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1

Kocatüurk, Emek, Pelin Kuteyla Ülkümen, Utkan Kizitaç, Tülin Yüksel, Ayşle Seza Kunter, and Selma Şlengiz Erhan. "In-Transit Metastasis from Primary Cutaneous Squamous Cell Carcinoma in a Nonimmunosuppressed Patient." Journal of Cutaneous Medicine and Surgery 19, no. 2 (2015): 167–70. http://dx.doi.org/10.2310/7750.2014.14047.

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Background In-transit metastases are dermal and subcutanous metastatic foci located between the tumor and the closest regional lymph node. Although in-transit metastasis has been commonly described for malignant melanoma, there have been some reports of in-transit metastases arising from primary cutaneous malignancies. The risk of development of in-transit metastases is higher in patients with high-risk squamous cell carcinoma. Case Report We present a case of in-transit metastasis in a nonimmunosuppressed patient with a primary cutaneous squamous cell carcinoma.
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2

Lejeune, F. J. "In transit metastases." European Journal of Cancer 37 (April 2001): S252. http://dx.doi.org/10.1016/s0959-8049(01)81423-4.

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3

Di Altobrando, Ambra, Federica Scarfì, Cosimo Misciali, Annalisa Patrizi, and Emi Dika. "In‐transit melanoma metastases." International Journal of Dermatology 58, no. 7 (2019): 844–45. http://dx.doi.org/10.1111/ijd.14377.

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4

Costa, Sergio Renato Pais, Sergio Henrique Couto Horta, and Alexandre Cruz Henriques. "Popliteal lymphadenectomy for treating metastatic melanoma: case report." Sao Paulo Medical Journal 126, no. 4 (2008): 232–35. http://dx.doi.org/10.1590/s1516-31802008000400009.

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CONTEXT: Regional lymph node involvement in patients with malignant melanomas has been associated with poor prognosis. In-transit metastases also lead to poor long-term survival. Whereas for nodal disease only regional lymphadenectomy offers adequate locoregional control, for in-transit metastasis both local excision and isolated limb perfusion with chemotherapy plus tumor necrosis factor-alpha can be used for disease control. In cases of tumors located in the distal region of the legs, the lymphatic dissemination most commonly observed is to the inguinal chain. Consequently, therapeutic ingui
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5

Queiroz, Marcello Moro, Eduardo Bertolli, Francisco Aparecido Belfort, and Rodrigo Ramella Munhoz. "Management of In-Transit Metastases." Current Oncology Reports 24, no. 5 (2022): 573–83. http://dx.doi.org/10.1007/s11912-022-01216-0.

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6

Trapeznikov, N., and L. Demidov. "Management of in-transit metastases." Melanoma Research 3, no. 1 (1993): 31. http://dx.doi.org/10.1097/00008390-199303000-00106.

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7

Al-Mondhiry, Jafar, Chelsea Stahl, Suraj S. Venna, and Sekwon Jang. "Detection of ctDNA in patients with stage III cutaneous melanoma with satellite/in-transit or nodal metastases." Journal of Clinical Oncology 41, no. 16_suppl (2023): e21559-e21559. http://dx.doi.org/10.1200/jco.2023.41.16_suppl.e21559.

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e21559 Background: Circulating tumor DNA (ctDNA) has emerged as a biomarker to monitor disease status in cancer patients. Limited data exists on the sensitivity of ctDNA for detection of satellite/in-transit or nodal metastases in melanoma. Methods: We conducted a retrospective study of stage III cutaneous melanomas with clinically detected satellite/in-transit and/or lymph node metastases who underwent ctDNA analysis using an mPCR-NGS-based ctDNA assay ("Signatera") prior to surgery or systemic therapy at Inova Schar Cancer Institute. Results: ctDNA was detected in 4 of 14 patients including
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8

Biswas, Bivas, Deepak Dabkara, and Sandip Ganguly. "In-transit metastases from malignant melanoma." National Medical Journal of India 30, no. 5 (2017): 297. http://dx.doi.org/10.4103/0970-258x.234405.

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9

Lee, Yunjae, Dongkyu Lee, Hyeonjung Yeo, Hannara Park, and Hyochun Park. "Extraordinarily aggressive cutaneous sarcomatoid squamous cell carcinoma of the face: a case report." Archives of Craniofacial Surgery 23, no. 2 (2022): 77–82. http://dx.doi.org/10.7181/acfs.2022.00059.

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Sarcomatoid squamous cell carcinoma (SSCC), a biphasic malignant tumor consisting of atypical squamous epithelial and mesenchymal elements mixed with epithelioid and spindle cells, is a variant of squamous cell carcinoma. Cutaneous SSCC is very rare and aggressive and has a poor prognosis. Here, we report a case of cutaneous SSCC with satellites and in-transit metastases. A 79-year-old woman presented with a protruding mass on the left temporal area sized 1.2× 1.0 cm. The punch biopsy report indicated keratoacanthoma or well-differentiated squamous cell carcinoma. The size of the tumor increas
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10

Mikkelsen, Joachim, Anne Lene Hagen Wagenblast, Nille Behrendt, and Jørgen Lock-Andersen. "Melanoma in situ with in-transit metastases." JPRAS Open 11 (March 2017): 37–42. http://dx.doi.org/10.1016/j.jpra.2017.01.006.

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11

Kumar, NSudhir, and ShilpaY Krishnegowda. "In-transit metastases of acral lentiginous melanoma." Pigment International 2, no. 1 (2015): 51. http://dx.doi.org/10.4103/2349-5847.159398.

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12

Pararajasingam, Abirami, and Richard Goodwin. "In-transit metastases: the migration of melanoma." British Journal of Hospital Medicine 81, no. 9 (2020): 1. http://dx.doi.org/10.12968/hmed.2020.0202.

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13

Letcă, Alina Florentina, Loredana Ungureanu, Lavinia Elena Grigore, Liliana Rogojan, and Rodica Cosgarea. "Melanoma with regression and in-transit metastasis." Medicine and Pharmacy Reports 89, no. 1 (2016): 165–68. http://dx.doi.org/10.15386/cjmed-525.

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Introduction. Melanoma is an aggressive tumor with an increasing incidence worldwide. In-transit metastases represent a unique pattern of dissemination.Case report. We report the case of a 42-year-old woman who presented with two lesions on the left latero-cervical region: a pigmented macule with irregular borders and colors and a firm, dome-shaped 5 mm nodule with an erythematous base and a black crust on top, at the periphery of the first lesion. The clinical picture supported the diagnosis of melanoma with in-transit metastasis, but the histopathology examination raised, initially, the prob
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14

Russano, Francesco, Paolo Del Fiore, Fortunato Cassalia, et al. "Do Tumor SURVIVIN and MDM2 Expression Levels Correlate with Treatment Response and Clinical Outcome in Isolated Limb Perfusion for In-Transit Cutaneous Melanoma Metastases?" Journal of Personalized Medicine 13, no. 12 (2023): 1657. http://dx.doi.org/10.3390/jpm13121657.

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Isolated limb perfusion (ILP) involves the local administration of high doses of anticancer drugs into a limb affected by unresectable locally advanced tumors (with special regard to in-transit melanoma metastases), minimizing systemic side effects. Tumor response to anticancer drugs may depend on the expression of apoptosis-related genes, such as SURVIVIN and MDM2. This retrospective cohort study investigated the association between tumor SURVIVIN and MDM2 expression levels and treatment response or clinical outcomes in patients undergoing ILP for in-transit melanoma metastases. The study coh
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15

Padmavathy, L., LLakshmana Rao, Sylvester, MDhana Lakshmi, and N. Ethirajan. "In-transit metastases from squamous cell carcinoma penis." Indian Journal of Dermatology 57, no. 4 (2012): 291. http://dx.doi.org/10.4103/0019-5154.97674.

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16

Nan Tie, Emilia, Michael A. Henderson, and David E. Gyorki. "Management of in‐transit melanoma metastases: a review." ANZ Journal of Surgery 89, no. 6 (2018): 647–52. http://dx.doi.org/10.1111/ans.14921.

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17

Testori, A., S. Ribero, and V. Bataille. "Diagnosis and treatment of in-transit melanoma metastases." European Journal of Surgical Oncology (EJSO) 43, no. 3 (2017): 544–60. http://dx.doi.org/10.1016/j.ejso.2016.10.005.

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18

Storey, Lucy, Mohammed Abdul-Latif, Sophia Kreft, et al. "Checkpoint inhibitor treatment in patients with isolated in-transit melanoma metastases." Journal of Clinical Oncology 38, no. 15_suppl (2020): 10070. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.10070.

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10070 Background: In the context of multiple in-transit melanoma metastases without nodal involvement, a variety of treatment modalities have historically been employed including surgery, laser, isolated limb perfusion/infusion, intralesional interleukin-2, T-VEC and electrochemotherapy. Unfortunately, most patients treated with these modalities experience subsequent disease progression. While checkpoint inhibitors (CPI) are a standard of care for bulky unresectable stage III and for stage IV melanoma, patients with isolated in-transit metastases were rarely included in registration studies. T
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19

Tarantino, Giuseppe, Anne Zaremba, Tuulia Vallius, et al. "Multi-modal and longitudinal characterization of the tumor and immune microenvironment from primary to in-transit and distant metastasis in acral melanoma." Journal of Clinical Oncology 41, no. 16_suppl (2023): e21518-e21518. http://dx.doi.org/10.1200/jco.2023.41.16_suppl.e21518.

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e21518 Background: Patients with in-transit metastases (ITM) in melanoma are a heterogeneous subset of patients where melanoma recurrence is anatomically detected between the site of the primary tumor and the draining lymph node. Notably, a significant subset of those patients has locoregional recurrences with long-term survival without progression to distant sites. The underlying mechanisms responsible for these distinct phenotypes are unknown. Methods: To understand the evolution from primary melanoma to in-transit and distant metastasis, we characterized the tumor and immune microenvironmen
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20

Barbosa, Joana, Miguel Coelho, Ricardo Vieira, and Victor Farricha. "Isolated Limb Perfusion for the Treatment of Unresectable In- Transit Metastases of Cutaneous Squamous Cell Carcinoma." Journal of the Portuguese Society of Dermatology and Venereology 79, no. 2 (2021): 159–61. http://dx.doi.org/10.29021/spdv.79.2.1305.

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Squamous cell carcinoma (SCC) is the second most common non-melanoma skin cancer and its incidence has been increasing over the past decades. SCC in-transit metastases are rare and predict a poor prognosis. We present the case of a 69-year-old patient with a right lower leg SCC, surgically excised with free margins. One month later, erythematous to violaceous, firm papules begin to erupt on the right lower leg, evolving to ulcerated nodules over a period of weeks. Homolateral inguinal and iliac nodal metastases were documented by percutaneous biopsy of an inguinal palpable lymph node and later
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21

El Moheb, Mohamad, Susan Kim, Chunyan Cao, et al. "Characterization of driver oncogenic mutations of in-transit melanoma metastases." Journal of Clinical Oncology 42, no. 16_suppl (2024): 9586. http://dx.doi.org/10.1200/jco.2024.42.16_suppl.9586.

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9586 Background: In-transit melanoma (ITM) is a distinctive form of melanoma metastasis, marked by aggressive locoregional progression and characterized by the entrapment of tumor cells within the lymphatic channels before reaching regional lymph nodes (LN). The mechanisms leading to lymphatic trapping rather than progression to distant metastasis are not well-understood. Previous research indicates a clonal origin for ITM, suggesting specific early-stage genetic alterations may drive this clinical phenotype. In this study, we sought to identify driver oncogenic mutations specific to ITM that
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22

Cohen, Max H., and Ronald B. Herberman: Deceased. "Skin test results with common and melanoma antigens compared to clinical outcomes of melanoma patients treated with intralesional (IL) dinitrochorobenzene (DNCB) or IL bacillus Calmette-Guerin (BCG)." Journal of Clinical Oncology 35, no. 7_suppl (2017): 59. http://dx.doi.org/10.1200/jco.2017.35.7_suppl.59.

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59 Background: In a previous study involving in vitro serial testing in patients receiving IL BCG or IL DNCB we determined that measurements of serial in vitro phytohemagglutinin stimulation levels correlated with the patients’ clinical courses. The current evaluation attempted to determine which in vivo skin test studies were useful in this setting. Methods: All patients had locally progressive melanoma satellosis, or in-transit metastases, but no evidence of distant metastasis past regional lymph nodes. Patients had been randomized to repeatedly receive either IL BCG (9 patients), or IL DNCB
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23

Russano, Francesco, Marco Rastrelli, Luigi Dall’Olmo, et al. "Therapeutic Treatment Options for In-Transit Metastases from Melanoma." Cancers 16, no. 17 (2024): 3065. http://dx.doi.org/10.3390/cancers16173065.

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In-transit metastases (ITM) in melanoma present a significant therapeutic challenge due to their advanced stage and complex clinical nature. From traditional management with surgical resection, ITM treatment has evolved with the advent of systemic therapies such as immune checkpoint inhibitors and targeted therapies, which have markedly improved survival outcomes. This study aims to review and highlight the efficacy of both systemic and locoregional treatment approaches for ITM. Methods include a comprehensive review of clinical studies examining the impact of treatments like immune checkpoint
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24

Hayes, A. J., M. A. Clark, M. Harries, and J. M. Thomas. "Management of in-transit metastases from cutaneous malignant melanoma." British Journal of Surgery 91, no. 6 (2004): 673–82. http://dx.doi.org/10.1002/bjs.4610.

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25

Testori, Alessandro, Mark B. Faries, John F. Thompson, et al. "Local and intralesional therapy of in-transit melanoma metastases." Journal of Surgical Oncology 104, no. 4 (2011): 391–96. http://dx.doi.org/10.1002/jso.22029.

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26

Feeney, Kendra J., and Michael J. Mastrangelo. "Intralesional Therapy for In-transit and Satellite Metastases in Melanoma." Surgical Oncology Clinics of North America 24, no. 2 (2015): 299–308. http://dx.doi.org/10.1016/j.soc.2014.12.007.

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27

Lyle, Megan, and Georgina V. Long. "Diagnosis and Treatment ofKIT-Mutant Metastatic Melanoma." Journal of Clinical Oncology 31, no. 26 (2013): 3176–81. http://dx.doi.org/10.1200/jco.2013.50.4662.

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A 52-year-old man has unresectable locally recurrent melanoma of the left foot ( Fig 1 ) and pulmonary metastases. Nine months before this presentation, he underwent a wide local excision and sentinel node biopsy for an acral melanoma on his left heel. Pathology disclosed Breslow thickness of 4.8 mm, Clark level IV, and tumor ulceration with a mitotic rate of 37 mitoses/mm2. Both sentinel nodes in the left groin were positive for melanoma cells, which expressed S100, HMB45, and melan A. At subsequent left inguinal dissection, seven more nodes showed no additional nodal metastases. Within 3 mon
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28

Thompson, John F., Robyn P.M. Saw, Johanna M. Dalton, et al. "Treatment of in-transit melanoma metastases using intralesional PV-10." Melanoma Research 31, no. 3 (2021): 232–41. http://dx.doi.org/10.1097/cmr.0000000000000729.

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29

Eggermont, A. M. M., and P. M. Schlag. "Treatment of melanoma in-transit metastases confined to the limb." European Surgery 28, no. 1 (1996): 9–13. http://dx.doi.org/10.1007/bf02625948.

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30

Royal, Richard Eldon, Luis M. Vence, Tara Wray, et al. "A toll-like receptor agonist to drive melanoma regression as a vaccination adjuvant or by direct tumor application." Journal of Clinical Oncology 35, no. 15_suppl (2017): 9582. http://dx.doi.org/10.1200/jco.2017.35.15_suppl.9582.

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9582 Background: Toll like receptor (TLR) agonists may enhance vaccination or direct immune activation at the tumor microenvironment. This trial evaluates the biologic and clinical effects of Resiquimod, a TLR 7/8 agonist that can activate both myeloid (mDC, TLR 8) and plasmacytoid (pDC, TLR 7) dendritic cells, in patients with advanced stage melanoma. Methods: Class I HLA-A0201+ subjects with in-transit melanoma metastases or high risk for recurrence were vaccinated weekly with peptide vaccination (class I restricted peptide GP100209-2m and, if HLA-DP4+, also with class II restricted peptide
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31

Tian, Jiabao, and Camelia Quek. "Understanding the Tumor Microenvironment in Melanoma Patients with In-Transit Metastases and Its Impacts on Immune Checkpoint Immunotherapy Responses." International Journal of Molecular Sciences 25, no. 8 (2024): 4243. http://dx.doi.org/10.3390/ijms25084243.

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Melanoma is the leading cause of global skin cancer-related death and currently ranks as the third most commonly diagnosed cancer in Australia. Melanoma patients with in-transit metastases (ITM), a type of locoregional metastasis located close to the primary tumor site, exhibit a high likelihood of further disease progression and poor survival outcomes. Immunotherapies, particularly immune checkpoint inhibitors (ICI), have demonstrated remarkable efficacy in ITM patients with reduced occurrence of further metastases and prolonged survival. The major challenge of immunotherapeutic efficacy lies
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32

Suojärvi, Nora J., Tiina A. Jahkola, Susanna Virolainen, Suvi K. Ilmonen, and Micaela M. Hernberg. "Outcome following local recurrence or in-transit metastases in cutaneous melanoma." Melanoma Research 22, no. 6 (2012): 447–53. http://dx.doi.org/10.1097/cmr.0b013e32835a310c.

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33

Hwang, Shelley J. E., Benjamin Y. Kong, Shaun Chou, Deepal Wakade, Matteo S. Carlino, and Pablo Fernandez-Penas. "Acute Truncal Lymphedema Secondary to Axillary Metastatic Melanoma Presenting Like Cellulitis." Case Reports in Medicine 2017 (2017): 1–3. http://dx.doi.org/10.1155/2017/5462929.

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There are reported cases of diphencyprone used in treating cutaneous metastases of melanoma. Here, we report a patient with previous primary melanoma on his left back treated with surgical excision and lymphadenectomy, followed by radiotherapy for the recurrent tumor on the primary site. Despite radiotherapy and treatment with dabrafenib and trametinib, in-transit metastases have developed and topical diphencyprone was applied to these metastases. Six weeks later, the patient developed fever and a spreading erythematous tender indurated plaque covering the left side of the body including axill
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34

Petrochenko, N. S., T. K. Kharatishvili, A. K. Valiev, et al. "Long-term results of isolated limb perfusion with hyperthermia in patients with limb melanoma." Bone and soft tissue sarcomas, tumors of the skin 15, no. 1 (2023): 38–43. http://dx.doi.org/10.17650/2219-4614-2023-15-1-38-43.

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Introduction. In patients with local recurrences of melanoma or with transit metastases of this tumor located distal to the axilla and inguinal region, the use of isolated regional limb perfusion is considered as one of the effective treatment options.Aim. To evaluate the long-term results of treatment extremities melanoma using the method of isolated regional perfusion of the extremities.Materials and methods. An analysis of the treatment and observation results of 72 patients (12 men and 60 women) with melanoma of the extremities was carried out, the median age was 56.7 years (from 25 to 78
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35

Mondal, Krishnendu, and Rupali Mandal. "Nodular melanoma on lip with retrograde in-transit metastases on face." Indian Journal of Dermatology, Venereology and Leprology 87 (July 1, 2021): 687–89. http://dx.doi.org/10.25259/ijdvl_64_20.

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36

Read, Rebecca L., Lauren Haydu, Robyn P. M. Saw, et al. "In-transit Melanoma Metastases: Incidence, Prognosis, and the Role of Lymphadenectomy." Annals of Surgical Oncology 22, no. 2 (2014): 475–81. http://dx.doi.org/10.1245/s10434-014-4100-0.

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37

Beasley, Georgia, and Douglas Tyler. "In-transit Melanoma Metastases: Incidence, Prognosis, and the Role of Lymphadenectomy." Annals of Surgical Oncology 22, no. 2 (2014): 358–60. http://dx.doi.org/10.1245/s10434-014-4110-y.

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38

Blackmon, Jonathan T., Michael S. Stratton, Young Kwak, et al. "Inflammatory melanoma in transit metastases with complete response to talimogene laherparepvec." JAAD Case Reports 3, no. 4 (2017): 280–83. http://dx.doi.org/10.1016/j.jdcr.2017.02.011.

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39

Tkachenko, Elizabeth, Jennifer Y. Lin, and Rebecca I. Hartman. "Regional vitiligo induced by imiquimod treatment for in-transit melanoma metastases." JAAD Case Reports 5, no. 5 (2019): 427–29. http://dx.doi.org/10.1016/j.jdcr.2019.03.015.

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40

Teng, Edward, Gloria R. Sue, Rajendra Sawh-Martinez, et al. "Scalp Melanoma and In-transit Metastases: A Retrospective Case-controlled Study." American Surgeon 80, no. 12 (2014): 1272–74. http://dx.doi.org/10.1177/000313481408001233.

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41

MOHS, FREDERIC E. "Micrographic Surgery for Satellites and In-Transit Metastases of Malignant Melanoma." Journal of Dermatologic Surgery and Oncology 12, no. 5 (1986): 471–76. http://dx.doi.org/10.1111/j.1524-4725.1986.tb01936.x.

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42

Kirov, K., E. Peycheva, and I. Gavrilova. "P024. Electro-immunotherapy with BCG of superficial in-transit melanoma metastases." Melanoma Research 21 (June 2011): e29-e30. http://dx.doi.org/10.1097/01.cmr.0000399485.18517.4b.

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43

Constantinescu, Anna, Roger Olofsson Bagge, and Anne Huibers. "Immunological phenotype as a predictor for response after isolated limb perfusion for patients with melanoma in-transit metastasis." Journal of Clinical Oncology 43, no. 16_suppl (2025): 9565. https://doi.org/10.1200/jco.2025.43.16_suppl.9565.

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9565 Background: Isolated limb perfusion (ILP) is a regional treatment for patients with melanoma in-transit metastases (ITM) confined to extremities, using a high dose of melphalan. ILP has a high response rate, with approximately 60% having a complete response (CR). This study aimed to validate if pre-operative immunological phenotype could be a predictive factor for CR after ILP. Methods: A total of 132 patients undergoing ILP as a first treatment for melanoma ITM between January 2012 and March 2023 were included in this study. The number and percentage of naïve and memory T and B cell subt
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44

Deroose, Jan P., Dirk J. Grünhagen, Alexander M. M. Eggermont, and Cornelis Verhoef. "Repeated isolated limb perfusion in melanoma patients with recurrent in-transit metastases." Melanoma Research 25, no. 5 (2015): 427–31. http://dx.doi.org/10.1097/cmr.0000000000000177.

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45

Marsden, J. "Management of in-transit limb metastases in melanoma: state of the art." Melanoma Research 20 (June 2010): e11-e12. http://dx.doi.org/10.1097/01.cmr.0000382767.08743.d0.

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46

Bagge, A. S. Lindqvist, D. Katsarelias, and R. Olofsson Bagge. "Quality of life in patients with in-transit metastases of malignant melanoma." European Journal of Surgical Oncology 45, no. 2 (2019): e133-e134. http://dx.doi.org/10.1016/j.ejso.2018.10.456.

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47

Gaudy, Cardine, Marie-Aleth Richard, Gilles Folchetti, Jean Jacques Bonerandi, and Jean-Jacques Grob. "Randomized Controlled Study of Electrochemotherapy in the Local Treatment of Skin Metastases of Melanoma." Journal of Cutaneous Medicine and Surgery 10, no. 3 (2006): 115–21. http://dx.doi.org/10.2310/7750.2006.00037.

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Background: Electrochemotherapy (ECT) combines intralesional injections of bleomycin with electroporation (EP), which permeabilizes tumor cells and thus increases the bleomycin efficacy at the tumor site. Objective: To assess whether EP therapy improves the local control of skin metastases of melanoma by intralesional bleomycin. The secondary objective was to evaluate tolerance of the treatments. Patients: Patients with at least two measurable skin metastases of melanoma that were previously untreated, either in stage III with in-transit melanoma skin metastases or stage IV with no efficacy of
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48

Lenga, Marisa, Esther Choi, Jeffrey Sosman, et al. "Successful treatment of in-transit metastatic melanoma with combination intralesional T-VEC and topical imiquimod immunotherapy." Journal for ImmunoTherapy of Cancer 12, no. 11 (2024): e009581. http://dx.doi.org/10.1136/jitc-2024-009581.

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In-transit metastases of malignant melanoma pose a significant clinical challenge, particularly in patients with contraindications to systemic therapies. While surgical excision and systemic immunotherapies remain standard treatments, localized therapies such as intralesional talimogene laherparepvec (T-VEC) and topical imiquimod, which stimulate tumor-specific T-cell responses, have garnered increasing attention for their potential efficacy and tolerability. Although the individual efficacy of these therapies is well-documented, their combined use and their synergistic effects have not been w
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49

Wain, E. M., N. K. Webber, C. M. Stefanato, P. Banerjee, and S. L. Morris. "Multiple in-transit cutaneous metastases from a primary cutaneous squamous cell carcinoma." Clinical and Experimental Dermatology 34, no. 4 (2009): 522–24. http://dx.doi.org/10.1111/j.1365-2230.2008.02967.x.

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50

Teng, E., S. Nishikawa, R. Sawh, et al. "150: SCALP MELANOMAS AND IN-TRANSIT METASTASES: A RETROSPECTIVE CASE-CONTROLLED STUDY." Plastic and Reconstructive Surgery 127 (May 2011): 83. http://dx.doi.org/10.1097/01.prs.0000396837.90492.cd.

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