Donor–derived small cell lung carcinoma in a kidney transplant recipient
BACKGROUND Transplantation of donor–derived malignancies during organ transplantation fortunately is very rare. Discontinuation of immunosuppressive medications under these circumstances has previously resulted in complete tumor rejection. Ectopic adrenocorticotropic hormone (ACTH) production may re...
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Veröffentlicht in: | Cancer 2001-11, Vol.92 (9), p.2429-2434 |
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creator | Bodvarsson, Sigurdur Burlingham, William Kusaka, Satoshi Hafez, Gholam‐Reza Becker, Bryan N. Pintar, Thomas Sollinger, Hans W. Albertini, Mark R. |
description | BACKGROUND
Transplantation of donor–derived malignancies during organ transplantation fortunately is very rare. Discontinuation of immunosuppressive medications under these circumstances has previously resulted in complete tumor rejection. Ectopic adrenocorticotropic hormone (ACTH) production may result in Cushing syndrome and is not an uncommon paraneoplastic feature of small cell carcinoma of the lung. Theoretically, in the organ transplantation setting, the resulting high cortisol levels could suppress a tumor‐rejection immune response. However, to the authors' knowledge, no such a clinical scenario has been described in the literature published to date.
METHODS
A 25–year–old living related kidney transplant recipient presented with Cushing syndrome 32 months after transplantation. The donor had been diagnosed with small cell carcinoma of the lung 22 months earlier. On further evaluation, the kidney recipient was diagnosed with donor–derived small cell lung carcinoma of the transplanted kidney. She was found to have extensive disease involving the liver and retroperitoneum. Despite discontinuation of immunosuppressive medications, the disease progressed and cortisol levels remained elevated during 6 weeks of observation.
RESULTS
The patient received six cycles of cisplatin and etoposide, which resulted in resolution of her hypercortisolemia and a complete remission of her donor–derived small cell carcinoma. At last follow‐up, she was 12 months from completing her therapy and continued in complete remission.
CONCLUSIONS
Donor–derived small cell carcinoma and ectopic ACTH production can occur in a patient after kidney transplantation. Cancer 2001;92:2429–34. © 2001 American Cancer Society.
Persistent ectopic adrenocorticotropic hormone (ACTH) production occurred in a kidney transplant recipient diagnosed as having a living related donor–derived small cell lung carcinoma. The donor–derived malignancy was not rejected after discontinuation of immune suppression. Ectopic ACTH production, clinical signs of Cushing syndrome, and radiographic evidence of metastatic disease completely resolved after the administration of systemic chemotherapy. |
doi_str_mv | 10.1002/1097-0142(20011101)92:9<2429::AID-CNCR1592>3.0.CO;2-G |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_72353703</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>72353703</sourcerecordid><originalsourceid>FETCH-LOGICAL-p2222-593f0ba1bc49646e52a9807fbe4b6f8da0c1c8ca6048f7dec7189494b4add7f33</originalsourceid><addsrcrecordid>eNpFkd1O2zAUgK2JaS1lrzDlCrGLdMc_qePCJqEApVNFpWmTEDdHjuNMhsTJkhbUu70Db8iTkKgt-OJYx-ezdXw-Qr5TGFMA9o2CkiFQwU4YAKUU6FfFpuqMCaam0_P5RZjcJL9opNgPPoZxsjxl4ewDGb7dOyBDAIjDSPDbATls2_sulSzin8iAUikiDjAkPy8qXzUv_58z27hHmwVtqYsiMLYLxdr_DYxujPNVqQPnAx08uMzbTbBqtG_rQvtV0Fjjamf96oh8zHXR2s-7fUT-XF3-Tq7DxXI2T84XYc26FUaK55BqmhqhJmJiI6ZVDDJPrUgneZxpMNTERk9AxLnMrJE0VkKJVOgskznnI3K8fbduqn9r266wdG3fsPa2WrcoGY-4hB78sgPXaWkzrBtX6maD-993wN0WeHKF3bzXAXsF2I8S-1HiXgEqhgp7BdgZwL0B5AiYLJHh7O2MvwKJ4X8v</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>72353703</pqid></control><display><type>article</type><title>Donor–derived small cell lung carcinoma in a kidney transplant recipient</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Wiley Free Content</source><source>Alma/SFX Local Collection</source><creator>Bodvarsson, Sigurdur ; Burlingham, William ; Kusaka, Satoshi ; Hafez, Gholam‐Reza ; Becker, Bryan N. ; Pintar, Thomas ; Sollinger, Hans W. ; Albertini, Mark R.</creator><creatorcontrib>Bodvarsson, Sigurdur ; Burlingham, William ; Kusaka, Satoshi ; Hafez, Gholam‐Reza ; Becker, Bryan N. ; Pintar, Thomas ; Sollinger, Hans W. ; Albertini, Mark R.</creatorcontrib><description>BACKGROUND
Transplantation of donor–derived malignancies during organ transplantation fortunately is very rare. Discontinuation of immunosuppressive medications under these circumstances has previously resulted in complete tumor rejection. Ectopic adrenocorticotropic hormone (ACTH) production may result in Cushing syndrome and is not an uncommon paraneoplastic feature of small cell carcinoma of the lung. Theoretically, in the organ transplantation setting, the resulting high cortisol levels could suppress a tumor‐rejection immune response. However, to the authors' knowledge, no such a clinical scenario has been described in the literature published to date.
METHODS
A 25–year–old living related kidney transplant recipient presented with Cushing syndrome 32 months after transplantation. The donor had been diagnosed with small cell carcinoma of the lung 22 months earlier. On further evaluation, the kidney recipient was diagnosed with donor–derived small cell lung carcinoma of the transplanted kidney. She was found to have extensive disease involving the liver and retroperitoneum. Despite discontinuation of immunosuppressive medications, the disease progressed and cortisol levels remained elevated during 6 weeks of observation.
RESULTS
The patient received six cycles of cisplatin and etoposide, which resulted in resolution of her hypercortisolemia and a complete remission of her donor–derived small cell carcinoma. At last follow‐up, she was 12 months from completing her therapy and continued in complete remission.
CONCLUSIONS
Donor–derived small cell carcinoma and ectopic ACTH production can occur in a patient after kidney transplantation. Cancer 2001;92:2429–34. © 2001 American Cancer Society.
Persistent ectopic adrenocorticotropic hormone (ACTH) production occurred in a kidney transplant recipient diagnosed as having a living related donor–derived small cell lung carcinoma. The donor–derived malignancy was not rejected after discontinuation of immune suppression. Ectopic ACTH production, clinical signs of Cushing syndrome, and radiographic evidence of metastatic disease completely resolved after the administration of systemic chemotherapy.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/1097-0142(20011101)92:9<2429::AID-CNCR1592>3.0.CO;2-G</identifier><identifier>PMID: 11745300</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Adrenocorticotropic Hormone - biosynthesis ; Adult ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Carcinoma, Small Cell - drug therapy ; Carcinoma, Small Cell - secondary ; chemotherapy ; Cisplatin - administration & dosage ; Cushing syndrome ; Cushing Syndrome - etiology ; ectopic adrenocorticotropic hormone (ACTH) production ; Etoposide - administration & dosage ; Female ; Humans ; Hydrocortisone - blood ; immunosuppression ; Immunosuppressive Agents - administration & dosage ; Immunosuppressive Agents - adverse effects ; Kidney Neoplasms - drug therapy ; Kidney Neoplasms - secondary ; Kidney Transplantation - adverse effects ; malignancy ; Tissue Donors ; transplantation</subject><ispartof>Cancer, 2001-11, Vol.92 (9), p.2429-2434</ispartof><rights>Copyright © 2001 American Cancer Society</rights><rights>Copyright 2001 American Cancer Society.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2F1097-0142%2820011101%2992%3A9%3C2429%3A%3AAID-CNCR1592%3E3.0.CO%3B2-G$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F1097-0142%2820011101%2992%3A9%3C2429%3A%3AAID-CNCR1592%3E3.0.CO%3B2-G$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,1430,27911,27912,45561,45562,46396,46820</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11745300$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bodvarsson, Sigurdur</creatorcontrib><creatorcontrib>Burlingham, William</creatorcontrib><creatorcontrib>Kusaka, Satoshi</creatorcontrib><creatorcontrib>Hafez, Gholam‐Reza</creatorcontrib><creatorcontrib>Becker, Bryan N.</creatorcontrib><creatorcontrib>Pintar, Thomas</creatorcontrib><creatorcontrib>Sollinger, Hans W.</creatorcontrib><creatorcontrib>Albertini, Mark R.</creatorcontrib><title>Donor–derived small cell lung carcinoma in a kidney transplant recipient</title><title>Cancer</title><addtitle>Cancer</addtitle><description>BACKGROUND
Transplantation of donor–derived malignancies during organ transplantation fortunately is very rare. Discontinuation of immunosuppressive medications under these circumstances has previously resulted in complete tumor rejection. Ectopic adrenocorticotropic hormone (ACTH) production may result in Cushing syndrome and is not an uncommon paraneoplastic feature of small cell carcinoma of the lung. Theoretically, in the organ transplantation setting, the resulting high cortisol levels could suppress a tumor‐rejection immune response. However, to the authors' knowledge, no such a clinical scenario has been described in the literature published to date.
METHODS
A 25–year–old living related kidney transplant recipient presented with Cushing syndrome 32 months after transplantation. The donor had been diagnosed with small cell carcinoma of the lung 22 months earlier. On further evaluation, the kidney recipient was diagnosed with donor–derived small cell lung carcinoma of the transplanted kidney. She was found to have extensive disease involving the liver and retroperitoneum. Despite discontinuation of immunosuppressive medications, the disease progressed and cortisol levels remained elevated during 6 weeks of observation.
RESULTS
The patient received six cycles of cisplatin and etoposide, which resulted in resolution of her hypercortisolemia and a complete remission of her donor–derived small cell carcinoma. At last follow‐up, she was 12 months from completing her therapy and continued in complete remission.
CONCLUSIONS
Donor–derived small cell carcinoma and ectopic ACTH production can occur in a patient after kidney transplantation. Cancer 2001;92:2429–34. © 2001 American Cancer Society.
Persistent ectopic adrenocorticotropic hormone (ACTH) production occurred in a kidney transplant recipient diagnosed as having a living related donor–derived small cell lung carcinoma. The donor–derived malignancy was not rejected after discontinuation of immune suppression. Ectopic ACTH production, clinical signs of Cushing syndrome, and radiographic evidence of metastatic disease completely resolved after the administration of systemic chemotherapy.</description><subject>Adrenocorticotropic Hormone - biosynthesis</subject><subject>Adult</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Carcinoma, Small Cell - drug therapy</subject><subject>Carcinoma, Small Cell - secondary</subject><subject>chemotherapy</subject><subject>Cisplatin - administration & dosage</subject><subject>Cushing syndrome</subject><subject>Cushing Syndrome - etiology</subject><subject>ectopic adrenocorticotropic hormone (ACTH) production</subject><subject>Etoposide - administration & dosage</subject><subject>Female</subject><subject>Humans</subject><subject>Hydrocortisone - blood</subject><subject>immunosuppression</subject><subject>Immunosuppressive Agents - administration & dosage</subject><subject>Immunosuppressive Agents - adverse effects</subject><subject>Kidney Neoplasms - drug therapy</subject><subject>Kidney Neoplasms - secondary</subject><subject>Kidney Transplantation - adverse effects</subject><subject>malignancy</subject><subject>Tissue Donors</subject><subject>transplantation</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkd1O2zAUgK2JaS1lrzDlCrGLdMc_qePCJqEApVNFpWmTEDdHjuNMhsTJkhbUu70Db8iTkKgt-OJYx-ezdXw-Qr5TGFMA9o2CkiFQwU4YAKUU6FfFpuqMCaam0_P5RZjcJL9opNgPPoZxsjxl4ewDGb7dOyBDAIjDSPDbATls2_sulSzin8iAUikiDjAkPy8qXzUv_58z27hHmwVtqYsiMLYLxdr_DYxujPNVqQPnAx08uMzbTbBqtG_rQvtV0Fjjamf96oh8zHXR2s-7fUT-XF3-Tq7DxXI2T84XYc26FUaK55BqmhqhJmJiI6ZVDDJPrUgneZxpMNTERk9AxLnMrJE0VkKJVOgskznnI3K8fbduqn9r266wdG3fsPa2WrcoGY-4hB78sgPXaWkzrBtX6maD-993wN0WeHKF3bzXAXsF2I8S-1HiXgEqhgp7BdgZwL0B5AiYLJHh7O2MvwKJ4X8v</recordid><startdate>20011101</startdate><enddate>20011101</enddate><creator>Bodvarsson, Sigurdur</creator><creator>Burlingham, William</creator><creator>Kusaka, Satoshi</creator><creator>Hafez, Gholam‐Reza</creator><creator>Becker, Bryan N.</creator><creator>Pintar, Thomas</creator><creator>Sollinger, Hans W.</creator><creator>Albertini, Mark R.</creator><general>John Wiley & Sons, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20011101</creationdate><title>Donor–derived small cell lung carcinoma in a kidney transplant recipient</title><author>Bodvarsson, Sigurdur ; Burlingham, William ; Kusaka, Satoshi ; Hafez, Gholam‐Reza ; Becker, Bryan N. ; Pintar, Thomas ; Sollinger, Hans W. ; Albertini, Mark R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p2222-593f0ba1bc49646e52a9807fbe4b6f8da0c1c8ca6048f7dec7189494b4add7f33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adrenocorticotropic Hormone - biosynthesis</topic><topic>Adult</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Carcinoma, Small Cell - drug therapy</topic><topic>Carcinoma, Small Cell - secondary</topic><topic>chemotherapy</topic><topic>Cisplatin - administration & dosage</topic><topic>Cushing syndrome</topic><topic>Cushing Syndrome - etiology</topic><topic>ectopic adrenocorticotropic hormone (ACTH) production</topic><topic>Etoposide - administration & dosage</topic><topic>Female</topic><topic>Humans</topic><topic>Hydrocortisone - blood</topic><topic>immunosuppression</topic><topic>Immunosuppressive Agents - administration & dosage</topic><topic>Immunosuppressive Agents - adverse effects</topic><topic>Kidney Neoplasms - drug therapy</topic><topic>Kidney Neoplasms - secondary</topic><topic>Kidney Transplantation - adverse effects</topic><topic>malignancy</topic><topic>Tissue Donors</topic><topic>transplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bodvarsson, Sigurdur</creatorcontrib><creatorcontrib>Burlingham, William</creatorcontrib><creatorcontrib>Kusaka, Satoshi</creatorcontrib><creatorcontrib>Hafez, Gholam‐Reza</creatorcontrib><creatorcontrib>Becker, Bryan N.</creatorcontrib><creatorcontrib>Pintar, Thomas</creatorcontrib><creatorcontrib>Sollinger, Hans W.</creatorcontrib><creatorcontrib>Albertini, Mark R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bodvarsson, Sigurdur</au><au>Burlingham, William</au><au>Kusaka, Satoshi</au><au>Hafez, Gholam‐Reza</au><au>Becker, Bryan N.</au><au>Pintar, Thomas</au><au>Sollinger, Hans W.</au><au>Albertini, Mark R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Donor–derived small cell lung carcinoma in a kidney transplant recipient</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2001-11-01</date><risdate>2001</risdate><volume>92</volume><issue>9</issue><spage>2429</spage><epage>2434</epage><pages>2429-2434</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><abstract>BACKGROUND
Transplantation of donor–derived malignancies during organ transplantation fortunately is very rare. Discontinuation of immunosuppressive medications under these circumstances has previously resulted in complete tumor rejection. Ectopic adrenocorticotropic hormone (ACTH) production may result in Cushing syndrome and is not an uncommon paraneoplastic feature of small cell carcinoma of the lung. Theoretically, in the organ transplantation setting, the resulting high cortisol levels could suppress a tumor‐rejection immune response. However, to the authors' knowledge, no such a clinical scenario has been described in the literature published to date.
METHODS
A 25–year–old living related kidney transplant recipient presented with Cushing syndrome 32 months after transplantation. The donor had been diagnosed with small cell carcinoma of the lung 22 months earlier. On further evaluation, the kidney recipient was diagnosed with donor–derived small cell lung carcinoma of the transplanted kidney. She was found to have extensive disease involving the liver and retroperitoneum. Despite discontinuation of immunosuppressive medications, the disease progressed and cortisol levels remained elevated during 6 weeks of observation.
RESULTS
The patient received six cycles of cisplatin and etoposide, which resulted in resolution of her hypercortisolemia and a complete remission of her donor–derived small cell carcinoma. At last follow‐up, she was 12 months from completing her therapy and continued in complete remission.
CONCLUSIONS
Donor–derived small cell carcinoma and ectopic ACTH production can occur in a patient after kidney transplantation. Cancer 2001;92:2429–34. © 2001 American Cancer Society.
Persistent ectopic adrenocorticotropic hormone (ACTH) production occurred in a kidney transplant recipient diagnosed as having a living related donor–derived small cell lung carcinoma. The donor–derived malignancy was not rejected after discontinuation of immune suppression. Ectopic ACTH production, clinical signs of Cushing syndrome, and radiographic evidence of metastatic disease completely resolved after the administration of systemic chemotherapy.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>11745300</pmid><doi>10.1002/1097-0142(20011101)92:9<2429::AID-CNCR1592>3.0.CO;2-G</doi><tpages>6</tpages></addata></record> |
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subjects | Adrenocorticotropic Hormone - biosynthesis Adult Antineoplastic Combined Chemotherapy Protocols - therapeutic use Carcinoma, Small Cell - drug therapy Carcinoma, Small Cell - secondary chemotherapy Cisplatin - administration & dosage Cushing syndrome Cushing Syndrome - etiology ectopic adrenocorticotropic hormone (ACTH) production Etoposide - administration & dosage Female Humans Hydrocortisone - blood immunosuppression Immunosuppressive Agents - administration & dosage Immunosuppressive Agents - adverse effects Kidney Neoplasms - drug therapy Kidney Neoplasms - secondary Kidney Transplantation - adverse effects malignancy Tissue Donors transplantation |
title | Donor–derived small cell lung carcinoma in a kidney transplant recipient |
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