The Impact of Neoadjuvant Hedgehog Inhibitor Therapy on the Surgical Treatment of Extensive Basal Cell Carcinoma

被引:15
|
作者
Ching, Jessica A. [1 ]
Curtis, Heather L. [1 ]
Braue, Jonathan A. [2 ]
Kudchadkar, Ragini R. [3 ]
Mendoza, Tania I. [4 ]
Messina, Jane L. [3 ,5 ]
Cruse, C. Wayne [1 ,3 ]
Smith, David J., Jr. [1 ]
Harrington, Michael A. [1 ,3 ]
机构
[1] Univ S Florida, Morsani Coll Med, Div Plast Surg, Tampa, FL USA
[2] Univ S Florida, Morsani Coll Med, Tampa, FL USA
[3] Univ S Florida, H Lee Moffitt Canc Ctr, Cutaneous Oncol Dept, Tampa, FL 33682 USA
[4] Univ S Florida, Morsani Coll Med, Dept Pathol, Tampa, FL USA
[5] Univ S Florida, H Lee Moffitt Canc Ctr, Dept Anat Pathol, Tampa, FL 33682 USA
关键词
HUMAN HOMOLOG; VISMODEGIB; PATHWAY; MUTATIONS;
D O I
10.1097/SAP.0000000000000452
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background Although hedgehog inhibitor therapy (HHIT) is offered as isolated medical treatment for extensive basal cell carcinoma (BCC), there is little evidence on the use of HHIT before definitive surgical intervention. In order to better define the utilization of HHIT for extensive BCC, we evaluated the impact of neoadjuvant HHIT on the subsequent surgical resection and reconstruction. Methods An IRB-approved, retrospective chart review was performed of patients who received HHIT as initial treatment for extensive BCC. Patients who discontinued HHIT and underwent surgical resection were included. Evaluation included BCC tumor response to HHIT, operative data, pathological data, radiation requirements, and evidence of tumor recurrence. Results Six patients were identified with tumors of the face/scalp (n = 4), trunk (n = 1) and upper extremity (n = 1). Hedgehog inhibitor therapy continued until tumors became unresponsive (n = 3, mean = 71 weeks) or side effects became intolerable (n = 3, mean = 31 weeks). In each case, a less extensive surgery was performed than estimated before HHIT. In 3 cases, significant bone resection was avoided. All resected specimens contained BCC. Four specimens exhibited clear margins. Postoperative radiation was performed in cases with positive margins (n = 2), and 1 patient experienced local recurrence. Length of follow-up was 5.7 to 11.8 months (mean = 8.23 months). Conclusions Although HHIT was not curative for extensive BCC, HHIT can decrease the morbidity of surgical treatment and increase the likelihood of curative resection. For patients with extensive BCC, a combined neoadjuvant use of HHIT and surgical treatment should be considered.
引用
收藏
页码:S193 / S197
页数:5
相关论文
共 50 条
  • [41] Epidermal activation of Hedgehog signaling establishes an immunosuppressive microenvironment in basal cell carcinoma by modulating skin immunity
    Grund-Groeschke, Sandra
    Ortner, Daniela
    Szenes-Nagy, Antal B.
    Zaborsky, Nadja
    Weiss, Richard
    Neureiter, Daniel
    Wipplinger, Martin
    Risch, Angela
    Hammerl, Peter
    Greil, Richard
    Sibilia, Maria
    Gratz, Iris K.
    Stoitzner, Patrizia
    Aberger, Fritz
    MOLECULAR ONCOLOGY, 2020, 14 (09) : 1930 - 1946
  • [42] Sonidegib, a novel smoothened inhibitor for the treatment of advanced basal cell carcinoma
    Doan, Hung Q.
    Silapunt, Sirunya
    Migden, Michael R.
    ONCOTARGETS AND THERAPY, 2016, 9 : 5671 - 5678
  • [43] Hedgehog Pathway Inhibitors Promote Adaptive Immune Responses in Basal Cell Carcinoma
    Otsuka, Atsushi
    Dreier, Jil
    Cheng, Phil F.
    Naegeli, Mirjam
    Lehmann, Holger
    Felderer, Lea
    Frew, Ian J.
    Matsushita, Shigeto
    Levesque, Mitchell P.
    Dummer, Reinhard
    CLINICAL CANCER RESEARCH, 2015, 21 (06) : 1289 - 1297
  • [44] Vismodegib, itraconazole and sonidegib as hedgehog pathway inhibitors and their relative competencies in the treatment of basal cell carcinomas
    Wahid, Mohd
    Jawed, Arshad
    Mandal, Raju K.
    Dar, Sajad A.
    Khan, Saif
    Akhter, Naseem
    Haque, Shafiul
    CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2016, 98 : 235 - 241
  • [45] Surgical management of basal cell carcinoma
    Amici, J-M
    ANNALES DE DERMATOLOGIE ET DE VENEREOLOGIE, 2018, 145 : 12 - 29
  • [46] Resistance to hedgehog inhibitors in basal cell carcinoma: strategies to adopt
    Villani, Alessia
    Fabbrocini, Gabriella
    Di Vico, Francesc
    Nastro, Francesca
    Scalvenzi, Massimiliano
    EXPERT OPINION ON DRUG SAFETY, 2022, 21 (04) : 583 - 584
  • [47] Medical treatment of advanced basal cell carcinoma
    Basset-Seguin, N.
    ANNALES DE DERMATOLOGIE ET DE VENEREOLOGIE, 2018, 145 : 36 - 41
  • [48] Sonidegib for the treatment of advanced basal cell carcinoma
    Ramelyte, Egle
    Amann, Valerie C.
    Dummer, Reinhard
    EXPERT OPINION ON PHARMACOTHERAPY, 2016, 17 (14) : 1963 - 1968
  • [49] Synergistic cross-talk of hedgehog and interleukin-6 signaling drives growth of basal cell carcinoma
    Sternberg, Christina
    Gruber, Wolfgang
    Eberl, Markus
    Tesanovic, Suzana
    Stadler, Manuela
    Elmer, Dominik P.
    Schlederer, Michaela
    Grund, Sandra
    Roos, Simone
    Wolff, Florian
    Kaur, Supreet
    Mangelberger, Doris
    Lehrach, Hans
    Hache, Hendrik
    Wierling, Christoph
    Laimer, Josef
    Lackner, Peter
    Wiederstein, Markus
    Kasper, Maria
    Risch, Angela
    Petzelbauer, Peter
    Moriggl, Richard
    Kenner, Lukas
    Aberger, Fritz
    INTERNATIONAL JOURNAL OF CANCER, 2018, 143 (11) : 2943 - 2954
  • [50] Genomic Analysis of Smoothened Inhibitor Resistance in Basal Cell Carcinoma
    Sharpe, Hayley J.
    Pau, Gregoire
    Dijkgraaf, Gerrit J.
    Basset-Seguin, Nicole
    Modrusan, Zora
    Januario, Thomas
    Tsui, Vickie
    Durham, Alison B.
    Dlugosz, Andrzej A.
    Haverty, Peter M.
    Bourgon, Richard
    Tang, Jean Y.
    Sarin, Kavita Y.
    Dirix, Luc
    Fisher, David C.
    Rudin, Charles M.
    Sofen, Howard
    Migden, Michael R.
    Yauch, Robert L.
    de Sauvage, Frederic J.
    CANCER CELL, 2015, 27 (03) : 327 - 341