Updates In Management
Of
Ca Rectum
Dr. Nabarun Biswas
Indoor Medical Officer
Surgery Dep. MMCH
ANATOMY
Nodes in the origin of inferior
mesenteric artery
Nodes in the origin of
sigmoid branches
Sacral nodes
Internal iliac nodes
Inguinal nodes
Rectal cancer
• 2nd most common malignancy in female & 3rd
most common in male
• 4th most common cause of cancer death after
lung, stomach & liver
Risk factor
• Red meat and saturated fatty acids
• Obesity
• Sedentary lifestyle
• Old age
• Alcohol and Smoking
• FAP - defect in APC gene on chromosome
5q21
• HNPCC - MSH2 & MLH1 gene defect
• Family history – 2 or more first degree relatives
• Inflammatory bowel disease – Ulcerative Colitis
• Adenomatous polyp
Premalignant conditions
1. Adenoma
2. Chronic IBD
3. Hereditary
 FAP
Pathogenesis
CRC
Hereditary
5%
Genetic
mutation
FAP,HNPCC,
PJS
Sporadic
95%
Adenoma
carcinoma
sequence
APC
K-ras
P 53
Adenoma - Carcinoma sequence
• Accounts for upto 75-95% of sporadic colo-rectal tumours and
typically arise form adenomatous polyp
•Mutation in wnt signaling pathway
1.APC mutation  activation of proto-oncogene (required
for normal cell renewal) over expression
2.Activation of oncogene k-ras  increase cell proliferation.
3.Suppression of P 53 (for apoptosis)  immortal cell
Staging
• Duke’s
• Astler-Coller
• TNM
Duke’s Staging
A B C1 C2 D
MUCOSA
SUBMUCOSA
MUSCULARIS
PROPRIA
SEROSA
LYMPHNODE
TNM Staging
N 0 N 1 N 2
T1 T2 T3 T4a T4b
MUCOSA
SUBMUCOSA
MUSCULARIS
PROPRIA
SEROSA/
Perirectal tissue
LYMPHNODE
AJCC Staging
• Stage I  100, 200 (T1 or 2 N0 M0)
• Stage II  300, 400 (T3 or 4 N0 M0)
• Stage III  any T, any N, M0
• Stage IV any T, any N, M1
Correlation between TNM, Duke’s &
DRE
Status Duke’s TNM DRE
Early A S-I (T1,N0,M0) Freely mobile over
rectal muscle
A S-I (T2,N0,M0) Moves with rectal
wall
Locally
advanced
B or C S-II, S-III
(T3/T4
or
N1/N2)
Slightly moves along
with pararectal fat
Advanced C or D S- IV (M1a/M1b) Fixed
Clinical features
• Early symptoms
1. Per rectal bleeding
3. Early morning diarrhoea
 Alteration of bowel habit
 Change to loose stool is common
 Stenosing ca may cause constipation
2. Tenesmus
 Lower half of rectum
 Spurious diarrhoea
 Bloody slime
Clinical features
• Late symptoms
1. Pain
 Colicky
 Severe , intractable
2. Weight loss
 Associated with metastatic disease
Examination
• Abdominal:
– Normal in early stage
– Obstructive feature in stenosing
recto-sigmoid tumour
• Rectal:
– Assessment of tumor size,
mobility and fixation, anterior
or posterior location,
relationship to sphincter
mechanism and the distance
from the anal verge.
Rigid Proctoscope
• Demonstrates the proximal
and distal levels of the mass
from anal verge
• Extent of circumferential
involvement
• Orientation within the lumen
• Aids in determining the feasibility
of local excision
Colonoscopy
Torule out
synchronous
cancers - which
occur 2 - 8% of the
time.
Virtual/ CT Colonoscopy
Transrectal Endoluminal
Ultrasound
Permits accurate characterization of the
primary tumor and the status of the
perirectal lymph nodes
MRI
• Investigation of choice for T staging
CT scan
• Regional tumor extension
• Lymphatic and
distant metastasis
• Tumor related complications -
perforation or fistula
formation
Laboratory studies
• Complete Blood count
• Serum Electrolytes
• Liver Enzymes
• CEA (Carcinoembryonic antigen)
Treatment
Management Protocol
1. Preoperative workup
2. Operative procedure
3. Post operative
management
4. Surveillance program
1. Counseling &
consent
2. Tumour board
formation
3. Correction of
co-morbidities
4. Prophylaxis
5. Bowel
preparation
Principle of Treatment
1. Surgery is the mainstay of curative Rx
2. Aim: radical excision of rectum + mesorectum+
lympho-vascular clearance
3. Widespread metastasis: palliative Rx 
stenting/RT/palliative resection
4. Liver/Lung metastasis: single/well localized 
resection with curative intent
5. Locally advanced (T3/4 or N1/2): neoadjuvent
CRT  surgery
Principle of Treatment
6. Watch & wait policy: after long course CRT if
CCR & CPR is found  intense surveillance
7. Early cancer(T1,T2 & N0): organ preserving
surgery by Local excision /TEMS (for T1)
8. If radical excision possible : APR or AR (High,
Low, Ultra low)
9. Sphincter saving possible if tumour margin ≥2
cm from ano-rectal junction
10. Defunctioning stoma: if tumour below
peritoneal reflection
Treatment modalities
• Surgery
• Chemotherapy
• Radiotherapy
• Targeted therapy
• Immuno therapy
• Alternative treatment
Surgery
• Surgery is the mainstay of treatment
• Radiation and chemotherapy are given before
or after surgery
• The type of surgery depends on the stage of
the cancer
Types of surgery
1. Local excision / TEMS / TAMIS
2. Anterior resection
 High AR
 Low AR
 Ultra Low AR
3. TME / Modified TME
4. APR
5. Surgery in advanced carcinoma
Approach
• Open
• Laparoscopic
• Robotic
• Trans anal
Trans anal endoscopic micro surgery:
TEMS
• For mid and lower rectal tumor
• For rectal adenomas and early rectal cancers
• Must below peritoneal reflection
TEMS
• Indication:
– Well differentiated
– Grade 1 or 2
– Not mucinous adenoma
– Lymphnode –ve
– Diameter < 3cm
– Tumor invades only
submucosa
Anterior Resection
• It is a sphincter saving operation
• Approach: open / laparoscopic / robotic
assistance
• Two terms: TME & CRM
Total Mesorectal Excision: TME
• Introduced by RJ Heald
in 1979
• For middle and lower third
rectal carcinoma
• Mesorectum: perirectal
fascia containing fat and
perirectal lymph nodes,
lymphatic
• Spread of carcinoma
rectum occurs in this area.
TME
Modified TME
• Distal spread of adenocarcinoma either in the
rectal wall or mesorectum greater than 2-3 cm
is rare.
• So the dissection continues to pelvic floor up to
ano-rectal junction (low AR) or 5 cm (3cm)
below the tomour margin (High AR) 
Modified TME
• Top to down manner
Modified TME
5 cm
5 cm
Ta TME
• Low anterior resection can be a challenging operation,
especially in obese male patients and in particular
after radiotherapy.
• Transanal total mesorectal excision (TaTME) might
offer technical advantages over laparoscopic or open
approaches particularly for tumors in the distal third
of the rectum.
• Defines the radial and distal margins more clearly.
• Bottom up manner
• TAMIS: modification of TaTME where SILS instruments
are used
TaTME
TaTME
Circumferential Resection Margin:
CRM
Circumferential Resection Margin:
CRM
• It is the radial distance between cancer tissue and
the non peritonalized margin of the resected
specimen
• CRM +ve when distance is ≤1 mm
• CRM –ve when distance is >1 mm
• CRM is an important prognostic factor for
recurrence
• CRM can be predicted preoperatively by thin slice
high resolution MRI
• In predicted CRM positivity neoadjuvant CRT is
indicated
Circumferential Resection Margin:
CRM
Anterior resection
• 3 types of 3 anterior resection
1. High  10cm from anal verge
2. Low  8 cm from anal verge
3. Ultra low  6cm from anal verge
• TME /modified TME is incorporated with AR
• Gastrointestinal continuity is maintained by
stapled anastomosis or hands sewn
Steps/ Technique in AR
• Lloyd-Davies position
• Good assistance
• Long midline incision
• Wide retraction
• Small bowel packed
out of the way
• Full laparotomy
Steps/ Technique in AR
• Assess for synchronous
lesion or spread
• Sigmoid and descending
colon mobilization lateral to
medial (in laparoscopic
method medial to lateral
after ligation of vessels)
• Protect left ureter and
gonadal vessel
• Splenic flexure mobilization
Colonic mobilisation
Steps/ Technique in AR….cont.
• next step is vascular
ligation
• High ligation and low
ligation of IMA
• High for proper
lymphatic clearance
& low for improve
vascularity
• 2 step ligation of IMV
for tension free
anastomosis
• Mesocolon divided &
lymphovascular
pedicle prepaired
Importance of vascular ligation in LN
+ve
Steps/ Technique in AR….cont.
• Next step is rectum &
mesorectal excision
• sharp dissection under direct
vision
• Preservation of hypogastric
nerve in 10 and 2 o’clock
position
• Retraction and counter
retraction given
Steps/ Technique in AR….cont.
• Posterior dissection
started 1st through holy
plane between presacral
fascia and waldayer’s
fascia
• middle rectal vessel is
ligated (20%)
• After completing
posterior dissection
anterior dissection
started in denonvillier’s
fascia between seminal
vesicle and rectum
Steps/ Technique in AR….cont.
• Next step is rectal
dissection &
anastomosis
• Rectum cross clamped
• Rectal wash given
• Dissection & specimen
removed
• Gut continuity
maintained by circular
stapler or hand sewn.
APR
• Tumour of the lower 3rd
having no adequate free
margin
• Sphincter involved
• 2 surgeon in 2 route
• Morbidity - 61%
• Mortality - 0 - 6.3%
• Urinary complications - 50%
• Perineal wound infections - 16%
APR technique
• Abdominal route 1st done by open / laparoscopic
& same way as AR except that the dissection
stops before pelvic floor is reached
• Perineal excision started with circum anal incision
• Depend into ischio-rectal fossa & out towards
levator muscles of pelvic side wall
• Extended posteriorly by incising waldeyer’s fascia
and anteriorly between rectum and prostate or
vagina
• Specimen delivered through perineal route
Projected lines of pelvic floor
resection in vertical plane
Anal
closure
Perineal incision
Incision line anterior to
coccyx through
anococcygeal ligament
through which scissors are
used to gain entrance to
the pelvis
Planes of pelvic dissection and
posterior plane of entry into
pelvis through the pelvic floor
Projected lines of
pelvic floor
transection
Lateral transection of
Levator ani muscle
Completion of anterior
dissection and removal
of rectum through
perineal wound
Anterior resection
of
rectourethralis,
puborectalis,
and
pubococcygeus
Pelvic floor closed
with two drains in
place
Advanced Ca Of The Rectum
En block resection
• in male cystectomy or prostatectomy and in
female posterior vaginectomy or hysterectomy
can be undertaken in combination with AR
• to achieve oncological clearance
Line of dissection, including
posterior wall of vagina for
low anterior rectal cancer
Posterior Vaginectomy
Lines of transection,
including posterior wall of
vagina
Pelvic Exenteration
•Morbidity - 20 - 40 %
•Mortality - 0 - 20%
• Aim is to remove pelvic
organs involved in the
malignant process
• Two types
 partial
 complete
• indication
 locally advanced
 recurrence
liver and lung resection
• Single or multiple well
localised metastasis
• long-term survival can be
achieved (40%)
• Performed synchronously at
the time of AR
Palliative resection
• Indication - stage IVb
• Bleeding, Localized perforation and Obstruction
• Options
• Permanent diversion followed by chemotherapy (+/-
radiotherapy demanding on local symptoms)
• Palliative resection with a permanent colostomy followed
by chemotherapy
• Palliative resection with restoration of GI continuity followed
by chemotherapy
• Obstructing cancer
• Loop ileostomy for diversion —> neoadjuvant chemoradiation —
> surgical resection
•
•
Metastatic cancer
• If life expectancy - > 6 months - palliative rectal
excision
• Rectal stents / laser destruction /Embolisation
Recurrent cancer
• Usually from residual cancer from pelvic wall
Radiotherapy
• Neoadjuvant ,adjuvant or palliative setting
• Neoadjuvant is short course and long course
chemoradiation
• Long course RT 45-50 Gy for 6 weeks + 1st & last
week chemo  6 weeks interval  surgery (down
staging)
• Short course RT 25 Gy for 5 day + 1st & 2nd day
chemo  surgery within 7-10 days (sterilize
tumour) or, 12 weeks later (down staging)
• Adjuvant is EBRT or IORT/ contact RT
Neoadjuvant CRT
Short course
Long course
External Beam Radiotherapy
Chemotherapy
• As Neoadjuvant with RT or adjuvant to reduce the
risk of disseminated disease
• 5 FU remain the 1st line therapy
• Oxaliplatin & Irinotcan is 2nd line
Targeted Therapy
• Target specific type of cancer cells
• Different targeted therapy work in different way
• one type stops the growth of new blood vessel
into rectal tumour
• second type stops the cancer cells from receiving
signal to grow
• less likely to harm normal cells than
chemotherapy
• not everyone will benefited from targeted
therapy
Immunotherapy
• increases the activity of immune system
• Improves body’s ability to find and destroy cancer
cell
• drugs are called checkpoint inhibitor
NCCN Guideline for the treatment
of Rectal Cancer
according to stage
Stage I (T1, T2, N0,M0 or Polyp)
High risk are
Fragmented
specimen
Poorly
differentiated
High grade (3)
Mucinous
adenoma
+ve margine
Lympho-
vasular invasion
Size >3 cm
Treatment After Transanal Local Excision And
Staging Update
Treatment After Transanal Local Excision And
Staging Update
Treatment After Abdominal Resection and
Staging Update
(T3,N0,M0)
Treatment After Abdominal Resection and
Staging Update
(T4 or N1, Mo)
Stage II & III
Less invasive:
1.T1 or T2 but LN +ve
2.T3 but CRM -ve
Stage II & III…..cont
Stage II & III…..cont
• More invasive:
– T3 + CRM +ve
– T4
– Cancer can not be removed with surgery
Option 1
Long course CRT then
After 6 wk imaging,
If CRM –ve then
Surgery
If surgery not possible, then
Systemic therapy
Option 2
12-16 wks of chemotherapy
(FOLFOX/CAPEOX/5FU-LV)
Then CRT
Next imaging
If possible  surgery
No further treatment
If surgery not possible
Then systemic therapy
Follow-up care
Follow-up care
Treatment for local recurrence
Treatment for metastatic cancer: Stage IV
Treatment for metastatic cancer: Stage IV
Treatment for Recurrence
Stage I (T1 or 2, N0, M0)
Stage II : (T3or4, N0, M0) &
Stage III: (any T, any N, M0)
Stage VI: (any T, any N, M1)
Metastatic Ca
Systemic chemotherapy
Stage VI: (any T, any N, M1)
Metastatic Ca
Recurrent Cancer
Conclusion
At present with the advancement in diagnostic
procedure and improvement of surgical
technique Rectal Carcinoma is regarded as
extremely curable malignant disease.
References
• Bailey’s And Love short practice of surgery 27th edi
• Cuschieri’s Essential Surgical practice 5th edi
• Current surgical Diagnosis & Treatment 14th edi
• American Cancer Society guideline
• National comprehensive Cancer Network (NCCN)
guideline
Ca rectum

Ca rectum

  • 1.
    Updates In Management Of CaRectum Dr. Nabarun Biswas Indoor Medical Officer Surgery Dep. MMCH
  • 2.
  • 6.
    Nodes in theorigin of inferior mesenteric artery Nodes in the origin of sigmoid branches Sacral nodes Internal iliac nodes Inguinal nodes
  • 8.
    Rectal cancer • 2ndmost common malignancy in female & 3rd most common in male • 4th most common cause of cancer death after lung, stomach & liver
  • 9.
    Risk factor • Redmeat and saturated fatty acids • Obesity • Sedentary lifestyle • Old age • Alcohol and Smoking • FAP - defect in APC gene on chromosome 5q21 • HNPCC - MSH2 & MLH1 gene defect • Family history – 2 or more first degree relatives • Inflammatory bowel disease – Ulcerative Colitis • Adenomatous polyp
  • 10.
    Premalignant conditions 1. Adenoma 2.Chronic IBD 3. Hereditary  FAP
  • 11.
  • 12.
    Adenoma - Carcinomasequence • Accounts for upto 75-95% of sporadic colo-rectal tumours and typically arise form adenomatous polyp •Mutation in wnt signaling pathway 1.APC mutation  activation of proto-oncogene (required for normal cell renewal) over expression 2.Activation of oncogene k-ras  increase cell proliferation. 3.Suppression of P 53 (for apoptosis)  immortal cell
  • 13.
  • 14.
    Duke’s Staging A BC1 C2 D MUCOSA SUBMUCOSA MUSCULARIS PROPRIA SEROSA LYMPHNODE
  • 15.
    TNM Staging N 0N 1 N 2 T1 T2 T3 T4a T4b MUCOSA SUBMUCOSA MUSCULARIS PROPRIA SEROSA/ Perirectal tissue LYMPHNODE
  • 16.
    AJCC Staging • StageI  100, 200 (T1 or 2 N0 M0) • Stage II  300, 400 (T3 or 4 N0 M0) • Stage III  any T, any N, M0 • Stage IV any T, any N, M1
  • 17.
    Correlation between TNM,Duke’s & DRE Status Duke’s TNM DRE Early A S-I (T1,N0,M0) Freely mobile over rectal muscle A S-I (T2,N0,M0) Moves with rectal wall Locally advanced B or C S-II, S-III (T3/T4 or N1/N2) Slightly moves along with pararectal fat Advanced C or D S- IV (M1a/M1b) Fixed
  • 18.
    Clinical features • Earlysymptoms 1. Per rectal bleeding 3. Early morning diarrhoea  Alteration of bowel habit  Change to loose stool is common  Stenosing ca may cause constipation 2. Tenesmus  Lower half of rectum  Spurious diarrhoea  Bloody slime
  • 19.
    Clinical features • Latesymptoms 1. Pain  Colicky  Severe , intractable 2. Weight loss  Associated with metastatic disease
  • 20.
    Examination • Abdominal: – Normalin early stage – Obstructive feature in stenosing recto-sigmoid tumour • Rectal: – Assessment of tumor size, mobility and fixation, anterior or posterior location, relationship to sphincter mechanism and the distance from the anal verge.
  • 21.
    Rigid Proctoscope • Demonstratesthe proximal and distal levels of the mass from anal verge • Extent of circumferential involvement • Orientation within the lumen • Aids in determining the feasibility of local excision
  • 22.
    Colonoscopy Torule out synchronous cancers -which occur 2 - 8% of the time.
  • 23.
  • 24.
    Transrectal Endoluminal Ultrasound Permits accuratecharacterization of the primary tumor and the status of the perirectal lymph nodes
  • 25.
    MRI • Investigation ofchoice for T staging
  • 26.
    CT scan • Regionaltumor extension • Lymphatic and distant metastasis • Tumor related complications - perforation or fistula formation
  • 27.
    Laboratory studies • CompleteBlood count • Serum Electrolytes • Liver Enzymes • CEA (Carcinoembryonic antigen)
  • 28.
  • 29.
    Management Protocol 1. Preoperativeworkup 2. Operative procedure 3. Post operative management 4. Surveillance program 1. Counseling & consent 2. Tumour board formation 3. Correction of co-morbidities 4. Prophylaxis 5. Bowel preparation
  • 30.
    Principle of Treatment 1.Surgery is the mainstay of curative Rx 2. Aim: radical excision of rectum + mesorectum+ lympho-vascular clearance 3. Widespread metastasis: palliative Rx  stenting/RT/palliative resection 4. Liver/Lung metastasis: single/well localized  resection with curative intent 5. Locally advanced (T3/4 or N1/2): neoadjuvent CRT  surgery
  • 31.
    Principle of Treatment 6.Watch & wait policy: after long course CRT if CCR & CPR is found  intense surveillance 7. Early cancer(T1,T2 & N0): organ preserving surgery by Local excision /TEMS (for T1) 8. If radical excision possible : APR or AR (High, Low, Ultra low) 9. Sphincter saving possible if tumour margin ≥2 cm from ano-rectal junction 10. Defunctioning stoma: if tumour below peritoneal reflection
  • 32.
    Treatment modalities • Surgery •Chemotherapy • Radiotherapy • Targeted therapy • Immuno therapy • Alternative treatment
  • 33.
    Surgery • Surgery isthe mainstay of treatment • Radiation and chemotherapy are given before or after surgery • The type of surgery depends on the stage of the cancer
  • 34.
    Types of surgery 1.Local excision / TEMS / TAMIS 2. Anterior resection  High AR  Low AR  Ultra Low AR 3. TME / Modified TME 4. APR 5. Surgery in advanced carcinoma
  • 35.
  • 36.
    Trans anal endoscopicmicro surgery: TEMS • For mid and lower rectal tumor • For rectal adenomas and early rectal cancers • Must below peritoneal reflection
  • 37.
    TEMS • Indication: – Welldifferentiated – Grade 1 or 2 – Not mucinous adenoma – Lymphnode –ve – Diameter < 3cm – Tumor invades only submucosa
  • 38.
    Anterior Resection • Itis a sphincter saving operation • Approach: open / laparoscopic / robotic assistance • Two terms: TME & CRM
  • 39.
    Total Mesorectal Excision:TME • Introduced by RJ Heald in 1979 • For middle and lower third rectal carcinoma • Mesorectum: perirectal fascia containing fat and perirectal lymph nodes, lymphatic • Spread of carcinoma rectum occurs in this area.
  • 40.
  • 41.
    Modified TME • Distalspread of adenocarcinoma either in the rectal wall or mesorectum greater than 2-3 cm is rare. • So the dissection continues to pelvic floor up to ano-rectal junction (low AR) or 5 cm (3cm) below the tomour margin (High AR)  Modified TME • Top to down manner
  • 42.
  • 43.
    Ta TME • Lowanterior resection can be a challenging operation, especially in obese male patients and in particular after radiotherapy. • Transanal total mesorectal excision (TaTME) might offer technical advantages over laparoscopic or open approaches particularly for tumors in the distal third of the rectum. • Defines the radial and distal margins more clearly. • Bottom up manner • TAMIS: modification of TaTME where SILS instruments are used
  • 44.
  • 45.
  • 46.
  • 47.
    Circumferential Resection Margin: CRM •It is the radial distance between cancer tissue and the non peritonalized margin of the resected specimen • CRM +ve when distance is ≤1 mm • CRM –ve when distance is >1 mm • CRM is an important prognostic factor for recurrence • CRM can be predicted preoperatively by thin slice high resolution MRI • In predicted CRM positivity neoadjuvant CRT is indicated
  • 48.
  • 49.
    Anterior resection • 3types of 3 anterior resection 1. High  10cm from anal verge 2. Low  8 cm from anal verge 3. Ultra low  6cm from anal verge • TME /modified TME is incorporated with AR • Gastrointestinal continuity is maintained by stapled anastomosis or hands sewn
  • 50.
    Steps/ Technique inAR • Lloyd-Davies position • Good assistance • Long midline incision • Wide retraction • Small bowel packed out of the way • Full laparotomy
  • 51.
    Steps/ Technique inAR • Assess for synchronous lesion or spread • Sigmoid and descending colon mobilization lateral to medial (in laparoscopic method medial to lateral after ligation of vessels) • Protect left ureter and gonadal vessel • Splenic flexure mobilization
  • 52.
  • 53.
    Steps/ Technique inAR….cont. • next step is vascular ligation • High ligation and low ligation of IMA • High for proper lymphatic clearance & low for improve vascularity • 2 step ligation of IMV for tension free anastomosis • Mesocolon divided & lymphovascular pedicle prepaired
  • 54.
    Importance of vascularligation in LN +ve
  • 55.
    Steps/ Technique inAR….cont. • Next step is rectum & mesorectal excision • sharp dissection under direct vision • Preservation of hypogastric nerve in 10 and 2 o’clock position • Retraction and counter retraction given
  • 56.
    Steps/ Technique inAR….cont. • Posterior dissection started 1st through holy plane between presacral fascia and waldayer’s fascia • middle rectal vessel is ligated (20%) • After completing posterior dissection anterior dissection started in denonvillier’s fascia between seminal vesicle and rectum
  • 57.
    Steps/ Technique inAR….cont. • Next step is rectal dissection & anastomosis • Rectum cross clamped • Rectal wash given • Dissection & specimen removed • Gut continuity maintained by circular stapler or hand sewn.
  • 58.
    APR • Tumour ofthe lower 3rd having no adequate free margin • Sphincter involved • 2 surgeon in 2 route • Morbidity - 61% • Mortality - 0 - 6.3% • Urinary complications - 50% • Perineal wound infections - 16%
  • 59.
    APR technique • Abdominalroute 1st done by open / laparoscopic & same way as AR except that the dissection stops before pelvic floor is reached • Perineal excision started with circum anal incision • Depend into ischio-rectal fossa & out towards levator muscles of pelvic side wall • Extended posteriorly by incising waldeyer’s fascia and anteriorly between rectum and prostate or vagina • Specimen delivered through perineal route
  • 60.
    Projected lines ofpelvic floor resection in vertical plane Anal closure Perineal incision
  • 61.
    Incision line anteriorto coccyx through anococcygeal ligament through which scissors are used to gain entrance to the pelvis Planes of pelvic dissection and posterior plane of entry into pelvis through the pelvic floor
  • 62.
    Projected lines of pelvicfloor transection Lateral transection of Levator ani muscle Completion of anterior dissection and removal of rectum through perineal wound Anterior resection of rectourethralis, puborectalis, and pubococcygeus Pelvic floor closed with two drains in place
  • 63.
    Advanced Ca OfThe Rectum
  • 64.
    En block resection •in male cystectomy or prostatectomy and in female posterior vaginectomy or hysterectomy can be undertaken in combination with AR • to achieve oncological clearance
  • 65.
    Line of dissection,including posterior wall of vagina for low anterior rectal cancer Posterior Vaginectomy Lines of transection, including posterior wall of vagina
  • 66.
    Pelvic Exenteration •Morbidity -20 - 40 % •Mortality - 0 - 20% • Aim is to remove pelvic organs involved in the malignant process • Two types  partial  complete • indication  locally advanced  recurrence
  • 67.
    liver and lungresection • Single or multiple well localised metastasis • long-term survival can be achieved (40%) • Performed synchronously at the time of AR
  • 68.
    Palliative resection • Indication- stage IVb • Bleeding, Localized perforation and Obstruction • Options • Permanent diversion followed by chemotherapy (+/- radiotherapy demanding on local symptoms) • Palliative resection with a permanent colostomy followed by chemotherapy • Palliative resection with restoration of GI continuity followed by chemotherapy
  • 69.
    • Obstructing cancer •Loop ileostomy for diversion —> neoadjuvant chemoradiation — > surgical resection • • Metastatic cancer • If life expectancy - > 6 months - palliative rectal excision • Rectal stents / laser destruction /Embolisation Recurrent cancer • Usually from residual cancer from pelvic wall
  • 70.
    Radiotherapy • Neoadjuvant ,adjuvantor palliative setting • Neoadjuvant is short course and long course chemoradiation • Long course RT 45-50 Gy for 6 weeks + 1st & last week chemo  6 weeks interval  surgery (down staging) • Short course RT 25 Gy for 5 day + 1st & 2nd day chemo  surgery within 7-10 days (sterilize tumour) or, 12 weeks later (down staging) • Adjuvant is EBRT or IORT/ contact RT
  • 71.
  • 72.
  • 73.
    Chemotherapy • As Neoadjuvantwith RT or adjuvant to reduce the risk of disseminated disease • 5 FU remain the 1st line therapy • Oxaliplatin & Irinotcan is 2nd line
  • 74.
    Targeted Therapy • Targetspecific type of cancer cells • Different targeted therapy work in different way • one type stops the growth of new blood vessel into rectal tumour • second type stops the cancer cells from receiving signal to grow • less likely to harm normal cells than chemotherapy • not everyone will benefited from targeted therapy
  • 76.
    Immunotherapy • increases theactivity of immune system • Improves body’s ability to find and destroy cancer cell • drugs are called checkpoint inhibitor
  • 77.
    NCCN Guideline forthe treatment of Rectal Cancer according to stage
  • 78.
    Stage I (T1,T2, N0,M0 or Polyp) High risk are Fragmented specimen Poorly differentiated High grade (3) Mucinous adenoma +ve margine Lympho- vasular invasion Size >3 cm
  • 79.
    Treatment After TransanalLocal Excision And Staging Update
  • 80.
    Treatment After TransanalLocal Excision And Staging Update
  • 81.
    Treatment After AbdominalResection and Staging Update (T3,N0,M0)
  • 82.
    Treatment After AbdominalResection and Staging Update (T4 or N1, Mo)
  • 83.
    Stage II &III Less invasive: 1.T1 or T2 but LN +ve 2.T3 but CRM -ve
  • 84.
    Stage II &III…..cont
  • 85.
    Stage II &III…..cont • More invasive: – T3 + CRM +ve – T4 – Cancer can not be removed with surgery Option 1 Long course CRT then After 6 wk imaging, If CRM –ve then Surgery If surgery not possible, then Systemic therapy Option 2 12-16 wks of chemotherapy (FOLFOX/CAPEOX/5FU-LV) Then CRT Next imaging If possible  surgery No further treatment If surgery not possible Then systemic therapy
  • 86.
  • 87.
  • 88.
  • 89.
    Treatment for metastaticcancer: Stage IV
  • 90.
    Treatment for metastaticcancer: Stage IV
  • 91.
  • 92.
    Stage I (T1or 2, N0, M0)
  • 93.
    Stage II :(T3or4, N0, M0) & Stage III: (any T, any N, M0)
  • 94.
    Stage VI: (anyT, any N, M1) Metastatic Ca Systemic chemotherapy
  • 95.
    Stage VI: (anyT, any N, M1) Metastatic Ca
  • 96.
  • 97.
    Conclusion At present withthe advancement in diagnostic procedure and improvement of surgical technique Rectal Carcinoma is regarded as extremely curable malignant disease.
  • 98.
    References • Bailey’s AndLove short practice of surgery 27th edi • Cuschieri’s Essential Surgical practice 5th edi • Current surgical Diagnosis & Treatment 14th edi • American Cancer Society guideline • National comprehensive Cancer Network (NCCN) guideline

Editor's Notes

  • #13 It is a stepwise pattern of genetic mutation  mutation in wnt signaling pathway APC mutation  activation of proto-oncogene (required for normal cell renewal) over expression Activation of oncogene k-ras  increase cell proliferation. Suppression of P 53 (for apoptosis)  immortal cell
  • #84 Less invasive: T1 or T2 but LN +ve T3 but CRM -ve