Home         Forums  

Go Back   Marrowforums > Treatments > Transplants
Register FAQ Search Today's Posts Mark Forums Read

Transplants Bone marrow and stem cell transplantation

Reply
 
Thread Tools Search this Thread
  #1  
Old Mon Jun 3, 2013, 06:07 PM
tytd tytd is offline
Member
 
Join Date: Jul 2009
Location: Southeast, USA
Posts: 132
transplant survival getting better

Here's an abstract to an article just published in May, 2013Journal of Clinical Oncology which indicates that transplant survival is improving and more are being done as we suspected from many on this forum having been through it. I have not read the full article yet but it give us hope that the treatments will continue to improve. These are however still old data up to 2005.not sure what the statistics are from 2005 until 2013----------- Significant Improvement in Survival After Allogeneic Hematopoietic Cell Transplantation During a Period of Significantly Increased Use, Older Recipient Age, and Use of Unrelated Donors
©American Society of Clinical Oncology
Purpose Over the past four decades, allogeneic hematopoietic cell transplantation (alloHCT) has evolved as a curative modality for patients with hematologic diseases. This study describes changes in use, technique, and survival in a population-based cohort.

Patients and Methods The study included 38,060 patients with hematologic malignancies or disorders who underwent first alloHCT in a US or Canadian center from 1994 to 2005 and were reported to the Center for International Blood and Marrow Transplant Research.

Results AlloHCT as treatment for acute lymphoblastic (ALL) and myeloid leukemias (AML), myelodysplastic syndrome (MDS), and Hodgkin and non-Hodgkin lymphomas increased by 45%, from 2,520 to 3,668 patients annually. From 1994 to 2005, use of both peripheral (7% to 65%) and cord blood increased (2% to 10%), whereas use of marrow decreased (90% to 27%). Despite a median age increase from 33 to 40 years and 263% increase in unrelated donors for alloHCT, overall survival (OS) at day 100 significantly improved for patients with AML in first complete remission after myeloablative sibling alloHCT (85% to 94%; P < .001) and unrelated alloHCT (63% to 86%; P < .001); 1-year OS improved among those undergoing unrelated alloHCT (48% to 63%; P = .003) but not among those undergoing sibling alloHCT. Similar results were seen for ALL and MDS. Day-100 OS after cord blood alloHCT improved significantly from 60% to 78% (P < .001) for AML, ALL, MDS, and chronic myeloid leukemia. Use of reduced-intensity regimens increased, yielding OS rates similar to those of myeloablative regimens.

Conclusion Survival for those undergoing alloHCT has significantly improved over time. However, new approaches are needed to further improve 1-year OS.

PDF
Citation Abstracts
•Download all citations on this page to my citation mana
__________________
possible low to int-1 MDS with predominant thrombocytopenia, mild anemia, dx 7/08, in watch and wait mode
Reply With Quote
  #2  
Old Mon Jun 3, 2013, 10:05 PM
Neil Cuadra Neil Cuadra is offline
Owner
 
Join Date: Jul 2006
Location: Los Angeles, California
Posts: 2,556
There are three reasons that the news is even better than this report shows:
  1. The data is from a few years back, as you point out. Recent data would contain even better statistics.

  2. As transplant success rates go up, the pool of patients eligible for transplants grows. That's why the median age rose from 33 to 40; older patients are getting transplants. If the ages of patients were still limited as in the past, the measured success rates would be even higher.

  3. For the same reasons, patients with less-ideal health conditions are now undergoing transplants, where in the past the tradeoffs wouldn't have warranted undergoing the risks of a transplant. If the restrictions of the past were still applied today, the measured success rates would be even higher.
Reply With Quote
  #3  
Old Mon Jun 10, 2013, 01:41 AM
KMac KMac is offline
Member
 
Join Date: Oct 2012
Location: Golden, Colorado
Posts: 103
This is such wonderful news. Thank you for posting! And thank you Neil for pointing out reasons why the outlook is even better than the article suggests.

I see people at my hospital with aplastic anemia doing very well after transplant. Two in particular, both over 40, neither with a sibling donor, and one with only a 9/10 match.

It seems that despite the risk & uncertainty, improvements in medicine offer us more reasons to be hopeful with every passing year.
__________________
Kevin, male age 45; dx SAA 02/2012 - Hgb 5.8, platelets 14, ANC 200, 1% cellularity. Received ATG 03/2012. As of 03/2015, significant improvement - Hgb 15, platelets 158, ANC fluctuates around 1000, Lymphocytes 620. Tapering cyclosporine. BMB 20-30% cellularity.
Reply With Quote
Reply


Thread Tools Search this Thread
Search this Thread:

Advanced Search

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

vB code is On
Smilies are On
[IMG] code is On
HTML code is Off
Forum Jump

Similar Threads
Thread Thread Starter Forum Replies Last Post
16 months past SCT and doing fairly well. The sage of my transplant, start to now rar MDS 7 Wed Nov 18, 2015 10:26 PM
From transplant to World Record in 6 years! squirrellypoo Transplants 4 Sat Sep 26, 2015 05:56 PM
New to site, Transplant Disappointment & Worries sveness Transplants 2 Sun Mar 4, 2012 11:05 AM
Transplant Survivors Conference, September 2008 Marrowforums News and Events 0 Fri Jun 6, 2008 02:27 AM
NMDP Provides Transplant Information Marrowforums Transplants 1 Tue May 8, 2007 04:00 AM


All times are GMT -4. The time now is 04:34 PM.


Powered by vBulletin® Version 3.6.7
Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.
Forum sites may contain non-authoritative and unverified information.
Medical decisions should be made in consultation with qualified medical professionals.
Site contents exclusive of member posts Copyright © 2006-2020 Marrowforums.org