Cited by 69Adrenal and Paraganglionic TumorsSarcoma Diagnosis and TreatmentAdrenal Hormones and Disorders

Radiation therapy for adjunctive treatment of adrenal cortical carcinoma

Markoe, Arnold M., Serber, William, Micaily, Bizhan, Brady, Luther W.·1991·American Journal of Clinical Oncology

Abstract

Adrenocortical carcinoma is a rare disease which is primarily approached surgically. There have been few reports of the efficacy of radiation therapy and, for the most part, these have been anecdotal. This paper reports on the potential adjuvant role of radiation therapy after surgical excision of primary adrenal cortical carcinoma and also comments about the efficacy of palliative radiation therapy for metastases. We have identified eight patients treated for adrenal cortical carcinomas at Hahnemann University Hospital (HUH) from 1962 until the present and have also identified five patients with the same diagnosis at Philadelphia General Hospital (PGH) from 1962 until its close in 1975. These two groups are examined separately. In the PGH group, in which two patients were diagnosed at autopsy and only one patient was treated by radiation therapy, the median survival was between 0 and 1 month for Stage IV disease with the only patient surviving to 6 months being that patient receiving radiation therapy. In the HUH group, five of eight patients were treated adjunctively after diagnosis, one was not and two received palliative therapy. The median survival for treated Stage III patients was between 34 months and 7 years. The suggestion, based on a limited patient series, is that patients treated postoperatively to the tumor bed and nodal areas in Stage III disease may have improved survival over historic series and improved local control.

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Crossref · 10.1097/00000421-199104000-00015

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  • Radiotherapy has been shown in several recent series to offer a significant improvement in disease control in both adjuvant and palliative settings, although such improvement has not been universally demonstrated.

    “Although traditionally considered ineffective for ACC (327–331), radiotherapy has been shown in several recent series to offer a significant improvement in disease control in both the adjuvant and palliative settings (247, 332–337), although such an improvement has not been universally demonstrated (338).”

    From Adrenocortical carcinoma (2014) · cites this paper as [334]

  • Markoe et al using doses of 30 to 50 Gy to treat bone metastases and unresectable tumors reported all 5 patients received adequate relief of pain.

    “They reported that all 5 patients that they treated received adequate relief of their pain (334).”

    From Adrenocortical carcinoma (2014) · cites this paper as [334]

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Authors
Markoe, A. M., Serber, W., Micaily, B., & Brady, L. W.
Affiliations
  • Hahnemann University Hospital (US)
  • University of Miami (US)
Venue
American Journal of Clinical Oncology
Published
1991-04
Volume
14
Issue
2
Pages
170-174
ISSN
0277-3732 (ISSN-L)
OpenAlex
W2017683047
Cited by
69
References
0
Citations by year
2024: 2 · 2022: 2 · 2021: 3 · 2019: 1 · 2018: 2 · 2017: 2 · 2016: 3 · 2015: 2 · 2014: 3 · 2013: 2 · 2012: 5
FWCI
1.51
Type
journal article
Language
en
Open access
closed
Locations
  • American Journal of Clinical Oncology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Surgery › Adrenal and Paraganglionic Tumors
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Sarcoma Diagnosis and Treatment
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
Keywords
adrenocortical carcinoma, adjuvant radiotherapy, postoperative radiotherapy, palliative radiotherapy, adrenal metastasis, survival, stage III disease, local tumor control
MeSH terms
Adrenal Gland Neoplasms, Aged, Aged, 80 and over, Carcinoma, Child, Combined Modality Therapy, Female, Humans, Lymph Nodes, Male, Middle Aged, Mitotane, Neoplasm Invasiveness, Neoplasm Recurrence, Local, Neoplasm Staging, Palliative Care, Radiotherapy Dosage, Survival Rate

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