Adrenocortical carcinoma surgery: Difference between revisions
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__NOTOC__ | __NOTOC__ | ||
{{Adrenocortical carcinoma}} | {{Adrenocortical carcinoma}} | ||
{{CMG}}; {{AE}} {{RT}} | {{CMG}}; {{AE}} {{RT}} {{MAD}} | ||
==Overview== | ==Overview== | ||
Surgery is the mainstay of treatment for adrenocortical carcinoma. | [[Surgery]] is the mainstay of treatment for adrenocortical carcinoma. Appropriate [[preoperative evaluation]] and operative planning are really important to assure the best outcome. [[Lymph nodes]] should be removed as part of the en bloc [[resection]]. Recurrence in the [[peritoneum]] outside the tumor bed has the worst survival. [[Surgery]] is indicated in those patients with [[disease]] confined to one site or [[Organ (anatomy)|organ]]. | ||
==Surgery== | ==Surgery== | ||
*Surgery is the mainstay of treatment for adrenocortical carcinoma. | *[[Surgery]] is the mainstay of treatment for adrenocortical carcinoma. | ||
* | *[[Adrenalectomy]] can also be performed even in the case of the [[invasion]] into large [[blood vessels]], such as the [[renal vein]] or [[inferior vena cava]]. | ||
*A large percentage of patients are not surgical candidates. | *A large percentage of patients are not surgical candidates. | ||
Appropriate preoperative evaluation and operative planning are the most important to assure the best outcome. | *Appropriate preoperative evaluation and operative planning are the most important to assure the best outcome. | ||
*Preoperative imaging should be obtained to evaluate the extent of the [[tumor]]. | |||
*[[Imaging]] should be done just before the [[surgery]] because ACC grow quickly and involvement of adjacent structures may change. | |||
*Optimization of [[hormone]] excess in patients with functional [[Mass|masses]] especially those with [[Cushing's syndrome|Cushing’s syndrome]] should be done. | |||
*Patients with widespread distant [[Metastasis|metastatic]] disease in multiple [[organs]] or those with multiple [[metastatic]] deposits in one [[Organ (anatomy)|organ]] system, unable to be completely resected, should not undergo [[adrenalectomy]]. The primary [[tumor]] can instead be treated with [[External beam radiotherapy|external beam radiation]] for [[Palliative care|palliation]] along with other adjuncts to improve local [[symptoms]] and for better control of [[hormone]] excess, if present.<ref name="pmid20675074">{{cite journal| author=Sabolch A, Feng M, Griffith K, Hammer G, Doherty G, Ben-Josef E| title=Adjuvant and definitive radiotherapy for adrenocortical carcinoma. | journal=Int J Radiat Oncol Biol Phys | year= 2011 | volume= 80 | issue= 5 | pages= 1477-84 | pmid=20675074 | doi=10.1016/j.ijrobp.2010.04.030 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20675074 }}</ref> | |||
*[[Obstruction]] of the [[Inferior vena cava|vena cava]] by [[tumor]] [[thrombus]] can lead to massive lower extremity [[edema]]. If [[tumor]] [[resection]] is not technically operable, [[Vena cavae|vena cava]] [[stents]] can be placed, leading to temporary prevention of [[occlusion]]. | |||
*[[Debulking]] for control of [[hormone]] excess in the setting of known [[Metastasis|metastatic]] disease is also performed in some situations. The benefits of [[debulking]] must outweigh the risks of [[surgery]] in patients who have [[Wound healing phases|poor wound healing]]. | |||
* [[Lymph nodes]] should be removed as part of the en bloc [[resection]]. The [[lymphadenectomy]] is performed based on the [[arterial]] supply of [[Adrenal mass causes|adrenal tumors]].<ref name="pmid22306837">{{cite journal| author=Gaujoux S, Brennan MF| title=Recommendation for standardized surgical management of primary adrenocortical carcinoma. | journal=Surgery | year= 2012 | volume= 152 | issue= 1 | pages= 123-32 | pmid=22306837 | doi=10.1016/j.surg.2011.09.030 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22306837 }}</ref> | |||
* Risk of severe [[bleeding]] and benefits of massive removal of [[Lymph node|lymph nodes]] should be balanced by surgeons in every case.<ref name="pmid22143204">{{cite journal| author=Reibetanz J, Jurowich C, Erdogan I, Nies C, Rayes N, Dralle H et al.| title=Impact of lymphadenectomy on the oncologic outcome of patients with adrenocortical carcinoma. | journal=Ann Surg | year= 2012 | volume= 255 | issue= 2 | pages= 363-9 | pmid=22143204 | doi=10.1097/SLA.0b013e3182367ac3 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22143204 }}</ref> | |||
* Published data comparing the [[efficacy]] of [[laparoscopic]] [[adrenalectomy]] (LA) vs open [[adrenalectomy]] (OA) for ACC are limited. | |||
* Lymph nodes | |||
* Risk of severe bleeding and benefits of massive removal of lymph nodes should be balanced by surgeons in every case. | |||
Published data comparing the efficacy of LA vs OA for ACC are limited. | |||
{| class="wikitable" | {| class="wikitable" | ||
!Laparoscopic adrenalectomy (LA) | ![[Laparoscopic surgery|Laparoscopic]] [[adrenalectomy]] (LA) | ||
!Open adrenalectomy (OA) | !Open [[adrenalectomy]] (OA) | ||
|- | |- | ||
| | | | ||
* LA has shown | * LA, when compared with open [[adrenalectomy]] has shown: | ||
* Application of laparoscopic instruments can result in the shedding of malignant cells. | ** Lower [[morbidity]] | ||
* | ** Less [[pain]] | ||
* | ** Shorter hospital stays | ||
* Peritoneal carcinomatosis occurred in only 25% | ** Decreased recovery time if compared with open [[adrenalectomy]]. | ||
* Recurrence rate of | * Application of [[laparoscopic]] instruments can result in the shedding of [[malignant]] [[cells]].<ref name="pmid23158185">{{cite journal| author=Miller BS, Gauger PG, Hammer GD, Doherty GM| title=Resection of adrenocortical carcinoma is less complete and local recurrence occurs sooner and more often after laparoscopic adrenalectomy than after open adrenalectomy. | journal=Surgery | year= 2012 | volume= 152 | issue= 6 | pages= 1150-7 | pmid=23158185 | doi=10.1016/j.surg.2012.08.024 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23158185 }}</ref> | ||
* 16% of patients had positive margins. | * Recurrence and [[Peritoneal|peritonea]]<nowiki/>l spread were more common in the LA group.<ref name="pmid16360394">{{cite journal| author=Gonzalez RJ, Shapiro S, Sarlis N, Vassilopoulou-Sellin R, Perrier ND, Evans DB et al.| title=Laparoscopic resection of adrenal cortical carcinoma: a cautionary note. | journal=Surgery | year= 2005 | volume= 138 | issue= 6 | pages= 1078-85; discussion 1085-6 | pmid=16360394 | doi=10.1016/j.surg.2005.09.012 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16360394 }}</ref> | ||
* Higher [[incidence]] of incomplete [[Resection|resections]] is found in LA. | |||
* [[Peritoneal carcinomatosis]] ([[Spread of the cancer|spread]]) occurred in only 25% of cases. | |||
* Recurrence rate is 100%.<ref name="pmid19851811">{{cite journal| author=Grubbs EG, Callender GG, Xing Y, Perrier ND, Evans DB, Phan AT et al.| title=Recurrence of adrenal cortical carcinoma following resection: surgery alone can achieve results equal to surgery plus mitotane. | journal=Ann Surg Oncol | year= 2010 | volume= 17 | issue= 1 | pages= 263-70 | pmid=19851811 | doi=10.1245/s10434-009-0716-x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19851811 }}</ref> | |||
* 16% of patients had positive margins after the [[surgery]]. | |||
| | | | ||
* American Association of Clinical Endocrinologists and the American Association of Endocrine Surgeons recommended OA as the procedure of choice | * American Association of Clinical Endocrinologists and the American Association of Endocrine Surgeons recommended OA as the procedure of choice.<ref name="pmid19632968">{{cite journal| author=Zeiger MA, Thompson GB, Duh QY, Hamrahian AH, Angelos P, Elaraj D et al.| title=American Association of Clinical Endocrinologists and American Association of Endocrine Surgeons Medical Guidelines for the Management of Adrenal Incidentalomas: executive summary of recommendations. | journal=Endocr Pract | year= 2009 | volume= 15 | issue= 5 | pages= 450-3 | pmid=19632968 | doi=10.4158/EP.15.5.450 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19632968 }}</ref> | ||
* Peritoneal spread is 60%with | * The [[Peritoneal carcinomatosis|peritoneal spread]] is 60% with significant earlier recurrence. | ||
* 30% of patients had positive margins. | * 30% of patients had positive margins. | ||
* Recurrence rate of 86% in the OA group. | |||
* Recurrence rate | * Survival for patients with stage 2 was longer in those undergoing OA. | ||
* Survival for patients with stage 2 was longer in those undergoing OA | |||
|} | |} | ||
==== '''''Surgical approach''''' ==== | ==== '''''Surgical approach''''' ==== | ||
1. Incision and exploration of the peritoneal cavity. | 1. [[Incision]] and [[exploration]] of the [[peritoneal cavity]]. | ||
2. Evaluation of liver for metastasis | 2. Evaluation of [[liver]] for [[metastasis]]. | ||
3. Containment | 3. Containment: a self-retaining retractor system with towels or [[laparotomy]] pads should be placed in such a way as to exclude the rest of the [[peritoneal cavity]] from the area of the [[tumor]] and other [[organs]] requiring [[resection]]. | ||
to | 4. Mobilization of [[organs]] adjacent to [[tumor]]. | ||
resection. | 5. En bloc [[resection]]. Preserve any [[Tissue (biology)|tissue]] overlying the [[tumor]]. | ||
6. Regional [[lymphadenectomy]]. | |||
7. Provide intact en bloc specimen for [[Pathology|pathologic]] review. | |||
8. Mark field to facilitate [[postsurgical]] [[External beam radiotherapy|external beam radiation therapy]]. | |||
9. Dictate operative report. | |||
==== '''''Recurrence of ACC''''' ==== | |||
* The number of [[organs]] involved by [[tumor]] at the time of the first [[metastasis]] is a predictor of survival.<ref name="pmid23150691">{{cite journal| author=Erdogan I, Deutschbein T, Jurowich C, Kroiss M, Ronchi C, Quinkler M et al.| title=The role of surgery in the management of recurrent adrenocortical carcinoma. | journal=J Clin Endocrinol Metab | year= 2013 | volume= 98 | issue= 1 | pages= 181-91 | pmid=23150691 | doi=10.1210/jc.2012-2559 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23150691 }}</ref> | |||
* University of Michigan data shows the site of first [[metastasis]] can also be used to predict the survival. | |||
* Recurrence in the [[peritoneum]] outside the [[tumor]] bed has the worst survival. | |||
* [[Surgery]] is indicated in those [[patients]] with [[disease]] confined to one site or [[Organ (anatomy)|organ]]. | |||
* Waiting 3 months while treating with [[chemotherapy]] to assess for [[tumor]] responsiveness of progression. If progression is not rapid, [[surgery]] may proceed with greater benefit.<ref name="pmid23158185" /> | |||
* The [[median]] survival of 74 months in those undergoing complete second resections and a median survival of 16 months in those undergoing incomplete second resection.<ref name="pmid17062775">{{cite journal| author=Assié G, Antoni G, Tissier F, Caillou B, Abiven G, Gicquel C et al.| title=Prognostic parameters of metastatic adrenocortical carcinoma. | journal=J Clin Endocrinol Metab | year= 2007 | volume= 92 | issue= 1 | pages= 148-54 | pmid=17062775 | doi=10.1210/jc.2006-0706 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17062775 }}</ref> | |||
== Video shows laparoscopic retroperitoneal adrenalectomy == | |||
{{#ev:youtube|aV2cL5z1lWo}} | |||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
{{WH}} | |||
{{WS}} | |||
{{ | |||
{{ | |||
Latest revision as of 12:31, 31 October 2017
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Adrenocortical carcinoma Microchapters |
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Differentiating Adrenocortical carcinoma from other Diseases |
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Adrenocortical carcinoma surgery On the Web |
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American Roentgen Ray Society Images of Adrenocortical carcinoma surgery |
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Risk calculators and risk factors for Adrenocortical carcinoma surgery |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2] Mohammed Abdelwahed M.D[3]
Overview
Surgery is the mainstay of treatment for adrenocortical carcinoma. Appropriate preoperative evaluation and operative planning are really important to assure the best outcome. Lymph nodes should be removed as part of the en bloc resection. Recurrence in the peritoneum outside the tumor bed has the worst survival. Surgery is indicated in those patients with disease confined to one site or organ.
Surgery
- Surgery is the mainstay of treatment for adrenocortical carcinoma.
- Adrenalectomy can also be performed even in the case of the invasion into large blood vessels, such as the renal vein or inferior vena cava.
- A large percentage of patients are not surgical candidates.
- Appropriate preoperative evaluation and operative planning are the most important to assure the best outcome.
- Preoperative imaging should be obtained to evaluate the extent of the tumor.
- Imaging should be done just before the surgery because ACC grow quickly and involvement of adjacent structures may change.
- Optimization of hormone excess in patients with functional masses especially those with Cushing’s syndrome should be done.
- Patients with widespread distant metastatic disease in multiple organs or those with multiple metastatic deposits in one organ system, unable to be completely resected, should not undergo adrenalectomy. The primary tumor can instead be treated with external beam radiation for palliation along with other adjuncts to improve local symptoms and for better control of hormone excess, if present.[1]
- Obstruction of the vena cava by tumor thrombus can lead to massive lower extremity edema. If tumor resection is not technically operable, vena cava stents can be placed, leading to temporary prevention of occlusion.
- Debulking for control of hormone excess in the setting of known metastatic disease is also performed in some situations. The benefits of debulking must outweigh the risks of surgery in patients who have poor wound healing.
- Lymph nodes should be removed as part of the en bloc resection. The lymphadenectomy is performed based on the arterial supply of adrenal tumors.[2]
- Risk of severe bleeding and benefits of massive removal of lymph nodes should be balanced by surgeons in every case.[3]
- Published data comparing the efficacy of laparoscopic adrenalectomy (LA) vs open adrenalectomy (OA) for ACC are limited.
| Laparoscopic adrenalectomy (LA) | Open adrenalectomy (OA) |
|---|---|
|
|
Surgical approach
1. Incision and exploration of the peritoneal cavity.
2. Evaluation of liver for metastasis.
3. Containment: a self-retaining retractor system with towels or laparotomy pads should be placed in such a way as to exclude the rest of the peritoneal cavity from the area of the tumor and other organs requiring resection.
4. Mobilization of organs adjacent to tumor.
5. En bloc resection. Preserve any tissue overlying the tumor.
6. Regional lymphadenectomy.
7. Provide intact en bloc specimen for pathologic review.
8. Mark field to facilitate postsurgical external beam radiation therapy.
9. Dictate operative report.
Recurrence of ACC
- The number of organs involved by tumor at the time of the first metastasis is a predictor of survival.[8]
- University of Michigan data shows the site of first metastasis can also be used to predict the survival.
- Recurrence in the peritoneum outside the tumor bed has the worst survival.
- Surgery is indicated in those patients with disease confined to one site or organ.
- Waiting 3 months while treating with chemotherapy to assess for tumor responsiveness of progression. If progression is not rapid, surgery may proceed with greater benefit.[4]
- The median survival of 74 months in those undergoing complete second resections and a median survival of 16 months in those undergoing incomplete second resection.[9]
Video shows laparoscopic retroperitoneal adrenalectomy
{{#ev:youtube|aV2cL5z1lWo}}
References
- ↑ Sabolch A, Feng M, Griffith K, Hammer G, Doherty G, Ben-Josef E (2011). "Adjuvant and definitive radiotherapy for adrenocortical carcinoma". Int J Radiat Oncol Biol Phys. 80 (5): 1477–84. doi:10.1016/j.ijrobp.2010.04.030. PMID 20675074.
- ↑ Gaujoux S, Brennan MF (2012). "Recommendation for standardized surgical management of primary adrenocortical carcinoma". Surgery. 152 (1): 123–32. doi:10.1016/j.surg.2011.09.030. PMID 22306837.
- ↑ Reibetanz J, Jurowich C, Erdogan I, Nies C, Rayes N, Dralle H; et al. (2012). "Impact of lymphadenectomy on the oncologic outcome of patients with adrenocortical carcinoma". Ann Surg. 255 (2): 363–9. doi:10.1097/SLA.0b013e3182367ac3. PMID 22143204.
- ↑ 4.0 4.1 Miller BS, Gauger PG, Hammer GD, Doherty GM (2012). "Resection of adrenocortical carcinoma is less complete and local recurrence occurs sooner and more often after laparoscopic adrenalectomy than after open adrenalectomy". Surgery. 152 (6): 1150–7. doi:10.1016/j.surg.2012.08.024. PMID 23158185.
- ↑ Gonzalez RJ, Shapiro S, Sarlis N, Vassilopoulou-Sellin R, Perrier ND, Evans DB; et al. (2005). "Laparoscopic resection of adrenal cortical carcinoma: a cautionary note". Surgery. 138 (6): 1078–85, discussion 1085-6. doi:10.1016/j.surg.2005.09.012. PMID 16360394.
- ↑ Grubbs EG, Callender GG, Xing Y, Perrier ND, Evans DB, Phan AT; et al. (2010). "Recurrence of adrenal cortical carcinoma following resection: surgery alone can achieve results equal to surgery plus mitotane". Ann Surg Oncol. 17 (1): 263–70. doi:10.1245/s10434-009-0716-x. PMID 19851811.
- ↑ Zeiger MA, Thompson GB, Duh QY, Hamrahian AH, Angelos P, Elaraj D; et al. (2009). "American Association of Clinical Endocrinologists and American Association of Endocrine Surgeons Medical Guidelines for the Management of Adrenal Incidentalomas: executive summary of recommendations". Endocr Pract. 15 (5): 450–3. doi:10.4158/EP.15.5.450. PMID 19632968.
- ↑ Erdogan I, Deutschbein T, Jurowich C, Kroiss M, Ronchi C, Quinkler M; et al. (2013). "The role of surgery in the management of recurrent adrenocortical carcinoma". J Clin Endocrinol Metab. 98 (1): 181–91. doi:10.1210/jc.2012-2559. PMID 23150691.
- ↑ Assié G, Antoni G, Tissier F, Caillou B, Abiven G, Gicquel C; et al. (2007). "Prognostic parameters of metastatic adrenocortical carcinoma". J Clin Endocrinol Metab. 92 (1): 148–54. doi:10.1210/jc.2006-0706. PMID 17062775.