Anal cancer radical
Radical chemoradiotherapy (any tumour above T1 margin tumour)
T1-T2 N0 = 50.4Gy/28#/5.5 weeks with concurrent IV mitomycin C 12mg/m2 (max 20mg) with oral capecitabine 825mg/m2 on days of RT.
T3-T4 or N+ = 53.2Gy/28#/5.5 weeks with concurrent IV mitomycin C 12mg/m2 (max 20mg) with oral capecitabine 825mg/m2 on days of RT. 53.2Gy to gross anal disease and CTVN3 (nodes >3cm), 50.4Gy to gross nodal disease.
Elective nodes (T2 plus) treated to 40Gy/28#/5.5 weeks.
CTVA includes entire anal canal.
Elective nodal areas should include: bilateral inguinal femoral, external iliac, internal iliac, obturator, pre sacral nodes and lower 5cm of mesorectum. If GTV extends into mesorectum the entire mesorectum should be in elective volume. This includes tumours which extend into the anorectal junction.
CI or PA nodes = M1
Anal cancer adjuvant
& indication
Consider if positive margin or close (<1mm) or unexpected finding.
Adjuvant chemoradiotherapy to anal margin and canal 41.4Gy/23#/4.5 weeks with concurrent IV mitomycin C 12mg/m2 (max 20mg) with oral capecitabine 825mg/m2 on days of RT.
Plus nodes if > 2cm (>/=T2)
Elective nodal areas should include: bilateral inguinal femoral, external iliac, internal iliac, obturator, pre sacral nodes and lower 5cm of mesorectum. If GTV extends into mesorectum the entire mesorectum should be in elective volume. This includes tumours which extend into the anorectal junction.
Anal cancer palliative RT?
30Gy/10#
Then usuals.
1L SACT carbo/taxol
2L cis/5FU
Rectal cancer low risk
Upto T3aN0 No EMVI, CRM not threatened
= surgery alone
Rectal cancer intermediate risk
> /= T3b, CRM not threatened, N and EMVI + or -
Short course radiotherapy 25Gy/5#/1 week followed by either immediate or delayed (6-8 weeks) surgery.
Rectal cancer high risk
CRM + or threatened (<1mm), tumour encroaching on intersphincteric plane or levator involvement.
Short course radiotherapy 25Gy/5#/1 week followed delayed (6-8 weeks) surgery.
Long course chemo-radiotherapy 50Gy/25#/5weeks with concurrent capecitabine 900mg/m2 BD PO on RT days.
Young, fit, high risk e.g. T4, N2 (pMMR only)
Total neoadjuvant therapy
Rapido protocol of Short course radiotherapy 25Gy/5#/1 week plus 3m CAPOX (D1 oxali 130mg/m2 IV, Capecitabine 1000 mg/m2 D1-D14, 21 day cycle x 4), followed by surgery.
Prodige protocol - 3m FOLFIRINOX chemotherapy (oxaliplatin 85 mg/m2, irinotecan 180 mg/m2, leucovorin 400 mg/m2, and fluorouracil 2400 mg/m2 intravenously every 14 days for 6 cycles), long course chemo-radiotherapy 50Gy/25#/5weeks with concurrent capecitabine 900mg/m2 BD PO on RT days, followed by surgery (total mesorectal excision).
Elective nodes: Int iliac, obturator, presacral and mesorectal
Spiel: I would outline the internal iliac and pre-sacral nodes from S1/2 junction. Int iliac, with 7mm margin around vessels down to obturator internus, presacral with 10mm roller ball down to the caudal border of mesorectum.
I would outline the mesorectum from S2/3 junction down to where mesoractal fat disappears (insertion of levator ani muscle into the external sphincter muscles). Obturator nodes, with a 17mm rollerball from the top of obturator internus to where obturator artery leaves the pelvis.
General - go 2cm above highest involved node - so may extend CTVe accordingly.
External iliac, CI considered metastatic.
Inguinal considered metastatic unless tumour is below the dentate line.
Presacral: 10mm rollerball (or 7mm ant to sup rectal art/IMA whichever is more anterior) from the S1/2 junction to caudal border of mesorectum.
Mesorectum: From S2/3 junction down to where mesoractal fat disappears (insertion of levator ani muscle into the external sphincter muscles).
Int iliac - From ant border of S1/2 to obturator internus muscle (top of obturator nodes). Outline vessels, plus 7mm margin.
Obturator - 17mm roller ball, Superiorly, from first slice showing obturator internus down to where obturator leaves the pelvis. Include areas of bladder if present.
Rectal adjuvant radiotherapy
If CRM + (or threatened <1mm) + no pre-op RT.
Adjuvant radiotherapy 45Gy/25#/5 weeks with a simultaneous integrated boost to 50Gy/25#/5 weeks to residual macroscopic disease or R1 resection.
Low risk endometrial
Stage IA (G1-G2) with endometrioid type (dMMR and NSMP) and no or focal LVSI
Stage I/II POLEmut cancer; for stage III POLEmut cancers
= No adjuvant therapy
Indications and dose/# for papillon radiotherapy
Low energy X ray contact brachytherapy.
When the tumour is 3 cm or less and has not spread beyond stage T3b N1 M0 (with limited nodal involvement), and:
- the person chooses not to have surgery, or
- the risks of surgery are unacceptably high.
People with larger tumours (with limited nodal involvement) may become eligible for this procedure if neoadjuvant treatment (external beam radiotherapy with or without chemotherapy) reduces the tumour to 3 cm or less and it has not spread beyond stage T3b N1 M0.
90-110Gy/3-4#/3-6 weeks, followed by EBRT.
RCR - can also be used for palliative tx for those with recurrence or mets.
Rectal cancer palliative RT?
PS0-1 consider higher doses including 45Gy/25# +/- conc. chemo, 30Gy/10#, 25Gy/5#, 20Gy/5#.
PS 2 20Gy/5
Very frail 8Gy/1.
1L SACT
dMMR - ipi/Nivo
Right sided - FOLFOX
Left sided KRAS WT - FOLFIRI + cetux
Intermediate risk endometrial cancer
Stage IA non-endometrioid type (serous, clear-cell, undifferentiated carcinoma, carcinosarcoma, mixed) and/or p53-abn cancers without myometrial invasion and no or focal LVSI.
Stage IA G3 with endometrioid type (dMMR and NSMP) and no or focal LVSI.
Stage IB (G1-G2) with endometrioid type (dMMR and NSMP) and no or focal LVSI.
Stage II G1 endometrioid type (dMMR and NSMP) and no or focal LVSI.
> 60 or non-endo, for surveillance
<60 and endo = Adjuvant vaginal vault brachytherapy 21Gy @5mm/3#/2-3 weeks
High - intermediate risk endometrial cancer
Stage I endometrioid type (dMMR and NSMP) any grade and any depth of invasion with substantial LVSI.
Stage IB G3 with endometrioid type (dMMR and NSMP) regardless of LVSI.
Stage II G1 endometrioid type (dMMR and NSMP) with substantial LVSI.
Stage II G2-G3 endometrioid type (dMMR and NSMP).
Adjuvant chemo-radiotherapy 45Gy/25#/5 weeks with concurrent cisplatin 40mg/m2 IV weekly.
With cervical involvement, plus HDR vault brachytherapy 8Gy at 5mm/2#.
Elective nodes:
Pelvic lymph nodes (i.e. obturator, internal, external and distal common iliac nodes (to the upper S1 level).
If posterior extension of the uterine tumour is present then the upper pre-sacral nodes are included.
(Margin of at least 20mm above the highest lymph node region involved).
High risk endometrial cancer
Non-endometroid and any p53Abn with myometrial invasion. (including undifferentiated carcinoma and carcinosarcoma).
All stage III and IVA with no residual tumour, regardless of histology and regardless of molecular subtype.
Adjuvant chemo-radiotherapy 45Gy/25#/5 weeks with concurrent cisplatin 40mg/m2 IV weekly.
With cervical involvement, plus HDR vault brachytherapy 8Gy at 5mm/2#.
If serous or stage III (+p53 abn as per Roshan) -
PORTEC 3 protocol of adjuvant chemoradiotherapy 48.6Gy/27#/5.5 weeks with concurrent cisplatin 50mg/m2 every 21 days followed by 4 cycles of adjuvant carboplatin (AUC5) and paclitaxel 175mg/m2 IV D1, 21 day cycle.
Definitive radiotherapy endometrial cancer
If inoperable due to comorbidity or advanced disease.
Brachytherapy alone
HDR:
* 36 Gy in 5 fractions (Grade C) prescribed to the uterine serosa
* 37.5 Gy in 6 fractions (Grade C) prescribed to the uterine serosa
If high grade, or deep myometrial invasion:
Combination therapy EBRT + Brachy
* 45 Gy in 25 fractions over 5 weeks (Grade C)
* 50 Gy in 25 fractions over 5 weeks (Grade C)
HDR Brachytherapy:
* 28 Gy in 4 fractions (Grade C) prescribed to the uterine serosa
* 25 Gy in 5 fractions (Grade C) prescribed to the uterine serosa
Salvage radiotherapy endometrial cancer
Salvage external beam radiotherapy 45 Gy in 25 fractions over 5 weeks.
If vaginal vault recurrence - with brachytherapy boost with interstitial needles.
(Gynae - For central pelvic or vaginal relapses consider interstitial brachy.)
Palliative RT re-treat endometrial cancer
Palliative re-irradiation dose 20Gy/10#/2weeks.
This is a re-irradiation case.
I would retrieve the previous radiotherapy plan.
I would convert the previous OAR doses to equivalent dose in 2-Gy fractions (EQD2) with assistance from the physics team.
Assess the elapsed time interval.
Calculate the cumulative EQD2 and compare with tolerance limits.
Discuss risks and benefits when consenting the patient
Adjuvant radiotherapy vulval cancer
Positive margins (<10mm, for re-resection if possible), ECS, >/=2 LN.
Also If SLNBx shows micromets (<2mm) can have adj RT, for lymphadenectomy if macromets.
Adjuvant radiotherapy to vulva, pelvic and inguinal nodes 50Gy/25#/5 weeks with concurrent cisplatin 40mg/m2 weekly (if 2+ nodes).
RCR dose/#, QART has variety of doses.
Primary radiotherapy vulval cancer
If inoperable.
50.4Gy/28#/5.5 weeks with SIB to the primary and involved nodes 63Gy/28#/5.5 weeks with concurrent cisplatin 40mg/m2 IV weekly. (CCC dose/#, 64.3Gy EQD2).
RCR: “The primary and involved nodes should be boosted using a simultaneous integrated
boost (SIB) with VMAT or brachytherapy to deliver a total dose of 60–68 Gy EQD2
(Grade C)”
Definitive radiotherapy of vaginal carcinoma:
Definitive radiotherapy of vaginal carcinoma:
* 45–50 Gy in 25 fractions over 5 weeks (Grade C)
can add concurrent cisplatin 40mg/m2 IV weekly.
Followed by HDR brachytherapy: A total EQD2 dose of 70–80 Gy should be the aim:
* Upper vagina: 24–28 Gy in 4 fractions (Grade C)
* Lower vagina: 18.75–20 Gy in 5 fractions (Grade C)
Note the lower vagina is less tolerant of very high
doses.
Radical chemo-radiotherapy cervical cancer
Stage 1B3 (>4cm)- IVa
Interlace protocol
Induction chemotherapy 6 cycles of weekly Carbo AUC 2 and paclitaxel 80mg/m2 IV.
Node negative:
Radical chemo-radiotherapy 45 Gy in 25 fractions over 5 weeks with concurrent cisplatin 40mg/m2 IV weekly
Node positive:
50.4 Gy in 28 fractions over 5.5 weeks with concurrent cisplatin 40mg/m2 IV weekly with SIB to 55Gy to involved nodes (CCC/RCR).
Followed by HDR Brachytherapy (</= 56 days max)
28 Gy in 4 fractions aiming for total dose of 85-90Gy to the high-risk CTV D90.
For small-volume tumours (<30 ml) a 3-fraction schedule may be considered (7.7 Gy × 3)
Elective nodes: Common iliac, Internal iliac, External Iliac, Obturator and if posterior extension of the cervical tumour is present then the upper pre-sacral nodes are included.
Where there is common iliac nodal involvement, a para-aortic nodal (PAN) volume is required. If there are 3 or more pelvic nodes involved a PAN should be strongly considered. The whole para-aortic strip extends usually to the level of the renal hilum at T12/L1 (or L1/L2 at least)
Includes the tumour (GTV), the entire uterine cervix, entire uterus, bilateral parametria, ovaries if seen, proximal half of the uterosacral ligaments and at least the upper half of the vagina depending on the extent of disease.
Incidental cervical cancer radiotherapy post hysterectomy
1A1, any LVSI or 1A2 no LVSI - no further mx.
1A2 w LVSI, clear margins - for LND.
>5mm (i.e. IB1 and above) for RT or CRT.
Believe it would be: adjuvant radiotherapy 45 Gy in 25 fractions over 5 weeks +/- concurrent cisplatin 40mg/m2 IV weekly
+ 6 Gy × 3 VB
Local recurrence cervical cancer - overall options
Consider pelvic exenterative surgery
OR
CRT if not had.
If solitary/oligomet - consider surgery or SBRT.
Cervical cancer pelvic LN mass post surgery
Salvage RT post surgery:
Salvage chemoradiotherapy to the pelvis 48.8Gy/30#/6 weeks with a SIB to the mass of 54Gy/30#/6 weeks with concurrent cisplatin 40mg/m2 IV weekly
Cervical cancer isolated PA node recurrence post CRT?
CRT to PA nodes 45Gy/25#/5 weeks with a match to the previous field with concurrent cisplatin 40mg/m2 IV weekly.