Herpes zoster and small cell bronchogenic carcinoma

In nine of 74 (12 per cent) consecutive, previously untreated patients with small cell bronchogenic carcinoma receiving combination chemotherapy herpes zoster developed. This is the highest frequency reported for this viral infection in patients with nonlymphoproliferative solid tumors. Cutaneous di...

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Published inThe American journal of medicine Vol. 68; no. 2; pp. 214 - 218
Main Authors Huberman, Mark, Fossieck, Byron E., Bunn, Paul A., Cohen, Martin H., Ihde, Daniel C., Minna, John D.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.01.1980
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Abstract In nine of 74 (12 per cent) consecutive, previously untreated patients with small cell bronchogenic carcinoma receiving combination chemotherapy herpes zoster developed. This is the highest frequency reported for this viral infection in patients with nonlymphoproliferative solid tumors. Cutaneous dissemination developed in six of the nine patients, but visceral involvement did not occur. The major difference between the patients with herpes zoster and those without was the superior duration of median survival for the infected patients. No relationship could be established between the development of herpes zoster and the extent of neoplastic disease, prior radiotherapy, treatment with specific chemotherapeutic agents or corticosteroids, cutaneous anergy or granulocytopenia. Serum specimens obtained from six of the nine patients prior to their infection demonstrated the preexistence of varicella zoster antibodies. As more effective and intensive chemotherapy prolongs the survival of patients with solid tumors, it is possible that the frequency of herpes zoster infection may approach that observed in patients with lymphoproliferative malignancies.
AbstractList In nine of 74 (12 per cent) consecutive, previously untreated patients with small cell bronchogenic carcinoma receiving combination chemotherapy herpes zoster developed. This is the highest frequency reported for this viral infection in patients with nonlymphoproliferative solid tumors. Cutaneous dissemination developed in six of the nine patients, but visceral involvement did not occur. The major difference between the patients with herpes zoster and those without was the superior duration of median survival for the infected patients. No relationship could be established between the development of herpes zoster and the extent of neoplastic disease, prior radiotherapy, treatment with specific chemotherapeutic agents or corticosteroids, cutaneous anergy or granulocytopenia. Serum specimens obtained from six of the nine patients prior to their infection demonstrated the preexistence of varicella zoster antibodies. As more effective and intensive chemotherapy prolongs the survival of patients with solid tumors, it is possible that the frequency of herpes zoster infection may approach that observed in patients with lymphoproliferative malignancies.
In nine of 74 (12 per cent) consecutive, previously untreated patients with small cell bronchogenic carcinoma receiving combination chemotherapy herpes zoster developed. This is the highest frequenzy reported for this viral infection in patients with nonlymphoproliferative solid tumors. Cutaneous dissemination developed in six of the nine patients, but visceral involvement did not occur. The major difference between the patients with herpes zoster and those without was the superior duration of median survival for the infected patients. No relationship could be established between the development of herpes zoster and the extent of neoplastic disease, prior radiotherapy, treatment with specific chemotherapeutic agents or corticosteroids, cutaneous anergy or granulocytopenia. Serum specimens obtained from six of the nine patients prior to their infection demonstrated the preexistence of varicella zoster antibodies. As more effective and intensive chemotherapy prolongs the survival of patients with solid tumors, it is possible that the frequency of herpes zoster infection may approach that observed in patients with lymphoproliferative malignancies.
Author Bunn, Paul A.
Fossieck, Byron E.
Minna, John D.
Huberman, Mark
Cohen, Martin H.
Ihde, Daniel C.
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Snippet In nine of 74 (12 per cent) consecutive, previously untreated patients with small cell bronchogenic carcinoma receiving combination chemotherapy herpes zoster...
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StartPage 214
SubjectTerms Adult
Aged
Antibodies, Viral - immunology
Antineoplastic Agents - administration & dosage
Carcinoma, Bronchogenic - complications
Carcinoma, Bronchogenic - drug therapy
Carcinoma, Bronchogenic - immunology
Carcinoma, Small Cell - complications
Carcinoma, Small Cell - drug therapy
Carcinoma, Small Cell - immunology
Drug Therapy, Combination
Female
Herpes Zoster - complications
Herpesvirus 3, Human - immunology
Humans
Lung Neoplasms - complications
Lung Neoplasms - drug therapy
Lung Neoplasms - immunology
Male
Middle Aged
Title Herpes zoster and small cell bronchogenic carcinoma
URI https://dx.doi.org/10.1016/0002-9343(80)90356-3
https://www.ncbi.nlm.nih.gov/pubmed/6243858
https://search.proquest.com/docview/74999636
Volume 68
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