rectal cancer : other therapies Flashcards
Aim of neo/adjuvant therapies
-for Operable disease – reduces local relapse rates
- for when (CRM) is involved/threatened – improved rates of R0 resection and local control
-for Inoperable disease (baseline) – improved rates of R0 resection, local control, and cancer-specific survival
Total Neoadjuvant Therapy (TNT) before surgery
-FOLFOX—>LCCRT (5FU) or SCRT
-LCCRT (5FU)—>FOLFOX(12-16 weeks)
-SCRT—>FOLFOX (12-16 weeks)
Why can’t chemo be given concurrently with SCRT
unsuitable for patients with inflammatory bowel disease and/or history of bowel obstruction
Why use RT?
Reduce the risk of local recurrence
◦ Involvement of the circumferential margin
◦ Lymph node status
◦ Extramural venous invasion
why use Neoadjuvant RT
◦ Induce tumour response prior to Sx
◦ Better definition of the target
◦ less small bowel toxicity as bowel adhesions more common after Sx
Stage I: T1 or 2 N0 M0
Primary tx:
-Local excision
-APR or sphincter sparing
Stage I: T1 or 2 N0 M0
-pT1-2 N0 with no high risk factors=Observation
-T1-2 with high risk factors=CRT
High Risk Features:
*+ve margin
*LVI
*Poorly diff
*Invasion into the lower ⅓ of submucosa
Locally advanced disease=
T3-4, node-negative (N0) or
node positive disease without distant metastasis (T any;N1-2M0)
Standard treatment for patients for CRM Clear: Greater than 1-2mm from MRF
NEOADJUVANT
LCCRT( infusional 5-FuP)
Or
SCRT
Standard treatment for patients for CRM Clear: Greater than 1-2mm from MRF
PRIMARY TREATMENT
a)Transabdominal resection
Or
b)Resection contraindicated
Standard treatment for patients for CRM Clear: Greater than 1-2mm from MRF
Adjuvant treatment
IF:
a)folfox then surveillance
B) systemic therapy
Standard treatment for patients for CRM Less than 1mm from MRF
additional therapies
Consolidation:
Chemotherapy for 12-16 weeks (after LCCRT OR SCRT)
induction: same but before
Rationale for TNT
Significant improvement in:
*Overall pathologic complete response rate
* Disease-free survival
* Distant metastasis-free survival
*Overall survival
LCCRT vs SCRT in terms of down-staging
-LCCRT is preferred for locally advanced tumours as ‘downstaging’ needed to ↓ chance of a +CRM or
↑ sphincter preservation
-The lesser ‘downstaging’ effect of SCRT may now be
better overcome with a longer delay to surgery or pre-operative/induction chemotherapy (i.e. TNT approach)
LCCRT vs SCRT
pt2
its preferred to administer CRT in the pre-operative setting because
improvement in locoregional control,
sphincter preservation,
reduced acute and late toxicity
Rationale for pre- or post-op concurrent chemo:
Ø Increases radiosensitivity
Ø Systemic control of disease
Ø Increased pCR and sphincter preservation
Oligometastatic Disease M1 Resectable disease CLEAR CRM
Chemo —>RT (25/5#) or C (5FU )/Pelvic RT—> Resection, if possible
Oligometastatic Disease M1 Resectable disease INVOLVED CRM
-Chemo (FOLFOX) then C (5FU) /RT (50.4/28#)
-RT (25/5#) or C (5FU )/Pelvic RT then Chemo (FOLFOX)
Oligometastatic Disease M1 Unresectable disease
Chemo then if resectable RT (25/5#) or C (5FU )/Pelvic RT THEN RESECT
Chemo then if unresectable then Systematic Tx
Unresectable?
-Tumour involving or extending beyond MRF
-Tumour within 1-2mm of MRF
-Involving nodes beyond MRF
-Invasion of pelvic organs