Kumka ◽  
...  

2021 ◽  
Vol 21 ◽  
pp. S254
Author(s):  
Felipe Peña-Muñoz ◽  
Luz Román-Molano ◽  
Danylo Palomino-Mendoza ◽  
Alberto Hernández-Sánchez ◽  
Borja Puertas-Martínez ◽  
...  

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