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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1259377 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type7 i6 u; m5 z) }& ?# q! D0 i
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 8 `8 N9 J4 x0 a6 X3 b$ C! Y
+ Author Affiliations) Z1 H1 O0 O- x# L& d" n

1 p9 {. \$ u* |1 G8 b; I4 b1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 5 ?" `$ S# J( B9 n# r
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 8 v1 i  v7 I" l7 R1 ~' k+ y
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
! c- `" P0 e/ o# [; e6 J# c  A4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
( s- A/ {. e0 X5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
. l  w2 S' P# d( m4 G6 d. C% i6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
! ?& {1 k9 j* d8 C) _7Kinki University School of Medicine, Osaka 589-8511, Japan 9 v* D6 A9 Z: K+ \
8Izumi Municipal Hospital, Osaka 594-0071, Japan
3 q- W: [  P" i5 e9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
/ P6 S# s' ?; f8 X0 n! F  d" u, bCorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp . ]. Y& P' I7 f4 s" s" }1 E0 L
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. , w# ?+ [" |% J& M* Q1 v

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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type 0 w/ ]+ T3 B3 j# z) v- s: u

! j: _* f# Z, ^0 g- B5 m5 pAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
! E% M6 `& t8 I8 v/ i6 @+ N$ q: u5 t
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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* _1 S; j4 w' g! w: U" d( c2 WPublished online on: Thursday, December 1, 2011
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' o, d5 y4 G0 ?6 {" gDoi: 10.3892/ol.2011.507 9 x$ k) g4 x' M% E6 `
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Pages: 405-410 : r2 ~5 ^; W; ?4 E0 Z  p) x

2 s2 j+ t, h+ F7 Y6 ZAbstract:
& {8 U: \2 d' K' A$ |! jS-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population
- D. w5 T* u2 YF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 . X' w6 W; W; @2 S( D% V! |
+ Author Affiliations
( a6 g) o6 `, W  I7 F1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
4 Z* \+ B1 Q+ P- `3 m2 T2Department of Thoracic Surgery, Kyoto University, Kyoto
) X+ [3 I" o- ^& E3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
) A1 t5 c  v! l# q# k&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
  o  a, Y$ N- }2 IReceived September 3, 2010. 3 i4 l5 @8 j' x* N  j5 E9 O
Revision received November 11, 2010. 3 J; O$ j  A5 s3 W+ a) n5 l: q
Accepted November 17, 2010.
& m' A% \( X! k9 VAbstract
% v: f/ o  y8 g% dBackground: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. " ^8 G" D  L) z8 p) W- r' I7 }
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.
/ p3 W4 b1 \2 |7 t( D0 MResults: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
9 r+ f* N1 X8 Q$ \2 \+ O  y4 r7 i( vConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
6 p( }- ]. S3 p& ^今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?1 L* D# _& v0 o1 a9 t
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy! U4 f: w2 f+ K( X" H: M: v
http://clinicaltrials.gov/ct2/show/NCT01523587- ]+ F+ W$ S2 p

; C' D2 [- i* H1 R3 @BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
& q% Z/ t7 ]7 \http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 ) K& }, L, ?/ K3 `) F
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
8 i  F* M$ E# c7 X9 t% v至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
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没有副作用是第一追求,效果显著是第二追求。4 H, p* V: K+ `2 v
不错。

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