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Isolated Limb Infusion: Efficacy, Toxicity and an Evolution in the Management of In-transit Melanoma

Overview
Specialty General Surgery
Date 2015 Mar 31
PMID 25821769
Citations 4
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Abstract

Background: Isolated limb infusion (ILI) delivers low-flow chemotherapy via percutaneous catheters to treat melanoma in-transit metastases.

Objective: To describe the experience of two regional referral centres with ILI.

Methods: A retrospective review of patients who underwent ILI between 2002 and 2012 was performed. Outcomes were measured using the WHO criteria for response, the Wieberdink toxicity score and long-term limb function using the Toronto Extremity Salvage Score (TESS).

Results: Fifty-two patients (mean age 66 years [range 27 to 90 years], female sex 65%, and lower [treated] limb in 86%) with 54 ILIs were reviewed. Wieberdink toxicity score was ≥3 in 21 (39%) procedures. Median follow-up was 18 months (range one to 117 months). Initial complete response (CR) was 29%, partial response 27%, stable disease 18% and progressive disease 27%. Predictors of better initial response were low disease burden and previous treatment. One or more treatments after ILI were common (65%). At 12 months, 19% of ILI patients had died from melanoma but 44% of surviving patients experienced limb CR. At 24 months, 57% of surviving patients experienced limb CR. The quality of life in the surviving, contactable patients according to the Toronto Extremity Salvage Score was 89%.

Conclusion: Even if ILI does not result in CR for melanoma intransit metastases. it may slow disease progression as a single therapy, but more frequently in combination with other modalities.

Citing Articles

Tumor Burden and Health-Related Quality of Life in Patients with Melanoma In-Transit Metastases.

Wesslau H, Carlander A, Ny L, Warnberg F, Olofsson Bagge R, Lindqvist Bagge A Cancers (Basel). 2023; 15(1).

PMID: 36612157 PMC: 9817978. DOI: 10.3390/cancers15010161.


The diagnostic value of modified systemic ınflammation score in predicting post-operative outcomes of cutaneous melanoma patients who underwent ısolated limb perfusion.

Morkavuk S, Culcu S, Esen E, Unal A World J Surg Oncol. 2021; 19(1):327.

PMID: 34781987 PMC: 8594072. DOI: 10.1186/s12957-021-02437-6.


Evaluation of Intra-Lesional Interleukin 2 for the Treatment of In-Transit Melanoma Disease: L'évaluation de l'interleukine-2 intralésionnelle pour traiter les mélanomes en transit.

Lopez-Obregon B, Barreto M, Fyfe A, McKinnon G, Webb C, Temple-Oberle C Plast Surg (Oakv). 2021; 29(1):4-9.

PMID: 33614534 PMC: 7874363. DOI: 10.1177/2292550320936669.


Locoregional management of in-transit metastasis in melanoma: an Ontario Health (Cancer Care Ontario) clinical practice guideline.

Wright F, Kellett S, Hong N, Sun A, Hanna T, Nessim C Curr Oncol. 2020; 27(3):e318-e325.

PMID: 32669939 PMC: 7339852. DOI: 10.3747/co.27.6523.

References
1.
Fraker D, Alexander H, Andrich M, Rosenberg S . Treatment of patients with melanoma of the extremity using hyperthermic isolated limb perfusion with melphalan, tumor necrosis factor, and interferon gamma: results of a tumor necrosis factor dose-escalation study. J Clin Oncol. 1996; 14(2):479-89. DOI: 10.1200/JCO.1996.14.2.479. View

2.
Kidner T, Morton D, Lee D, Hoban M, Foshag L, Turner R . Combined intralesional Bacille Calmette-Guérin (BCG) and topical imiquimod for in-transit melanoma. J Immunother. 2012; 35(9):716-20. PMC: 3674843. DOI: 10.1097/CJI.0b013e31827457bd. View

3.
Turley R, Raymond A, Tyler D . Regional treatment strategies for in-transit melanoma metastasis. Surg Oncol Clin N Am. 2010; 20(1):79-103. PMC: 3023884. DOI: 10.1016/j.soc.2010.09.008. View

4.
Vohra N, Turaga K, Gonzalez R, Conley A, Reed D, Bui M . The use of isolated limb infusion in limb threatening extremity sarcomas. Int J Hyperthermia. 2012; 29(1):1-7. PMC: 4509503. DOI: 10.3109/02656736.2012.740548. View

5.
Boyd K, Wehrli B, Temple C . Intra-lesional interleukin-2 for the treatment of in-transit melanoma. J Surg Oncol. 2011; 104(7):711-7. DOI: 10.1002/jso.21968. View