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Tell me the diagnosis and treatment plan

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"cervical cancer" AND "chemoradiation" AND "FIGO stage"

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"cervical cancer" AND "concurrent chemoradiotherapy"

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cervical cancer FIGO 2023 staging IIB treatment chemoradiation guidelines cisplatin brachytherapy

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Patient Summary

Patient: Ms. Mithu Devi | Female, 48 years 6 months | Referred by Dr. Alok Narang Study: Whole Body FDG PET-CT (Pretreatment evaluation for known carcinoma cervix) Date: 20 July 2026

PET-CT Findings (Key Points)

RegionFinding
Cervix / PelvisFDG-avid heterogeneously enhancing soft tissue lesion involving uterine cervix, extending into adjacent upper vagina - size: 2.8 (AP) x 4.2 (TR) x 3.4 (CC) cm, SUVmax 13.3
Adjacent structuresClosely abutting posterior urinary bladder wall and rectum - no obvious infiltration; bilateral lower ureters uninvolved
Lymph nodesMetabolically active left external iliac lymph node (~1.5 x 1.0 cm, SUVmax 14.3) - likely metastatic; other nodes in aortocaval/paraaortic/bilateral iliac regions are subcentimetric and FDG-negative (likely reactive)
Distant metastasisNone. No FDG-avid lesions in lung, bone, liver, or distant nodes
LiverEnlarged (~17.1 cm craniocaudal), diffuse fatty changes - no focal FDG uptake; no metastatic disease
Brain / Thorax / BoneNo abnormal FDG uptake

Diagnosis

Primary Malignant Pathology: Carcinoma of the Uterine Cervix

FIGO Staging (2018 system):

Based on the PET-CT findings:
  • Cervical tumor extending into the upper vagina = at minimum Stage II
  • Parametrial involvement - not explicitly stated; the tumor is large (>4 cm) and abutting rectum/bladder without clear infiltration
  • Pelvic lymph node metastasis (left external iliac) = under FIGO 2018, pelvic LN positivity upstages to Stage IIIC1
Most likely stage: FIGO Stage IIIC1r (pelvic lymph node metastasis confirmed on imaging - 'r' suffix denotes radiological staging)
This corresponds to the diagram shown below (IIIC1 = pelvic LN involvement):
FIGO Cervical Cancer Staging 2018
Berek & Novak's Gynecology - FIGO Cervical Cancer Staging 2018
Note: The FIGO 2018 staging system - which is incorporated into this report - uses imaging and pathologic measurements to determine pelvic/para-aortic nodal involvement. The left external iliac node (SUVmax 14.3) strongly indicates metastatic disease, placing this patient in Stage IIIC1.

Treatment Plan

As per NCCN Guidelines (v1.2024) and ESGO/SEOM Guidelines (2023) for Stage IIIC1 Locally Advanced Cervical Cancer:

1. Primary Treatment: Concurrent Chemoradiotherapy (CCRT)

This is the standard of care for Stage IIB and above (including IIIC1), supported by multiple RCTs showing a 30-50% reduction in risk of death compared to radiation alone.

Radiotherapy

  • External Beam Radiation Therapy (EBRT): 45-50 Gy to the pelvis in 25-28 fractions
    • Field should cover the primary tumor, parametria, upper vagina, and pelvic lymph nodes (including the left external iliac node)
    • Extended-field RT to para-aortic nodes may be considered if para-aortic nodes are suspicious (they are not significantly enlarged here, but close monitoring is warranted)
  • Brachytherapy (intracavitary/interstitial): Given after EBRT - this is an essential component. Total EQD2 to point A: typically ≥85 Gy. Omission of brachytherapy significantly worsens outcomes.

Concurrent Chemotherapy (Radiosensitizer)

  • Cisplatin 40 mg/m² IV weekly (max 70 mg/week) x 5-6 cycles - preferred agent
  • Alternative if cisplatin-intolerant: Carboplatin (AUC 2 weekly)

2. Additional Systemic Therapy (Consider)

Based on the KEYNOTE-A18 trial (2023), the NCCN guidelines now allow pembrolizumab (anti-PD-1) in combination with chemoradiation for locally advanced cervical cancer (Stage IIIC1). This should be discussed and considered in fit patients:
  • Pembrolizumab 200 mg every 3 weeks x 5 cycles concurrent with CCRT, then 400 mg every 6 weeks maintenance x 15 cycles

3. Pre-treatment Work-Up Required

Before initiating treatment:
  • Histopathology/biopsy confirmation (squamous cell carcinoma vs adenocarcinoma vs other - guides PD-L1 testing)
  • MRI pelvis (preferred for local staging and treatment planning - better soft tissue delineation than PET-CT alone; Grainger & Allison's Diagnostic Radiology)
  • PD-L1 testing (CPS score) if pembrolizumab is being considered
  • Renal function tests (creatinine, GFR) before cisplatin - note serum creatinine is 0.70 mg/dL (normal here)
  • Complete blood count, LFTs (fatty liver noted - monitor hepatotoxicity)
  • USG abdomen - for gallbladder/biliary system evaluation (liver is enlarged with fatty changes)
  • Fertility counseling - patient is 48 years, likely perimenopausal; ovarian function/hormone status discussion
  • Consider para-aortic lymph node dissection/biopsy for pathological staging if upstaging would change field borders

4. Response Assessment

  • PET-CT reassessment 3 months after completion of CCRT
  • If complete metabolic response: surveillance
  • If residual disease: assess for salvage (exenteration in selected cases; additional systemic therapy)

Summary Table

ParameterDetail
DiagnosisCarcinoma cervix, likely squamous cell (confirm on biopsy)
FIGO StageIIIC1r (pelvic LN metastasis on imaging)
Primary treatmentConcurrent Chemoradiotherapy (CCRT)
RadiationEBRT 45-50 Gy + Brachytherapy boost (intracavitary)
ChemotherapyCisplatin 40 mg/m² weekly x 5-6 cycles
Add-on (consider)Pembrolizumab (KEYNOTE-A18 regimen)
PrognosisStage IIIC1 5-year survival ~40-50% with CCRT; improved with immunotherapy in PD-L1+ disease

Sources: Berek & Novak's Gynecology (FIGO 2018 staging) | Grainger & Allison's Diagnostic Radiology (cervical cancer imaging) | NCCN Guidelines Cervical Cancer v1.2024 | SEOM-GEICO Clinical Guidelines 2023 | PubMed PMID 39351236 (chemoradiation + immune checkpoint inhibitors in locally advanced cervical cancer, 2024)
Disclaimer: This analysis is based on imaging findings only. Final clinical staging, treatment decisions, and all therapeutic interventions must be made by the treating oncologist/gynecologic oncologist in conjunction with a multidisciplinary tumor board, following clinical examination, histopathological confirmation, and institutional protocols.
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