Factors influencing haematological recovery after allogeneic haemopoietic stem cell transplants: graft‐versus‐host disease, donor type, cytomegalovirus infections and cell dose

Platelet recovery after allogeneic haemopoietic stem cell transplant (HSCT) and predictive factors were analysed in 342 patients with haematological malignancies. All patients were prepared with cyclophosphamide plus total body irradiation, and received an unmanipulated HSCT from an HLA‐identical si...

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Veröffentlicht in:British journal of haematology 2001-01, Vol.112 (1), p.219-227
Hauptverfasser: Dominietto, Alida, Raiola, Anna Maria, Van Lint, Maria Teresa, Lamparelli, Teresa, Gualandi, Francesca, Berisso, Giovanni, Bregante, Stefania, Frassoni, Francesco, Casarino, Lucia, Verdiani, Simonetta, Bacigalupo, Andrea
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container_title British journal of haematology
container_volume 112
creator Dominietto, Alida
Raiola, Anna Maria
Van Lint, Maria Teresa
Lamparelli, Teresa
Gualandi, Francesca
Berisso, Giovanni
Bregante, Stefania
Frassoni, Francesco
Casarino, Lucia
Verdiani, Simonetta
Bacigalupo, Andrea
description Platelet recovery after allogeneic haemopoietic stem cell transplant (HSCT) and predictive factors were analysed in 342 patients with haematological malignancies. All patients were prepared with cyclophosphamide plus total body irradiation, and received an unmanipulated HSCT from an HLA‐identical sibling (n = 270), a matched unrelated donor (n = 67) or an identical twin (n = 5). The source of stem cells was peripheral blood (n = 15) or bone marrow (n = 327). Graft‐vs.‐host disease (GvHD) prophylaxis consisted of cyclosporin A with or without methotrexate. The proportion of patients with
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All patients were prepared with cyclophosphamide plus total body irradiation, and received an unmanipulated HSCT from an HLA‐identical sibling (n = 270), a matched unrelated donor (n = 67) or an identical twin (n = 5). The source of stem cells was peripheral blood (n = 15) or bone marrow (n = 327). Graft‐vs.‐host disease (GvHD) prophylaxis consisted of cyclosporin A with or without methotrexate. The proportion of patients with < 50 × 109/l platelets on d +50, d +100, d +200 and d +365 after HSCT was 26%, 27%, 14% and 11% respectively. Thrombocytopenia was independent of the degree of complete donor chimaerism. Four variables were predictive of platelet recovery: donor type, acute GvHD, cytomegalovirus (CMV) infection and number of cells infused at transplant. Recipients of an unrelated graft had lower platelet counts (49 × 109/l) on d +50 than identical sibling grafts (108 × 109/l) (P < 0·001) and twin grafts (149 × 109/l) (P < 0·001). Patients with GvHD grades 0, I, II, III and IV had significantly different platelet counts on d +50 (153 × 109/l, 102 × 109/l, 85 × 109/l, 32 × 109/l and 22 × 109/l; P < 0·001) and thereafter. Thrombocytopenia was more frequent in patients with high‐level CMV antigenaemia (> four positive cells/2 × 105) (P < 0·0001) and in patients who received a low cell dose at transplant (≤ 4·1 × 108/kg) (P = 0·009). Platelet counts predicted transplant‐related mortality (TRM) and were higher at all time intervals in patients surviving the transplant. Patients with grade II GvHD and > 50 × 109/l platelets had a lower TRM than patients with grade II GvHD and ≤ 50 × 109/l platelets (14% vs. 40%, P < 0·0001). In conclusion, (i) a significant proportion of allogeneic HSCT recipients are thrombocytopenic long‐term, irrespective of complete donor chimaerism, (ii) thrombocytopenia identifies patients at greater risk of lethal complications, and (iii) platelet recovery is influenced by GvHD, donor type, CMV infections and cell dose, not by stem cell source or other patient–disease‐related variables.]]></description><identifier>ISSN: 0007-1048</identifier><identifier>EISSN: 1365-2141</identifier><identifier>DOI: 10.1046/j.1365-2141.2001.02468.x</identifier><identifier>PMID: 11167808</identifier><identifier>CODEN: BJHEAL</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Adolescent ; Adult ; allogeneic bone marrow transplantation ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Bone Marrow Transplantation - mortality ; Bone marrow, stem cells transplantation. Graft versus host reaction ; Child ; Chimera ; Cytomegalovirus Infections - complications ; Female ; Graft vs Host Disease ; graft‐versus‐host disease ; haematopoietic recovery ; Hematologic Neoplasms - blood ; Hematologic Neoplasms - mortality ; Hematologic Neoplasms - surgery ; Hematology ; Hematopoietic Stem Cell Transplantation - mortality ; Histocompatibility Testing ; Humans ; Male ; Medical sciences ; Middle Aged ; Platelet Count ; Prognosis ; Thrombocytopenia - complications ; Time Factors ; Tissue Donors ; Transfusions. Complications. Transfusion reactions. Cell and gene therapy ; Transplantation, Homologous ; Twins, Monozygotic</subject><ispartof>British journal of haematology, 2001-01, Vol.112 (1), p.219-227</ispartof><rights>2001 INIST-CNRS</rights><rights>Copyright Blackwell Scientific Publications Ltd. Jan 2001</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4708-4bd56ff29087ede4518faf12c0f56b9a0ed5a97add68ccc453cb70d48d4c6b883</citedby><cites>FETCH-LOGICAL-c4708-4bd56ff29087ede4518faf12c0f56b9a0ed5a97add68ccc453cb70d48d4c6b883</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1365-2141.2001.02468.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1365-2141.2001.02468.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,4024,27923,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=961626$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11167808$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dominietto, Alida</creatorcontrib><creatorcontrib>Raiola, Anna Maria</creatorcontrib><creatorcontrib>Van Lint, Maria Teresa</creatorcontrib><creatorcontrib>Lamparelli, Teresa</creatorcontrib><creatorcontrib>Gualandi, Francesca</creatorcontrib><creatorcontrib>Berisso, Giovanni</creatorcontrib><creatorcontrib>Bregante, Stefania</creatorcontrib><creatorcontrib>Frassoni, Francesco</creatorcontrib><creatorcontrib>Casarino, Lucia</creatorcontrib><creatorcontrib>Verdiani, Simonetta</creatorcontrib><creatorcontrib>Bacigalupo, Andrea</creatorcontrib><title>Factors influencing haematological recovery after allogeneic haemopoietic stem cell transplants: graft‐versus‐host disease, donor type, cytomegalovirus infections and cell dose</title><title>British journal of haematology</title><addtitle>Br J Haematol</addtitle><description><![CDATA[Platelet recovery after allogeneic haemopoietic stem cell transplant (HSCT) and predictive factors were analysed in 342 patients with haematological malignancies. All patients were prepared with cyclophosphamide plus total body irradiation, and received an unmanipulated HSCT from an HLA‐identical sibling (n = 270), a matched unrelated donor (n = 67) or an identical twin (n = 5). The source of stem cells was peripheral blood (n = 15) or bone marrow (n = 327). Graft‐vs.‐host disease (GvHD) prophylaxis consisted of cyclosporin A with or without methotrexate. The proportion of patients with < 50 × 109/l platelets on d +50, d +100, d +200 and d +365 after HSCT was 26%, 27%, 14% and 11% respectively. Thrombocytopenia was independent of the degree of complete donor chimaerism. Four variables were predictive of platelet recovery: donor type, acute GvHD, cytomegalovirus (CMV) infection and number of cells infused at transplant. Recipients of an unrelated graft had lower platelet counts (49 × 109/l) on d +50 than identical sibling grafts (108 × 109/l) (P < 0·001) and twin grafts (149 × 109/l) (P < 0·001). Patients with GvHD grades 0, I, II, III and IV had significantly different platelet counts on d +50 (153 × 109/l, 102 × 109/l, 85 × 109/l, 32 × 109/l and 22 × 109/l; P < 0·001) and thereafter. Thrombocytopenia was more frequent in patients with high‐level CMV antigenaemia (> four positive cells/2 × 105) (P < 0·0001) and in patients who received a low cell dose at transplant (≤ 4·1 × 108/kg) (P = 0·009). Platelet counts predicted transplant‐related mortality (TRM) and were higher at all time intervals in patients surviving the transplant. Patients with grade II GvHD and > 50 × 109/l platelets had a lower TRM than patients with grade II GvHD and ≤ 50 × 109/l platelets (14% vs. 40%, P < 0·0001). In conclusion, (i) a significant proportion of allogeneic HSCT recipients are thrombocytopenic long‐term, irrespective of complete donor chimaerism, (ii) thrombocytopenia identifies patients at greater risk of lethal complications, and (iii) platelet recovery is influenced by GvHD, donor type, CMV infections and cell dose, not by stem cell source or other patient–disease‐related variables.]]></description><subject>Adolescent</subject><subject>Adult</subject><subject>allogeneic bone marrow transplantation</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow Transplantation - mortality</subject><subject>Bone marrow, stem cells transplantation. Graft versus host reaction</subject><subject>Child</subject><subject>Chimera</subject><subject>Cytomegalovirus Infections - complications</subject><subject>Female</subject><subject>Graft vs Host Disease</subject><subject>graft‐versus‐host disease</subject><subject>haematopoietic recovery</subject><subject>Hematologic Neoplasms - blood</subject><subject>Hematologic Neoplasms - mortality</subject><subject>Hematologic Neoplasms - surgery</subject><subject>Hematology</subject><subject>Hematopoietic Stem Cell Transplantation - mortality</subject><subject>Histocompatibility Testing</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Platelet Count</subject><subject>Prognosis</subject><subject>Thrombocytopenia - complications</subject><subject>Time Factors</subject><subject>Tissue Donors</subject><subject>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</subject><subject>Transplantation, Homologous</subject><subject>Twins, Monozygotic</subject><issn>0007-1048</issn><issn>1365-2141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAURiMEokPhFZAFEitmsPPjOEgsaEUpqBIbWFuOfTP1KLGDr1OaXR-Bh-GJeBKcmVGRWLHytXy-6086WUYY3TBa8je7DSt4tc5ZyTY5pWxD85KLze2DbHX_8DBbUUrrdQqIk-wJ4i6BBa3Y4-yEMcZrQcUq-3WhdPQBiXVdP4HT1m3JtYJBRd_7rdWqJwG0v4EwE9VFCET16QEcWL0H_egtxHTBCAPR0PckBuVw7JWL-JZsQ4r9vvuZNuCEabj2GImxCArhNTHe-UDiPKZZz9EPsFW9v7Fh2ncCHa13SJQzh93GIzzNHnWqR3h2PE-zbxcfvp5frq--fPx0_v5qrcuainXZmop3Xd5QUYOBsmKiUx3LNe0q3jaKgqlUUytjuNBal1Wh25qaUphS81aI4jR7ddg7Bv99AoxysLi0UA78hLKmPOd5wRP44h9w56fgUjfJGlE1TVXlCRIHSAePGKCTY7CDCrNkVC5a5U4u9uRiTy5a5V6rvE3R58f9UzuA-Rs8ekzAyyOgMCnrkgBt8Z5rOEtNE_XuQP2wPcz__b08-3y5TMUfMkTFFg</recordid><startdate>200101</startdate><enddate>200101</enddate><creator>Dominietto, Alida</creator><creator>Raiola, Anna Maria</creator><creator>Van Lint, Maria Teresa</creator><creator>Lamparelli, Teresa</creator><creator>Gualandi, Francesca</creator><creator>Berisso, Giovanni</creator><creator>Bregante, Stefania</creator><creator>Frassoni, Francesco</creator><creator>Casarino, Lucia</creator><creator>Verdiani, Simonetta</creator><creator>Bacigalupo, Andrea</creator><general>Blackwell Science Ltd</general><general>Blackwell</general><general>Blackwell Publishing Ltd</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200101</creationdate><title>Factors influencing haematological recovery after allogeneic haemopoietic stem cell transplants: graft‐versus‐host disease, donor type, cytomegalovirus infections and cell dose</title><author>Dominietto, Alida ; Raiola, Anna Maria ; Van Lint, Maria Teresa ; Lamparelli, Teresa ; Gualandi, Francesca ; Berisso, Giovanni ; Bregante, Stefania ; Frassoni, Francesco ; Casarino, Lucia ; Verdiani, Simonetta ; Bacigalupo, Andrea</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4708-4bd56ff29087ede4518faf12c0f56b9a0ed5a97add68ccc453cb70d48d4c6b883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>allogeneic bone marrow transplantation</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Bone Marrow Transplantation - mortality</topic><topic>Bone marrow, stem cells transplantation. Graft versus host reaction</topic><topic>Child</topic><topic>Chimera</topic><topic>Cytomegalovirus Infections - complications</topic><topic>Female</topic><topic>Graft vs Host Disease</topic><topic>graft‐versus‐host disease</topic><topic>haematopoietic recovery</topic><topic>Hematologic Neoplasms - blood</topic><topic>Hematologic Neoplasms - mortality</topic><topic>Hematologic Neoplasms - surgery</topic><topic>Hematology</topic><topic>Hematopoietic Stem Cell Transplantation - mortality</topic><topic>Histocompatibility Testing</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Platelet Count</topic><topic>Prognosis</topic><topic>Thrombocytopenia - complications</topic><topic>Time Factors</topic><topic>Tissue Donors</topic><topic>Transfusions. Complications. Transfusion reactions. 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All patients were prepared with cyclophosphamide plus total body irradiation, and received an unmanipulated HSCT from an HLA‐identical sibling (n = 270), a matched unrelated donor (n = 67) or an identical twin (n = 5). The source of stem cells was peripheral blood (n = 15) or bone marrow (n = 327). Graft‐vs.‐host disease (GvHD) prophylaxis consisted of cyclosporin A with or without methotrexate. The proportion of patients with < 50 × 109/l platelets on d +50, d +100, d +200 and d +365 after HSCT was 26%, 27%, 14% and 11% respectively. Thrombocytopenia was independent of the degree of complete donor chimaerism. Four variables were predictive of platelet recovery: donor type, acute GvHD, cytomegalovirus (CMV) infection and number of cells infused at transplant. Recipients of an unrelated graft had lower platelet counts (49 × 109/l) on d +50 than identical sibling grafts (108 × 109/l) (P < 0·001) and twin grafts (149 × 109/l) (P < 0·001). Patients with GvHD grades 0, I, II, III and IV had significantly different platelet counts on d +50 (153 × 109/l, 102 × 109/l, 85 × 109/l, 32 × 109/l and 22 × 109/l; P < 0·001) and thereafter. Thrombocytopenia was more frequent in patients with high‐level CMV antigenaemia (> four positive cells/2 × 105) (P < 0·0001) and in patients who received a low cell dose at transplant (≤ 4·1 × 108/kg) (P = 0·009). Platelet counts predicted transplant‐related mortality (TRM) and were higher at all time intervals in patients surviving the transplant. Patients with grade II GvHD and > 50 × 109/l platelets had a lower TRM than patients with grade II GvHD and ≤ 50 × 109/l platelets (14% vs. 40%, P < 0·0001). In conclusion, (i) a significant proportion of allogeneic HSCT recipients are thrombocytopenic long‐term, irrespective of complete donor chimaerism, (ii) thrombocytopenia identifies patients at greater risk of lethal complications, and (iii) platelet recovery is influenced by GvHD, donor type, CMV infections and cell dose, not by stem cell source or other patient–disease‐related variables.]]></abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>11167808</pmid><doi>10.1046/j.1365-2141.2001.02468.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
allogeneic bone marrow transplantation
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Biological and medical sciences
Bone Marrow Transplantation - mortality
Bone marrow, stem cells transplantation. Graft versus host reaction
Child
Chimera
Cytomegalovirus Infections - complications
Female
Graft vs Host Disease
graft‐versus‐host disease
haematopoietic recovery
Hematologic Neoplasms - blood
Hematologic Neoplasms - mortality
Hematologic Neoplasms - surgery
Hematology
Hematopoietic Stem Cell Transplantation - mortality
Histocompatibility Testing
Humans
Male
Medical sciences
Middle Aged
Platelet Count
Prognosis
Thrombocytopenia - complications
Time Factors
Tissue Donors
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
Transplantation, Homologous
Twins, Monozygotic
title Factors influencing haematological recovery after allogeneic haemopoietic stem cell transplants: graft‐versus‐host disease, donor type, cytomegalovirus infections and cell dose
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