Infection Risk in Lymphoproliferative Diseases (LPD) Treated with Targeted Drugs. Geltamo Real-Life Experience
Introduction:Recently there has been a renewal of therapeutic tools for the treatment of lymphoid neoplasms to increase the antitumor efficacy and reduce the toxicity generated by conventional chemotherapies, which adds to the intrinsic immunological dysfunction of the disease itself. To date, few d...
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| Veröffentlicht in: | Blood 2020-11, Vol.136 (Supplement 1), p.37-40 |
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| creator | Infante, Maria Stefania Fernandez-Cruz, Ana Nuñez, Lucia Carpio, Cecilia Jimenez-Ubieto, Ana Lopez Jimenez, Javier Vázquez, Lourdes Del Campo, Raquel Romero, Samuel Alonso Prieto, Carmen Murillo, Daniel Prat, Margarita Plana Cuenca, Jose Luis Villaverde Gutiérrez, Paola Bastidas, Gabriela Bocanegra, Ana Serna, Ángel de Nicolas, Rodrigo Marquet Palomanes, Juan Garcia-Suarez, Julio Mas Ochoa, Maria Carmen Comai, Alessandra Martin, Xabier Seri, Cristina Navarro Matilla, Belen Hernandez-Rivas, Jose Angel Lopez-Guillermo, Armando Ruiz-Campos, Isabel Grande, Carlos |
| description | Introduction:Recently there has been a renewal of therapeutic tools for the treatment of lymphoid neoplasms to increase the antitumor efficacy and reduce the toxicity generated by conventional chemotherapies, which adds to the intrinsic immunological dysfunction of the disease itself. To date, few data are published about infection risk of these new drugs, and the need for infectious prophylaxis is unknown.
The aim of the study is to analyze the infectious complications in patients with LPD treated with monoclonal antibodies (obinutuzumab, ofatumumab, brentuximab, nivolumab and pembrolizumab), BTK inhibitors (ibrutinib, acalabrutinib) and PI3K inhibitors (idelalisib).
Methods: Multicenter retrospective study in patients with LPD treated with targeted therapies (single agents or combination) in 18 Hematology centers in Spain, from the time of their commercial availability to March 2020. Patients in clinical trials were excluded as well as patients with active infections at the beginning of treatment.
Results:During the study period, 380 patients were included.Baseline characteristics of the entire cohort are shown in Table 1.Median follow-up was 17.3 months (range 0-103), the longest follow-up corresponding to CLL patients (24 months, range 0-98) and the shortest to LBCL (5 months, range 0-25). Median exposure to target drugs was 8 months (range 0-72).Ibrutinib was administered to 219 patients(1 FL, 147 CLL, 27 MCL, 10 DLBCL, 1 TL and 32 WM, 1 HL),Brentuximab to 49(31 HL, 14 TL and 4 DLBCL) andIdelalisibto 35 patients (16 affected by chronic lymphocytic leukemia - CLL, 15 FL and 1 DLBCL, 1 WM, 1MCL, 1HL).Obinutuzumabcombinations were used in 10 (6 CLL, 3 FL, 1 MCL) and 5 HL patients (of which 4/5 underwent previous BMT) receivedNivolumab.
A total number of 237 infectious events occurred in 148/380 patients (38.9%), 39% of which were grade 3 and 54/148 (36.4%) experienced 2 or more infective episodes: of those 54, 21 (38%) had underwent 3 or more lines of therapy and 28 (51%) had hypogammaglobulinemia. Hospitalization was required in 59.2% events. A bacterial cause of infection was reported in 40% of cases, and viral in 16%, including 11/237 (4,6%) SARS-CoV-2 infection. Invasive fungal infection (IFI) occurred in 3.3% (8/237). Noteworthy, no case of PJP was identified. Lung was the most frequent site of infection in 24% of cases (57/237) while the upper respiratory tract was involved in 17% of events (41/237). Urinary tract infections were diagnosed in 10% ( |
| doi_str_mv | 10.1182/blood-2020-134729 |
| format | Article |
| fullrecord | <record><control><sourceid>elsevier_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1182_blood_2020_134729</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0006497118729546</els_id><sourcerecordid>S0006497118729546</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1379-abbf77cb618780ae719f7d840c3df38c6798598aab34d3d5d74d5372104615883</originalsourceid><addsrcrecordid>eNp9kEFLwzAYhoMoOKc_wFuOeshMmrZJ8STbnIOCMuY5pMnXLdo1I6nT_Xu7zbOnj_eD5-XlQeiW0RFjMnmoGu8tSWhCCeOpSIozNGBZIgntX-doQCnNSVoIdomuYvyglKU8yQaonbc1mM75Fi9c_MSuxeV-s137bfCNqyHozu0AT1wEHSHiu_Jtco-XAXQHFn-7bo2XOqzgkCbhaxVHeAZNpzceL0A3pOw78PRnC8FBa-AaXdS6iXDzd4fo_Xm6HL-Q8nU2Hz-VxDAuCqKrqhbCVDmTQlINghW1sDKlhtuaS5OLQmaF1LriqeU2syK1GRcJo2nOMin5ELFTrwk-xgC12ga30WGvGFUHYeooTB2EqZOwnnk8MdAP2zkIKprjaOtCr0hZ7_6hfwGP6HNu</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Infection Risk in Lymphoproliferative Diseases (LPD) Treated with Targeted Drugs. Geltamo Real-Life Experience</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Infante, Maria Stefania ; Fernandez-Cruz, Ana ; Nuñez, Lucia ; Carpio, Cecilia ; Jimenez-Ubieto, Ana ; Lopez Jimenez, Javier ; Vázquez, Lourdes ; Del Campo, Raquel ; Romero, Samuel ; Alonso Prieto, Carmen ; Murillo, Daniel ; Prat, Margarita ; Plana Cuenca, Jose Luis ; Villaverde Gutiérrez, Paola ; Bastidas, Gabriela ; Bocanegra, Ana ; Serna, Ángel ; de Nicolas, Rodrigo ; Marquet Palomanes, Juan ; Garcia-Suarez, Julio ; Mas Ochoa, Maria Carmen ; Comai, Alessandra ; Martin, Xabier ; Seri, Cristina ; Navarro Matilla, Belen ; Hernandez-Rivas, Jose Angel ; Lopez-Guillermo, Armando ; Ruiz-Campos, Isabel ; Grande, Carlos</creator><creatorcontrib>Infante, Maria Stefania ; Fernandez-Cruz, Ana ; Nuñez, Lucia ; Carpio, Cecilia ; Jimenez-Ubieto, Ana ; Lopez Jimenez, Javier ; Vázquez, Lourdes ; Del Campo, Raquel ; Romero, Samuel ; Alonso Prieto, Carmen ; Murillo, Daniel ; Prat, Margarita ; Plana Cuenca, Jose Luis ; Villaverde Gutiérrez, Paola ; Bastidas, Gabriela ; Bocanegra, Ana ; Serna, Ángel ; de Nicolas, Rodrigo ; Marquet Palomanes, Juan ; Garcia-Suarez, Julio ; Mas Ochoa, Maria Carmen ; Comai, Alessandra ; Martin, Xabier ; Seri, Cristina ; Navarro Matilla, Belen ; Hernandez-Rivas, Jose Angel ; Lopez-Guillermo, Armando ; Ruiz-Campos, Isabel ; Grande, Carlos</creatorcontrib><description>Introduction:Recently there has been a renewal of therapeutic tools for the treatment of lymphoid neoplasms to increase the antitumor efficacy and reduce the toxicity generated by conventional chemotherapies, which adds to the intrinsic immunological dysfunction of the disease itself. To date, few data are published about infection risk of these new drugs, and the need for infectious prophylaxis is unknown.
The aim of the study is to analyze the infectious complications in patients with LPD treated with monoclonal antibodies (obinutuzumab, ofatumumab, brentuximab, nivolumab and pembrolizumab), BTK inhibitors (ibrutinib, acalabrutinib) and PI3K inhibitors (idelalisib).
Methods: Multicenter retrospective study in patients with LPD treated with targeted therapies (single agents or combination) in 18 Hematology centers in Spain, from the time of their commercial availability to March 2020. Patients in clinical trials were excluded as well as patients with active infections at the beginning of treatment.
Results:During the study period, 380 patients were included.Baseline characteristics of the entire cohort are shown in Table 1.Median follow-up was 17.3 months (range 0-103), the longest follow-up corresponding to CLL patients (24 months, range 0-98) and the shortest to LBCL (5 months, range 0-25). Median exposure to target drugs was 8 months (range 0-72).Ibrutinib was administered to 219 patients(1 FL, 147 CLL, 27 MCL, 10 DLBCL, 1 TL and 32 WM, 1 HL),Brentuximab to 49(31 HL, 14 TL and 4 DLBCL) andIdelalisibto 35 patients (16 affected by chronic lymphocytic leukemia - CLL, 15 FL and 1 DLBCL, 1 WM, 1MCL, 1HL).Obinutuzumabcombinations were used in 10 (6 CLL, 3 FL, 1 MCL) and 5 HL patients (of which 4/5 underwent previous BMT) receivedNivolumab.
A total number of 237 infectious events occurred in 148/380 patients (38.9%), 39% of which were grade 3 and 54/148 (36.4%) experienced 2 or more infective episodes: of those 54, 21 (38%) had underwent 3 or more lines of therapy and 28 (51%) had hypogammaglobulinemia. Hospitalization was required in 59.2% events. A bacterial cause of infection was reported in 40% of cases, and viral in 16%, including 11/237 (4,6%) SARS-CoV-2 infection. Invasive fungal infection (IFI) occurred in 3.3% (8/237). Noteworthy, no case of PJP was identified. Lung was the most frequent site of infection in 24% of cases (57/237) while the upper respiratory tract was involved in 17% of events (41/237). Urinary tract infections were diagnosed in 10% (24/237). Other sites involved were skin and soft tissue 7%, gastrointestinal tract 5,4%, bloodstream infections 3% and catheter related infections 2,5%.
Considering drugs individually, 86 patients that receivedIbrutinib(39.2 %)experienced a total of 137 infectious episodes: 30% bacterial, 19% viral, 5% fungal and 45% clinical and image-based infections; the 17(34.6%of those who received Brentuximab, experienced a total of 16 infectious episodes: 56% bacterial, 37.5% viral infections and one catheter-related sepsis. Of those who receivedIdelalisib,18 (51.4%)experienced a total of 28 episodes: 42% bacterial, 14% viral and 7% fungal. Four patients treated withObinutuzumabcombinations (40%) experienced one infection during treatment (25% bacterial and 75% viral). Only one patient treated withNivolumabexperienced more than three infections, he was also under corticosteroid treatment.
Focusing on IFI (Table 2): 7/8 infections were identified in CLL patients, 6 out 7 being on ibrutinib treatment and 1/7 on Idelalisib.Aspergilluswas the fungus most frequently isolated. The targeted drug was discontinued temporarily in 4 patients and indefinitely in 3. Twenty three (6%) patients died due to infection in our series.
Conclusions:
1. We identified 38.7% infections in our LPD patients treated with targeted drugs, with a median drug-exposure time of 8 months (range 0-72), with a non-negligible incidence of bacterial infections.
2. The highest rates of infection were found in patients treated with with Idelalisib and Ibrutinib (51.4% and 39.2% respectively).
3. IFI (3.3%) occurred with low frequency, mostly in CLL patients during ibrutinib treatment, leading to its temporal discontinuation in most of the cases.
4. No case of PJP was identified in our cohort.
5. An analysis to determine risk factors for infection and the optimal monitoring and prophylaxis for these patients is ongoing.
[Display omitted]
Hernandez-Rivas:Janssen:Membership on an entity's Board of Directors or advisory committees;Abbvie:Membership on an entity's Board of Directors or advisory committees;Roche:Membership on an entity's Board of Directors or advisory committees;AstraZeneca:Membership on an entity's Board of Directors or advisory committees;Gilead:Membership on an entity's Board of Directors or advisory committees;Celgene/BMS:Membership on an entity's Board of Directors or advisory committees;Rovi:Membership on an entity's Board of Directors or advisory committees.Lopez-Guillermo:novartis:Consultancy;celgene:Consultancy, Research Funding;roche:Consultancy, Research Funding;gilead:Consultancy, Research Funding.</description><identifier>ISSN: 0006-4971</identifier><identifier>EISSN: 1528-0020</identifier><identifier>DOI: 10.1182/blood-2020-134729</identifier><language>eng</language><publisher>Elsevier Inc</publisher><ispartof>Blood, 2020-11, Vol.136 (Supplement 1), p.37-40</ispartof><rights>2020 American Society of Hematology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Infante, Maria Stefania</creatorcontrib><creatorcontrib>Fernandez-Cruz, Ana</creatorcontrib><creatorcontrib>Nuñez, Lucia</creatorcontrib><creatorcontrib>Carpio, Cecilia</creatorcontrib><creatorcontrib>Jimenez-Ubieto, Ana</creatorcontrib><creatorcontrib>Lopez Jimenez, Javier</creatorcontrib><creatorcontrib>Vázquez, Lourdes</creatorcontrib><creatorcontrib>Del Campo, Raquel</creatorcontrib><creatorcontrib>Romero, Samuel</creatorcontrib><creatorcontrib>Alonso Prieto, Carmen</creatorcontrib><creatorcontrib>Murillo, Daniel</creatorcontrib><creatorcontrib>Prat, Margarita</creatorcontrib><creatorcontrib>Plana Cuenca, Jose Luis</creatorcontrib><creatorcontrib>Villaverde Gutiérrez, Paola</creatorcontrib><creatorcontrib>Bastidas, Gabriela</creatorcontrib><creatorcontrib>Bocanegra, Ana</creatorcontrib><creatorcontrib>Serna, Ángel</creatorcontrib><creatorcontrib>de Nicolas, Rodrigo</creatorcontrib><creatorcontrib>Marquet Palomanes, Juan</creatorcontrib><creatorcontrib>Garcia-Suarez, Julio</creatorcontrib><creatorcontrib>Mas Ochoa, Maria Carmen</creatorcontrib><creatorcontrib>Comai, Alessandra</creatorcontrib><creatorcontrib>Martin, Xabier</creatorcontrib><creatorcontrib>Seri, Cristina</creatorcontrib><creatorcontrib>Navarro Matilla, Belen</creatorcontrib><creatorcontrib>Hernandez-Rivas, Jose Angel</creatorcontrib><creatorcontrib>Lopez-Guillermo, Armando</creatorcontrib><creatorcontrib>Ruiz-Campos, Isabel</creatorcontrib><creatorcontrib>Grande, Carlos</creatorcontrib><title>Infection Risk in Lymphoproliferative Diseases (LPD) Treated with Targeted Drugs. Geltamo Real-Life Experience</title><title>Blood</title><description>Introduction:Recently there has been a renewal of therapeutic tools for the treatment of lymphoid neoplasms to increase the antitumor efficacy and reduce the toxicity generated by conventional chemotherapies, which adds to the intrinsic immunological dysfunction of the disease itself. To date, few data are published about infection risk of these new drugs, and the need for infectious prophylaxis is unknown.
The aim of the study is to analyze the infectious complications in patients with LPD treated with monoclonal antibodies (obinutuzumab, ofatumumab, brentuximab, nivolumab and pembrolizumab), BTK inhibitors (ibrutinib, acalabrutinib) and PI3K inhibitors (idelalisib).
Methods: Multicenter retrospective study in patients with LPD treated with targeted therapies (single agents or combination) in 18 Hematology centers in Spain, from the time of their commercial availability to March 2020. Patients in clinical trials were excluded as well as patients with active infections at the beginning of treatment.
Results:During the study period, 380 patients were included.Baseline characteristics of the entire cohort are shown in Table 1.Median follow-up was 17.3 months (range 0-103), the longest follow-up corresponding to CLL patients (24 months, range 0-98) and the shortest to LBCL (5 months, range 0-25). Median exposure to target drugs was 8 months (range 0-72).Ibrutinib was administered to 219 patients(1 FL, 147 CLL, 27 MCL, 10 DLBCL, 1 TL and 32 WM, 1 HL),Brentuximab to 49(31 HL, 14 TL and 4 DLBCL) andIdelalisibto 35 patients (16 affected by chronic lymphocytic leukemia - CLL, 15 FL and 1 DLBCL, 1 WM, 1MCL, 1HL).Obinutuzumabcombinations were used in 10 (6 CLL, 3 FL, 1 MCL) and 5 HL patients (of which 4/5 underwent previous BMT) receivedNivolumab.
A total number of 237 infectious events occurred in 148/380 patients (38.9%), 39% of which were grade 3 and 54/148 (36.4%) experienced 2 or more infective episodes: of those 54, 21 (38%) had underwent 3 or more lines of therapy and 28 (51%) had hypogammaglobulinemia. Hospitalization was required in 59.2% events. A bacterial cause of infection was reported in 40% of cases, and viral in 16%, including 11/237 (4,6%) SARS-CoV-2 infection. Invasive fungal infection (IFI) occurred in 3.3% (8/237). Noteworthy, no case of PJP was identified. Lung was the most frequent site of infection in 24% of cases (57/237) while the upper respiratory tract was involved in 17% of events (41/237). Urinary tract infections were diagnosed in 10% (24/237). Other sites involved were skin and soft tissue 7%, gastrointestinal tract 5,4%, bloodstream infections 3% and catheter related infections 2,5%.
Considering drugs individually, 86 patients that receivedIbrutinib(39.2 %)experienced a total of 137 infectious episodes: 30% bacterial, 19% viral, 5% fungal and 45% clinical and image-based infections; the 17(34.6%of those who received Brentuximab, experienced a total of 16 infectious episodes: 56% bacterial, 37.5% viral infections and one catheter-related sepsis. Of those who receivedIdelalisib,18 (51.4%)experienced a total of 28 episodes: 42% bacterial, 14% viral and 7% fungal. Four patients treated withObinutuzumabcombinations (40%) experienced one infection during treatment (25% bacterial and 75% viral). Only one patient treated withNivolumabexperienced more than three infections, he was also under corticosteroid treatment.
Focusing on IFI (Table 2): 7/8 infections were identified in CLL patients, 6 out 7 being on ibrutinib treatment and 1/7 on Idelalisib.Aspergilluswas the fungus most frequently isolated. The targeted drug was discontinued temporarily in 4 patients and indefinitely in 3. Twenty three (6%) patients died due to infection in our series.
Conclusions:
1. We identified 38.7% infections in our LPD patients treated with targeted drugs, with a median drug-exposure time of 8 months (range 0-72), with a non-negligible incidence of bacterial infections.
2. The highest rates of infection were found in patients treated with with Idelalisib and Ibrutinib (51.4% and 39.2% respectively).
3. IFI (3.3%) occurred with low frequency, mostly in CLL patients during ibrutinib treatment, leading to its temporal discontinuation in most of the cases.
4. No case of PJP was identified in our cohort.
5. An analysis to determine risk factors for infection and the optimal monitoring and prophylaxis for these patients is ongoing.
[Display omitted]
Hernandez-Rivas:Janssen:Membership on an entity's Board of Directors or advisory committees;Abbvie:Membership on an entity's Board of Directors or advisory committees;Roche:Membership on an entity's Board of Directors or advisory committees;AstraZeneca:Membership on an entity's Board of Directors or advisory committees;Gilead:Membership on an entity's Board of Directors or advisory committees;Celgene/BMS:Membership on an entity's Board of Directors or advisory committees;Rovi:Membership on an entity's Board of Directors or advisory committees.Lopez-Guillermo:novartis:Consultancy;celgene:Consultancy, Research Funding;roche:Consultancy, Research Funding;gilead:Consultancy, Research Funding.</description><issn>0006-4971</issn><issn>1528-0020</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kEFLwzAYhoMoOKc_wFuOeshMmrZJ8STbnIOCMuY5pMnXLdo1I6nT_Xu7zbOnj_eD5-XlQeiW0RFjMnmoGu8tSWhCCeOpSIozNGBZIgntX-doQCnNSVoIdomuYvyglKU8yQaonbc1mM75Fi9c_MSuxeV-s137bfCNqyHozu0AT1wEHSHiu_Jtco-XAXQHFn-7bo2XOqzgkCbhaxVHeAZNpzceL0A3pOw78PRnC8FBa-AaXdS6iXDzd4fo_Xm6HL-Q8nU2Hz-VxDAuCqKrqhbCVDmTQlINghW1sDKlhtuaS5OLQmaF1LriqeU2syK1GRcJo2nOMin5ELFTrwk-xgC12ga30WGvGFUHYeooTB2EqZOwnnk8MdAP2zkIKprjaOtCr0hZ7_6hfwGP6HNu</recordid><startdate>20201105</startdate><enddate>20201105</enddate><creator>Infante, Maria Stefania</creator><creator>Fernandez-Cruz, Ana</creator><creator>Nuñez, Lucia</creator><creator>Carpio, Cecilia</creator><creator>Jimenez-Ubieto, Ana</creator><creator>Lopez Jimenez, Javier</creator><creator>Vázquez, Lourdes</creator><creator>Del Campo, Raquel</creator><creator>Romero, Samuel</creator><creator>Alonso Prieto, Carmen</creator><creator>Murillo, Daniel</creator><creator>Prat, Margarita</creator><creator>Plana Cuenca, Jose Luis</creator><creator>Villaverde Gutiérrez, Paola</creator><creator>Bastidas, Gabriela</creator><creator>Bocanegra, Ana</creator><creator>Serna, Ángel</creator><creator>de Nicolas, Rodrigo</creator><creator>Marquet Palomanes, Juan</creator><creator>Garcia-Suarez, Julio</creator><creator>Mas Ochoa, Maria Carmen</creator><creator>Comai, Alessandra</creator><creator>Martin, Xabier</creator><creator>Seri, Cristina</creator><creator>Navarro Matilla, Belen</creator><creator>Hernandez-Rivas, Jose Angel</creator><creator>Lopez-Guillermo, Armando</creator><creator>Ruiz-Campos, Isabel</creator><creator>Grande, Carlos</creator><general>Elsevier Inc</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20201105</creationdate><title>Infection Risk in Lymphoproliferative Diseases (LPD) Treated with Targeted Drugs. 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Geltamo Real-Life Experience</atitle><jtitle>Blood</jtitle><date>2020-11-05</date><risdate>2020</risdate><volume>136</volume><issue>Supplement 1</issue><spage>37</spage><epage>40</epage><pages>37-40</pages><issn>0006-4971</issn><eissn>1528-0020</eissn><abstract>Introduction:Recently there has been a renewal of therapeutic tools for the treatment of lymphoid neoplasms to increase the antitumor efficacy and reduce the toxicity generated by conventional chemotherapies, which adds to the intrinsic immunological dysfunction of the disease itself. To date, few data are published about infection risk of these new drugs, and the need for infectious prophylaxis is unknown.
The aim of the study is to analyze the infectious complications in patients with LPD treated with monoclonal antibodies (obinutuzumab, ofatumumab, brentuximab, nivolumab and pembrolizumab), BTK inhibitors (ibrutinib, acalabrutinib) and PI3K inhibitors (idelalisib).
Methods: Multicenter retrospective study in patients with LPD treated with targeted therapies (single agents or combination) in 18 Hematology centers in Spain, from the time of their commercial availability to March 2020. Patients in clinical trials were excluded as well as patients with active infections at the beginning of treatment.
Results:During the study period, 380 patients were included.Baseline characteristics of the entire cohort are shown in Table 1.Median follow-up was 17.3 months (range 0-103), the longest follow-up corresponding to CLL patients (24 months, range 0-98) and the shortest to LBCL (5 months, range 0-25). Median exposure to target drugs was 8 months (range 0-72).Ibrutinib was administered to 219 patients(1 FL, 147 CLL, 27 MCL, 10 DLBCL, 1 TL and 32 WM, 1 HL),Brentuximab to 49(31 HL, 14 TL and 4 DLBCL) andIdelalisibto 35 patients (16 affected by chronic lymphocytic leukemia - CLL, 15 FL and 1 DLBCL, 1 WM, 1MCL, 1HL).Obinutuzumabcombinations were used in 10 (6 CLL, 3 FL, 1 MCL) and 5 HL patients (of which 4/5 underwent previous BMT) receivedNivolumab.
A total number of 237 infectious events occurred in 148/380 patients (38.9%), 39% of which were grade 3 and 54/148 (36.4%) experienced 2 or more infective episodes: of those 54, 21 (38%) had underwent 3 or more lines of therapy and 28 (51%) had hypogammaglobulinemia. Hospitalization was required in 59.2% events. A bacterial cause of infection was reported in 40% of cases, and viral in 16%, including 11/237 (4,6%) SARS-CoV-2 infection. Invasive fungal infection (IFI) occurred in 3.3% (8/237). Noteworthy, no case of PJP was identified. Lung was the most frequent site of infection in 24% of cases (57/237) while the upper respiratory tract was involved in 17% of events (41/237). Urinary tract infections were diagnosed in 10% (24/237). Other sites involved were skin and soft tissue 7%, gastrointestinal tract 5,4%, bloodstream infections 3% and catheter related infections 2,5%.
Considering drugs individually, 86 patients that receivedIbrutinib(39.2 %)experienced a total of 137 infectious episodes: 30% bacterial, 19% viral, 5% fungal and 45% clinical and image-based infections; the 17(34.6%of those who received Brentuximab, experienced a total of 16 infectious episodes: 56% bacterial, 37.5% viral infections and one catheter-related sepsis. Of those who receivedIdelalisib,18 (51.4%)experienced a total of 28 episodes: 42% bacterial, 14% viral and 7% fungal. Four patients treated withObinutuzumabcombinations (40%) experienced one infection during treatment (25% bacterial and 75% viral). Only one patient treated withNivolumabexperienced more than three infections, he was also under corticosteroid treatment.
Focusing on IFI (Table 2): 7/8 infections were identified in CLL patients, 6 out 7 being on ibrutinib treatment and 1/7 on Idelalisib.Aspergilluswas the fungus most frequently isolated. The targeted drug was discontinued temporarily in 4 patients and indefinitely in 3. Twenty three (6%) patients died due to infection in our series.
Conclusions:
1. We identified 38.7% infections in our LPD patients treated with targeted drugs, with a median drug-exposure time of 8 months (range 0-72), with a non-negligible incidence of bacterial infections.
2. The highest rates of infection were found in patients treated with with Idelalisib and Ibrutinib (51.4% and 39.2% respectively).
3. IFI (3.3%) occurred with low frequency, mostly in CLL patients during ibrutinib treatment, leading to its temporal discontinuation in most of the cases.
4. No case of PJP was identified in our cohort.
5. An analysis to determine risk factors for infection and the optimal monitoring and prophylaxis for these patients is ongoing.
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Hernandez-Rivas:Janssen:Membership on an entity's Board of Directors or advisory committees;Abbvie:Membership on an entity's Board of Directors or advisory committees;Roche:Membership on an entity's Board of Directors or advisory committees;AstraZeneca:Membership on an entity's Board of Directors or advisory committees;Gilead:Membership on an entity's Board of Directors or advisory committees;Celgene/BMS:Membership on an entity's Board of Directors or advisory committees;Rovi:Membership on an entity's Board of Directors or advisory committees.Lopez-Guillermo:novartis:Consultancy;celgene:Consultancy, Research Funding;roche:Consultancy, Research Funding;gilead:Consultancy, Research Funding.</abstract><pub>Elsevier Inc</pub><doi>10.1182/blood-2020-134729</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0006-4971 |
| ispartof | Blood, 2020-11, Vol.136 (Supplement 1), p.37-40 |
| issn | 0006-4971 1528-0020 |
| language | eng |
| recordid | cdi_crossref_primary_10_1182_blood_2020_134729 |
| source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
| title | Infection Risk in Lymphoproliferative Diseases (LPD) Treated with Targeted Drugs. Geltamo Real-Life Experience |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T01%3A17%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Infection%20Risk%20in%20Lymphoproliferative%20Diseases%20(LPD)%20Treated%20with%20Targeted%20Drugs.%20Geltamo%20Real-Life%20Experience&rft.jtitle=Blood&rft.au=Infante,%20Maria%20Stefania&rft.date=2020-11-05&rft.volume=136&rft.issue=Supplement%201&rft.spage=37&rft.epage=40&rft.pages=37-40&rft.issn=0006-4971&rft.eissn=1528-0020&rft_id=info:doi/10.1182/blood-2020-134729&rft_dat=%3Celsevier_cross%3ES0006497118729546%3C/elsevier_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_els_id=S0006497118729546&rfr_iscdi=true |