Clinical outcome of childhood lymphoblastic lymphoma in Shanghai China 2001–2010. Issue 4 (14th November 2013)
- Record Type:
- Journal Article
- Title:
- Clinical outcome of childhood lymphoblastic lymphoma in Shanghai China 2001–2010. Issue 4 (14th November 2013)
- Main Title:
- Clinical outcome of childhood lymphoblastic lymphoma in Shanghai China 2001–2010
- Authors:
- Gao, Yi‐Jin
Pan, Ci
Tang, Jing‐Yan
Lu, Feng‐Juan
Chen, Jing
Xue, Hui‐Liang
Zhai, Xiao‐Wen
Li, Jun
Ye, Qi‐Dong
Zhou, Min
Wang, Hong‐Sheng
Miao, Hui
Qian, Xiao‐Wen
Xu, Zhou
Meng, Jian‐Hua - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="pbc24848-sec-0001" sec-type="section"> <title>Background</title> <p>This retrospective cohort study analysed the clinical characteristics and outcomes of patients with childhood lymphoblastic lymphoma (LBL) treated in Shanghai, China.</p> </sec> <sec id="pbc24848-sec-0002" sec-type="section"> <title>Procedure</title> <p>From 2001 to 2010, 108 evaluable patients ≤16 years of age who were newly diagnosed with biopsy‐proven LBL were treated with one of three treatment protocols: CCCG‐99, SCMC‐T‐NHL‐2002, or LBL‐CHOF‐2006.</p> </sec> <sec id="pbc24848-sec-0003" sec-type="section"> <title>Results</title> <p>Two patients had Stage I disease, 5 had Stage II, 55 had Stage III, and 46 had Stage IV. The immunophenotype was T‐cell LBL in 92 patients (85.2%) and precursor B‐cell LBL in 16 (14.8%). The abandonment rate was 11.5%. Twenty‐five patients (23.2%) suffered from resistant disease, including 1 with isolated central nervous system (CNS) relapse. At a median follow‐up of 40.4 months (range, 0–114 months), the 5‐year probability of event‐free survival (pEFS) was 63.9 ± 4.6% in all patients. The 5‐year pEFS for patients with pB‐LBL was better than for patients with T‐LBL (100% vs. 61.3 ± 5.1%, <italic>P</italic> = 0.007). Patients who had achieved complete remission on day 33 of induction had significantly better pEFS than those who had not (78.8 ± 4.6% vs. 28.2 ± 9.0%, <italic>P</italic> = 0.000). Three<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="pbc24848-sec-0001" sec-type="section"> <title>Background</title> <p>This retrospective cohort study analysed the clinical characteristics and outcomes of patients with childhood lymphoblastic lymphoma (LBL) treated in Shanghai, China.</p> </sec> <sec id="pbc24848-sec-0002" sec-type="section"> <title>Procedure</title> <p>From 2001 to 2010, 108 evaluable patients ≤16 years of age who were newly diagnosed with biopsy‐proven LBL were treated with one of three treatment protocols: CCCG‐99, SCMC‐T‐NHL‐2002, or LBL‐CHOF‐2006.</p> </sec> <sec id="pbc24848-sec-0003" sec-type="section"> <title>Results</title> <p>Two patients had Stage I disease, 5 had Stage II, 55 had Stage III, and 46 had Stage IV. The immunophenotype was T‐cell LBL in 92 patients (85.2%) and precursor B‐cell LBL in 16 (14.8%). The abandonment rate was 11.5%. Twenty‐five patients (23.2%) suffered from resistant disease, including 1 with isolated central nervous system (CNS) relapse. At a median follow‐up of 40.4 months (range, 0–114 months), the 5‐year probability of event‐free survival (pEFS) was 63.9 ± 4.6% in all patients. The 5‐year pEFS for patients with pB‐LBL was better than for patients with T‐LBL (100% vs. 61.3 ± 5.1%, <italic>P</italic> = 0.007). Patients who had achieved complete remission on day 33 of induction had significantly better pEFS than those who had not (78.8 ± 4.6% vs. 28.2 ± 9.0%, <italic>P</italic> = 0.000). Three of 25 patients who experienced resistant disease were alive at the end of the study period.</p> </sec> <sec id="pbc24848-sec-0004" sec-type="section"> <title>Conclusions</title> <p>The abandonment rate was lower for patients with LBL than for patients with acute lymphoblastic leukemia. Prophylactic cranial radiation can be omitted for patients with LBL even when advanced‐stage disease is present, as intensive systemic chemotherapy with intrathecal therapy is sufficient to prevent CNS relapse. The survival of patients with resistant disease was very poor. Pediatr Blood Cancer 2014;61:659–663. © 2013 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Pediatric blood & cancer. Volume 61:Issue 4(2014:Apr.)
- Journal:
- Pediatric blood & cancer
- Issue:
- Volume 61:Issue 4(2014:Apr.)
- Issue Display:
- Volume 61, Issue 4 (2014)
- Year:
- 2014
- Volume:
- 61
- Issue:
- 4
- Issue Sort Value:
- 2014-0061-0004-0000
- Page Start:
- 659
- Page End:
- 663
- Publication Date:
- 2013-11-14
- Subjects:
- Tumors in children -- Periodicals
Blood -- Diseases -- Periodicals
Cancer in children -- Periodicals
618.92 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1545-5017 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pbc.24848 ↗
- Languages:
- English
- ISSNs:
- 1545-5009
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6417.533500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3561.xml