Appendix cancer medical therapy: Difference between revisions

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__NOTOC__
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{{Appendix cancer}}
{{Appendix cancer}}
{{CMG}}; {{AE}}
{{CMG}}; {{AE}} {{Soroush}}


==Overview==
==Overview==
There is no treatment for [disease name]; the mainstay of therapy is supportive care.


OR
Medical therapy in appendix cancer could be either supportive, [[Palliative care|palliative]], or curative. While [[Carcinoid Tumor|carcinoid]] tumors rarely need [[chemotherapy]], systemic [[chemotherapy]] as well as [[Intraperitoneal hyperthermic chemoperfusion|hyperthermic intraperitoneal]] [[chemotherapy]] plus/minus early postoperative intraperitoneal [[chemotherapy]] (EPIC) and/or [[Adjuvant therapy|concomitant intravenous chemotherapy]] are mainstream of medical treatment in [[adenocarcinoma]] of [[Vermiform appendix|appendix]]. Medical therapy is generally administered to control the [[Symptom|symptoms]] in patients with [[Carcinoid Tumor|carcinoid]] tumors and [[carcinoid syndrome]].


Supportive therapy for [disease name] includes [therapy 1], [therapy 2], and [therapy 3].


OR


The majority of cases of [disease name] are self-limited and require only supportive care.
==Medical Therapy ==
*'''Supportive medical therapy''' for appendix cancer, may include:<ref name="pmid3696178">{{cite journal |vauthors=Moertel CG, Weiland LH, Nagorney DM, Dockerty MB |title=Carcinoid tumor of the appendix: treatment and prognosis |journal=N. Engl. J. Med. |volume=317 |issue=27 |pages=1699–701 |year=1987 |pmid=3696178 |doi=10.1056/NEJM198712313172704 |url=}}</ref><ref>Treatment Option Overview for GI Carcinoid Tumors
. NATIONAL CANCER INSTITUTE . http://www.cancer.gov/types/gi-carcinoid-tumors/hp/gi-carcinoid-treatment-pdq#link/_97_toc Accessed on September 22, 2015</ref>
:*[[Somatostatin]] analogs
::*[[Octreotide]] or [[lanreotide]]
:*[[Loperamide]] or [[diphenoxylate]] for primary [[diarrhea]]
:* [[Somatostatin]] analogs for symptom control in patients with [[carcinoid syndrome]].  


OR
*'''Curative and palliative chemotherapy'''
:*Systemic [[chemotherapy]]
:*[[Intraperitoneal hyperthermic chemoperfusion|Hyperthermic intraperitoneal]] [[chemotherapy]]<ref name="pmid21160924">González-Moreno S, González-Bayón LA, Ortega-Pérez G (2010) [https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=21160924 Hyperthermic intraperitoneal chemotherapy: Rationale and technique.] ''World J Gastrointest Oncol'' 2 (2):68-75. [http://dx.doi.org/10.4251/wjgo.v2.i2.68 DOI:10.4251/wjgo.v2.i2.68] PMID: [https://pubmed.gov/21160924 21160924]</ref>


[Disease name] is a medical emergency and requires prompt treatment.
*'''Systemic chemotherapy'''
*Systemic [[chemotherapy]] has not been generally recommended for carcionid tumors, but patients with non-cacinoid tumors are usually receive [[chemotherapy]].
:*Nevertheless systemic [[chemotherapy]] for metastatic appendiceal [[adenocarcinoma]] has not been studied appropriately.
:*Many experts refer to current [[colorectal cancer]] [[chemotherapy]] approaches for [[adenocarcinoma]] of appendix.
:*'''Current colon cancer chemotherapy agents are as follows:'''


OR
::*5-fluorouracil ([[Fluorouracil|5-FU]]) : Traditional active agent
::*[[Irinotecan]]
::*[[Oxaliplatin]]
::*[[Vascular endothelial growth factor]] receptor inhibitors ([[bevacizumab]])
::*[[Epidermal growth factor]] receptor [[Enzyme inhibitor|inhibitor]]<nowiki/>s ([[cetuximab]] and  [[panitumumab]]),
::*[[Aflibercept]] 
::*[[Regorafenib]]: inhibitor of [[Tyrosine kinase|angiogenic tyrosine kinase]]<nowiki/>s (including the [[Vascular endothelial growth factor|VEGF]] receptors 1,2, and 3),
::*[[Capecitabine]] or [[Fluorouracil|5-FU]] with or without a platinum drug


The mainstay of treatment for [disease name] is [therapy].
*'''[[FOLFOX regimen|FOLFOX]]-6 has been widely recommended in patients with [[Vermiform appendix|appendix]] [[adenocarcinoma]].''' 


OR
:*[[Oxaliplatin]], [[Fluorouracil|5-FU]] and [[leucovorin]] or [[capecitabine]] are active agents of the FOLFOX regime. <math>\blacktriangledown</math>
 
The optimal therapy for [malignancy name] depends on the stage at diagnosis.


OR


[Therapy] is recommended among all patients who develop [disease name].
*


OR
{| class="wikitable"
|+
!'''Modified FOLFOX-6'''<ref name="pmid12177775">Cheeseman SL, Joel SP, Chester JD, Wilson G, Dent JT, Richards FJ et al. (2002) [https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=12177775 A 'modified de Gramont' regimen of fluorouracil, alone and with oxaliplatin, for advanced colorectal cancer.] ''Br J Cancer'' 87 (4):393-9. [http://dx.doi.org/10.1038/sj.bjc.6600467 DOI:10.1038/sj.bjc.6600467] PMID: [https://pubmed.gov/12177775 12177775]</ref><ref name="pmid18640933">Hochster HS, Hart LL, Ramanathan RK, Childs BH, Hainsworth JD, Cohn AL et al. (2008) [https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=18640933 Safety and efficacy of oxaliplatin and fluoropyrimidine regimens with or without bevacizumab as first-line treatment of metastatic colorectal cancer: results of the TREE Study.] ''J Clin Oncol'' 26 (21):3523-9. [http://dx.doi.org/10.1200/JCO.2007.15.4138 DOI:10.1200/JCO.2007.15.4138] PMID: [https://pubmed.gov/18640933 18640933]</ref>
|-
|
*'''[[Oxaliplatin]]''' 85 mg/m <sup>2</sup> IV
:*Dilute with 250 mL 5 percent dextrose in water (D5W)
:*Administer over 2 hrs
:*''Avoid extravasation: May cause significant tissue damage''
|-
|
*'''[[Leucovorin]]''' 400  mg/m <sup>2</sup> IV  (d,l-racemic mixture)  / 200 mg/m <sup>2</sup> IV  (l-[[leucovorin]])
:*Dilute with 250 mL D5W
:*Administer over 2 hrs concurrent with [[oxaliplatin]].
|-
|
*'''[[Fluorouracil]] (FU)''' 400 mg/m <sup>2</sup> IV bolus<ref name="pmid14657227">Tournigand C, André T, Achille E, Lledo G, Flesh M, Mery-Mignard D et al. (2004) [https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=14657227 FOLFIRI followed by FOLFOX6 or the reverse sequence in advanced colorectal cancer: a randomized GERCOR study.] ''J Clin Oncol'' 22 (2):229-37. [http://dx.doi.org/10.1200/JCO.2004.05.113 DOI:10.1200/JCO.2004.05.113] PMID: [https://pubmed.gov/14657227 14657227]</ref>
:*Slow IV push over 5 mins (administer immediately after [[leucovorin]])
|-
|
*'''[[Fluorouracil]] (FU)''' 2400 mg/m <sup>2</sup> IV
:*Administer immediately after FU IV bolus
:*Dilute with 500 to 1000 mL D5W
:*Administer over 46 hours
|}
:*'''''Cycle length is 14 days'''''
:*'''Doses should be recalculated if there is a 10 percent or more change in body weight.'''


Pharmacologic medical therapy is recommended among patients with [disease subclass 1], [disease subclass 2], and [disease subclass 3].
*'''Prior to each treatment<math>\blacktriangledown</math>'''
::* Assess changes in [[Neurology|neurologic]] function.
::* Assess [[Electrolyte disturbance|electrolyte]]<nowiki/>s and [[liver]] and [[renal function]].
::* [[Complete blood count|CBC]] with differential and [[platelet]] count.  


OR
*'''Common complications and approaches to complications'''
:* '''Diarrhea:''' 
::* Grade 2 or worse diarrhea: <math>\blacktriangledown</math>
::** Withhold treatment.
::** Restart at a lower dose of FU after complete resolution.
::* '''[[Diarrhea|Severe diarrhea]], [[mucositis]], and [[Bone marrow suppression|myelosuppression]] after FU''':<math>\blacktriangledown</math>
::** Evaluate for [[dihydropyrimidine dehydrogenase]] deficiency.


Pharmacologic medical therapies for [disease name] include (either) [therapy 1], [therapy 2], and/or [therapy 3].
:*'''Neurologic [[toxicity]]'''
::*In order to decrease chance of developing [[oxaliplatin]] induced [[neuropathy]] recommend patients to avoid exposure to cold up to 48 hours after each infusion.
::*Transient grade 3 [[paresthesia]]/[[dysesthesia]] / grade 2 symptoms lasting longer than 1 week:<math>\blacktriangledown</math>
::**Decrease [[oxaliplatin]] dose by 25 percent.
::*Grade 4 or persistent grade 3 [[paresthesia]]/[[dysesthesia]]:<math>\blacktriangledown</math>
::**Discontinue [[oxaliplatin]].


OR
:*'''[[Bone marrow suppression|Myelotoxicity]]'''
::*Total white [[Complete blood count|blood cell count]] <3000 cells/mm <sup>3</sup> , absolute [[neutrophil]] count <1500 cells/mm <sup>3</sup> , or [[Platelet|platelets]] <100,000 /mm <sup>3</sup> on the day of treatment:<math>\blacktriangledown</math>
::**Delay treatment cycle by one week.
::*''If treatment is delayed for '''two weeks''' or delayed '''for one week on two separate occasions,''' eliminate FU bolus.''
::*''If occurred again:''<math>\blacktriangledown</math>
:::*Reduce infusional [[Fluorouracil|5-FU]] by 20 percent ''and''
:::*Reduce [[oxaliplatin]] dose from 65 mg/m <sup>2</sup>


Empiric therapy for [disease name] depends on [disease factor 1] and [disease factor 2].
*[[Intraperitoneal hyperthermic chemoperfusion|'''Hyperthermic intraperitoneal''']] '''[[chemotherapy]] (HIPEC)'''<ref name="pmid21160924">González-Moreno S, González-Bayón LA, Ortega-Pérez G (2010) [https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&retmode=ref&cmd=prlinks&id=21160924 Hyperthermic intraperitoneal chemotherapy: Rationale and technique.] ''World J Gastrointest Oncol'' 2 (2):68-75. [http://dx.doi.org/10.4251/wjgo.v2.i2.68 DOI:10.4251/wjgo.v2.i2.68] PMID: [https://pubmed.gov/21160924 21160924]</ref>
:*Delivered in the operating room after cytoreductive surgery.
:*In selected cases is accompanied by early postoperative intraperitoneal chemotherapy (EPIC) as well as concomitant intravenous chemotherapy (CIVC).
{| class="wikitable"
|+
!'''Common HIPEC current regimens'''
|-
|
*[[Oxaliplatin]], 130 mg/m <sup>2</sup> for 60 minutes
*Concomitant intravenous [[chemotherapy]] (CIVC) 5-FU, 400 mg/m <sup>2</sup>
* Early postoperative intraperitoneal [[chemotherapy]] (EPIC) with 5-FU
|-
|
* [[Mitomycin]] C, 35 mg/m <sup>2</sup> for 90 minutes
*Concomitant intravenous [[chemotherapy]] 5-FU, 400 mg/m <sup>2</sup>
* Early postoperative intraperitoneal chemotherapy (EPIC) with 5-FU
|-
|
*[[Mitomycin]] C, 35 mg/m <sup>2</sup>  for 90 minutes without EPIC or CIVC
|-
|
*[[Mitomycin]] C, 3.3 mg//m <sup>2</sup>/L for 90 minutes without EPIC or CIVC
|}
*'''''Infuse the fluid at 43-45°Ci n order to maintain the intraperitoneal fluid temperature at 41-43°C.'''''
*'''''To avoid renal toxicity maintain urine output higher than 100 cc (desirable 150 cc) every 15 min during HIPEC.'''''


OR
Patients with [disease subclass 1] are treated with [therapy 1], whereas patients with [disease subclass 2] are treated with [therapy 2].
==Medical Therapy==
*Pharmacologic medical therapy is recommended among patients with [disease subclass 1], [disease subclass 2], and [disease subclass 3].
*Pharmacologic medical therapies for [disease name] include (either) [therapy 1], [therapy 2], and/or [therapy 3].
*Empiric therapy for [disease name] depends on [disease factor 1] and [disease factor 2].
*Patients with [disease subclass 1] are treated with [therapy 1], whereas patients with [disease subclass 2] are treated with [therapy 2].
===Disease Name===
* '''1 Stage 1 - Name of stage'''
** 1.1 '''Specific Organ system involved 1'''
*** 1.1.1 '''Adult'''
**** Preferred regimen (1): [[drug name]] 100 mg PO q12h for 10-21 days '''(Contraindications/specific instructions)''' 
**** Preferred regimen (2): [[drug name]] 500 mg PO q8h for 14-21 days
**** Preferred regimen (3): [[drug name]] 500 mg q12h for 14-21 days
**** Alternative regimen (1): [[drug name]] 500 mg PO q6h for 7–10 days 
**** Alternative regimen (2): [[drug name]] 500 mg PO q12h for 14–21 days
**** Alternative regimen (3): [[drug name]] 500 mg PO q6h for 14–21 days
*** 1.1.2 '''Pediatric'''
**** 1.1.2.1 (Specific population e.g. '''children < 8 years of age''')
***** Preferred regimen (1): [[drug name]] 50 mg/kg PO per day q8h (maximum, 500 mg per dose) 
***** Preferred regimen (2): [[drug name]] 30 mg/kg PO per day in 2 divided doses (maximum, 500 mg per dose)
***** Alternative regimen (1): [[drug name]]10 mg/kg PO q6h (maximum, 500 mg per day)
***** Alternative regimen (2): [[drug name]] 7.5 mg/kg PO q12h (maximum, 500 mg per dose)
***** Alternative regimen (3): [[drug name]] 12.5 mg/kg PO q6h (maximum, 500 mg per dose)
****1.1.2.2 (Specific population e.g. '<nowiki/>'''''children < 8 years of age'''''')
***** Preferred regimen (1): [[drug name]] 4 mg/kg/day PO q12h（maximum, 100 mg per dose）
***** Alternative regimen (1): [[drug name]] 10 mg/kg PO q6h (maximum, 500 mg per day)
***** Alternative regimen (2): [[drug name]] 7.5 mg/kg PO q12h (maximum, 500 mg per dose) 
***** Alternative regimen (3): [[drug name]] 12.5 mg/kg PO q6h (maximum, 500 mg per dose)
** 1.2 '''Specific Organ system involved 2'''
*** 1.2.1 '''Adult'''
**** Preferred regimen (1): [[drug name]] 500 mg PO q8h
*** 1.2.2  '''Pediatric'''
**** Preferred regimen (1): [[drug name]] 50 mg/kg/day PO q8h (maximum, 500 mg per dose)
* 2 '''Stage 2 - Name of stage'''
** 2.1 '''Specific Organ system involved 1 '''
**: '''Note (1):'''
**: '''Note (2)''':
**: '''Note (3):'''
*** 2.1.1 '''Adult'''
**** Parenteral regimen
***** Preferred regimen (1): [[drug name]] 2 g IV q24h for 14 (14–21) days
***** Alternative regimen (1): [[drug name]] 2 g IV q8h for 14 (14–21) days
***** Alternative regimen (2): [[drug name]] 18–24 MU/day IV q4h for 14 (14–21) days
**** Oral regimen
***** Preferred regimen (1): [[drug name]] 500 mg PO q8h for 14 (14–21) days
***** Preferred regimen (2): [[drug name]] 100 mg PO q12h for 14 (14–21) days
***** Preferred regimen (3): [[drug name]] 500 mg PO q12h for 14 (14–21) days
***** Alternative regimen (1): [[drug name]] 500 mg PO q6h for 7–10 days 
***** Alternative regimen (2): [[drug name]] 500 mg PO q12h for 14–21 days
***** Alternative regimen (3):[[drug name]] 500 mg PO q6h for 14–21 days
*** 2.1.2 '''Pediatric'''
**** Parenteral regimen
***** Preferred regimen (1): [[drug name]] 50–75 mg/kg IV q24h for 14 (14–21) days (maximum, 2 g)
***** Alternative regimen (1): [[drug name]] 150–200 mg/kg/day IV q6–8h for 14 (14–21) days (maximum, 6 g per day)
***** Alternative regimen (2):  [[drug name]] 200,000–400,000 U/kg/day IV q4h for 14 (14–21) days (maximum, 18–24 million U per day) '<nowiki/>'''''(Contraindications/specific instructions)''''''
**** Oral regimen
***** Preferred regimen (1):  [[drug name]] 50 mg/kg/day PO q8h for 14 (14–21) days  (maximum, 500 mg per dose)
***** Preferred regimen (2): [[drug name]] '''(for children aged ≥ 8 years)''' 4 mg/kg/day PO q12h for 14 (14–21) days (maximum, 100 mg per dose)
***** Preferred regimen (3): [[drug name]] 30 mg/kg/day PO q12h for 14 (14–21) days  (maximum, 500 mg per dose)
***** Alternative regimen (1):  [[drug name]] 10 mg/kg PO q6h 7–10 days  (maximum, 500 mg per day)
***** Alternative regimen (2): [[drug name]] 7.5 mg/kg PO q12h for 14–21 days  (maximum, 500 mg per dose)
***** Alternative regimen (3): [[drug name]] 12.5 mg/kg PO q6h for 14–21 days  (maximum,500 mg per dose)
** 2.2  '<nowiki/>'''''Other Organ system involved 2''''''
**: '''Note (1):'''
**: '''Note (2)''':
**: '''Note (3):'''
*** 2.2.1 '''Adult'''
**** Parenteral regimen
***** Preferred regimen (1): [[drug name]] 2 g IV q24h for 14 (14–21) days
***** Alternative regimen (1): [[drug name]] 2 g IV q8h for 14 (14–21) days
***** Alternative regimen (2): [[drug name]] 18–24 MU/day IV q4h for 14 (14–21) days
**** Oral regimen
***** Preferred regimen (1): [[drug name]] 500 mg PO q8h for 14 (14–21) days
***** Preferred regimen (2): [[drug name]] 100 mg PO q12h for 14 (14–21) days
***** Preferred regimen (3): [[drug name]] 500 mg PO q12h for 14 (14–21) days
***** Alternative regimen (1): [[drug name]] 500 mg PO q6h for 7–10 days 
***** Alternative regimen (2): [[drug name]] 500 mg PO q12h for 14–21 days
***** Alternative regimen (3):[[drug name]] 500 mg PO q6h for 14–21 days
*** 2.2.2 '''Pediatric'''
**** Parenteral regimen
***** Preferred regimen (1): [[drug name]] 50–75 mg/kg IV q24h for 14 (14–21) days (maximum, 2 g)
***** Alternative regimen (1): [[drug name]] 150–200 mg/kg/day IV q6–8h for 14 (14–21) days (maximum, 6 g per day)
***** Alternative regimen (2):  [[drug name]] 200,000–400,000 U/kg/day IV q4h for 14 (14–21) days (maximum, 18–24 million U per day)
**** Oral regimen
***** Preferred regimen (1):  [[drug name]] 50 mg/kg/day PO q8h for 14 (14–21) days  (maximum, 500 mg per dose)
***** Preferred regimen (2): [[drug name]] 4 mg/kg/day PO q12h for 14 (14–21) days (maximum, 100 mg per dose)
***** Preferred regimen (3): [[drug name]] 30 mg/kg/day PO q12h for 14 (14–21) days  (maximum, 500 mg per dose)
***** Alternative regimen (1):  [[drug name]] 10 mg/kg PO q6h 7–10 days  (maximum, 500 mg per day)
***** Alternative regimen (2): [[drug name]] 7.5 mg/kg PO q12h for 14–21 days  (maximum, 500 mg per dose)
***** Alternative regimen (3): [[drug name]] 12.5 mg/kg PO q6h for 14–21 days  (maximum,500 mg per dose)


==References==
==References==
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{{WH}}
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{{WS}}
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[[Category: (name of the system)]]
[[Category:Surgery]]
[[Category:Medicine]]
[[Category:Emergency medicine]]
[[Category:Oncology]]
[[Category:Up-To-Date]]

Latest revision as of 18:07, 22 February 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Soroush Seifirad, M.D.[2]

Overview

Medical therapy in appendix cancer could be either supportive, palliative, or curative. While carcinoid tumors rarely need chemotherapy, systemic chemotherapy as well as hyperthermic intraperitoneal chemotherapy plus/minus early postoperative intraperitoneal chemotherapy (EPIC) and/or concomitant intravenous chemotherapy are mainstream of medical treatment in adenocarcinoma of appendix. Medical therapy is generally administered to control the symptoms in patients with carcinoid tumors and carcinoid syndrome.


Medical Therapy

  • Supportive medical therapy for appendix cancer, may include:[1][2]
  • Curative and palliative chemotherapy
  • Systemic chemotherapy
  • Systemic chemotherapy has not been generally recommended for carcionid tumors, but patients with non-cacinoid tumors are usually receive chemotherapy.


Modified FOLFOX-6[4][5]
  • Dilute with 250 mL 5 percent dextrose in water (D5W)
  • Administer over 2 hrs
  • Avoid extravasation: May cause significant tissue damage
  • Dilute with 250 mL D5W
  • Administer over 2 hrs concurrent with oxaliplatin.
  • Slow IV push over 5 mins (administer immediately after leucovorin)
  • Administer immediately after FU IV bolus
  • Dilute with 500 to 1000 mL D5W
  • Administer over 46 hours
  • Cycle length is 14 days
  • Doses should be recalculated if there is a 10 percent or more change in body weight.
  • Prior to each treatment<math>\blacktriangledown</math>
  • Common complications and approaches to complications
  • Diarrhea:
  • Total white blood cell count <3000 cells/mm 3 , absolute neutrophil count <1500 cells/mm 3 , or platelets <100,000 /mm 3 on the day of treatment:<math>\blacktriangledown</math>
    • Delay treatment cycle by one week.
  • If treatment is delayed for two weeks or delayed for one week on two separate occasions, eliminate FU bolus.
  • If occurred again:<math>\blacktriangledown</math>
  • Reduce infusional 5-FU by 20 percent and
  • Reduce oxaliplatin dose from 65 mg/m 2
  • Delivered in the operating room after cytoreductive surgery.
  • In selected cases is accompanied by early postoperative intraperitoneal chemotherapy (EPIC) as well as concomitant intravenous chemotherapy (CIVC).
Common HIPEC current regimens
  • Mitomycin C, 35 mg/m 2 for 90 minutes
  • Concomitant intravenous chemotherapy 5-FU, 400 mg/m 2
  • Early postoperative intraperitoneal chemotherapy (EPIC) with 5-FU
  • Mitomycin C, 35 mg/m 2 for 90 minutes without EPIC or CIVC
  • Mitomycin C, 3.3 mg//m 2/L for 90 minutes without EPIC or CIVC
  • Infuse the fluid at 43-45°Ci n order to maintain the intraperitoneal fluid temperature at 41-43°C.
  • To avoid renal toxicity maintain urine output higher than 100 cc (desirable 150 cc) every 15 min during HIPEC.


References

  1. ↑ Moertel CG, Weiland LH, Nagorney DM, Dockerty MB (1987). "Carcinoid tumor of the appendix: treatment and prognosis". N. Engl. J. Med. 317 (27): 1699–701. doi:10.1056/NEJM198712313172704. PMID 3696178.
  2. ↑ Treatment Option Overview for GI Carcinoid Tumors . NATIONAL CANCER INSTITUTE . http://www.cancer.gov/types/gi-carcinoid-tumors/hp/gi-carcinoid-treatment-pdq#link/_97_toc Accessed on September 22, 2015
  3. ↑ 3.0 3.1 González-Moreno S, González-Bayón LA, Ortega-Pérez G (2010) Hyperthermic intraperitoneal chemotherapy: Rationale and technique. World J Gastrointest Oncol 2 (2):68-75. DOI:10.4251/wjgo.v2.i2.68 PMID: 21160924
  4. ↑ Cheeseman SL, Joel SP, Chester JD, Wilson G, Dent JT, Richards FJ et al. (2002) A 'modified de Gramont' regimen of fluorouracil, alone and with oxaliplatin, for advanced colorectal cancer. Br J Cancer 87 (4):393-9. DOI:10.1038/sj.bjc.6600467 PMID: 12177775
  5. ↑ Hochster HS, Hart LL, Ramanathan RK, Childs BH, Hainsworth JD, Cohn AL et al. (2008) Safety and efficacy of oxaliplatin and fluoropyrimidine regimens with or without bevacizumab as first-line treatment of metastatic colorectal cancer: results of the TREE Study. J Clin Oncol 26 (21):3523-9. DOI:10.1200/JCO.2007.15.4138 PMID: 18640933
  6. ↑ Tournigand C, André T, Achille E, Lledo G, Flesh M, Mery-Mignard D et al. (2004) FOLFIRI followed by FOLFOX6 or the reverse sequence in advanced colorectal cancer: a randomized GERCOR study. J Clin Oncol 22 (2):229-37. DOI:10.1200/JCO.2004.05.113 PMID: 14657227

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