Short Communication
Ann Hematol Oncol. 2018; 5(8): 1222.
Autologous Stem Cell Transplantation in Elderly Patients is Safe and is not associated with a Higher Frequency of Readmission Compared to Younger Patients. A Single Center Experience
Farina M*, Crippa C, Cerqui E, Daffini R, Soverini G, Dalceggio D, Pelizzari AM, Cattaneo C, Belotti A, Ribolla R and Rossi G
Department of Hematology, Spedali Civili Brescia, Italy
*Corresponding author: Mirko Farina, Department of Hematology, Spedali Civili Brescia, Italy
Received: October 03, 2018; Accepted: November 01, 2018; Published: November 08, 2018
Background
High dose chemotherapy and Autologous Stem Cell Transplantation (ASCT) is an effective treatment strategy for many adult Patients (pts) with Non-Hodgkin Lymphoma (NHL) and Multiple Myeloma (MM) and it is increasingly performed also in selected patients older than 65 years.
Aims
Data on toxicity and complications rate of ASCT in elderly patients are scarce. Herein we evaluated complications and rehospitalization rate within 3 months in patients older than 65 yrs undergoing ASCT.
Methods
We retrospectively analyzed 231 consecutive patients who underwent ASCT at our Institution between January 2016 and December 2017, focusing on the group of pts aged > 65 yrs. Their characteristics, clinical course and outcome were analysed and compared with younger pts.
Results
Seventy-two of 231 (31%) ASCT pts were > 65 yrs. Diagnosis was MM in 52 (72%) and NHL in 20 pts (28%) respectively. Median age was 69 (range 65-76). Patients’ comorbidities or significant laboratory abnormalities are summarized in (Table 1). Based on clinical judgement, conditioning regimen dose intensity was reduced in 10 pts (14%). In 12% (6/52) of MM pts melphalan dose was reduced to 140 mg/m² (4) or 100 mg/m² (2). FEAM dose was reduced at 75% in 4 NHL pts (20%) [1,2]. Pts achieved hematology recovery after a median of 10 days (6-13) and were discharged after 13 days (9- 29). Infectious complications were the most frequent adverse event during the aplastic phase [3-5].
n (72)
%
Hypertension
26
36
Diabetes mellitus
9
12.5
HBsAg seropositivity
4
5
Thyroids dysfunction
4
5
Sleep apnea syndrome
3
4
Lupus anticoagulant
2
2.7
Chronic renal failure
2
2.7
Cardiac arrhythmia
5
7
Parkinson disease
1
1
Primary biliary cirrhosis
9
12.5
Ischemic heart disease
6
8
Previous Neoplasia Previous Pulmonary Embolia/Venus thrombosis
6
8
Previous Transient ischemic attack/ictus
5
7
Table 1:
Fever of Unknown Origin (FUO) developed in 31 pts (43%), sepsis in 16 (22%) and pneumonia in 10 (14%). Among noninfectious complications, WHO grade >III mucositis occurred in 12 pts (17%), neutropenic enteritis in 4 (5.5%) and cardiac arrhythmia (atrial fibrillation or TPSV) in 3 (4%).
Readmission to the Hematology Unit within 3 months from ASCT occurred after a median of 32 days (14-120 [s2] days) in 16 of 72 pts (22%) [6]. Most of the re-admissions were due to FUO (37.5%) or infections (sepsis in 12.5%, pneumonia in 19%, diarrhea in 12.5%, Human Respiratory Syncytial Virus infection in 6%). Other causes included: hyporexia/vomiting, respiratory distress, disease relapse, acute cholecystitis, appendicitis and unrelated neoplasia. Table 2 compares the characteristics of elderly pts needing readmission or not after ASCT. The risk of being re-admitted did not vary according to age, type of disease, time to neutrophil recovery, time to discharge or number of comorbidities at ASCT, whereas the development of neutropenic enteritis (p 0.05; HR 3.84, 0.98-15.06) or WHO grade III mucositis (p 0.04; HR 2.79, 1.06-7.37) during ASCT were significantly associated with subsequent re-admission.
n (72)
%
Hypertension
26
36
Diabetes mellitus
9
12.5
HBsAg seropositivity
4
5
Thyroid?s dysfunction
4
5
Sleep apnea syndrome
3
4
Lupus anticoagulant
2
2.7
Chronic renal failure
2
2.7
Cardiac arrhythmia
5
7
Parkinson disease
1
1
Primary biliary cirrhosis
9
12.5
Ischemic heart disease
6
8
Previous Neoplasia Previous Pulmonary Embolia/Venus thrombosis
6
8
Previous Transient ischemic attack/ictus
5
7
Table 2:
The re-hospitalization rate after ASCT of pts aged <65 was 18% (29/159), not significantly different from elderly pts. Moreover, no differences were found in time to re-admission (median 30 vs. 32 days), and in the causes of re-hospitalization [FUO/sepsis (45% vs. 50%), diarrhea (17 vs. 12.5%), pneumonia (10% vs. 19%), disease progression (21% vs. 6%, p: 0.39)] in younger vs. elderly pts, respectively. No transplant-related death was observed in pts over 65 yrs, while 1 younger pts died of within 3 months from ASCT.
Conclusion
ASCT performed in pts older than 65 yrs shows a low rate of short-term complications without unexpected adverse events. The rate of post-ASCT readmission is similar to younger pts and its risk is higher in pts developing severe mucositis or neutropenic enteritis during ASCT.
References
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