PULMONARY FUNCTION TESTS (PFTS) PRIOR TO AUTOLOGOUS STEM CELL TRANSPLANT AS PREDICTOR OF PULMONARY COMPLICATIONS AND SURVIVAL IN ADULTS WITH HEMATOLOGICAL MALIGNANCIES
Author(s): ,
Ombretta Annibali
Affiliations:
Hematology Unit,UNIVERSITY CAMPUS BIO-MEDICO ROMA,Rome,Italy
,
Francesca Chiodi
Affiliations:
Hematology Unit,UNIVERSITY CAMPUS BIO-MEDICO ROMA,Rome,Italy
,
Simone Scarlata
Affiliations:
Geriatric Unit of Respiratory Pathophisiology,UNIVERSITY CAMPUS BIO-MEDICO ROMA,Rome,Italy
,
Simona Santangelo
Affiliations:
Geriatric Unit of Respiratory Pathophisiology,UNIVERSITY CAMPUS BIO-MEDICO ROMA,Rome,Italy
,
Chiara Sarlo
Affiliations:
Hematology Unit,UNIVERSITY CAMPUS BIO-MEDICO ROMA,Rome,Italy
,
Daniele Armiento
Affiliations:
Hematology Unit,UNIVERSITY CAMPUS BIO-MEDICO ROMA,Rome,Italy
,
Elisabetta Cerchiara
Affiliations:
Hematology Unit,UNIVERSITY CAMPUS BIO-MEDICO ROMA,Rome,Italy
,
Silvia Ferraro
Affiliations:
Hematology Unit,UNIVERSITY CAMPUS BIO-MEDICO ROMA,Rome,Italy
,
Maria Cristina Tirindelli
Affiliations:
Hematology Unit,UNIVERSITY CAMPUS BIO-MEDICO ROMA,Rome,Italy
,
Raffaele Antonelli Incalzi
Affiliations:
Geriatric Unit of Respiratory Pathophisiology,UNIVERSITY CAMPUS BIO-MEDICO ROMA,Rome,Italy
,
William Arcese
Affiliations:
Hematology Unit ,UNIVERSITY Tor Vergata on behalf of Rome Transplant Network (RTN),Rome,Italy
Giuseppe Avvisati
Affiliations:
Hematology Unit ,UNIVERSITY CAMPUS BIO-MEDICO ROMA,Rome,Italy
(Abstract release date: 05/21/15) EHA Library. Annibali O. 06/12/15; 103002; PB2050 Disclosure(s): UNIVERSITÀ CAMPUS BIO-MEDICO ROMA
Ematologia
Dr. Ombretta Annibali
Dr. Ombretta Annibali
Contributions
Abstract
Abstract: PB2050

Type: Publication Only

Background
Autologous Stem Cell Transplantation (ASCT) represents a standard-of-care for Multiple Myeloma patients eligible to receive high-dose chemotherapy, Lymphoma patients undergoing second-line treatments and for a small proportion of Acute Leukemia patients. Although all canditates to an ASCT are carefully evaluated for their eligibility with a complete screening of clinical, laboratory, imaging and functional tests to check comorbidities, global organ function and infections, pulmonary and infective complications are a significant cause of morbidity and mortality after ASCT. However, the relationship between pre-transplant Pulmonary Function Tests (PFTs), development of post-ASCT complications and mortality is unknown.

Aims
The aim of this study was to evaluate the role of  pre ASCT PFTs on  post-ASCT complications and mortality

Methods
We collected data for 88 patients undergoing ASCT between March 2008 and February 2015 in our Institution. Complete PFTs were obtained in 62 patients ( 74% males; median age 57 yrs, range, 18-69): Multiple Myeloma n=44, Non-Hodgkin Lymphoma n=18, Hodgkin Lymphoma n=4, Acute Myeloid Leukemia n=1).  ASCT was  performed as first line treatment  in 42 (67%)  patients, after first relapse in 17 (28%) and as salvage treatment after ≥2 relapse in 3 (5%). Previous regimens including drugs known to induce pulmonary toxicity, such as bortezomib and bleomycin had been administered to 34/62 (55%) patients

Results
Of the 62 transplanted patients, 9 (13.4%) had abnormal PFTs at baseline (5 obstructive and 4 restrictive PFTs) and 19 (28.4%) had two or more major chronic comorbidities (metabolic and cardiovascular disease). Infective complications occurred in 40/62 (64.5%) and respiratory complications in 9/62 (14.5%) cases. After a median follow-up of 25 months (range, 4-111), 48 out of 62 patients (77,4%) are alive. Post-ASCT respiratory complications  were significantly higher (97% vs  83 %; P=0.05)  in patients with reduced pre-ASCT FEV1

Summary

To reduce the risk of respiratory complications after ASCT, these patients might benefit from the use of a reduced intensity conditioning .

 



Keyword(s): Autologous bone marrow transplant

Session topic: Publication Only
Abstract: PB2050

Type: Publication Only

Background
Autologous Stem Cell Transplantation (ASCT) represents a standard-of-care for Multiple Myeloma patients eligible to receive high-dose chemotherapy, Lymphoma patients undergoing second-line treatments and for a small proportion of Acute Leukemia patients. Although all canditates to an ASCT are carefully evaluated for their eligibility with a complete screening of clinical, laboratory, imaging and functional tests to check comorbidities, global organ function and infections, pulmonary and infective complications are a significant cause of morbidity and mortality after ASCT. However, the relationship between pre-transplant Pulmonary Function Tests (PFTs), development of post-ASCT complications and mortality is unknown.

Aims
The aim of this study was to evaluate the role of  pre ASCT PFTs on  post-ASCT complications and mortality

Methods
We collected data for 88 patients undergoing ASCT between March 2008 and February 2015 in our Institution. Complete PFTs were obtained in 62 patients ( 74% males; median age 57 yrs, range, 18-69): Multiple Myeloma n=44, Non-Hodgkin Lymphoma n=18, Hodgkin Lymphoma n=4, Acute Myeloid Leukemia n=1).  ASCT was  performed as first line treatment  in 42 (67%)  patients, after first relapse in 17 (28%) and as salvage treatment after ≥2 relapse in 3 (5%). Previous regimens including drugs known to induce pulmonary toxicity, such as bortezomib and bleomycin had been administered to 34/62 (55%) patients

Results
Of the 62 transplanted patients, 9 (13.4%) had abnormal PFTs at baseline (5 obstructive and 4 restrictive PFTs) and 19 (28.4%) had two or more major chronic comorbidities (metabolic and cardiovascular disease). Infective complications occurred in 40/62 (64.5%) and respiratory complications in 9/62 (14.5%) cases. After a median follow-up of 25 months (range, 4-111), 48 out of 62 patients (77,4%) are alive. Post-ASCT respiratory complications  were significantly higher (97% vs  83 %; P=0.05)  in patients with reduced pre-ASCT FEV1

Summary

To reduce the risk of respiratory complications after ASCT, these patients might benefit from the use of a reduced intensity conditioning .

 



Keyword(s): Autologous bone marrow transplant

Session topic: Publication Only

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